General Information of Drug Transporter (DT)
DT ID DTD0025 Transporter Info
Gene Name SLC22A8
Transporter Name Organic anion transporter 3
Gene ID
9376
UniProt ID
Q8TCC7
Exogenous factors (drugs, dietary constituents, etc.) Modulation of This DT (EGM)

Chemical Compound

  DT Modulation1

Probenecid inhibits the reaction SLC22A8 protein affects the transport of Cimetidine [76]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Probenecid inhibits the reaction SLC22A8 protein affects the transport of estrone sulfate [72]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

Probenecid inhibits the reaction SLC22A8 protein affects the transport of Famotidine [76]

Regulation Mechanism

Transcription Factor Info

  DT Modulation4

Probenecid inhibits the reaction SLC22A8 protein affects the transport of traumatic acid [91]

Regulation Mechanism

Transcription Factor Info

  DT Modulation5

Probenecid inhibits the reaction SLC22A8 protein results in increased import of 6-carboxyfluorescein [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation6

Probenecid inhibits the reaction SLC22A8 protein results in increased import of estrone sulfate [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation7

Probenecid inhibits the reaction SLC22A8 protein results in increased uptake of 6-carboxyfluorescein [65]

Regulation Mechanism

Transcription Factor Info

  DT Modulation8

Probenecid inhibits the reaction SLC22A8 protein results in increased uptake of 7-hydroxycoumarin glucuronide [65]

Regulation Mechanism

Transcription Factor Info

  DT Modulation9

Probenecid inhibits the reaction SLC22A8 protein results in increased uptake of 7-hydroxycoumarin metabolite [65]

Regulation Mechanism

Transcription Factor Info

  DT Modulation10

Probenecid inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [56]

Regulation Mechanism

Transcription Factor Info

  DT Modulation11

Probenecid inhibits the reaction SLC22A8 protein results in increased uptake of methyl 2-(1-(5-fluoropentyl)-1H-indazole-3-carboxamide)-3,3-dimethylbutanoate metabolite [92]

Regulation Mechanism

Transcription Factor Info

  DT Modulation12

Probenecid inhibits the reaction SLC22A8 results in increased uptake of Aristolochic Acids which results in increased chemical synthesis of 7-(deoxyadenosin-N(6)-yl)aristolactam I [67]

Regulation Mechanism

Transcription Factor Info

  DT Modulation13

Probenecid inhibits the reaction SLC22A8 results in increased uptake of Aristolochic Acids which results in increased chemical synthesis of 7-(deoxyguanosin-N(2)-yl)aristolactam I [67]

Regulation Mechanism

Transcription Factor Info

  DT Modulation14

Probenecid results in decreased activity of SLC22A8 protein [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation15

Probenecid results in decreased expression of SLC22A8 mRNA [93]

Regulation Mechanism

Transcription Factor Info

  DT Modulation16

Probenecid results in decreased expression of SLC22A8 protein [93]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Bumetanide inhibits the reaction SLC22A8 protein affects the transport of estrone sulfate [72]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Furosemide inhibits the reaction SLC22A8 protein affects the transport of estrone sulfate [72]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Novobiocin inhibits the reaction SLC22A8 protein results in increased uptake of 4-carboxyfluorescein [64]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Diclofenac inhibits the reaction SLC22A8 protein affects the transport of estrone sulfate [72]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Indomethacin inhibits the reaction SLC22A8 protein affects the transport of estrone sulfate [72]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

SLC22A8 protein results in increased uptake of Cefazolin [73]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Cephaloridine inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [73]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

SLC22A8 protein results in increased uptake of Cephaloridine [73]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Cimetidine inhibits the reaction SLC22A8 protein affects the transport of estrone sulfate [75]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Probenecid inhibits the reaction SLC22A8 protein affects the transport of Cimetidine [76]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

SLC22A8 protein affects the transport of Cimetidine [72]

Regulation Mechanism

Transcription Factor Info

  DT Modulation4

SLC22A8 protein results in increased uptake of Cimetidine [76]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Valsartan results in increased expression of SLC22A8 protein [97]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Cefaclor inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [73]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

SLC22A8 protein results in increased uptake of Cefaclor [73]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Linoleic Acid results in decreased activity of SLC22A8 protein [38]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Omeprazole results in decreased activity of SLC22A8 protein which results in decreased uptake of Indican [83]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Lansoprazole results in decreased activity of SLC22A8 protein which results in decreased uptake of Indican [83]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Toluene results in decreased methylation of SLC22A8 gene [55]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

2-amino-1-methyl-6-phenylimidazo(4,5-b)pyridine inhibits the reaction SLC22A8 protein results in increased import of 6-carboxyfluorescein [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

2-amino-1-methyl-6-phenylimidazo(4,5-b)pyridine promotes the reaction 2-amino-9H-pyrido(2,3-b)indole inhibits the reaction SLC22A8 protein results in increased import of 6-carboxyfluorescein [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

2-amino-1-methyl-6-phenylimidazo(4,5-b)pyridine promotes the reaction 2-amino-9H-pyrido(2,3-b)indole results in decreased activity of SLC22A8 protein [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation4

2-amino-1-methyl-6-phenylimidazo(4,5-b)pyridine results in decreased activity of SLC22A8 protein [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation5

2-amino-9H-pyrido(2,3-b)indole promotes the reaction 2-amino-1-methyl-6-phenylimidazo(4,5-b)pyridine inhibits the reaction SLC22A8 protein results in increased import of 6-carboxyfluorescein [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation6

2-amino-9H-pyrido(2,3-b)indole promotes the reaction 2-amino-1-methyl-6-phenylimidazo(4,5-b)pyridine results in decreased activity of SLC22A8 protein [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Emodin results in decreased activity of SLC22A8 protein [38]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Benzo(a)pyrene affects the methylation of SLC22A8 exon [71]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Benzo(a)pyrene affects the methylation of SLC22A8 promoter [71]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

Benzo(a)pyrene results in decreased activity of SLC22A8 protein [58]

Regulation Mechanism

Transcription Factor Info

  DT Modulation4

Benzo(a)pyrene results in decreased methylation of SLC22A8 5' UTR [71]

Regulation Mechanism

Transcription Factor Info

  DT Modulation5

Benzo(a)pyrene results in increased methylation of SLC22A8 3' UTR [71]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Luteolin results in decreased activity of SLC22A8 protein [59]

Regulation Mechanism

Transcription Factor Info

  2-amino-9H-pyrido(2,3-b)indole

           6 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

2-amino-1-methyl-6-phenylimidazo(4,5-b)pyridine promotes the reaction 2-amino-9H-pyrido(2,3-b)indole inhibits the reaction SLC22A8 protein results in increased import of 6-carboxyfluorescein [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

2-amino-1-methyl-6-phenylimidazo(4,5-b)pyridine promotes the reaction 2-amino-9H-pyrido(2,3-b)indole results in decreased activity of SLC22A8 protein [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

2-amino-9H-pyrido(2,3-b)indole inhibits the reaction SLC22A8 protein results in increased import of 6-carboxyfluorescein [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation4

2-amino-9H-pyrido(2,3-b)indole promotes the reaction 2-amino-1-methyl-6-phenylimidazo(4,5-b)pyridine inhibits the reaction SLC22A8 protein results in increased import of 6-carboxyfluorescein [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation5

2-amino-9H-pyrido(2,3-b)indole promotes the reaction 2-amino-1-methyl-6-phenylimidazo(4,5-b)pyridine results in decreased activity of SLC22A8 protein [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation6

2-amino-9H-pyrido(2,3-b)indole results in decreased activity of SLC22A8 protein [36]

Regulation Mechanism

Transcription Factor Info

  3-amino-1-methyl-5H-pyrido(4,3-b)indole

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

3-amino-1-methyl-5H-pyrido(4,3-b)indole inhibits the reaction SLC22A8 protein results in increased import of 6-carboxyfluorescein [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

3-amino-1-methyl-5H-pyrido(4,3-b)indole results in decreased activity of SLC22A8 protein [36]

Regulation Mechanism

Transcription Factor Info

  4-carboxyfluorescein

           7 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Niclosamide inhibits the reaction SLC22A8 protein results in increased uptake of 4-carboxyfluorescein [64]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Novobiocin inhibits the reaction SLC22A8 protein results in increased uptake of 4-carboxyfluorescein [64]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

quercetin 3-O-glucuronide analog inhibits the reaction SLC22A8 protein results in increased transport of 4-carboxyfluorescein [18]

Regulation Mechanism

Transcription Factor Info

  DT Modulation4

quercetin 3-O-glucuronide inhibits the reaction SLC22A8 protein results in increased transport of 4-carboxyfluorescein [18]

Regulation Mechanism

Transcription Factor Info

  DT Modulation5

quercetin 3'-sulfate inhibits the reaction SLC22A8 protein results in increased transport of 4-carboxyfluorescein [18]

Regulation Mechanism

Transcription Factor Info

  DT Modulation6

SLC22A8 protein results in increased transport of 4-carboxyfluorescein [18]

Regulation Mechanism

Transcription Factor Info

  DT Modulation7

SLC22A8 protein results in increased uptake of 4-carboxyfluorescein [64]

Regulation Mechanism

Transcription Factor Info

  5,7-dihydroxy-6-methoxy-2-phenylchromen-4-one

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

5,7-dihydroxy-6-methoxy-2-phenylchromen-4-one inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [63]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

5,7-dihydroxy-6-methoxy-2-phenylchromen-4-one results in decreased activity of SLC22A8 protein [59]

Regulation Mechanism

Transcription Factor Info

  6-carboxyfluorescein

         17 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

2-amino-1-methyl-6-phenylimidazo(4,5-b)pyridine inhibits the reaction SLC22A8 protein results in increased import of 6-carboxyfluorescein [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

2-amino-1-methyl-6-phenylimidazo(4,5-b)pyridine promotes the reaction 2-amino-9H-pyrido(2,3-b)indole inhibits the reaction SLC22A8 protein results in increased import of 6-carboxyfluorescein [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

