EMBL-EBI | Chemical Biology | ChEBI
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| ChEBI ID | CHEBI:202940 |
| ChEBI Name | carbovir |
| Stars | |
| Definition | Cyclopent-2-en-1-ylmethanol in which the 4-position is substituted by a 2-amino-6-hydroxy-9H-purin-9-yl group such that the two substitutents on the cyclopentene ring are in a cis relationship. The (−)-enantiomer, also known as carbovir, is a potent inhibitor of HIV replication replication in cell cultures. |
| Last Modified | 27 September 2010 |
| Formula | |
| Net Charge | 0 |
| Average Mass | 247.253 |
| Roles Classification |
|---|
| Biological Role: | HIV-1 reverse transcriptase inhibitor An entity which inhibits the activity of HIV-1 reverse transcriptase. |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| carbovir (CHEBI:202940) has role HIV-1 reverse transcriptase inhibitor (CHEBI:53756) |
| carbovir (CHEBI:202940) is a 2-aminopurines (CHEBI:20702) |
| Incoming Relation(s) |
| (−)-carbovir (CHEBI:421843) is a carbovir (CHEBI:202940) |
| IUPAC Name |
|---|
| 2-amino-9-[rel-(1R,4S)-4-(hydroxymethyl)cyclopent-2-en-1-yl]-1,9-dihydro-6H-purin-6-one |
| Synonyms | Source |
|---|---|
| 2-amino-9-[rel-(1R,4S)-4-(hydroxymethyl)cyclopent-2-en-1-yl]-9H-purin-6-ol | IUPAC |
| cis-2-amino-9-(4-hydroxymethylcyclopent-2-enyl)-9H-purin-6-ol | ChEBI |
| cis-2-amino-1,9-dihydro-9-(4-(hydroxymethyl)-2-cyclopenten-1-yl)-6H-purin-6-one | ChEBI |
| cis-(±)-2-amino-1,9-dihydro-9-(4-(hydroxymethyl)-2-cyclopenten-1-yl)-6H-purin-6-one | ChEBI |
| carbovir | ChemIDplus |
| (±)-carbovir | ChEBI |
| Registry Numbers | Sources |
|---|---|
| CAS:118353-05-2 | ChemIDplus |
| Citations |
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