General Information of Drug Transporter (DT)
DT ID DTD0009 Transporter Info
Gene Name SLC22A3
Transporter Name Organic cation transporter 3
Gene ID
6581
UniProt ID
O75751
Exogenous factors (drugs, dietary constituents, etc.) Modulation of This DT (EGM)

Approved Drug

  Quinine

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

  DT Modulation1

Quinine inhibits the transportation of N-methylpyridinium by SLC22A3 (IC50 = 18.3 microM) [1]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Oocytes-OCT3

  DT Modulation2

Quinine inhibits the transportation of N-methylpyridinium by SLC22A3 (IC50 = 37 microM) [2]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Chinese hamster ovary (CHO) cells-OCT3

  DT Modulation3

Quinine inhibits the transportation of N-methylpyridinium by SLC22A3 (IC50 = 22.7 microM) [3]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Chinese hamster ovary (CHO) cells-OCT3

  DT Modulation4

Quinine inhibits the activity of SLC22A3 [4]

  Clonidine

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

  DT Modulation1

Clonidine inhibits the transportation of N-methylpyridinium by SLC22A3 (Ki = 373 microM) [5]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Human retinal pigment epithelial (HRPE) cells-OCT3

  DT Modulation2

Clonidine inhibits the transportation of N-methylpyridinium by SLC22A3 (IC50 = 110 microM) [2]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Chinese hamster ovary (CHO) cells-OCT3

  Desipramine

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

  DT Modulation1

Desipramine inhibits the transportation of N-methylpyridinium by SLC22A3 (Ki = 14 microM) [5]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Human retinal pigment epithelial (HRPE) cells-OCT3

  DT Modulation2

Desipramine inhibits the activity of SLC22A3 [7]

  Metformin

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

  DT Modulation1

Metformin inhibits the transportation of N-methylpyridinium by SLC22A3 (IC50 = 2332 microM) [1]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Oocytes-OCT3

  DT Modulation2

Metformin inhibits the transportation of N-methylpyridinium by SLC22A3 (Ki = 904 microM) [6]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OCT3

  DT Modulation3

Carvedilol inhibits the reaction SLC22A3 protein results in increased uptake of Metformin [38]

Regulation Mechanism

Transcription Factor Info

  DT Modulation4

Cimetidine inhibits the reaction SLC22A3 protein results in increased uptake of Metformin [38]

Regulation Mechanism

Transcription Factor Info

  DT Modulation5

Imipramine inhibits the reaction SLC22A3 protein results in increased uptake of Metformin [38]

Regulation Mechanism

Transcription Factor Info

  DT Modulation6

Metformin inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [1]

Regulation Mechanism

Transcription Factor Info

  DT Modulation7

SLC22A3 protein results in increased uptake of Metformin [38]

Regulation Mechanism

Transcription Factor Info

  DT Modulation8

Verapamil inhibits the reaction SLC22A3 protein results in increased uptake of Metformin [38]

Regulation Mechanism

Transcription Factor Info

  Ranitidine

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

  DT Modulation1

Ranitidine inhibits the transportation of N-methylpyridinium by SLC22A3 (IC50 = 290 microM) [1]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Oocytes-OCT3

  DT Modulation2

Ranitidine inhibits the transportation of N-methylpyridinium by SLC22A3 (IC50 = 372 microM) [2]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Chinese hamster ovary (CHO) cells-OCT3

  Estradiol

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

  DT Modulation1

Estradiol inhibits the transportation of 1-Methyl-4-phenylpyridinium by SLC22A3 (IC50 = 2.88 microM) [8]

Affected Drug/Substrate

1-Methyl-4-phenylpyridinium Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OCT3

  Phenoxybenzamine

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

  DT Modulation1

Phenoxybenzamine inhibits the transportation of 1-Methyl-4-phenylpyridinium by SLC22A3 (IC50 = 6.13 microM) [8]

Affected Drug/Substrate

1-Methyl-4-phenylpyridinium Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OCT3

  Progesterone

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

  DT Modulation1

Progesterone inhibits the transportation of 1-Methyl-4-phenylpyridinium by SLC22A3 (IC50 = 4.28 microM) [8]

Affected Drug/Substrate

1-Methyl-4-phenylpyridinium Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OCT3

  Ergotidine

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

  DT Modulation1

Ergotidine inhibits the transportation of N-methylpyridinium by SLC22A3 (Ki = 140 microM) [9]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OCT3

  Imipramine

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

  DT Modulation1

Imipramine inhibits the transportation of N-methylpyridinium by SLC22A3 (Ki = 42 microM) [5]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Human retinal pigment epithelial (HRPE) cells-OCT3

  Procainamide

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

  DT Modulation1

Procainamide inhibits the transportation of N-methylpyridinium by SLC22A3 (Ki = 738 microM) [5]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Human retinal pigment epithelial (HRPE) cells-OCT3

  Famotidine

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

  DT Modulation1

Famotidine inhibits the transportation of N-methylpyridinium by SLC22A3 (IC50 = 6.7 microM) [1]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Oocytes-OCT3

  Atropine

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

  DT Modulation1

Atropine inhibits the transportation of N-methylpyridinium by SLC22A3 (IC50 = 466 microM) [2]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Chinese hamster ovary (CHO) cells-OCT3

  Diphenhydramine

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

  DT Modulation1

Diphenhydramine inhibits the transportation of N-methylpyridinium by SLC22A3 (IC50 = 695 microM) [2]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Chinese hamster ovary (CHO) cells-OCT3

  Amantadine

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

  DT Modulation1

Amantadine inhibits the transportation of N-methylpyridinium by SLC22A3 (Ki > 1000 microM) [10]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OCT3

  Cocaine

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

  DT Modulation1

Cocaine inhibits the transportation of N-methylpyridinium by SLC22A3 (Ki > 1000 microM) [10]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OCT3

  Dextroamphetamine

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

  DT Modulation1

Dextroamphetamine inhibits the transportation of N-methylpyridinium by SLC22A3 (Ki = 460 microM) [10]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OCT3

  Ketamine

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

  DT Modulation1

Ketamine inhibits the transportation of N-methylpyridinium by SLC22A3 (Ki = 225.7 microM) [10]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OCT3

  Memantine

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

  DT Modulation1

Memantine inhibits the transportation of N-methylpyridinium by SLC22A3 (Ki = 236 microM) [10]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OCT3