2-amino-9H-pyrido(2,3-b)indole inhibits the reaction SLC22A8 protein results in increased import of 6-carboxyfluorescein [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation4

2-amino-9H-pyrido(2,3-b)indole promotes the reaction 2-amino-1-methyl-6-phenylimidazo(4,5-b)pyridine inhibits the reaction SLC22A8 protein results in increased import of 6-carboxyfluorescein [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation5

3-amino-1-methyl-5H-pyrido(4,3-b)indole inhibits the reaction SLC22A8 protein results in increased import of 6-carboxyfluorescein [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation6

7-hydroxycoumarin glucuronide inhibits the reaction SLC22A8 protein results in increased uptake of 6-carboxyfluorescein [65]

Regulation Mechanism

Transcription Factor Info

  DT Modulation7

7-hydroxycoumarin inhibits the reaction SLC22A8 protein results in increased uptake of 6-carboxyfluorescein [65]

Regulation Mechanism

Transcription Factor Info

  DT Modulation8

7-hydroxycoumarin metabolite inhibits the reaction SLC22A8 protein results in increased uptake of 6-carboxyfluorescein [65]

Regulation Mechanism

Transcription Factor Info

  DT Modulation9

Cadmium Chloride promotes the reaction SLC22A8 protein results in increased import of 6-carboxyfluorescein [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation10

glutaric acid promotes the reaction SLC22A8 protein results in increased import of 6-carboxyfluorescein [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation11

lead chloride promotes the reaction SLC22A8 protein results in increased import of 6-carboxyfluorescein [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation12

Probenecid inhibits the reaction SLC22A8 protein results in increased import of 6-carboxyfluorescein [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation13

Probenecid inhibits the reaction SLC22A8 protein results in increased uptake of 6-carboxyfluorescein [65]

Regulation Mechanism

Transcription Factor Info

  DT Modulation14

SLC22A8 protein results in increased import of 6-carboxyfluorescein [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation15

SLC22A8 protein results in increased uptake of 6-carboxyfluorescein [66]

Regulation Mechanism

Transcription Factor Info

  DT Modulation16

sodium arsenate promotes the reaction SLC22A8 protein results in increased import of 6-carboxyfluorescein [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation17

Unithiol analog inhibits the reaction SLC22A8 protein results in increased uptake of 6-carboxyfluorescein [66]

Regulation Mechanism

Transcription Factor Info

  7-(deoxyadenosin-N(6)-yl)aristolactam I

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Probenecid inhibits the reaction SLC22A8 results in increased uptake of Aristolochic Acids which results in increased chemical synthesis of 7-(deoxyadenosin-N(6)-yl)aristolactam I [67]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

SLC22A8 results in increased uptake of Aristolochic Acids which results in increased chemical synthesis of 7-(deoxyadenosin-N(6)-yl)aristolactam I [67]

Regulation Mechanism

Transcription Factor Info

  7-(deoxyguanosin-N(2)-yl)aristolactam I

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Probenecid inhibits the reaction SLC22A8 results in increased uptake of Aristolochic Acids which results in increased chemical synthesis of 7-(deoxyguanosin-N(2)-yl)aristolactam I [67]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

SLC22A8 results in increased uptake of Aristolochic Acids which results in increased chemical synthesis of 7-(deoxyguanosin-N(2)-yl)aristolactam I [67]

Regulation Mechanism

Transcription Factor Info

  7-hydroxycoumarin

           4 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

7-hydroxycoumarin inhibits the reaction SLC22A8 protein results in increased uptake of 6-carboxyfluorescein [65]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

7-hydroxycoumarin metabolite inhibits the reaction SLC22A8 protein results in increased uptake of 6-carboxyfluorescein [65]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

Probenecid inhibits the reaction SLC22A8 protein results in increased uptake of 7-hydroxycoumarin metabolite [65]

Regulation Mechanism

Transcription Factor Info

  DT Modulation4

SLC22A8 protein results in increased uptake of 7-hydroxycoumarin metabolite [65]

Regulation Mechanism

Transcription Factor Info

  7-hydroxycoumarin glucuronide

           3 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

7-hydroxycoumarin glucuronide inhibits the reaction SLC22A8 protein results in increased uptake of 6-carboxyfluorescein [65]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Probenecid inhibits the reaction SLC22A8 protein results in increased uptake of 7-hydroxycoumarin glucuronide [65]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

SLC22A8 protein results in increased uptake of 7-hydroxycoumarin glucuronide [65]

Regulation Mechanism

Transcription Factor Info

  acetamiprid

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

acetamiprid results in decreased activity of SLC22A8 protein [57]

Regulation Mechanism

Transcription Factor Info

  adefovir

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

SLC22A8 protein results in increased susceptibility to adefovir [68]

Regulation Mechanism

Transcription Factor Info

  aristolochic acid I

           4 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

aristolochic acid I inhibits the reaction SLC22A8 results in increased uptake of estrone sulfate [67]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

aristolochic acid I promotes the reaction SLC22A8 results in increased export of p-Aminohippuric Acid [67]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

wedelolactone results in decreased activity of SLC22A8 protein which results in increased susceptibility to and results in increased activity of aristolochic acid I [59]

Regulation Mechanism

Transcription Factor Info

  DT Modulation4

wogonin results in decreased activity of SLC22A8 protein which results in increased susceptibility to and results in increased activity of aristolochic acid I [59]

Regulation Mechanism

Transcription Factor Info

  aurantio-obtusin

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

aurantio-obtusin results in decreased activity of SLC22A8 protein [38]

Regulation Mechanism

Transcription Factor Info

  bisphenol A

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

bisphenol A inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [56]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

bisphenol A results in decreased activity of SLC22A8 protein [56]

Regulation Mechanism

Transcription Factor Info

  bisphenol F

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

bisphenol F inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [56]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

bisphenol F results in decreased activity of SLC22A8 protein [56]

Regulation Mechanism

Transcription Factor Info

  bisphenol S

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

bisphenol S inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [56]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

bisphenol S results in decreased activity of SLC22A8 protein [56]

Regulation Mechanism

Transcription Factor Info

  Cadmium Chloride

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Cadmium Chloride promotes the reaction SLC22A8 protein results in increased import of 6-carboxyfluorescein [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Cadmium Chloride results in increased activity of SLC22A8 protein [36]

Regulation Mechanism

Transcription Factor Info

  Cefdinir

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Cefdinir inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [73]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

SLC22A8 protein results in increased uptake of Cefdinir [73]

Regulation Mechanism

Transcription Factor Info

  cefoselis

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

cefoselis inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [73]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

SLC22A8 protein results in increased uptake of cefoselis [73]

Regulation Mechanism

Transcription Factor Info

  Cefotiam

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Cefotiam inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [73]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

SLC22A8 protein results in increased uptake of Cefotiam [73]

Regulation Mechanism

Transcription Factor Info

  Ceftibuten

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Ceftibuten inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [73]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

SLC22A8 protein results in increased uptake of Ceftibuten [73]

Regulation Mechanism

Transcription Factor Info

  Ceftizoxime

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Ceftizoxime inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [73]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

SLC22A8 protein results in increased uptake of Ceftizoxime [73]

Regulation Mechanism

Transcription Factor Info

  Cephalosporins

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

SLC22A8 protein affects the secretion of Cephalosporins [73]

Regulation Mechanism

Transcription Factor Info

  CGP 52608

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

CGP 52608 promotes the reaction RORA protein binds to SLC22A8 gene [74]

Regulation Mechanism

Transcription Factor Info

  chrysophanic acid

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

chrysophanic acid results in decreased activity of SLC22A8 protein [38]

Regulation Mechanism

Transcription Factor Info

  Cidofovir

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

SLC22A8 protein results in increased susceptibility to Cidofovir [68]

Regulation Mechanism

Transcription Factor Info

  Cisplatin

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Cisplatin results in decreased expression of SLC22A8 protein [77]

Regulation Mechanism

Transcription Factor Info

  clothianidin

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

clothianidin results in decreased activity of SLC22A8 protein [57]

Regulation Mechanism

Transcription Factor Info

  cyazofamid

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

cyazofamid inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [78]

Regulation Mechanism

Transcription Factor Info

  Cyclic AMP

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

SLC22A8 protein affects the transport of Cyclic AMP [72]

Regulation Mechanism

Transcription Factor Info

  daidzein

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

SLC22A8 protein results in increased uptake of daidzein analog [18]

Regulation Mechanism

Transcription Factor Info

  Dehydroepiandrosterone

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Dehydroepiandrosterone inhibits the reaction SLC22A8 protein affects the transport of estrone sulfate [72]

Regulation Mechanism

Transcription Factor Info

  Dehydroepiandrosterone Sulfate

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

SLC22A8 protein affects the transport of Dehydroepiandrosterone Sulfate [72]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

SLC22A8 protein results in increased uptake of Dehydroepiandrosterone Sulfate [73]

Regulation Mechanism

Transcription Factor Info

  Diazinon

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Diazinon results in increased methylation of SLC22A8 gene [79]

Regulation Mechanism

Transcription Factor Info

  Dinoprostone

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

SLC22A8 protein affects the transport of Dinoprostone [72]

Regulation Mechanism

Transcription Factor Info

  dioscorealide B

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

dioscorealide B results in decreased activity of SLC22A8 protein [59]

Regulation Mechanism

Transcription Factor Info

  Enalaprilat

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

SLC22A8 protein results in increased uptake of Enalaprilat [80]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

verlukast inhibits the reaction SLC22A8 protein results in increased uptake of Enalaprilat [80]

Regulation Mechanism

Transcription Factor Info

  estrone sulfate

         36 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

5,7-dihydroxy-6-methoxy-2-phenylchromen-4-one inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [63]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

aristolochic acid I inhibits the reaction SLC22A8 results in increased uptake of estrone sulfate [67]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

bisphenol A inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [56]

Regulation Mechanism

Transcription Factor Info

  DT Modulation4

bisphenol F inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [56]

