Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C11H13N5O2 |
| Molecular Weight | 247.2532 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC1=NC2=C(N=CN2[C@H]3C[C@@H](CO)C=C3)C(=O)N1
InChI
InChIKey=XSSYCIGJYCVRRK-NKWVEPMBSA-N
InChI=1S/C11H13N5O2/c12-11-14-9-8(10(18)15-11)13-5-16(9)7-2-1-6(3-7)4-17/h1-2,5-7,17H,3-4H2,(H3,12,14,15,18)/t6-,7+/m0/s1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Asymmetric synthesis and antiviral activities of L-carbocyclic 2', 3'-didehydro-2',3'-dideoxy and 2',3'-dideoxy nucleosides. | 1999-08-26 |
|
| Activities of (-)-carbovir and 3'-azido-3'-deoxythymidine against human immunodeficiency virus in vitro. | 1990-06 |
|
| Resolution of racemic carbovir and selective inhibition of human immunodeficiency virus by the (-) enantiomer. | 1990-05-16 |
Patents
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
CPG1J3583K
Created by
admin on Mon Mar 31 20:21:42 GMT 2025 , Edited by admin on Mon Mar 31 20:21:42 GMT 2025
|
PRIMARY | |||
|
135538685
Created by
admin on Mon Mar 31 20:21:42 GMT 2025 , Edited by admin on Mon Mar 31 20:21:42 GMT 2025
|
PRIMARY | |||
|
124915-24-8
Created by
admin on Mon Mar 31 20:21:42 GMT 2025 , Edited by admin on Mon Mar 31 20:21:42 GMT 2025
|
PRIMARY |
SUBSTANCE RECORD
