Name | SureCN82803 |
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Synonyms |
(3S,11aR)-N-(2,4-Difluorobenzyl)-6-hydroxy-3-methyl-5,7-dioxo-2,3,5,7,11,11a-hexahydro[1,3]oxazolo[3,2-a]pyrido[1,2-d]pyrazine-8-carboxamide
Cabotegravir 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-, (3S,11aR)- GSK1265744A unii-hmh0132z1q |
Description | Cabotegravir is a potent HIV integrase inhibitor as an oral lead-in tablet and long-acting injectable for the treatment and prevention of HIV infection. Cabotegravir is an inhibitor of OAT1 (IC50 0.81 μM) and OAT3 (IC50 0.41 μM).IC50 value: 0.81 μM (OAT1), 0.41 μM (OAT3) [1]Target: OAT1, OAT3Cabotegravir is a potent HIV integrase inhibitor in clinical development as an oral lead-in tablet and long-acting injectable for the treatment and prevention of HIV infection.[2] Cabotegravir is an HIV-1 integrase inhibitor under development as a tablet for both oral lead-in therapy and long-acting (LA) injectable for intramuscular dosing.[3] |
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Related Catalog | |
References |
Density | 1.6±0.1 g/cm3 |
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Boiling Point | 664.0±55.0 °C at 760 mmHg |
Molecular Formula | C19H17F2N3O5 |
Molecular Weight | 405.352 |
Flash Point | 355.4±31.5 °C |
Exact Mass | 405.113617 |
PSA | 104.36000 |
LogP | -1.70 |
Vapour Pressure | 0.0±2.1 mmHg at 25°C |
Index of Refraction | 1.661 |
Storage condition | -20℃ |