Regulation Mechanism

Transcription Factor Info

  DT Modulation5

bisphenol S inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [56]

Regulation Mechanism

Transcription Factor Info

  DT Modulation6

Bumetanide inhibits the reaction SLC22A8 protein affects the transport of estrone sulfate [72]

Regulation Mechanism

Transcription Factor Info

  DT Modulation7

Cefaclor inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [73]

Regulation Mechanism

Transcription Factor Info

  DT Modulation8

Cefdinir inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [73]

Regulation Mechanism

Transcription Factor Info

  DT Modulation9

cefoselis inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [73]

Regulation Mechanism

Transcription Factor Info

  DT Modulation10

Cefotiam inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [73]

Regulation Mechanism

Transcription Factor Info

  DT Modulation11

Ceftibuten inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [73]

Regulation Mechanism

Transcription Factor Info

  DT Modulation12

Ceftizoxime inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [73]

Regulation Mechanism

Transcription Factor Info

  DT Modulation13

Cephaloridine inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [73]

Regulation Mechanism

Transcription Factor Info

  DT Modulation14

Cholates inhibits the reaction SLC22A8 protein affects the transport of estrone sulfate [72]

Regulation Mechanism

Transcription Factor Info

  DT Modulation15

Cimetidine inhibits the reaction SLC22A8 protein affects the transport of estrone sulfate [75]

Regulation Mechanism

Transcription Factor Info

  DT Modulation16

cyazofamid inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [78]

Regulation Mechanism

Transcription Factor Info

  DT Modulation17

Dehydroepiandrosterone inhibits the reaction SLC22A8 protein affects the transport of estrone sulfate [72]

Regulation Mechanism

Transcription Factor Info

  DT Modulation18

Diclofenac inhibits the reaction SLC22A8 protein affects the transport of estrone sulfate [72]

Regulation Mechanism

Transcription Factor Info

  DT Modulation19

estrone sulfate inhibits the reaction SLC22A8 protein results in increased uptake of Famotidine [75]

Regulation Mechanism

Transcription Factor Info

  DT Modulation20

estrone sulfate promotes the reaction SLC22A8 results in increased export of p-Aminohippuric Acid [67]

Regulation Mechanism

Transcription Factor Info

  DT Modulation21

Famotidine inhibits the reaction SLC22A8 protein affects the transport of estrone sulfate [75]

Regulation Mechanism

Transcription Factor Info

  DT Modulation22

Furosemide inhibits the reaction SLC22A8 protein affects the transport of estrone sulfate [72]

Regulation Mechanism

Transcription Factor Info

  DT Modulation23

Ibuprofen inhibits the reaction SLC22A8 protein affects the transport of estrone sulfate [72]

Regulation Mechanism

Transcription Factor Info

  DT Modulation24

Indomethacin inhibits the reaction SLC22A8 protein affects the transport of estrone sulfate [72]

Regulation Mechanism

Transcription Factor Info

  DT Modulation25

Probenecid inhibits the reaction SLC22A8 protein affects the transport of estrone sulfate [72]

Regulation Mechanism

Transcription Factor Info

  DT Modulation26

Probenecid inhibits the reaction SLC22A8 protein results in increased import of estrone sulfate [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation27

Probenecid inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [56]

Regulation Mechanism

Transcription Factor Info

  DT Modulation28

Quercetin inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [81]

Regulation Mechanism

Transcription Factor Info

  DT Modulation29

rhein inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [82]

Regulation Mechanism

Transcription Factor Info

  DT Modulation30

rhein metabolite inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [82]

Regulation Mechanism

Transcription Factor Info

  DT Modulation31

SLC22A8 protein affects the transport of estrone sulfate [72]

Regulation Mechanism

Transcription Factor Info

  DT Modulation32

SLC22A8 protein results in increased import of estrone sulfate [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation33

SLC22A8 protein results in increased uptake of estrone sulfate [73]

Regulation Mechanism

Transcription Factor Info

  DT Modulation34

SLC22A8 results in increased uptake of estrone sulfate [67]

Regulation Mechanism

Transcription Factor Info

  DT Modulation35

tetrabromobisphenol A inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [56]

Regulation Mechanism

Transcription Factor Info

  DT Modulation36

Tobacco Smoke Pollution inhibits the reaction SLC22A8 protein results in increased import of estrone sulfate [36]

Regulation Mechanism

Transcription Factor Info

  Famotidine

           4 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

estrone sulfate inhibits the reaction SLC22A8 protein results in increased uptake of Famotidine [75]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Famotidine inhibits the reaction SLC22A8 protein affects the transport of estrone sulfate [75]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

Probenecid inhibits the reaction SLC22A8 protein affects the transport of Famotidine [76]

Regulation Mechanism

Transcription Factor Info

  DT Modulation4

SLC22A8 protein results in increased uptake of Famotidine [75]

Regulation Mechanism

Transcription Factor Info

  glutaric acid

           3 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

glutaric acid promotes the reaction SLC22A8 protein results in increased import of 6-carboxyfluorescein [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

glutaric acid results in increased activity of SLC22A8 protein [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

SLC22A8 protein results in increased import of glutaric acid [36]

Regulation Mechanism

Transcription Factor Info

  glycitein

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

SLC22A8 protein results in increased uptake of glycitein analog [18]

Regulation Mechanism

Transcription Factor Info

  Indican

           3 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Lansoprazole results in decreased activity of SLC22A8 protein which results in decreased uptake of Indican [83]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Omeprazole results in decreased activity of SLC22A8 protein which results in decreased uptake of Indican [83]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

Pantoprazole results in decreased activity of SLC22A8 protein which results in decreased uptake of Indican [83]

Regulation Mechanism

Transcription Factor Info

  lead chloride

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

lead chloride promotes the reaction SLC22A8 protein results in increased import of 6-carboxyfluorescein [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

lead chloride results in increased activity of SLC22A8 protein [36]

Regulation Mechanism

Transcription Factor Info

  Leucovorin

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

SLC22A8 protein results in increased uptake of Leucovorin [73]

Regulation Mechanism

Transcription Factor Info

  Methotrexate

           5 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Resveratrol inhibits the reaction SLC22A8 protein results in increased uptake of Methotrexate [86]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

rhein metabolite inhibits the reaction SLC22A8 protein results in increased uptake of Methotrexate [82]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

SLC22A8 protein affects the transport of Methotrexate [72]

Regulation Mechanism

Transcription Factor Info

  DT Modulation4

SLC22A8 protein results in increased susceptibility to Methotrexate [86]

Regulation Mechanism

Transcription Factor Info

  DT Modulation5

SLC22A8 protein results in increased uptake of Methotrexate [73]

Regulation Mechanism

Transcription Factor Info

  Niclosamide

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Niclosamide inhibits the reaction SLC22A8 protein results in increased uptake of 4-carboxyfluorescein [64]

Regulation Mechanism

Transcription Factor Info

  obtusifolin

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

obtusifolin results in decreased activity of SLC22A8 protein [38]

Regulation Mechanism

Transcription Factor Info

  p-Aminohippuric Acid

           6 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

aristolochic acid I promotes the reaction SLC22A8 results in increased export of p-Aminohippuric Acid [67]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

estrone sulfate promotes the reaction SLC22A8 results in increased export of p-Aminohippuric Acid [67]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

SLC22A8 protein affects the transport of p-Aminohippuric Acid [72]

Regulation Mechanism

Transcription Factor Info

  DT Modulation4

SLC22A8 protein results in increased uptake of p-Aminohippuric Acid [73]

Regulation Mechanism

Transcription Factor Info

  DT Modulation5

SLC22A8 results in increased export of p-Aminohippuric Acid [67]

Regulation Mechanism

Transcription Factor Info

  DT Modulation6

Succinic Acid results in increased activity of SLC22A8 protein which results in increased uptake of p-Aminohippuric Acid [87]

Regulation Mechanism

Transcription Factor Info

  Pantoprazole

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Pantoprazole results in decreased activity of SLC22A8 protein which results in decreased uptake of Indican [83]

Regulation Mechanism

Transcription Factor Info

  penconazole

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

penconazole results in decreased activity of SLC22A8 protein [88]

Regulation Mechanism

Transcription Factor Info

  Penicillin G

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Resveratrol inhibits the reaction SLC22A8 protein results in increased uptake of Penicillin G [86]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

SLC22A8 protein results in increased uptake of Penicillin G [89]

Regulation Mechanism

Transcription Factor Info

  perfluorohexanesulfonic acid

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

SLC22A8 protein results in increased uptake of perfluorohexanesulfonic acid [90]

Regulation Mechanism

Transcription Factor Info

  perfluoro-n-heptanoic acid

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

SLC22A8 protein results in increased uptake of perfluoro-n-heptanoic acid [90]

Regulation Mechanism

Transcription Factor Info

  perfluorooctanoic acid

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

SLC22A8 protein results in increased uptake of perfluorooctanoic acid [90]

Regulation Mechanism

Transcription Factor Info

  quercetin 3-O-glucuronide

           3 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

quercetin 3-O-glucuronide analog inhibits the reaction SLC22A8 protein results in increased transport of 4-carboxyfluorescein [18]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

quercetin 3-O-glucuronide inhibits the reaction SLC22A8 protein results in increased transport of 4-carboxyfluorescein [18]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

SLC22A8 protein results in increased uptake of quercetin 3-O-glucuronide analog [18]

Regulation Mechanism

Transcription Factor Info

  quercetin 3'-sulfate

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

quercetin 3'-sulfate inhibits the reaction SLC22A8 protein results in increased transport of 4-carboxyfluorescein [18]

Regulation Mechanism

Transcription Factor Info

  Ranitidine

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

SLC22A8 protein results in increased uptake of Ranitidine [76]

Regulation Mechanism

Transcription Factor Info

  rhein

           3 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

rhein inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [82]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

rhein metabolite inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [82]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

rhein metabolite inhibits the reaction SLC22A8 protein results in increased uptake of Methotrexate [82]

