Term Name: entecavir (anhydrous)
Synonyms: 2-amino-9-[(1S,3R,4S)-4-hydroxy-3-(hydroxymethyl)-2-methylidenecyclopentyl]-1,9-dihydro-6H-purin-6-one, entecavir
Definition: Guanine substituted at the 9 position by a 4-hydroxy-3-(hydroxymethyl)-2-methylidenecyclopentyl group. A synthetic analogue of 2'-deoxyguanosine, it is a nucleoside reverse transcriptase inhibitor with selective antiviral activity against hepatitis B virus. Entecavir is phosphorylated intracellularly to the active triphosphate form, which competes with deoxyguanosine triphosphate, the natural substrate of hepatitis B virus reverse transcriptase, inhibiting every stage of the enzyme's activity, although it has no activity against HIV. It is used for the treatment of chronic hepatitis B.
Ontology: ChEBI [CHEBI:473990]  ( EBI )

Relationships
is a type of: 2-aminopurines oxopurine primary alcohol secondary alcohol
has_role: antiviral drug EC 2.7.7.49 (RNA-directed DNA polymerase) inhibitor
inverse has_part: entecavir hydrate