CHEBI:202940 - carbovir

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ChEBI Name carbovir
ChEBI ID CHEBI:202940
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.
Stars This entity has been manually annotated by the ChEBI Team.
Roles Classification
Biological Role(s): HIV-1 reverse transcriptase inhibitor
An entity which inhibits the activity of HIV-1 reverse transcriptase.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing carbovir (CHEBI:202940) has role HIV-1 reverse transcriptase inhibitor (CHEBI:53756)
carbovir (CHEBI:202940) is a 2-aminopurines (CHEBI:20702)
Incoming (−)-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 Sources
(±)-carbovir ChEBI
2-amino-9-[rel-(1R,4S)-4-(hydroxymethyl)cyclopent-2-en-1-yl]-9H-purin-6-ol IUPAC
carbovir ChemIDplus
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
cis-2-amino-9-(4-hydroxymethylcyclopent-2-enyl)-9H-purin-6-ol ChEBI
Registry Number Type Source
118353-05-2 CAS Registry Number ChemIDplus
Citations Types Sources
15916425 PubMed citation ChEMBL
18549801 PubMed citation Europe PMC
2296018 PubMed citation ChEMBL
Last Modified
27 September 2010