  Pentamidine

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

  DT Modulation1

Pentamidine inhibits the transportation of N-methylpyridinium by SLC22A3 (IC50 = 14.8 microM) [3]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Chinese hamster ovary (CHO) cells-OCT3

  Prazosin

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

  DT Modulation1

Prazosin inhibits the transportation of N-methylpyridinium by SLC22A3 (IC50 = 12.6 microM) [8]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OCT3

  Mifepristone

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

  DT Modulation1

Mifepristone inhibits the expression of SLC22A3 [12]

  Phenobarbital

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

  DT Modulation1

Phenobarbital affects the expression of SLC22A3 [13]

  Copper Sulfate

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

  DT Modulation1

Copper Sulfate inhibits the expression of SLC22A3 [14]

  Cisplatin

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

  DT Modulation1

Cisplatin inhibits the expression of SLC22A3 [15]

  Acetaminophen

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

  DT Modulation1

Acetaminophen inhibits the expression of SLC22A3 [16]

  Decitabine

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

  DT Modulation1

Decitabine affects the expression of SLC22A3 [17]

  Hydrogen Peroxide

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

  DT Modulation1

Hydrogen Peroxide affects the expression of SLC22A3 [18]

  Menadione

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

  DT Modulation1

Menadione affects the expression of SLC22A3 [18]

  Valproic Acid

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

  DT Modulation1

Valproic Acid affects the expression of SLC22A3 [19]

  Mdv-3100

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

  DT Modulation1

Mdv-3100 inhibits the expression of SLC22A3 [20]

  Doxorubicin

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

  DT Modulation1

Doxorubicin affects the expression of SLC22A3 [21]

  Cyclosporine

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

  DT Modulation1

Cyclosporine inhibits the expression of SLC22A3 [22]

  Atorvastatin

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

  DT Modulation1

Atorvastatin inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [37]

Regulation Mechanism

Transcription Factor Info

Drug in Phase 3 Trial

  Corticosterone

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

  DT Modulation1

Corticosterone inhibits the activity of SLC22A3 [8]

  Triclosan

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

  DT Modulation1

Triclosan inhibits the expression of SLC22A3 [28]

Drug in Phase 2 Trial

  YM155

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

  DT Modulation1

YM155 inhibits the transportation of N-methylpyridinium by SLC22A3 (IC50 = 108 microM) [11]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OCT3

  MeIQx

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

  DT Modulation1

MeIQx inhibits the activity of SLC22A3 [27]

Drug in Phase 1 Trial

  Quercetin

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

  DT Modulation1

Quercetin inhibits the expression of SLC22A3 [23]

  Sodium arsenite

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

  DT Modulation1

Sodium arsenite inhibits the expression of SLC22A3 [30]

Drug in Preclinical Test

  Beta-carboline

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

  DT Modulation1

Beta-carboline inhibits the activity of SLC22A3 [27]

Discontinued Drug

  Dizocilpine

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

  DT Modulation1

Dizocilpine inhibits the transportation of N-methylpyridinium by SLC22A3 (Ki = 224 microM) [10]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OCT3

  Antiparasitics

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

  DT Modulation1

Antiparasitics inhibits the transportation of N-methylpyridinium by SLC22A3 (IC50 = 20.4 microM) [3]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Chinese hamster ovary (CHO) cells-OCT3

Investigative Drug

  Tetraethylammonium

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

  DT Modulation1

Tetraethylammonium inhibits the transportation of N-methylpyridinium by SLC22A3 (Ki = 1372 microM) [5]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Human retinal pigment epithelial (HRPE) cells-OCT3

  DT Modulation2

Tetraethylammonium inhibits the transportation of N-methylpyridinium by SLC22A3 (IC50 = 1237 microM) [1]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Oocytes-OCT3

  DT Modulation3

Tetraethylammonium inhibits the transportation of N-methylpyridinium by SLC22A3 (IC50 = 1476.6 microM) [3]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Chinese hamster ovary (CHO) cells-OCT3

  Phencyclidine

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

  DT Modulation1

Phencyclidine inhibits the transportation of N-methylpyridinium by SLC22A3 (Ki = 333 microM) [10]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OCT3

Drug Withdrawn

  Etilefrine

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

  DT Modulation1

Etilefrine inhibits the transportation of N-methylpyridinium by SLC22A3 (IC50 = 4448 microM) [2]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Chinese hamster ovary (CHO) cells-OCT3

  Phenformin

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

  DT Modulation1

Phenformin inhibits the transportation of N-methylpyridinium by SLC22A3 (Ki = 134 microM) [6]

Affected Drug/Substrate

N-methylpyridinium Modulation Type Inhibition

Cell System

Human embryonic kidney 293 cells (HEK293)-OCT3

Natural Product

  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 expression of SLC22A3 [29]

  Particulate Matter

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

  DT Modulation1

Particulate Matter inhibits the expression of SLC22A3 [34]

Environmental toxicant

  Polychlorinated dibenzodioxin

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

  DT Modulation1

Polychlorinated dibenzodioxin inhibits the expression of SLC22A3 [32]

Mycotoxins

  Aflatoxin B1

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

  DT Modulation1

Aflatoxin B1 inhibits the expression of SLC22A3 [33]

  DT Modulation2

Aflatoxin B1 affects the expression of SLC22A3 protein [40]

Regulation Mechanism

Transcription Factor Info

  Zearalenone

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

  DT Modulation1

Zearalenone results in increased expression of SLC22A3 mRNA [46]

Regulation Mechanism

Transcription Factor Info

Acute Toxic Substance

  Oxyquinoline

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

  DT Modulation1

Oxyquinoline inhibits the expression of SLC22A3 [23]

  Formaldehyde

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

  DT Modulation1

Formaldehyde increases the expression of SLC22A3 [24]

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

           3 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 SLC22A3 [27]

Carcinogen

  2-amino-3-methylimidazo(4,5-f)quinoline

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

  DT Modulation1

2-amino-3-methylimidazo(4,5-f)quinoline inhibits the activity of SLC22A3 [27]

  Benzo(a)pyrene

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

  DT Modulation1

Benzo(a)pyrene inhibits the expression of SLC22A3 [31]

  Cadmium

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

  DT Modulation1

Cadmium Chloride results in increased abundance of Cadmium which results in increased expression of SLC22A3 mRNA [48]