Regulation Mechanism

Transcription Factor Info

  sodium arsenate

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

sodium arsenate promotes the reaction SLC22A8 protein results in increased import of 6-carboxyfluorescein [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

sodium arsenate results in increased activity of SLC22A8 protein [36]

Regulation Mechanism

Transcription Factor Info

  Succinic Acid

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Succinic Acid results in increased activity of SLC22A8 protein [87]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Succinic Acid results in increased activity of SLC22A8 protein which results in increased uptake of p-Aminohippuric Acid [87]

Regulation Mechanism

Transcription Factor Info

  Taurocholic Acid

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

SLC22A8 protein affects the transport of Taurocholic Acid [72]

Regulation Mechanism

Transcription Factor Info

  Tenofovir

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

SLC22A8 protein results in increased import of Tenofovir [94]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

SLC22A8 protein results in increased susceptibility to Tenofovir [68]

Regulation Mechanism

Transcription Factor Info

  tetrabromobisphenol A

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

tetrabromobisphenol A inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [56]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

tetrabromobisphenol A results in decreased activity of SLC22A8 protein [56]

Regulation Mechanism

Transcription Factor Info

  Tetracycline

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

SLC22A8 protein results in increased uptake of Tetracycline [95]

Regulation Mechanism

Transcription Factor Info

  thiacloprid

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

thiacloprid metabolite results in decreased activity of SLC22A8 protein [57]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

thiacloprid results in decreased activity of SLC22A8 protein [57]

Regulation Mechanism

Transcription Factor Info

  traumatic acid

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Probenecid inhibits the reaction SLC22A8 protein affects the transport of traumatic acid [91]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

SLC22A8 protein affects the transport of traumatic acid [91]

Regulation Mechanism

Transcription Factor Info

  uniconazole

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

uniconazole results in decreased activity of SLC22A8 protein [88]

Regulation Mechanism

Transcription Factor Info

  Unithiol

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Unithiol analog inhibits the reaction SLC22A8 protein results in increased uptake of 6-carboxyfluorescein [66]

Regulation Mechanism

Transcription Factor Info

  Uric Acid

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

SLC22A8 protein affects the transport of Uric Acid [72]

Regulation Mechanism

Transcription Factor Info

  Valproic Acid

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Valproic Acid results in increased methylation of SLC22A8 gene [96]

Regulation Mechanism

Transcription Factor Info

  verlukast

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

verlukast inhibits the reaction SLC22A8 protein results in increased uptake of Enalaprilat [80]

Regulation Mechanism

Transcription Factor Info

  wedelolactone

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

wedelolactone results in decreased activity of SLC22A8 protein [59]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

wedelolactone results in decreased activity of SLC22A8 protein which results in increased susceptibility to and results in increased activity of aristolochic acid I [59]

Regulation Mechanism

Transcription Factor Info

  wogonin

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

wogonin results in decreased activity of SLC22A8 protein [59]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

wogonin results in decreased activity of SLC22A8 protein which results in increased susceptibility to and results in increased activity of aristolochic acid I [59]

Regulation Mechanism

Transcription Factor Info

Nanoparticle

  perfluoro-n-nonanoic acid

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

SLC22A8 protein results in increased uptake of perfluoro-n-nonanoic acid [90]

Regulation Mechanism

Transcription Factor Info

Fungicide

  tebuconazole

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

tebuconazole results in decreased activity of SLC22A8 protein [88]

Regulation Mechanism

Transcription Factor Info

Approved Drug

  Probenecid

         27 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Probenecid inhibits the transportation of Cimetidine by SLC22A8 (IC50 = 3.1 microM) [1]

Affected Drug/Substrate

Cimetidine Modulation Type Inhibition

Cell System

Chinese hamster ovary (CHO) cells-OAT3

  DT Modulation2

Probenecid inhibits the transportation of Dimesna by SLC22A8 (Ki = 32 microM) [2]

Affected Drug/Substrate

Dimesna Modulation Type Inhibition

Cell System

Human cervical cancer cell line (Hela)-OAT3

  DT Modulation3

Probenecid inhibits the transportation of Estrone sulfate by SLC22A8 (Ki = 9 microM) [3]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  DT Modulation4

Probenecid inhibits the transportation of Fexofenadine by SLC22A8 (Ki = 1.3 microM) [4]

Affected Drug/Substrate

Fexofenadine Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OAT3

  DT Modulation5

Probenecid inhibits the transportation of Ochratoxin A by SLC22A8 (Ki = 4.41 microM) [5]

Affected Drug/Substrate

Ochratoxin A Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  DT Modulation6

Probenecid inhibits the transportation of Sitagliptin by SLC22A8 (IC50 = 5.6 microM) [1]

Affected Drug/Substrate

Sitagliptin Modulation Type Inhibition

Cell System

Chinese hamster ovary (CHO) cells-OAT3

  DT Modulation7

Probenecid inhibits the transportation of Estrone sulfate by SLC22A8 [6]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OAT3

  DT Modulation8

Probenecid inhibits the transportation of Fluorescein by SLC22A8 [7]

Affected Drug/Substrate

Fluorescein Modulation Type Inhibition

Cell System

Chinese hamster ovary (CHO) cells-OAT3

  DT Modulation9

Probenecid inhibits the activity of SLC22A8 [1], [8]

  DT Modulation10

Probenecid blocks the activity of SLC22A8 [9], [10]

  DT Modulation11

Probenecid inhibits the activity of SLC22A8 [21]

  Bumetanide

           4 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Bumetanide inhibits the transportation of Estrone sulfate by SLC22A8 (IC50 = 0.75 microM) [11]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  DT Modulation2

Bumetanide inhibits the transportation of Estrone sulfate by SLC22A8 (IC50 = 7.8 microM) [13]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

Oocytes-OAT3

  DT Modulation3

Bumetanide inhibits the transportation of Methotrexate by SLC22A8 (IC50 = 5.4 microM) [13]

Affected Drug/Substrate

Methotrexate Modulation Type Inhibition

Cell System

Oocytes-OAT3

  Furosemide

           4 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Furosemide inhibits the transportation of Estrone sulfate by SLC22A8 (IC50 = 7.31 microM) [11]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  DT Modulation2

Furosemide inhibits the transportation of Sitagliptin by SLC22A8 (IC50 = 1.7 microM) [1]

Affected Drug/Substrate

Sitagliptin Modulation Type Inhibition

Cell System

Chinese hamster ovary (CHO) cells-OAT3

  DT Modulation3

Furosemide inhibits the activity of SLC22A8 [1], [16]

  Ibuprofen

           4 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Ibuprofen inhibits the transportation of Estrone sulfate by SLC22A8 (IC50 = 6 microM) [12]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  DT Modulation2

Ibuprofen inhibits the transportation of Sitagliptin by SLC22A8 (IC50 = 3.7 microM) [1]

Affected Drug/Substrate

Sitagliptin Modulation Type Inhibition

Cell System

Chinese hamster ovary (CHO) cells-OAT3

  DT Modulation3

Ibuprofen inhibits the activity of SLC22A8 [1], [16]

  DT Modulation4

Ibuprofen inhibits the reaction SLC22A8 protein affects the transport of estrone sulfate [72]

Regulation Mechanism

Transcription Factor Info

  Cefadroxil

           3 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Cefadroxil inhibits the transportation of Prostaglandin F2alpha by SLC22A8 (Ki = 8620 microM) [15]

Affected Drug/Substrate

Prostaglandin F2alpha Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  DT Modulation2

Cefadroxil inhibits the transportation of Fluorescein by SLC22A8 [7]

Affected Drug/Substrate

Fluorescein Modulation Type Inhibition

Cell System

Chinese hamster ovary (CHO) cells-OAT3

  DT Modulation3

Cefadroxil inhibits the transportation of Estrone sulfate by SLC22A8 [7]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

  Piroxicam

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Piroxicam inhibits the transportation of Estrone sulfate by SLC22A8 (IC50 = 2.52 microM) [12]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  DT Modulation2

Piroxicam inhibits the transportation of Ochratoxin A by SLC22A8 (Ki = 4.88 microM) [5]

Affected Drug/Substrate

Ochratoxin A Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Fluvastatin

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Fluvastatin inhibits the transportation of Estrone sulfate by SLC22A8 (IC50 = 5.79 microM) [19]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  DT Modulation2

Fluvastatin inhibits the activity of SLC22A8 [19]

  Simvastatin

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Simvastatin inhibits the transportation of Estrone sulfate by SLC22A8 (IC50 = 32.3 microM) [19]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  DT Modulation2

Simvastatin inhibits the activity of SLC22A8 [19]

  Sulfasalazine

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Sulfasalazine inhibits the transportation of Methotrexate by SLC22A8 (IC50 = 3 microM) [13]

Affected Drug/Substrate

Methotrexate Modulation Type Inhibition

Cell System

Oocytes-OAT3

  DT Modulation2

Sulfasalazine inhibits the activity of SLC22A8 [13]

  Gemfibrozil

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Gemfibrozil inhibits the transportation of Pravastatin by SLC22A8 (IC50 = 6.8 microM) [20]

Affected Drug/Substrate

Pravastatin Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  DT Modulation2

Gemfibrozil inhibits the activity of SLC22A8 [22]

  Sitagliptin

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Sitagliptin inhibits the transportation of Cimetidine by SLC22A8 (IC50 = 160 microM) [1]

Affected Drug/Substrate

Cimetidine Modulation Type Inhibition

Cell System

Chinese hamster ovary (CHO) cells-OAT3

  Betamipron

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Betamipron inhibits the transportation of Estrone sulfate by SLC22A8 (Ki = 48.3 microM) [3]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Cilastatin

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Cilastatin inhibits the transportation of Estrone sulfate by SLC22A8 (Ki = 231 microM) [3]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  DT Modulation2

Cilastatin inhibits the uptake of diclofenac acyl glucuronide by SLC22A8 [32]

Affected Drug/Substrate

Diclofenac acyl glucuronide Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OAT3

