General Information
Drug ID
DR01175
Drug Name
Didanosine
Synonyms
69655-05-6; 9-(2,3-Dideoxy-beta-D-ribofuranosyl)-6-oxopurine; 9-[(2R,5R)-5-(HYDROXYMETHYL)TETRAHYDROFURAN-2-YL]-1,9-DIHYDRO-6H-PURIN-6-ONE; 9-[(2R,5S)-5-(hydroxymethyl)tetrahydrofuran-2-yl]-1,9-dihydro-6H-purin-6-one; BMY 40900; BMY-40900; CHEBI:490877; DDI; DIDEOXYINOSINE; DRG-0016; DSSTox_CID_2927; Didanosina; Didanosina [INN-Spanish]; Didanosinum; Didanosinum [INN-Latin]; Inosine, 2',3'-dideoxy-; K3GDH6OH08; NCGC00090691-03; NCGC00159514-02; NSC 612049; UNII-K3GDH6OH08; Videx; Videx EC; ddIno; didanosine
Drug Type
Small molecular drug
Indication Human immunodeficiency virus infection [ICD11:1C62.Z] Approved [1]
Therapeutic Class
Anti-HIV Agents
Structure
3D MOL 2D MOL
Formula
C10H12N4O3
Canonical SMILES
C1CC(OC1CO)N2C=NC3=C2N=CNC3=O
InChI
InChI=1S/C10H12N4O3/c15-3-6-1-2-7(17-6)14-5-13-8-9(14)11-4-12-10(8)16/h4-7,15H,1-3H2,(H,11,12,16)/t6-,7+/m0/s1
InChIKey
BXZVVICBKDXVGW-NKWVEPMBSA-N
CAS Number
CAS 69655-05-6
Pharmaceutical Properties Molecular Weight 236.23 Topological Polar Surface Area 88.7
Heavy Atom Count 17 Rotatable Bond Count 2
Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 5
XLogP
-1.2
PubChem CID
135398739
PubChem SID
103529091 ,12014245 ,14847321 ,15121787 ,15121788 ,15196316 ,17389541 ,22431600 ,25819905 ,26719672 ,26754510 ,26757698 ,29215491 ,34715128 ,46386730 ,46506255 ,46508438 ,48415887 ,48422196 ,48422428 ,48423223 ,48424479 ,49681777 ,49718183 ,56463354 ,57313303 ,58717761 ,595889 ,596438 ,596681 ,597344 ,601538 ,602978 ,622273 ,77794640 ,7847362 ,7885163 ,7979070 ,7979071 ,81093234 ,833736 ,87351572 ,87559876 ,90451743 ,91612512 ,9168 ,92308421 ,92308956 ,92711314 ,92729668
ChEBI ID
CHEBI:490877
TTD Drug ID
D06FDR
DT(s) Transporting This Drug CNT2 Transporter Info Concentrative nucleoside transporter 2 Substrate [2]
References
1 Didanosine was approved by FDA. The official website of the U.S. Food and Drug Administration. (2019)
2 Clinical Nephrotoxins: Renal Injury from Drugs and Chemicals.

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