General Information
Drug ID
DR01330
Drug Name
Clofarabine
Synonyms
(2R,3R,4S,5R)-5-(6-amino-2-chloropurin-9-yl)-4-fluoro-2-(hydroxymethyl)oxolan-3-ol; 2-Chloro-9-(2-deoxy-2-fluoro-b-D-arabinofuranosyl)-9H-purin-6-amine; 2-Chloro-9-(2-deoxy-2-fluoro-beta-D-arabinofuranosyl)-9H-purin-6-amine; 2-Chloro-9-(2-deoxy-2-fluoro-beta-D-arabinofuranosyl)adenine; 2-Cl-2'-F-araA; 2-chloro-9-(2'-deoxy-2'-fluoro-beta-D-arabinofuranosyl)adenine; 3S211048; CAFdA; CFB; Cl-F-Ara-A; Clofarabina; Clofarabine (USAN/INN); Clofarabine [USAN]; Clofarabinum; Clofarex; Clolar; Clolar (TN); Clolar, Evoltra, Clofarabine; Evoltra; Evoltra (TN)
Drug Type
Small molecular drug
Indication Acute lymphoblastic leukemia [ICD11:2B33.0] Approved [1]
Juvenile myelomonocytic leukemia [ICD11:2A42] Approved [1]
Therapeutic Class
Anticancer Agents
Structure
3D MOL 2D MOL
Formula
C10H11ClFN5O3
Canonical SMILES
C1=NC2=C(N=C(N=C2N1C3C(C(C(O3)CO)O)F)Cl)N
InChI
InChI=1S/C10H11ClFN5O3/c11-10-15-7(13)5-8(16-10)17(2-14-5)9-4(12)6(19)3(1-18)20-9/h2-4,6,9,18-19H,1H2,(H2,13,15,16)/t3-,4+,6-,9-/m1/s1
InChIKey
WDDPHFBMKLOVOX-AYQXTPAHSA-N
CAS Number
CAS 123318-82-1
Pharmaceutical Properties Molecular Weight 303.68 Topological Polar Surface Area 119
Heavy Atom Count 20 Rotatable Bond Count 2
Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 8
XLogP
0.9
PubChem CID
119182
PubChem SID
8149071 ,10238376 ,10317422 ,12014412 ,14800615 ,14800616 ,29300120 ,46504968 ,47205855 ,50027432 ,56459308 ,57339361 ,71821361 ,77716344 ,81092867 ,92309003 ,92719465 ,93608050 ,99437031 ,99444025 ,103707445 ,104407717 ,109610765 ,118048878 ,124757091 ,125163895 ,126584329 ,126620778 ,126652234 ,126671067 ,129564367 ,134223319 ,134338128 ,135073562 ,135698306 ,136920392 ,136946661 ,136949087 ,137005624 ,141857409 ,143493352 ,144115841 ,144205735 ,152058774 ,152237732 ,152258941 ,160647786 ,160963976 ,162011506 ,162176704
ChEBI ID
CHEBI:681569
TTD Drug ID
D0R5RR
DT(s) Transporting This Drug BCRP Transporter Info Breast cancer resistance protein Substrate [2]
CNT3 Transporter Info Concentrative Na(+)-nucleoside cotransporter 3 Substrate [3]
ENT1 Transporter Info Equilibrative nucleoside transporter 1 Substrate [3]
ENT2 Transporter Info Equilibrative nucleoside transporter 2 Substrate [3]
References
1 Clofarabine was approved by FDA. The official website of the U.S. Food and Drug Administration. (2019)
2 Contribution of the drug transporter ABCG2 (breast cancer resistance protein) to resistance against anticancer nucleosides. Mol Cancer Ther. 2008 Sep;7(9):3092-102.
3 Cytarabine-resistant leukemia cells are moderately sensitive to clofarabine in vitro. Anticancer Res. 2014 Apr;34(4):1657-62.

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