  Acetazolamide

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Acetazolamide inhibits the transportation of Estrone sulfate by SLC22A8 (IC50 = 816 microM) [11]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Chlorothiazide

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Chlorothiazide inhibits the transportation of Estrone sulfate by SLC22A8 (IC50 = 65.3 microM) [11]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Cyclothiazide

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Cyclothiazide inhibits the transportation of Estrone sulfate by SLC22A8 (IC50 = 27.9 microM) [11]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Ethacrynic Acid

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Ethacrynic acid inhibits the transportation of Estrone sulfate by SLC22A8 (IC50 = 0.58 microM) [11]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Hydrochlorothiazide

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Hydrochlorothiazide inhibits the transportation of Estrone sulfate by SLC22A8 (IC50 = 942 microM) [11]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Methazolamide

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Methazolamide inhibits the transportation of Estrone sulfate by SLC22A8 (IC50 = 97.5 microM) [11]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Trichlormethiazide

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Trichloromethiazide inhibits the transportation of Estrone sulfate by SLC22A8 (IC50 = 71.2 microM) [11]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Novobiocin

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Novobiocin inhibits the transportation of Estrone sulfate by SLC22A8 (IC50 = 4.99 microM; Ki = 4.77 microM) [23]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

Monkey kidney tissue Fibroblast-like cell lines (COS)7-OAT3

  Diclofenac

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Diclofenac inhibits the transportation of Estrone sulfate by SLC22A8 (IC50 = 7.78 microM) [12]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Indomethacin

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Indomethacin inhibits the transportation of Estrone sulfate by SLC22A8 (IC50 = 0.61 microM) [12]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Ketoprofen

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Ketoprofen inhibits the transportation of Estrone sulfate by SLC22A8 (IC50 = 5.98 microM) [12]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Mefenamic Acid

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Mefenamic acid inhibits the transportation of Estrone sulfate by SLC22A8 (IC50 = 0.78 microM) [12]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Naproxen

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Naproxen inhibits the transportation of Estrone sulfate by SLC22A8 (IC50 = 4.67 microM) [12]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Sulindac

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Sulindac inhibits the transportation of Estrone sulfate by SLC22A8 (IC50 = 3.62 microM) [12]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Pravastatin

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Pravastatin inhibits the transportation of Estrone sulfate by SLC22A8 (IC50 = 13.7 microM) [19]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Phenylbutazone

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Phenylbutazone inhibits the transportation of Methotrexate by SLC22A8 (Ki = 34.7 microM) [14]

Affected Drug/Substrate

Methotrexate Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Cefamandole

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Cefamandole inhibits the transportation of Prostaglandin F2alpha by SLC22A8 (Ki = 50 microM) [15]

Affected Drug/Substrate

Prostaglandin F2alpha Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Cefazolin

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Cefazolin inhibits the transportation of Prostaglandin F2alpha by SLC22A8 (Ki = 550 microM) [15]

Affected Drug/Substrate

Prostaglandin F2alpha Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Cefoperazone

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Cefoperazone inhibits the transportation of Prostaglandin F2alpha by SLC22A8 (Ki = 1890 microM) [15]

Affected Drug/Substrate

Prostaglandin F2alpha Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Cefotaxime

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Cefotaxime inhibits the transportation of Prostaglandin F2alpha by SLC22A8 (Ki = 290 microM) [15]

Affected Drug/Substrate

Prostaglandin F2alpha Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Ceftriaxone

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Ceftriaxone inhibits the transportation of Prostaglandin F2alpha by SLC22A8 (Ki = 4390 microM) [15]

Affected Drug/Substrate

Prostaglandin F2alpha Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Cephalothin

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Cephalothin inhibits the transportation of Prostaglandin F2alpha by SLC22A8 (Ki = 40 microM) [15]

Affected Drug/Substrate

Prostaglandin F2alpha Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Cimetidine

           5 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Cimetidine inhibits the transportation of Sitagliptin by SLC22A8 (IC50 = 79 microM) [1]

Affected Drug/Substrate

Sitagliptin Modulation Type Inhibition

Cell System

Chinese hamster ovary (CHO) cells-OAT3

  Fenofibric acid

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Fenofibric acid inhibits the transportation of Sitagliptin by SLC22A8 (IC50 = 2.2 microM) [1]

Affected Drug/Substrate

Sitagliptin Modulation Type Inhibition

Cell System

Chinese hamster ovary (CHO) cells-OAT3

  Indapamide

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Indapamide inhibits the transportation of Sitagliptin by SLC22A8 (IC50 = 11 microM) [1]

Affected Drug/Substrate

Sitagliptin Modulation Type Inhibition

Cell System

Chinese hamster ovary (CHO) cells-OAT3

  Quinapril

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Quinapril inhibits the transportation of Sitagliptin by SLC22A8 (IC50 = 6.2 microM) [1]

Affected Drug/Substrate

Sitagliptin Modulation Type Inhibition

Cell System

Chinese hamster ovary (CHO) cells-OAT3

  Piperacillin

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Piperacillin inhibits the transporation of tazobactam by SLC22A8 (IC50 = 89.04 microM; Ki = 172 microM) [29]

Affected Drug/Substrate

Tazobactam Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)

  Candesartan

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Candesartan inhibits the transportation of Uric acid by SLC22A8 (IC50 = 0.3 microM) [30]

Affected Drug/Substrate

Uric acid Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OAT3

  Losartan

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Losartan inhibits the transportation of Uric acid by SLC22A8 (IC50 = 1.6 microM) [30]

Affected Drug/Substrate

Uric acid Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OAT3

  Olmesartan medoxomil

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Olmesartan medoxomil inhibits the transportation of Uric acid by SLC22A8 (IC50 = 0.027 microM) [30]

Affected Drug/Substrate

Uric acid Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OAT3

  Telmisartan

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Telmisartan inhibits the transportation of Uric acid by SLC22A8 (IC50 = 1.6 microM) [30]

Affected Drug/Substrate

Uric acid Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OAT3

  Valsartan

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Valsartan inhibits the transportation of Uric acid by SLC22A8 (IC50 = 0.2 microM) [30]

Affected Drug/Substrate

Uric acid Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OAT3

  Imipenem

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Imipenem significantly inhibits the uptake of cilastatin by SLC22A8 [31]

Affected Drug/Substrate

Cilastatin Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OAT3

  Zidovudine

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Zidovudine inhibits the transportation of Estrone sulfate by SLC22A8 [33]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Linagliptin

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Linagliptin inhibits the transportation of Estrone sulfate by SLC22A8 [6]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OAT3

  Carbenicillin

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Carbenicillin inhibits the transportation of Fluorescein by SLC22A8 [7]

Affected Drug/Substrate

Fluorescein Modulation Type Inhibition

Cell System

Chinese hamster ovary (CHO) cells-OAT3

  Cefaclor

           3 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Cefaclor inhibits the transportation of Fluorescein by SLC22A8 [7]

Affected Drug/Substrate

Fluorescein Modulation Type Inhibition

Cell System

Chinese hamster ovary (CHO) cells-OAT3

  Dicloxacillin

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Dicloxacillin inhibits the transportation of Fluorescein by SLC22A8 [7]

Affected Drug/Substrate

Fluorescein Modulation Type Inhibition

Cell System

Chinese hamster ovary (CHO) cells-OAT3

  Oxacillin

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Oxacillin inhibits the transportation of Fluorescein by SLC22A8 [7]

Affected Drug/Substrate

Fluorescein Modulation Type Inhibition

Cell System

Chinese hamster ovary (CHO) cells-OAT3

  Aspirin

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Aspirin inhibits the transportation of Cilostazol by SLC22A8 [34]

Affected Drug/Substrate

Cilostazol Modulation Type Inhibition

  DT Modulation2

Aspirin results in increased expression of SLC22A8 mRNA [70]

Regulation Mechanism

Transcription Factor Info

  Bendroflumethiazide

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Bendroflumethiazide inhibits the transportation of Polycyclic aromatic hydrocarbons by SLC22A8 [35]

Affected Drug/Substrate

Polycyclic aromatic hydrocarbons Modulation Type Inhibition

  Folic Acid

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Folic Acid inhibits the expression of SLC22A8 [37]

  Testosterone

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Testosterone inhibits the expression of SLC22A8 [39]

  Fluorescein

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Fluorescein inhibits the activity of SLC22A8 [40]

  Ciprofloxacin

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Ciprofloxacin inhibits the activity of SLC22A8 [41]

  Gatifloxacin

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Gatifloxacin inhibits the activity of SLC22A8 [41]

  Torasemide

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Torsemide inhibits the activity of SLC22A8 [42]

  Etoricoxib

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Etoricoxib inhibits the activity of SLC22A8 [43]

  Celecoxib

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Celecoxib inhibits the activity of SLC22A8 [44], [45]

  Rofecoxib

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Rofecoxib inhibits the activity of SLC22A8 [45]

  Valdecoxib

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Valdecoxib inhibits the activity of SLC22A8 [45]

  Vancomycin

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Vancomycin inhibits the activity of SLC22A8 [46]

  Sulfadiazine

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Sulfadiazine inhibits the activity of SLC22A8 [47]

  Nitrofurantoin

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Nitrofurantoin inhibits the activity of SLC22A8 [48]

  Metronidazole

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Metronidazole inhibits the activity of SLC22A8 [49]

  Selexipag

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Selexipag inhibits the activity of SLC22A8 [50]

  Omeprazole

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Esomeprazole inhibits the activity of SLC22A8 [51]

  Lansoprazole

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Lansoprazole inhibits the activity of SLC22A8 [51]

  Itraconazole

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Itraconazole inhibits the activity of SLC22A8 [52]

  Ketoconazole

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Ketoconazole inhibits the activity of SLC22A8 [52]

Drug Marketed but not Approved by US FDA

  Linoleic Acid

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Linoleic Acid inhibits the activity of SLC22A8 [38]

Drug in Phase 4 Trial

  DT Modulation1

Benzylpenicillin inhibits the uptake of cilastatin by SLC22A8 [31]