Regulation Mechanism

Transcription Factor Info

Health and Environmental Toxicant

  Butyraldehyde

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

  DT Modulation1

Butyraldehyde inhibits the expression of SLC22A3 [25]

  tris(1,3-dichloro-2-propyl)phosphate

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

  DT Modulation1

tris(1,3-dichloro-2-propyl)phosphate inhibits the expression of SLC22A3 [26]

  Endosulfan

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

  DT Modulation1

Endosulfan inhibits the reaction Tetrachlorodibenzodioxin results in decreased expression of SLC22A3 mRNA [32]

Regulation Mechanism

Transcription Factor Info

Chemical Compound

  DT Modulation1

Quinine inhibits the reaction SLC22A3 protein results in increased transport of 1-Methyl-4-phenylpyridinium [2]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Quinine inhibits the reaction SLC22A3 protein results in increased uptake of Ethidium [35]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

SLC22A3 protein results in increased uptake of Tetraethylammonium [5]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Tetraethylammonium inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [1]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

Tetraethylammonium inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium analog [5]

Regulation Mechanism

Transcription Factor Info

  DT Modulation4

Tetraethylammonium inhibits the reaction SLC22A3 protein results in increased uptake of Ethidium [35]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Clonidine inhibits the reaction SLC22A3 protein results in increased transport of 1-Methyl-4-phenylpyridinium [2]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Clonidine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium analog [5]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Desipramine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium analog [5]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Ranitidine inhibits the reaction SLC22A3 protein affects the transport of 1-Methyl-4-phenylpyridinium [1]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Ranitidine inhibits the reaction SLC22A3 protein results in increased transport of 1-Methyl-4-phenylpyridinium [2]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

Ranitidine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [1]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Estradiol co-treated with TGFB1 protein results in increased expression of SLC22A3 mRNA [56]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Estradiol inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [8]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

Estradiol results in decreased activity of SLC22A3 protein [8]

Regulation Mechanism

Transcription Factor Info

  DT Modulation4

Estradiol results in decreased expression of SLC22A3 mRNA [40]

Regulation Mechanism

Transcription Factor Info

  DT Modulation5

Estradiol results in increased expression of SLC22A3 mRNA [46]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Phenoxybenzamine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [8]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Phenoxybenzamine results in decreased activity of SLC22A3 protein [8]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Progesterone inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [8]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Progesterone results in decreased activity of SLC22A3 protein [8]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Imipramine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [38]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Imipramine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium analog [5]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

Imipramine inhibits the reaction SLC22A3 protein results in increased uptake of Metformin [38]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Procainamide inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium analog [5]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Famotidine inhibits the reaction SLC22A3 protein affects the transport of 1-Methyl-4-phenylpyridinium [1]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Famotidine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [1]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

Famotidine results in decreased activity of SLC22A3 protein [1]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Atropine inhibits the reaction SLC22A3 protein results in increased transport of 1-Methyl-4-phenylpyridinium [2]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

SLC22A3 protein results in increased uptake of Atropine [2]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Diphenhydramine inhibits the reaction SLC22A3 protein results in increased transport of 1-Methyl-4-phenylpyridinium [2]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Etilefrine inhibits the reaction SLC22A3 protein results in increased transport of 1-Methyl-4-phenylpyridinium [2]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

SLC22A3 protein results in increased uptake of Etilefrine [2]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Prazosin inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [8]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Prazosin results in decreased activity of SLC22A3 protein [8]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Cisplatin affects the expression of SLC22A3 mRNA [17]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Cisplatin co-treated with jinfukang results in decreased expression of SLC22A3 mRNA [52]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

SLC22A3 affects the susceptibility to Cisplatin [15]

Regulation Mechanism

Transcription Factor Info

  DT Modulation4

SLC22A3 results in increased uptake of Cisplatin [15]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Cyclosporine results in increased expression of SLC22A3 mRNA [54]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Corticosterone inhibits the reaction SLC22A3 protein results in increased import of 4-(4-(dimethylamino)styryl)-1-methylpyridinium iodide [27]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Corticosterone inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [8]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

Corticosterone inhibits the reaction SLC22A3 protein results in increased uptake of Formoterol Fumarate [47]

Regulation Mechanism

Transcription Factor Info

  DT Modulation4

Corticosterone results in decreased activity of SLC22A3 protein [8]

Regulation Mechanism

Transcription Factor Info

  Pentanal

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

  DT Modulation1

Pentanal inhibits the expression of SLC22A3 [25]

  DT Modulation1

2-amino-1-methyl-6-phenylimidazo(4,5-b)pyridine inhibits the reaction SLC22A3 protein results in increased import of 4-(4-(dimethylamino)styryl)-1-methylpyridinium iodide [27]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

2-amino-1-methyl-6-phenylimidazo(4,5-b)pyridine results in decreased activity of SLC22A3 protein [27]

Regulation Mechanism

Transcription Factor Info

  DT Modulation1

Benzo(a)pyrene co-treated with benzo(b)fluoranthene affects the expression of SLC22A3 mRNA [43]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Benzo(a)pyrene results in increased methylation of SLC22A3 exon [44]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

Benzo(a)pyrene results in increased methylation of SLC22A3 promoter [44]

Regulation Mechanism

Transcription Factor Info

  1-Methyl-4-phenylpyridinium

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

  DT Modulation1

1-Methyl-4-phenylpyridinium analog inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium analog [5]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

1-Methyl-4-phenylpyridinium inhibits the reaction SLC22A3 protein results in increased uptake of Ethidium [35]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

4-(1H-imidazol-4-ylmethyl)piperidine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation4

Atorvastatin inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [37]

Regulation Mechanism

Transcription Factor Info

  DT Modulation5

Atropine inhibits the reaction SLC22A3 protein results in increased transport of 1-Methyl-4-phenylpyridinium [2]

Regulation Mechanism

Transcription Factor Info

  DT Modulation6

BU 224 inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation7

Carvedilol inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [37]

Regulation Mechanism

Transcription Factor Info

  DT Modulation8

Cimetidine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [38]

Regulation Mechanism

Transcription Factor Info

  DT Modulation9

clobenpropit inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation10

Clonidine inhibits the reaction SLC22A3 protein results in increased transport of 1-Methyl-4-phenylpyridinium [2]

Regulation Mechanism

Transcription Factor Info

  DT Modulation11

Clonidine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium analog [5]

Regulation Mechanism

Transcription Factor Info

  DT Modulation12

Corticosterone inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [8]

Regulation Mechanism

Transcription Factor Info

  DT Modulation13

Desipramine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium analog [5]

Regulation Mechanism

Transcription Factor Info

  DT Modulation14

Digoxin inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [37]

Regulation Mechanism

Transcription Factor Info

  DT Modulation15

Diphenhydramine inhibits the reaction SLC22A3 protein results in increased transport of 1-Methyl-4-phenylpyridinium [2]

Regulation Mechanism

Transcription Factor Info

  DT Modulation16

disprocynium 24 inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation17

Estradiol inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [8]

Regulation Mechanism

Transcription Factor Info

  DT Modulation18

Etilefrine inhibits the reaction SLC22A3 protein results in increased transport of 1-Methyl-4-phenylpyridinium [2]

Regulation Mechanism

Transcription Factor Info

  DT Modulation19

Famotidine inhibits the reaction SLC22A3 protein affects the transport of 1-Methyl-4-phenylpyridinium [1]

Regulation Mechanism

Transcription Factor Info

  DT Modulation20

Famotidine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [1]

Regulation Mechanism

Transcription Factor Info

  DT Modulation21

Flecainide inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [37]

Regulation Mechanism

Transcription Factor Info

  DT Modulation22

Guanidine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium analog [5]

Regulation Mechanism

Transcription Factor Info

  DT Modulation23

Histamine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation24

Imipramine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [38]

Regulation Mechanism

Transcription Factor Info

  DT Modulation25

Imipramine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium analog [5]

Regulation Mechanism

Transcription Factor Info

  DT Modulation26

Ipratropium inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [37]

Regulation Mechanism

Transcription Factor Info

  DT Modulation27

Lidocaine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [37]

Regulation Mechanism

Transcription Factor Info

  DT Modulation28

Metformin inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [1]

Regulation Mechanism

Transcription Factor Info

  DT Modulation29

metiprenaline inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [8]

Regulation Mechanism

Transcription Factor Info

  DT Modulation30

Molsidomine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [37]

Regulation Mechanism

Transcription Factor Info

  DT Modulation31

Nifedipine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [37]

Regulation Mechanism

Transcription Factor Info

  DT Modulation32

Papaverine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation33

Phenoxybenzamine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [8]

Regulation Mechanism

Transcription Factor Info

  DT Modulation34

Phentolamine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation35

Prazosin inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [8]

Regulation Mechanism

Transcription Factor Info

  DT Modulation36

Procainamide inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium analog [5]

Regulation Mechanism

Transcription Factor Info

  DT Modulation37

Progesterone inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [8]

Regulation Mechanism

Transcription Factor Info

  DT Modulation38

Propafenone inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [37]

Regulation Mechanism

Transcription Factor Info

  DT Modulation39

Propranolol inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [37]

Regulation Mechanism

Transcription Factor Info

  DT Modulation40

pseudoisocyanine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [8]

Regulation Mechanism

Transcription Factor Info

  DT Modulation41

Quinidine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [1]

Regulation Mechanism

Transcription Factor Info

  DT Modulation42

Quinine inhibits the reaction SLC22A3 protein results in increased transport of 1-Methyl-4-phenylpyridinium [2]

Regulation Mechanism

Transcription Factor Info

  DT Modulation43

Ranitidine inhibits the reaction SLC22A3 protein affects the transport of 1-Methyl-4-phenylpyridinium [1]

Regulation Mechanism

Transcription Factor Info

  DT Modulation44

Ranitidine inhibits the reaction SLC22A3 protein results in increased transport of 1-Methyl-4-phenylpyridinium [2]

Regulation Mechanism

Transcription Factor Info

  DT Modulation45

Ranitidine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [1]

Regulation Mechanism

Transcription Factor Info

  DT Modulation46

SK&F 550 inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [8]

Regulation Mechanism

Transcription Factor Info

  DT Modulation47

SLC22A3 protein polymorphism affects the uptake of 1-Methyl-4-phenylpyridinium [39]

Regulation Mechanism

Transcription Factor Info

  DT Modulation48

SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [8]

Regulation Mechanism

Transcription Factor Info

  DT Modulation49

SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium analog [5]

Regulation Mechanism

Transcription Factor Info

  DT Modulation50

Spironolactone inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [37]

Regulation Mechanism

Transcription Factor Info

  DT Modulation51

Tetraethylammonium inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [1]

Regulation Mechanism

Transcription Factor Info

  DT Modulation52

Tetraethylammonium inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium analog [5]

Regulation Mechanism

Transcription Factor Info

  DT Modulation53

thioperamide inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation54

trimazosin inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation55

Verapamil inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [37]

Regulation Mechanism

Transcription Factor Info

  2-amino-3,4-dimethylimidazo(4,5-f)quinoline

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

  DT Modulation1

2-amino-3,4-dimethylimidazo(4,5-f)quinoline inhibits the reaction SLC22A3 protein results in increased import of 4-(4-(dimethylamino)styryl)-1-methylpyridinium iodide [27]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

2-amino-3,4-dimethylimidazo(4,5-f)quinoline results in decreased activity of SLC22A3 protein [27]

Regulation Mechanism

Transcription Factor Info

  2-amino-3,7,8-trimethylimidazo(4,5-f)quinoxaline

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

  DT Modulation1

2-amino-3,7,8-trimethylimidazo(4,5-f)quinoxaline inhibits the reaction SLC22A3 protein results in increased import of 4-(4-(dimethylamino)styryl)-1-methylpyridinium iodide [27]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

2-amino-3,7,8-trimethylimidazo(4,5-f)quinoxaline results in decreased activity of SLC22A3 protein [27]

Regulation Mechanism

Transcription Factor Info

  2-amino-3,8-dimethylimidazo(4,5-f)quinoxaline

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

  DT Modulation1

2-amino-3,8-dimethylimidazo(4,5-f)quinoxaline inhibits the reaction SLC22A3 protein results in increased import of 4-(4-(dimethylamino)styryl)-1-methylpyridinium iodide [27]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

2-amino-3,8-dimethylimidazo(4,5-f)quinoxaline results in decreased activity of SLC22A3 protein [27]

Regulation Mechanism

Transcription Factor Info

  2-amino-3-methyl-3H-imidazo(4,5-f)quinoline

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

  DT Modulation1

2-amino-3-methyl-3H-imidazo(4,5-f)quinoline inhibits the reaction SLC22A3 protein results in increased import of 4-(4-(dimethylamino)styryl)-1-methylpyridinium iodide [27]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

