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
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
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
Title | Date | PubMed |
---|---|---|
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
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 09:47:49 GMT 2023
by
admin
on
Sat Dec 16 09:47:49 GMT 2023
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Record UNII |
C7BPP68MLT
|
Record Status |
Validated (UNII)
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Record Version |
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-
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451819
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DTXSID60157443
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C7BPP68MLT
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admin on Sat Dec 16 09:47:50 GMT 2023 , Edited by admin on Sat Dec 16 09:47:50 GMT 2023
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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
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Related Record | Type | Details | ||
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ACTIVE MOIETY |