Affected Drug/Substrate

Cilastatin Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OAT3

  Dihydrotestosterone

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Dihydrotestosterone induces the activity of SLC22A8 [61]

Drug in Phase 3 Trial

  Benzylpenicillin

           4 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Benzylpenicillin inhibits the transportation of Methotrexate by SLC22A8 (Ki = 97.6 microM) [14]

Affected Drug/Substrate

Methotrexate Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  DT Modulation2

Benzylpenicillin inhibits the transportation of Fluorescein by SLC22A8 [7]

Affected Drug/Substrate

Fluorescein Modulation Type Inhibition

Cell System

Chinese hamster ovary (CHO) cells-OAT3

  DT Modulation3

Benzylpenicillin inhibits the activity of SLC22A8 [17]

  Pratosartan

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Pratosartan inhibits the transportation of Uric acid by SLC22A8 (IC50 = 0.095 microM) [30]

Affected Drug/Substrate

Uric acid Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OAT3

Drug in Phase 2 Trial

  Bisphenol A

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Bisphenol A inhibits the activity of SLC22A8 [56]

Drug in Phase 1/2 Trial

  PRI-724

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

PRI-724 inhibits the activity of SLC22A8 [53]

Cell System

Human embryonic kidney 293 cells (HEK293)-

Drug in Phase 1 Trial

  Luteolin

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Luteolin inhibits the activity of SLC22A8 [59]

  Quercetin

           3 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Quercetin inhibits the activity of SLC22A8 [59]

Drug in Preclinical Test

  Emodin

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Emodin inhibits the activity of SLC22A8 [38]

Investigative Drug

  Adipate

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Adipate inhibits the transportation of Estrone sulfate by SLC22A8 (IC50 = 136 microM) [24]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OAT3

  Alpha-ketoglutaric acid

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Alpha-ketoglutaric acid inhibits the transportation of Estrone sulfate by SLC22A8 (IC50 = 92.8 microM) [24]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OAT3

  Glutarate

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Glutarate inhibits the transportation of Estrone sulfate by SLC22A8 (IC50 = 78.5 microM) [24]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OAT3

  Aminohippuric acid

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Aminohippuric acid inhibits the transportation of Ochratoxin A by SLC22A8 (Ki = 19.6 microM) [5]

Affected Drug/Substrate

Ochratoxin A Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Angiotensinamide

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Angiotensinamide inhibits the activity of SLC22A8 [62]

  21H7

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

21H7 inhibits the activity of SLC22A8 [53]

Cell System

Human embryonic kidney 293 cells (HEK293)-

  FH535

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

FH535 inhibits the activity of SLC22A8 [53]

Cell System

Human embryonic kidney 293 cells (HEK293)-

  JBP485

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

JBP485 inhibits the uptake of imipenem by SLC22A6 [98]

Affected Drug/Substrate

Imipenem Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OAT3

Drug Withdrawn

  Phenacetin

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Phenacetin inhibits the transportation of Estrone sulfate by SLC22A8 (IC50 = 19.4 microM) [12]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Cephaloridine

           3 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Cephaloridine inhibits the transportation of Prostaglandin F2alpha by SLC22A8 (Ki = 2460 microM) [15]

Affected Drug/Substrate

Prostaglandin F2alpha Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Retigabine

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Ezogabine inhibits the activity of SLC22A8 [60]

Natural Product

  Quercetin-3-O-glucuronide

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Quercetin-3-O-glucuronide inhibits the transportation of 5-carboxyfluorescein by SLC22A8 (IC50 = 1.31 microM) [18]

Affected Drug/Substrate

5-carboxyfluorescein Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OAT3

  DT Modulation2

Quercetin-3-O-glucuronide inhibits the transportation of 5-carboxyfluorescein by SLC22A8 (IC50 = 0.43 microM) [18]

Affected Drug/Substrate

5-carboxyfluorescein Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OAT3

  Quercetin-3-O-sulfate

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Quercetin-3-O-sulfate inhibits the transportation of 5-carboxyfluorescein by SLC22A8 (IC50 = 0.75 microM) [18]

Affected Drug/Substrate

5-carboxyfluorescein Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OAT3

  Gallic Acid

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Gallic acid inhibits the transportation of Estrone sulfate by SLC22A8 (IC50 = 9 microM) [25]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OAT3

  Rosmarinic acid

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Rosmarinic acid inhibits the transportation of Estrone sulfate by SLC22A8 (Ki= 0.55 microM) [25]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OAT3

  Ursolic acid

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Ursolic acid inhibits the transportation of Estrone sulfate by SLC22A8 (IC50 = 19 microM) [25]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OAT3

  Rhein

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Rhubarb inhibits the transportation of Estrone sulfate by SLC22A8 in a competitive manner (IC50 = 0.008 microM) [26]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OAT3

  Allethrin

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Allethrin inhibits the transportation of Fluorescein by SLC22A8 (IC50 = 69.4 microM) [27]

Affected Drug/Substrate

Fluorescein Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OAT3

  Tetramethrin

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Tetramethrin inhibits the transportation of Fluorescein by SLC22A8 (IC50 = 77.6 microM) [27]

Affected Drug/Substrate

Fluorescein Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OAT3

  Citreoverdine

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Citreoverdine inhibits the transportation of Organic anion by SLC22A8 (IC50 = 6.63 microM) [28]

Affected Drug/Substrate

Organic anion Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Cyclopiazonic acid

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Cyclopiazonic acid inhibits the transportation of Organic anion by SLC22A8 (IC50 = 1.9 microM) [28]

Affected Drug/Substrate

Organic anion Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Fumonisin B1

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Fumonisin B1 inhibits the transportation of Organic anion by SLC22A8 (IC50 = 181 microM) [28]

Affected Drug/Substrate

Organic anion Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Daidzein-7-O-Glucuronide

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Daidzein-7-O-Glucuronide inhibits the transportation of 5-carboxyfluorescein by SLC22A8 [18]

Affected Drug/Substrate

5-carboxyfluorescein Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OAT3

  Genistein-7-O-glucuronide

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Genistein-7-O-glucuronide inhibits the transportation of 5-carboxyfluorescein by SLC22A8 [18]

Affected Drug/Substrate

5-carboxyfluorescein Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OAT3

  Glycitein-7-O-glucuronide

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Glycitein-7-O-glucuronide inhibits the transportation of 5-carboxyfluorescein by SLC22A8 [18]

Affected Drug/Substrate

5-carboxyfluorescein Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OAT3

  Cigarette smoke condensate (0.08mg/ml)

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Cigarette smoke condensate (0.08mg/ml) inhibits the activity of SLC22A8 [36]

Cell System

Human embryonic kidney 293 cells (HEK293)-OAT3

  Cigarette smoke condensate (0.32mg/ml)

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Cigarette smoke condensate (0.32mg/ml) inhibits the activity of SLC22A8 [36]

Cell System

Human embryonic kidney 293 cells (HEK293)-OAT3

  Tobacco Smoke Pollution

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Tobacco Smoke Pollution inhibits the activity of SLC22A8 [36]

  Chrysophanic acid

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Chrysophanic acid inhibits the activity of SLC22A8 [38]

  DT Modulation1

Quercetin inhibits the reaction SLC22A8 protein results in increased uptake of estrone sulfate [81]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Quercetin results in decreased activity of SLC22A8 protein [59]

Regulation Mechanism

Transcription Factor Info

  Wogonin

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Wogonin inhibits the activity of SLC22A8 [59]

  Oroxylin A

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Oroxylin A inhibits the activity of SLC22A8 (IC50 = 0.112 microM) [63]

Cell System

Human embryonic kidney 293 cells (HEK293)-SLC22A8

  Resveratrol

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Resveratrol inhibits the reaction SLC22A8 protein results in increased uptake of Methotrexate [86]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Resveratrol inhibits the reaction SLC22A8 protein results in increased uptake of Penicillin G [86]

Regulation Mechanism

Transcription Factor Info

Dietary Constituent

  Danshen

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Danshen inhibits the transportation of Estrone sulfate by SLC22A8 (Ki = 8.6 microM) [25]

Affected Drug/Substrate

Estrone sulfate Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OAT3

Environmental toxicant

  Bisphenol F

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Bisphenol F inhibits the activity of SLC22A8 [56]

  Tetrabromobisphenol A

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Tetrabromobisphenol A inhibits the activity of SLC22A8 [56]

  Sodium arsenate

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Sodium arsenate increases the activity of SLC22A8 [36]

  Mercury

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

SLC22A8 gene SNP affects the susceptibility to and affects the abundance of Mercury [84]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

SLC22A8 gene SNP affects the susceptibility to Mercury which affects the abundance of Mercury [85]

Regulation Mechanism

Transcription Factor Info

Mycotoxins

  DT Modulation1

Cyclopiazonic acid inhibits the transportation of Organic anion by SLC22A8 (IC50 = 1.9 microM) [28]

Affected Drug/Substrate

Organic anion Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  DT Modulation1

Fumonisin B1 inhibits the transportation of Organic anion by SLC22A8 (IC50 = 181 microM) [28]

Affected Drug/Substrate

Organic anion Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Aflatoxin B1

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Aflatoxin B1 inhibits the transportation of Organic anion by SLC22A8 (IC50 = 13.1 microM) [28]

Affected Drug/Substrate

Organic anion Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  DT Modulation2

Aflatoxin B1 affects the methylation of SLC22A8 intron [69]

Regulation Mechanism

Transcription Factor Info

  Alpha-zearalenol

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Alpha-zearalenol inhibits the transportation of Organic anion by SLC22A8 (IC50 = 4.55 microM) [28]

Affected Drug/Substrate

Organic anion Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Citrioveridine

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Citrioveridine inhibits the transportation of Organic anion by SLC22A8 (IC50 = 6.63 microM) [28]

Affected Drug/Substrate

Organic anion Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Patulin

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Patulin inhibits the transportation of Organic anion by SLC22A8 (IC50 > 1000 microM) [28]

