Name | CABOTEGRAVIR SODIUM |
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Synonyms |
S-265744B
Oxazolo[3,2-a]pyrido[1,2-d]pyrazine-8-carboxamide, N-[(2,4-difluorophenyl)methyl]-2,3,5,7,11,11a-hexahydro-6-hydroxy-3-methyl-5,7-dioxo-, sodium salt, (3S,11aR)- (1:1) 3L12PT535M CABOTEGRAVIR SODIUM Sodium (3S,11aR)-8-[(2,4-difluorobenzyl)carbamoyl]-3-methyl-5,7-dioxo-2,3,5,7,11,11a-hexahydro[1,3]oxazolo[3,2-a]pyrido[1,2-d]pyrazin-6-olate GSK1265744B |
Description | Cabotegravir sodium is a highly potent HIV integrase inhibitor with an IC50 value of 2.5 nM for HIVADA. Cabotegravir sodium is primarily metabolized by uridine diphosphate glucuronosyltransferase (UGT) 1A1, with low potential to interact with other antiretroviral drugs (ARVs)[1]. |
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Related Catalog | |
Target |
IC50: 2.5 nM (HIVADA)[1] |
References |
Molecular Formula | C19H16F2N3NaO5 |
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Molecular Weight | 427.334 |
Exact Mass | 427.095581 |