2-amino-3-methyl-3H-imidazo(4,5-f)quinoline results in decreased activity of SLC22A3 protein [27]

Regulation Mechanism

Transcription Factor Info

  2-amino-3-methylimidazo(4,5-f)quinoxaline

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

  DT Modulation1

2-amino-3-methylimidazo(4,5-f)quinoxaline inhibits the reaction SLC22A3 protein results in increased import of 4-(4-(dimethylamino)styryl)-1-methylpyridinium iodide [27]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

2-amino-3-methylimidazo(4,5-f)quinoxaline results in decreased activity of SLC22A3 protein [27]

Regulation Mechanism

Transcription Factor Info

  2-amino-6-methyldipyrido(1,2-a-3',2'-d)imidazole

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

  DT Modulation1

2-amino-6-methyldipyrido(1,2-a-3',2'-d)imidazole inhibits the reaction SLC22A3 protein results in increased import of 4-(4-(dimethylamino)styryl)-1-methylpyridinium iodide [27]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

2-amino-6-methyldipyrido(1,2-a-3',2'-d)imidazole results in decreased activity of SLC22A3 protein [27]

Regulation Mechanism

Transcription Factor Info

  3,4,8-trimethylimidazo(4,5-f)quinoxalin-2-amine

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

  DT Modulation1

3,4,8-trimethylimidazo(4,5-f)quinoxalin-2-amine inhibits the reaction SLC22A3 protein results in increased import of 4-(4-(dimethylamino)styryl)-1-methylpyridinium iodide [27]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

3,4,8-trimethylimidazo(4,5-f)quinoxalin-2-amine results in decreased activity of SLC22A3 protein [27]

Regulation Mechanism

Transcription Factor Info

  3-amino-1,4-dimethyl-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-1,4-dimethyl-5H-pyrido(4,3-b)indole inhibits the reaction SLC22A3 protein results in increased import of 4-(4-(dimethylamino)styryl)-1-methylpyridinium iodide [27]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

3-amino-1,4-dimethyl-5H-pyrido(4,3-b)indole results in decreased activity of SLC22A3 protein [27]

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 SLC22A3 protein results in increased import of 4-(4-(dimethylamino)styryl)-1-methylpyridinium iodide [27]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

3-amino-1-methyl-5H-pyrido(4,3-b)indole results in decreased activity of SLC22A3 protein [27]

Regulation Mechanism

Transcription Factor Info

  4-(1H-imidazol-4-ylmethyl)piperidine

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

  DT Modulation1

4-(1H-imidazol-4-ylmethyl)piperidine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [36]

Regulation Mechanism

Transcription Factor Info

  Aldehydes

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

  DT Modulation1

Aldehydes results in decreased expression of SLC22A3 mRNA [41]

Regulation Mechanism

Transcription Factor Info

  beclomethasone 17-monopropionate

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

  DT Modulation1

SLC22A3 protein results in increased susceptibility to beclomethasone 17-monopropionate results in decreased transport of Formoterol Fumarate [42]

Regulation Mechanism

Transcription Factor Info

  benzo(b)fluoranthene

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

  DT Modulation1

Benzo(a)pyrene co-treated with benzo(b)fluoranthene affects the expression of SLC22A3 mRNA [43]

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 co-treated with Fulvestrant affects the methylation of SLC22A3 gene [45]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

bisphenol A results in increased expression of SLC22A3 mRNA [46]

Regulation Mechanism

Transcription Factor Info

  bisphenol S

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

  DT Modulation1

bisphenol S results in increased methylation of SLC22A3 gene [45]

Regulation Mechanism

Transcription Factor Info

  BU 224

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

  DT Modulation1

BU 224 inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [36]

Regulation Mechanism

Transcription Factor Info

  Budesonide

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

  DT Modulation1

Budesonide inhibits the reaction SLC22A3 protein results in increased uptake of Formoterol Fumarate [47]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

SLC22A3 protein results in increased susceptibility to Budesonide results in decreased transport of Formoterol Fumarate [42]

Regulation Mechanism

Transcription Factor Info

  butyraldehyde

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

  DT Modulation1

butyraldehyde results in decreased expression of SLC22A3 mRNA [25]

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 results in increased abundance of Cadmium which results in increased expression of SLC22A3 mRNA [48]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Cadmium Chloride results in increased expression of SLC22A3 mRNA [49]

Regulation Mechanism

Transcription Factor Info

  Cannabidiol

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

  DT Modulation1

Cannabidiol results in increased expression of SLC22A3 mRNA [50]

Regulation Mechanism

Transcription Factor Info

  Carvedilol

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

  DT Modulation1

Carvedilol inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [37]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Carvedilol inhibits the reaction SLC22A3 protein results in increased uptake of Metformin [38]

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 SLC22A3 gene [51]

Regulation Mechanism

Transcription Factor Info

  Cimetidine

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

  DT Modulation1

Cimetidine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [38]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Cimetidine inhibits the reaction SLC22A3 protein results in increased uptake of Ethidium [35]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

Cimetidine inhibits the reaction SLC22A3 protein results in increased uptake of Metformin [38]

Regulation Mechanism

Transcription Factor Info

  clobenpropit

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

  DT Modulation1

clobenpropit inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [36]

Regulation Mechanism

Transcription Factor Info

  cobaltous chloride

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

  DT Modulation1

cobaltous chloride results in decreased expression of SLC22A3 mRNA [53]

Regulation Mechanism

Transcription Factor Info

  desisobutyrylciclesonide

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

  DT Modulation1

SLC22A3 protein results in increased susceptibility to desisobutyrylciclesonide results in decreased transport of Formoterol Fumarate [42]

Regulation Mechanism

Transcription Factor Info

  Digoxin

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

  DT Modulation1

Digoxin inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [37]

Regulation Mechanism

Transcription Factor Info

  disprocynium 24

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

  DT Modulation1

disprocynium 24 inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [36]

Regulation Mechanism

Transcription Factor Info

  Dopamine

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

  DT Modulation1

SLC22A3 protein results in increased uptake of Dopamine [55]

Regulation Mechanism

Transcription Factor Info

  enzalutamide

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

  DT Modulation1

enzalutamide results in decreased expression of SLC22A3 mRNA [20]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

KDM1A protein promotes the reaction enzalutamide results in decreased expression of SLC22A3 mRNA [20]

Regulation Mechanism

Transcription Factor Info

  Epinephrine

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

  DT Modulation1

SLC22A3 protein results in increased uptake of Epinephrine [55]