Affected Drug/Substrate

Organic anion Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Gliotoxin

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Gliotoxin inhibits the transportation of Organic anion by SLC22A8 (IC50 = 73.9 microM) [28]

Affected Drug/Substrate

Organic anion Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  Zearalenone

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Zearalenone inhibits the transportation of Organic anion by SLC22A8 (IC50 = 6.71 microM) [28]

Affected Drug/Substrate

Organic anion Modulation Type Inhibition

Cell System

The Proximal Tubule (S2) Cells-OAT3

  aflatoxin B2

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

aflatoxin B2 results in increased methylation of SLC22A8 intron [69]

Regulation Mechanism

Transcription Factor Info

  ochratoxin A

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

SLC22A8 protein affects the transport of ochratoxin A [72]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

SLC22A8 protein results in increased uptake of ochratoxin A [73]

Regulation Mechanism

Transcription Factor Info

Acute Toxic Substance

  2-amino-1-methyl-6-phenylimidazo(4,5-b)pyridine

           7 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

2-amino-1-methyl-6-phenylimidazo(4,5-b)pyridine inhibits the activity of SLC22A8 [36]

Carcinogen

  Benzo(a)pyrene

           6 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Benzo(a)pyrene inhibits the activity of SLC22A8 [58]

Pesticide/Insecticide

  Clothianidin

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Clothianidin inhibits the activity of SLC22A8 [57]

  Imidacloprid

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Imidacloprid inhibits the activity of SLC22A8 [57]

  imidacloprid

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

imidacloprid results in decreased activity of SLC22A8 protein [57]

Regulation Mechanism

Transcription Factor Info

Health and Environmental Toxicant

  Toluene

           2 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Toluene increases the expression of SLC22A8 [55]

  Lead chloride

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Lead chloride increases the activity of SLC22A8 [36]

