Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C10H10N4O3 |
| Molecular Weight | 234.2114 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC[C@H]1O[C@H](C=C1)N2C=NC3=C2N=CNC3=O
InChI
InChIKey=TYQPBHYPIRLWKU-NKWVEPMBSA-N
InChI=1S/C10H10N4O3/c15-3-6-1-2-7(17-6)14-5-13-8-9(14)11-4-12-10(8)16/h1-2,4-7,15H,3H2,(H,11,12,16)/t6-,7+/m0/s1
| Molecular Formula | C10H10N4O3 |
| Molecular Weight | 234.2114 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| cycloSal-Pronucleotides of 2',3'-dideoxyadenosine and 2', 3'-dideoxy-2',3'-didehydroadenosine: synthesis and antiviral evaluation of a highly efficient nucleotide delivery system. | 1999-05-06 |
|
| Comparative activity of 2',3'-saturated and unsaturated pyrimidine and purine nucleosides against human immunodeficiency virus type 1 in peripheral blood mononuclear cells. | 1988-10-01 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:18:42 GMT 2025
by
admin
on
Mon Mar 31 21:18:42 GMT 2025
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| Record UNII |
849Y7EQ734
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| Record Status |
Validated (UNII)
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| Record Version |
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| Code System | Code | Type | Description | ||
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DTXSID80195544
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135418295
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849Y7EQ734
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42867-68-5
Created by
admin on Mon Mar 31 21:18:42 GMT 2025 , Edited by admin on Mon Mar 31 21:18:42 GMT 2025
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| Related Record | Type | Details | ||
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PARENT -> IMPURITY |
In the chromatogram obtained with solution (2), the following peaks are eluted at the following relative retention with reference to didanosine (retention time about 13-15 min): impurity F about 0.8.
The area of any individual peak corresponding to impurity F is not greater than 0.2 times the area of the principal peak obtained with solution (4) (0.2%).
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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