Regulation Mechanism

Transcription Factor Info

  Ethidium

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

  DT Modulation1

1-Methyl-4-phenylpyridinium inhibits the reaction SLC22A3 protein results in increased uptake of Ethidium [35]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Cimetidine inhibits the reaction SLC22A3 protein results in increased uptake of Ethidium [35]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

Quinine inhibits the reaction SLC22A3 protein results in increased uptake of Ethidium [35]

Regulation Mechanism

Transcription Factor Info

  DT Modulation4

SLC22A3 protein results in increased uptake of Ethidium [35]

Regulation Mechanism

Transcription Factor Info

  DT Modulation5

Tetraethylammonium inhibits the reaction SLC22A3 protein results in increased uptake of Ethidium [35]

Regulation Mechanism

Transcription Factor Info

  Flecainide

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

  DT Modulation1

Flecainide inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [37]

Regulation Mechanism

Transcription Factor Info

  Fluticasone

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

  DT Modulation1

Fluticasone inhibits the reaction SLC22A3 protein results in increased uptake of Formoterol Fumarate [47]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

SLC22A3 protein results in increased susceptibility to Fluticasone results in decreased transport of Formoterol Fumarate [42]

Regulation Mechanism

Transcription Factor Info

  Fonofos

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

  DT Modulation1

Fonofos results in increased methylation of SLC22A3 promoter [57]

Regulation Mechanism

Transcription Factor Info

  Formoterol Fumarate

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

  DT Modulation1

Budesonide inhibits the reaction SLC22A3 protein results in increased uptake of Formoterol Fumarate [47]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Corticosterone inhibits the reaction SLC22A3 protein results in increased uptake of Formoterol Fumarate [47]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

Fluticasone inhibits the reaction SLC22A3 protein results in increased uptake of Formoterol Fumarate [47]

Regulation Mechanism

Transcription Factor Info

  DT Modulation4

SLC22A3 protein results in increased susceptibility to beclomethasone 17-monopropionate results in decreased transport of Formoterol Fumarate [42]

Regulation Mechanism

Transcription Factor Info

  DT Modulation5

SLC22A3 protein results in increased susceptibility to Budesonide results in decreased transport of Formoterol Fumarate [42]

Regulation Mechanism

Transcription Factor Info

  DT Modulation6

SLC22A3 protein results in increased susceptibility to desisobutyrylciclesonide results in decreased transport of Formoterol Fumarate [42]

Regulation Mechanism

Transcription Factor Info

  DT Modulation7

SLC22A3 protein results in increased susceptibility to Fluticasone results in decreased transport of Formoterol Fumarate [42]

Regulation Mechanism

Transcription Factor Info

  DT Modulation8

SLC22A3 protein results in increased uptake of Formoterol Fumarate [47]

Regulation Mechanism

Transcription Factor Info

  Fulvestrant

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

  DT Modulation1

bisphenol A co-treated with Fulvestrant affects the methylation of SLC22A3 gene [45]

Regulation Mechanism

Transcription Factor Info

  Glu-P-2

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

  DT Modulation1

Glu-P-2 inhibits the reaction SLC22A3 protein results in increased import of 4-(4-(dimethylamino)styryl)-1-methylpyridinium iodide [27]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Glu-P-2 results in decreased activity of SLC22A3 protein [27]

Regulation Mechanism

Transcription Factor Info

  Guanidine

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

  DT Modulation1

Guanidine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium analog [5]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

SLC22A3 protein results in increased uptake of Guanidine [5]

Regulation Mechanism

Transcription Factor Info

  Histamine

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

  DT Modulation1

Histamine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [36]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

SLC22A3 protein polymorphism affects the uptake of Histamine [39]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

SLC22A3 protein results in increased uptake of Histamine [55]

Regulation Mechanism

Transcription Factor Info

  Ipratropium

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

  DT Modulation1

Ipratropium inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [37]

Regulation Mechanism

Transcription Factor Info

  Lamivudine

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

  DT Modulation1

SLC22A3 protein results in increased uptake of Lamivudine [58]

Regulation Mechanism

Transcription Factor Info

  lead acetate

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

  DT Modulation1

lead acetate co-treated with zinc protoporphyrin results in increased expression of SLC22A3 mRNA [59]

Regulation Mechanism

Transcription Factor Info

  Lidocaine

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

  DT Modulation1

Lidocaine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [37]

Regulation Mechanism

Transcription Factor Info

  metiprenaline

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

  DT Modulation1

metiprenaline inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [8]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

metiprenaline results in decreased activity of SLC22A3 protein [8]

Regulation Mechanism

Transcription Factor Info

  Molsidomine

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

  DT Modulation1

Molsidomine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [37]

Regulation Mechanism

Transcription Factor Info

  Nifedipine

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

  DT Modulation1

Nifedipine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [37]

Regulation Mechanism

Transcription Factor Info

  Norepinephrine

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

  DT Modulation1

SLC22A3 protein results in increased uptake of Norepinephrine [55]

Regulation Mechanism

Transcription Factor Info

  norharman

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

  DT Modulation1

norharman inhibits the reaction SLC22A3 protein results in increased import of 4-(4-(dimethylamino)styryl)-1-methylpyridinium iodide [27]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

norharman results in decreased activity of SLC22A3 protein [27]

Regulation Mechanism

Transcription Factor Info

  Paclitaxel

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

  DT Modulation1

SLC22A3 protein affects the susceptibility to Paclitaxel [60]

Regulation Mechanism

Transcription Factor Info

  Papaverine

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

  DT Modulation1

Papaverine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [36]

Regulation Mechanism

Transcription Factor Info

  Parathion

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

  DT Modulation1

Parathion results in increased methylation of SLC22A3 promoter [57]

Regulation Mechanism

Transcription Factor Info

  pentanal

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

  DT Modulation1

pentanal results in decreased expression of SLC22A3 mRNA [25]

Regulation Mechanism

Transcription Factor Info

  Phentolamine

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

  DT Modulation1

Phentolamine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [36]

Regulation Mechanism

Transcription Factor Info

  Propafenone

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

  DT Modulation1

Propafenone inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [37]

Regulation Mechanism

Transcription Factor Info

  propionaldehyde

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

  DT Modulation1

propionaldehyde results in decreased expression of SLC22A3 mRNA [25]

Regulation Mechanism

Transcription Factor Info

  Propranolol

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

  DT Modulation1

Propranolol inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [37]