Herbicide

  Atrazine

           1 DT Activity Modulations Related to This Exogenous Factor Click to Show/Hide the Full List

  DT Modulation1

Atrazine increases the expression of SLC22A8 [54]
References
1 Transport of the dipeptidyl peptidase-4 inhibitor sitagliptin by human organic anion transporter 3, organic anion transporting polypeptide 4C1, and multidrug resistance P-glycoprotein. J Pharmacol Exp Ther. 2007 May;321(2):673-83.
2 In vitro and in vivo assessment of renal drug transporters in the disposition of mesna and dimesna. J Clin Pharmacol. 2012 Apr;52(4):530-42.
3 Characterization of organic anion transport inhibitors using cells stably expressing human organic anion transporters. Eur J Pharmacol. 2001 May 11;419(2-3):113-20.
4 Inhibition of oat3-mediated renal uptake as a mechanism for drug-drug interaction between fexofenadine and probenecid. Drug Metab Dispos. 2006 May;34(5):743-7.
5 Characterization of ochratoxin A transport by human organic anion transporters. Life Sci. 2001 Sep 21;69(18):2123-35.
6 Evaluation and prediction of potential drug-drug interactions of linagliptin using in vitro cell culture methods. Drug Metab Dispos. 2013 Jan;41(1):149-58.
7 Organic anion transporter 3 interacts selectively with lipophilic beta-lactam antibiotics. Drug Metab Dispos. 2013 Apr;41(4):791-800.
8 Preclinical and clinical evidence for the collaborative transport and renal secretion of an oxazolidinone antibiotic by organic anion transporter 3 (OAT3/SLC22A8) and multidrug and toxin extrusion protein 1 (MATE1/SLC47A1). J Pharmacol Exp Ther. 2010 Sep 1;334(3):936-44.
9 Transport of organic anions across the basolateral membrane of proximal tubule cells. Rev Physiol Biochem Pharmacol. 2003;146:95-158.
10 Interactions of organic anions with the organic cation transporter in renal BBMV. Am J Physiol. 1988 Jan;254(1 Pt 2):F56-61.
11 Interactions of human organic anion transporters with diuretics. J Pharmacol Exp Ther. 2004 Mar;308(3):1021-9.
12 Interactions of human organic anion transporters and human organic cation transporters with nonsteroidal anti-inflammatory drugs. J Pharmacol Exp Ther. 2002 Nov;303(2):534-9.
13 In vitro risk assessment of AZD9056 perpetrating a transporter-mediated drug-drug interaction with methotrexate. Eur J Pharm Sci. 2011 May 18;43(1-2):41-9.
14 Characterization of methotrexate transport and its drug interactions with human organic anion transporters. J Pharmacol Exp Ther. 2002 Aug;302(2):666-71.
15 Interaction of human and rat organic anion transporter 2 with various cephalosporin antibiotics. Eur J Pharmacol. 2003 Mar 28;465(1-2):1-7.
16 Scintillation proximity assay for measuring uptake by the human drug transporters hOCT1, hOAT3, and hOATP1B1. Anal Biochem. 2007 Jul 15;366(2):117-25.
17 Involvement of multispecific organic anion transporter, Oatp14 (Slc21a14), in the transport of thyroxine across the blood-brain barrier. Endocrinology. 2004 Sep;145(9):4384-91.
18 Flavonoid conjugates interact with organic anion transporters (OATs) and attenuate cytotoxicity of adefovir mediated by organic anion transporter 1 (OAT1/SLC22A6). Biochem Pharmacol. 2011 Apr 1;81(7):942-9.
19 Evidence for a role of human organic anion transporters in the muscular side effects of HMG-CoA reductase inhibitors. Eur J Pharmacol. 2004 Jan 12;483(2-3):133-8.
20 Inhibition of human organic anion transporter 3 mediated pravastatin transport by gemfibrozil and the metabolites in humans. Xenobiotica. 2007 Apr;37(4):416-26.
21 Blockade of Organic Anion Transport in Humans After Treatment With the Drug Probenecid Leads to Major Metabolic Alterations in Plasma and Urine. Clin Pharmacol Ther. 2022 Sep;112(3):653-664.
22 Factors Associated With Neurological Outcome After Childhood Stroke-Reply. JAMA Neurol. 2016 Oct 1;73(10):1257-1258.
23 Novobiocin is a potent inhibitor for human organic anion transporters. Drug Metab Dispos. 2009 Jun;37(6):1203-10.
24 Differential interaction of dicarboxylates with human sodium-dicarboxylate cotransporter 3 and organic anion transporters 1 and 3. Am J Physiol Renal Physiol. 2011 Nov;301(5):F1026-34.
25 Organic solute carrier 22 (SLC22) family: Potential for interactions with food, herbal/dietary supplements, endogenous compounds, and drugs. J Food Drug Anal. 2018 Apr;26(2S):S45-S60.
26 The anthraquinone drug rhein potently interferes with organic anion transporter-mediated renal elimination. Biochem Pharmacol. 2013 Oct 1;86(7):991-6.
27 Inhibition of Human Drug Transporter Activities by the Pyrethroid Pesticides Allethrin and Tetramethrin. PLoS One. 2017 Jan 18;12(1):e0169480.
28 Interactions of organic anion transporters and organic cation transporters with mycotoxins. J Pharmacol Sci. 2008 Mar;106(3):435-43.
29 OAT1 and OAT3 also mediate the drug-drug interaction between piperacillin and tazobactam. Int J Pharm. 2018 Feb 15;537(1-2):172-182.
30 Involvement of uric acid transporters in alteration of serum uric acid level by angiotensin II receptor blockers. Pharm Res. 2008 Mar;25(3):639-46.
31 Organic anion transporters also mediate the drug-drug interaction between imipenem and cilastatin. Asian J Pharm Sci. 2020 Mar;15(2):252-263.
32 Overcoming ABCB1-mediated multidrug resistance by transcription factor BHLHE40. Neoplasia. 2023 May;39:100891.
33 Human organic anion transporters and human organic cation transporters mediate renal antiviral transport. J Pharmacol Exp Ther. 2002 Mar;300(3):918-24.
34 Aspirin and probenecid inhibit organic anion transporter 3-mediated renal uptake of cilostazol and probenecid induces metabolism of cilostazol in the rat. Drug Metab Dispos. 2014 Jun;42(6):996-1007.
35 Overlapping in vitro and in vivo specificities of the organic anion transporters OAT1 and OAT3 for loop and thiazide diuretics. Am J Physiol Renal Physiol. 2008 Apr;294(4):F867-73.
36 Inhibition of organic anion transporter (OAT) activity by cigarette smoke condensate. Toxicol In Vitro. 2017 Oct;44:27-35.
37 Folic acid supplementation dysregulates gene expression in lymphoblastoid cells--implications in nutrition. Biochem Biophys Res Commun. 2011 Sep 9;412(4):688-92.
38 From the Cover: Identification of Natural Products as Inhibitors of Human Organic Anion Transporters (OAT1 and OAT3) and Their Protective Effect on Mercury-Induced Toxicity. Toxicol Sci. 2018 Feb 1;161(2):321-334.
39 The exosome-like vesicles derived from androgen exposed-prostate stromal cells promote epithelial cells proliferation and epithelial-mesenchymal transition. Toxicol Appl Pharmacol. 2021 Jan 15;411:115384.
40 Structural variation governs substrate specificity for organic anion transporter (OAT) homologs. Potential remote sensing by OAT family members. J Biol Chem. 2007 Aug 17;282(33):23841-53.
41 Organic anion transporter 3 (oat3/slc22a8) interacts with carboxyfluoroquinolones, and deletion increases systemic exposure to ciprofloxacin. Mol Pharmacol. 2008 Jul;74(1):122-31.
42 Torsemide renal clearance and genetic variation in luminal and basolateral organic anion transporters. Br J Clin Pharmacol. 2006 Sep;62(3):323-35.
43 Inhibitory effect of selective cyclooxygenase-2 inhibitor etoricoxib on human organic anion transporter 3 (hOAT3). Drug Metab Lett. 2011 Apr;5(2):140-37.
44 Drug interaction between celecoxib and methotrexate in organic anion transporter 3-transfected renal cells and in rats in vivo. Eur J Pharmacol. 2010 Aug 25;640(1-3):168-71.
45 Inhibitory effect of selective cyclooxygenase-2 inhibitor lumiracoxib on human organic anion transporters hOAT1 and hOAT3. Drug Metab Pharmacokinet. 2010;25(5):450-5.
46 JBP485 attenuates vancomycin-induced nephrotoxicity by regulating the expressions of organic anion transporter (Oat) 1, Oat3, organic cation transporter 2 (Oct2), multidrug resistance-associated protein 2 (Mrp2) and P-glycoprotein (P-gp) in rats. Toxicol Lett. 2018 Oct 1;295:195-204.
47 The inhibitory effects of eighteen front-line antibiotics on the substrate uptake mediated by human Organic anion/cation transporters, Organic anion transporting polypeptides and Oligopeptide transporters in in vitro models. Eur J Pharm Sci. 2018 Mar 30;115:132-143.
48 Role of efflux transporters in the absorption, distribution and elimination in rodents of a novel PDE4 inhibitor, CHF6001. Eur J Pharm Sci. 2018 Mar 30;115:100-108.
49 Evidence of post-transcriptional readthrough regulation in FGF5 gene of alpaca. Gene. 2018 Mar 20;647:121-128.
50 The metabolism and drug-drug interaction potential of the selective prostacyclin receptor agonist selexipag. Xenobiotica. 2018 Jul;48(7):704-719.
51 Lansoprazole Exacerbates Pemetrexed-Mediated Hematologic Toxicity by Competitive Inhibition of Renal Basolateral Human Organic Anion Transporter 3. Drug Metab Dispos. 2016 Oct;44(10):1543-9.
52 Evaluation of Ketoconazole and Its Alternative Clinical CYP3A4/5 Inhibitors as Inhibitors of Drug Transporters: The In Vitro Effects of Ketoconazole, Ritonavir, Clarithromycin, and Itraconazole on 13 Clinically-Relevant Drug Transporters. Drug Metab Dispos. 2016 Mar;44(3):453-9.
53 Impaired Transport Activity of Human Organic Anion Transporters (OATs) and Organic Anion Transporting Polypeptides (OATPs) by Wnt Inhibitors. J Pharm Sci. 2021 Feb;110(2):914-924.
54 Endoplasmic reticulum stress impairs insulin signaling through mitochondrial damage in SH-SY5Y cells. Neurosignals. 2012;20(4):265-80.
55 Association analysis of toluene exposure time with high-throughput mRNA expressions and methylation patterns using in vivo samples. Environ Res. 2016 Apr;146:59-64.
56 Inhibition of SLC drug transporter activities by environmental bisphenols. Toxicol In Vitro. 2017 Apr;40:34-44.
57 Neonicotinoid pesticides poorly interact with human drug transporters. J Biochem Mol Toxicol. 2019 Oct;33(10):e22379.
58 Involvement of aryl hydrocarbon receptor in the cytotoxicity of corannulene and its derivatives. Toxicol Lett. 2020 Mar 15;321:114-121.
59 Potent Inhibitors of Organic Anion Transporters 1 and 3 From Natural Compounds and Their Protective Effect on Aristolochic Acid Nephropathy. Toxicol Sci. 2020 Jun 1;175(2):279-291.
60 KEGG: new perspectives on genomes, pathways, diseases and drugs. Nucleic Acids Res. 2017 Jan 4;45(D1):D353-D361. (dg:DG02866)
61 Dominant expression of androgen receptors and their functional regulation of organic anion transporter 3 in rat brain capillary endothelial cells; comparison of gene expression between the blood-brain and -retinal barriers. J Cell Physiol. 2005 Sep;204(3):896-900.
62 Angiotensin II inhibits activity of human organic anion transporter 3 through activation of protein kinase Calpha: accelerating endocytosis of the transporter. Eur J Pharmacol. 2010 Feb 10;627(1-3):49-55.
63 Interactions between Oroxylin A with the solute carrier transporters and ATP-binding cassette transporters: Drug transporters profile for this flavonoid. Chem Biol Interact. 2020 Jun 1;324:109097.
64 Pharmacokinetic interactions of niclosamide in rats: Involvement of organic anion transporters 1 and 3 and organic cation transporter 2. Chem Biol Interact. 2024;390:110886.
65 7-Hydroxycoumarin and its conjugated metabolites interact with organic anion transporters 1 and 3 in vitro and in vivo. Chem Biol Interact. 2025;405:111293.
66 Organic anion transporter 3 (OAT3) and renal transport of the metal chelator 2,3-dimercapto-1-propanesulfonic acid (DMPS). Can J Physiol Pharmacol. 2010;88(2):141-6.
67 Molecular evidence for an involvement of organic anion transporters (OATs) in aristolochic acid nephropathy. Toxicology. 2009;264(1-2):74-9.
68 Intracellular concentrations determine the cytotoxicity of adefovir, cidofovir and tenofovir. Toxicol In Vitro. 2015;29(1):251-8.
69 Effect of aflatoxin B(1), benzo[a]pyrene, and methapyrilene on transcriptomic and epigenetic alterations in human liver HepaRG cells. Food Chem Toxicol. 2018;121:214-223.
70 Expression profile analysis of colon cancer cells in response to sulindac or aspirin. Biochem Biophys Res Commun. 2002 Mar 29;292(2):498-512.
71 Air pollution and DNA methylation alterations in lung cancer: A systematic and comparative study. Oncotarget. 2017;8(1):1369-1391.
72 Identification and characterization of human organic anion transporter 3 expressing predominantly in the kidney. Mol Pharmacol. 2001 May;59(5):1277-86.
73 Human organic anion transporter hOAT3 is a potent transporter of cephalosporin antibiotics, in comparison with hOAT1. Biochem Pharmacol. 2005 Oct 1;70(7):1104-13.
74 Identification of potential target genes of ROR-alpha in THP1 and HUVEC cell lines. Exp Cell Res. 2017;353(1):6-15.
75 Different transport properties between famotidine and cimetidine by human renal organic ion transporters (SLC22A). Eur J Pharmacol. 2004 Oct 25;503(1-3):25-30.
76 A species difference in the transport activities of H2 receptor antagonists by rat and human renal organic anion and cation transporters. J Pharmacol Exp Ther. 2005 Oct;315(1):337-45.
77 The toxicity of cisplatin derives from effects on renal organic ion transporters expression and serum endogenous substance levels. Food Chem Toxicol. 2024;192:114949.
78 Interactions between cyazofamid and human drug transporters. J Biochem Mol Toxicol. 2020;34(4):e22459.
79 Genome-wide study of DNA methylation alterations in response to diazinon exposure in vitro. Environ Toxicol Pharmacol. 2012;34(3):959-68.
80 Completing the Enalaprilat Excretion Pathway-Renal Handling by the Proximal Tubule. Pharmaceutics. 2020;12(10).
81 Allopurinol, rutin, and quercetin attenuate hyperuricemia and renal dysfunction in rats induced by fructose intake: renal organic ion transporter involvement. Am J Physiol Renal Physiol. 2009;297(4):F1080-91.
82 Interaction between rhein acyl glucuronide and methotrexate based on human organic anion transporters. Chem Biol Interact. 2017;277:79-84.
83 Proton pump inhibitor-induced risk of chronic kidney disease is associated with increase of indoxyl sulfate synthesis via inhibition of CYP2E1 protein degradation. Chem Biol Interact. 2022;368:110219.
84 Polymorphisms in genes encoding potential mercury transporters and urine mercury concentrations in populations exposed to mercury vapor from gold mining. Environ Health Perspect. 2013;121(1):85-91.
85 Genetic Polymorphisms in Multispecific Transporters Mitigate Mercury Nephrotoxicity in an Artisanal and Small-Scale Gold Mining Community in Colombia. Toxicol Sci. 2020;178(2):338-346.
86 P-gp, MRP2 and OAT1/OAT3 mediate the drug-drug interaction between resveratrol and methotrexate. Toxicol Appl Pharmacol. 2016;306:27-35.
87 Lack of efflux of diglycolic acid from proximal tubule cells leads to its accumulation and to toxicity of diethylene glycol. Toxicol Lett. 2023;379:48-55.
88 Studies on the interaction of five triazole fungicides with human renal transporters in cells. Toxicol In Vitro. 2023;88:105555.
89 Characterization of the uptake of organic anion transporter (OAT) 1 and OAT3 substrates by human kidney slices. J Pharmacol Exp Ther. 2007;321(1):362-9.
90 In vitro and in silico characterization of the transport of selected perfluoroalkyl carboxylic acids and perfluoroalkyl sulfonic acids by human organic anion transporter 1 (OAT1), OAT2 and OAT3. Toxicology. 2024;509:153961.
91 Identification of a substrate of the renal tubular transporters for detecting drug-induced early acute kidney injury. Toxicol Sci. 2024;201(2):190-205.
92 Diagnosing intake and rationalizing toxicities associated with 5F-MDMB-PINACA and 4F-MDMB-BINACA abuse. Arch Toxicol. 2021;95(2):489-508.
93 Targeting organic anion transporter 3 with probenecid as a novel anti-influenza a virus strategy. Antimicrob Agents Chemother. 2013;57(1):475-83.
94 Transporter-dependent cytotoxicity of antiviral drugs in primary cultures of human proximal tubular cells. Toxicology. 2018;404-405:10-24.
95 Human organic anion transporters mediate the transport of tetracycline. Jpn J Pharmacol. 2002 Jan;88(1):69-76.
96 Integrative omics data analyses of repeated dose toxicity of valproic acid in vitro reveal new mechanisms of steatosis induction. Toxicology. 2018 Jan 15;393:160-170.
97 Uric acid accumulation in the kidney triggers mast cell degranulation and aggravates renal oxidative stress. Toxicology. 2023;483:153387.
98 JBP485, A Dual Inhibitor of Organic Anion Transporters (OATs) and Renal Dehydropeptidase-I (DHP-I), Protects Against Imipenem-Induced Nephrotoxicity. Front Pharmacol. 2022 Jun 8;13:938813.

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