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Details

Stereochemistry ABSOLUTE
Molecular Formula C10H15N3O4
Molecular Weight 241.2438
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BEA-005

SMILES

NC1=NC(=O)N(C=C1)[C@H]2C[C@H](CO)[C@@H](CO)O2

InChI

InChIKey=WZGBNAXNHRMYLG-ZXFLCMHBSA-N
InChI=1S/C10H15N3O4/c11-8-1-2-13(10(16)12-8)9-3-6(4-14)7(5-15)17-9/h1-2,6-7,9,14-15H,3-5H2,(H2,11,12,16)/t6-,7-,9-/m1/s1

HIDE SMILES / InChI

Molecular Formula C10H15N3O4
Molecular Weight 241.2438
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 3 / 3
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Comparative studies of 2',3'-didehydro-2',3'-dideoxythymidine (D4T) with other pyrimidine nucleoside analogues.
1990
Prevention of simian immunodeficiency virus, SIVsm, or HIV-2 infection in cynomolgus monkeys by pre- and postexposure administration of BEA-005.
1997 Feb
Synthesis and antiviral activity of prodrugs of the nucleoside 1-[2',3'-dideoxy-3'-C-(hydroxymethyl)-beta-D-erythropentofuranosyl] cytosine.
1998 May
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 09:47:49 GMT 2023
Edited
by admin
on Sat Dec 16 09:47:49 GMT 2023
Record UNII
C7BPP68MLT
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BEA-005
Common Name English
CYTIDINE, 2',3'-DIDEOXY-3'-(HYDROXYMETHYL)-
Systematic Name English
Code System Code Type Description
PUBCHEM
451819
Created by admin on Sat Dec 16 09:47:50 GMT 2023 , Edited by admin on Sat Dec 16 09:47:50 GMT 2023
PRIMARY
EPA CompTox
DTXSID60157443
Created by admin on Sat Dec 16 09:47:50 GMT 2023 , Edited by admin on Sat Dec 16 09:47:50 GMT 2023
PRIMARY
FDA UNII
C7BPP68MLT
Created by admin on Sat Dec 16 09:47:50 GMT 2023 , Edited by admin on Sat Dec 16 09:47:50 GMT 2023
PRIMARY
CAS
132235-73-5
Created by admin on Sat Dec 16 09:47:50 GMT 2023 , Edited by admin on Sat Dec 16 09:47:50 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY