Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C10H13ClN2O4 |
| Molecular Weight | 260.674 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CN([C@H]2C[C@H](Cl)[C@@H](CO)O2)C(=O)NC1=O
InChI
InChIKey=KQVJDKGDGLWBQT-XLPZGREQSA-N
InChI=1S/C10H13ClN2O4/c1-5-3-13(10(16)12-9(5)15)8-2-6(11)7(4-14)17-8/h3,6-8,14H,2,4H2,1H3,(H,12,15,16)/t6-,7+,8+/m0/s1
| Molecular Formula | C10H13ClN2O4 |
| Molecular Weight | 260.674 |
| 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 |
|---|---|---|
| Synthesis and in vitro antiviral activities of 3'-fluoro (or chloro) and 2',3'-difluoro 2',3'-dideoxynucleoside analogs against hepatitis B and C viruses. | 2010-11-01 |
|
| 3'-bromo analogues of pyrimidine nucleosides as a new class of potent inhibitors of Mycobacterium tuberculosis. | 2010-05-27 |
|
| 3'-substituted 2',3'-dideoxynucleoside analogues as potential anti-HIV (HTLV-III/LAV) agents. | 1987-08 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:31:13 GMT 2025
by
admin
on
Mon Mar 31 18:31:13 GMT 2025
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| Record UNII |
8GQZ0LXH0C
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| Record Status |
Validated (UNII)
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25526-94-7
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DTXSID10180226
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1724521
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| Related Record | Type | Details | ||
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PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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