dideoxyadenosine

PubChem Notes:

Dideoxyadenosine A dideoxynucleoside compound in which the 3'-hydroxy group on the sugar moiety has been replaced by a hydrogen. This modification prevents the formation of phosphodiester linkages which are needed for the completion of nucleic acid chains. The compound is an inhibitor of HIV replication, acting as a chain-terminator of viral DNA by binding to reverse transcriptase. Its principal side effect is nephrotoxicity. In vivo, dideoxyadenosine is rapidly metabolized to DIDANOSINE (ddI) by enzymatic deamination; ddI is then converted to dideoxyinosine monophosphate and ultimately to dideoxyadenosine triphosphate, the putative active metabolite.

Molecular Formula: C10H13N5O2


InChI: InChI=1/C10H13N5O2/c11-9-8-10(13-4-12-9)15(5-14-8)7-2-1-6(3-16)17-7/h4-7,16H,1-3H2,(H2,11,12,13)/t6-,7+/m0/s1/f/h11H2

InChIKey: InChIKey=WVXRAFOPTSTNLL-JANDEZSGDA
SMILES: C1CC(OC1CO)N2C=NC3=C2N=CN=C3N

Names:
    ADENOSINE, 2',3'-DIDEOXY-
    BRN 0619924
    CCRIS 428
    ddAdo
    dideoxyadenosine
    DRG-0039
    EINECS 223-853-2
    NSC 98700
    NSC-98700
    2',3'-Dideoxyadenosine
    [(2S,5R)-5-(6-aminopurin-9-yl)oxolan-2-yl]methanol

Registries:
    PubChem CID 20039
    PubChem ID 162883