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
CC1=CN([C@H]2C[C@H](N)[C@@H](CO)O2)C(=O)NC1=O
InChI
InChIKey=ADVCGXWUUOVPPB-XLPZGREQSA-N
InChI=1S/C10H15N3O4/c1-5-3-13(10(16)12-9(5)15)8-2-6(11)7(4-14)17-8/h3,6-8,14H,2,4,11H2,1H3,(H,12,15,16)/t6-,7+,8+/m0/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 |
|---|---|---|
| 3D-QSAR studies on antitubercular thymidine monophosphate kinase inhibitors based on different alignment methods. | 2006-02-15 |
|
| Thymidine and thymidine-5'-O-monophosphate analogues as inhibitors of Mycobacterium tuberculosis thymidylate kinase. | 2003-09-15 |
|
| Prophylactic contraceptives for HIV/AIDS. | 1999-12-03 |
|
| Aryl phosphate derivatives of bromo-methoxy-azidothymidine are dual-function spermicides with potent anti-human immunodeficiency virus. | 1998-09 |
|
| Enhanced in vitro inhibition of HIV-1 replication by 3'-fluoro-3'-deoxythymidine compared to several other nucleoside analogs. | 1988-12 |
|
| Synthesis and antiviral activity of various 3'-azido, 3'-amino, 2',3'-unsaturated, and 2',3'-dideoxy analogues of pyrimidine deoxyribonucleosides against retroviruses. | 1987-02 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:34:15 GMT 2025
by
admin
on
Mon Mar 31 21:34:15 GMT 2025
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| Record UNII |
7W21M0C25B
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| Record Status |
Validated (UNII)
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| Record Version |
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DTXSID00966879
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7W21M0C25B
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108074
Created by
admin on Mon Mar 31 21:34:15 GMT 2025 , Edited by admin on Mon Mar 31 21:34:15 GMT 2025
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