Regulation Mechanism

Transcription Factor Info

  pseudoisocyanine

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

  DT Modulation1

pseudoisocyanine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [8]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

SLC22A3 protein results in increased uptake of pseudoisocyanine [61]

Regulation Mechanism

Transcription Factor Info

  Quinidine

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

  DT Modulation1

Quinidine inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [1]

Regulation Mechanism

Transcription Factor Info

  Salmeterol Xinafoate

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

  DT Modulation1

SLC22A3 protein results in increased uptake of Salmeterol Xinafoate [47]

Regulation Mechanism

Transcription Factor Info

  Serotonin

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

  DT Modulation1

SLC22A3 protein results in increased uptake of Serotonin [55]

Regulation Mechanism

Transcription Factor Info

  Silicon Dioxide

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

  DT Modulation1

Silicon Dioxide analog results in decreased expression of SLC22A3 mRNA [62]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Silicon Dioxide analog results in increased expression of SLC22A3 mRNA [63]

Regulation Mechanism

Transcription Factor Info

  SK&F 550

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

  DT Modulation1

SK&F 550 inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [8]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

SK&F 550 results in decreased activity of SLC22A3 protein [8]

Regulation Mechanism

Transcription Factor Info

  sodium arsenite

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

  DT Modulation1

sodium arsenite results in decreased expression of SLC22A3 mRNA [30]

Regulation Mechanism

Transcription Factor Info

  Sodium Dodecyl Sulfate

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

  DT Modulation1

Sodium Dodecyl Sulfate results in decreased expression of SLC22A3 mRNA [64]

Regulation Mechanism

Transcription Factor Info

  Spironolactone

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

  DT Modulation1

Spironolactone inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [37]

Regulation Mechanism

Transcription Factor Info

  Sulpiride

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

  DT Modulation1

SLC22A3 protein results in increased uptake of Sulpiride [61]

Regulation Mechanism

Transcription Factor Info

  terbufos

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

  DT Modulation1

terbufos results in increased methylation of SLC22A3 promoter [57]

Regulation Mechanism

Transcription Factor Info

  tert-Butylhydroperoxide

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

  DT Modulation1

tert-Butylhydroperoxide affects the expression of SLC22A3 mRNA [18]

Regulation Mechanism

Transcription Factor Info

  Tetrachlorodibenzodioxin

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

  DT Modulation1

Endosulfan inhibits the reaction Tetrachlorodibenzodioxin results in decreased expression of SLC22A3 mRNA [32]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Tetrachlorodibenzodioxin affects the expression of SLC22A3 mRNA [65]

Regulation Mechanism

Transcription Factor Info

  DT Modulation3

Tetrachlorodibenzodioxin results in decreased expression of SLC22A3 mRNA [40]

Regulation Mechanism

Transcription Factor Info

  thioperamide

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

  DT Modulation1

thioperamide inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [36]

Regulation Mechanism

Transcription Factor Info

  trimazosin

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

  DT Modulation1

trimazosin inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [36]

Regulation Mechanism

Transcription Factor Info

  Trimethoprim

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

  DT Modulation1

SLC22A3 protein results in increased transport of Trimethoprim [66]

Regulation Mechanism

Transcription Factor Info

  Verapamil

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

  DT Modulation1

Verapamil inhibits the reaction SLC22A3 protein results in increased uptake of 1-Methyl-4-phenylpyridinium [37]

Regulation Mechanism

Transcription Factor Info

  DT Modulation2

Verapamil inhibits the reaction SLC22A3 protein results in increased uptake of Metformin [38]

Regulation Mechanism

Transcription Factor Info

  Vinblastine

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

  DT Modulation1

SLC22A3 protein affects the susceptibility to Vinblastine [60]

Regulation Mechanism

Transcription Factor Info

  Vitamin K 3

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

  DT Modulation1

Vitamin K 3 affects the expression of SLC22A3 mRNA [18]

Regulation Mechanism

Transcription Factor Info

  zinc protoporphyrin

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

  DT Modulation1

lead acetate co-treated with zinc protoporphyrin results in increased expression of SLC22A3 mRNA [59]

Regulation Mechanism

Transcription Factor Info
References
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2 Drug specificity and intestinal membrane localization of human organic cation transporters (OCT). Biochem Pharmacol. 2005 Dec 5;70(12):1851-60.
3 Transport of dicationic drugs pentamidine and furamidine by human organic cation transporters. Drug Metab Dispos. 2009 Feb;37(2):424-30.
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10 Differential pharmacological in vitro properties of organic cation transporters and regional distribution in rat brain. Neuropharmacology. 2006 Jun;50(8):941-52.
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12 Mifepristone induced progesterone withdrawal reveals novel regulatory pathways in human endometrium. Mol Hum Reprod. 2007 Sep;13(9):641-54.
13 Reproducible chemical-induced changes in gene expression profiles in human hepatoma HepaRG cells under various experimental conditions. Toxicol In Vitro. 2009 Apr;23(3):466-75.
14 Physiological and toxicological transcriptome changes in HepG2 cells exposed to copper. Physiol Genomics. 2009 Aug 7;38(3):386-401.
15 Contribution of organic cation transporter 3 to cisplatin cytotoxicity in human cervical cancer cells. J Pharm Sci. 2012 Jan;101(1):394-404.
16 Predictive toxicology using systemic biology and liver microfluidic "on chip" approaches: application to acetaminophen injury. Toxicol Appl Pharmacol. 2012 Mar 15;259(3):270-80.
17 Acute hypersensitivity of pluripotent testicular cancer-derived embryonal carcinoma to low-dose 5-aza deoxycytidine is associated with global DNA Damage-associated p53 activation, anti-pluripotency and DNA demethylation. PLoS One. 2012;7(12):e53003.
18 Time series analysis of oxidative stress response patterns in HepG2: a toxicogenomics approach. Toxicology. 2013 Apr 5;306:24-34.
19 Gene Expression Regulation and Pathway Analysis After Valproic Acid and Carbamazepine Exposure in a Human Embryonic Stem Cell-Based Neurodevelopmental Toxicity Assay. Toxicol Sci. 2015 Aug;146(2):311-20.
20 LSD1 activates a lethal prostate cancer gene network independently of its demethylase function. Proc Natl Acad Sci U S A. 2018 May 1;115(18):E4179-E4188.
21 Bringing in vitro analysis closer to in vivo: Studying doxorubicin toxicity and associated mechanisms in 3D human microtissues with PBPK-based dose modelling. Toxicol Lett. 2018 Sep 15;294:184-192.
22 Integrating multiple omics to unravel mechanisms of Cyclosporin A induced hepatotoxicity in vitro. Toxicol In Vitro. 2015 Apr;29(3):489-501.
23 Comparison of phenotypic and transcriptomic effects of false-positive genotoxins, true genotoxins and non-genotoxins using HepG2 cells. Mutagenesis. 2011 Sep;26(5):593-604.
24 Characterization of formaldehyde's genotoxic mode of action by gene expression analysis in TK6 cells. Arch Toxicol. 2013 Nov;87(11):1999-2012.
25 Integrated analysis of microRNA and mRNA expression profiles highlights aldehyde-induced inflammatory responses in cells relevant for lung toxicity. Toxicology. 2015 Aug 6;334:111-21.
26 Defensive and adverse energy-related molecular responses precede tris (1, 3-dichloro-2-propyl) phosphate cytotoxicity. J Appl Toxicol. 2016 May;36(5):649-58.
27 Inhibition of organic cation transporter (OCT) activities by carcinogenic heterocyclic aromatic amines. Toxicol In Vitro. 2019 Feb;54:10-22.
28 Transcriptome and DNA Methylome Dynamics during Triclosan-Induced Cardiomyocyte Differentiation Toxicity. Stem Cells Int. 2018 Oct 29;2018:8608327.
29 Assessment of a 72-hour repeated exposure to Swedish snus extract and total particulate matter from 3R4F cigarette smoke on gingival organotypic cultures. Food Chem Toxicol. 2019 Mar;125:252-270.
30 Dynamic alteration in miRNA and mRNA expression profiles at different stages of chronic arsenic exposure-induced carcinogenesis in a human cell culture model of skin cancer. Arch Toxicol. 2021 Jul;95(7):2351-2365.
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33 Identification of early target genes of aflatoxin B1 in human hepatocytes, inter-individual variability and comparison with other genotoxic compounds. Toxicol Appl Pharmacol. 2012 Jan 15;258(2):176-87.
34 Transcriptional profiling of human bronchial epithelial cell BEAS-2B exposed to diesel and biomass ultrafine particles. BMC Genomics. 2018 Apr 27;19(1):302.
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36 Activation of the extraneuronal monoamine transporter (EMT) from rat expressed in 293 cells. Br J Pharmacol. 2002;137(6):910-8.
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41 Transcriptome profile analysis of saturated aliphatic aldehydes reveals carbon number-specific molecules involved in pulmonary toxicity. Chem Res Toxicol. 2014 Aug 18;27(8):1362-70.
42 Rapid nongenomic actions of inhaled corticosteroids on long-acting (2)-agonist transport in the airway. Pulm Pharmacol Ther. 2011;24(6):654-9.
43 Binary PAH mixtures cause additive or antagonistic effects on gene expression but synergistic effects on DNA adduct formation. Carcinogenesis. 2007;28(12):2632-40.
44 Air pollution and DNA methylation alterations in lung cancer: A systematic and comparative study. Oncotarget. 2017;8(1):1369-1391.
45 DNA methylome-wide alterations associated with estrogen receptor-dependent effects of bisphenols in breast cancer. Clin Epigenetics. 2019;11(1):138.
46 Comparative Analysis of Transcriptomic Changes including mRNA and microRNA Expression Induced by the Xenoestrogens Zearalenone and Bisphenol A in Human Ovarian Cells. Toxins (Basel). 2023;15(2).
47 The effect of corticosteroids on the disposal of long-acting beta2-agonists by airway smooth muscle cells. J Allergy Clin Immunol. 2007;120(5):1103-9.
48 Cadmium acute exposure induces metabolic and transcriptomic perturbations in human mature adipocytes. Toxicology. 2022;470:153153.
49 Evaluation of Cd-induced cytotoxicity in primary human keratinocytes. Hum Exp Toxicol. 2024;43:9603271231224458.
50 Cannabidiol disrupts tryptophan metabolism in the human term placenta. Toxicology. 2024;505:153813.
51 Identification of potential target genes of ROR-alpha in THP1 and HUVEC cell lines. Exp Cell Res. 2017;353(1):6-15.
52 Activation of AIFM2 enhances apoptosis of human lung cancer cells undergoing toxicological stress. Toxicol Lett. 2016 Sep 6;258:227-236.
53 Alterations of histone modifications by cobalt compounds. Carcinogenesis. 2009;30(7):1243-51.
54 Integrative "-Omics" Analysis in Primary Human Hepatocytes Unravels Persistent Mechanisms of Cyclosporine A-Induced Cholestasis. Chem Res Toxicol. 2016 Dec 19;29(12):2164-2174.
55 Selective transport of monoamine neurotransmitters by human plasma membrane monoamine transporter and organic cation transporter 3. J Pharmacol Exp Ther. 2010;335(3):743-53.
56 Transforming growth factor beta1 targets estrogen receptor signaling in bronchial epithelial cells. Respir Res. 2018 Aug 30;19(1):160.
57 DNA methylation alterations in response to pesticide exposure in vitro. Environ Mol Mutagen. 2012;53(7):542-9.
58 Transport of lamivudine [(-)-beta-L-2',3'-dideoxy-3'-thiacytidine] and high-affinity interaction of nucleoside reverse transcriptase inhibitors with human organic cation transporters 1, 2, and 3. J Pharmacol Exp Ther. 2009;329(1):252-61.
59 Analysis of lead toxicity in human cells. BMC Genomics. 2012;13:344.
60 Gene expression profiling of 30 cancer cell lines predicts resistance towards 11 anticancer drugs at clinically achieved concentrations. Int J Cancer. 2006;118(7):1699-712.
61 Multiple drug transporters mediate the placental transport of sulpiride. Arch Toxicol. 2017 Dec;91(12):3873-3884.
62 High-throughput, quantitative assessment of the effects of low-dose silica nanoparticles on lung cells: grasping complex toxicity with a great depth of field. BMC Genomics. 2015;16(1):315.
63 Transcriptional responses of human aortic endothelial cells to nanoconstructs used in biomedical applications. Mol Pharm. 2013;10(8):3242-52.
64 CXCL14 downregulation in human keratinocytes is a potential biomarker for a novel in vitro skin sensitization test. Toxicol Appl Pharmacol. 2020;386:114828.
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