ChemicalBook--->CAS DataBase List--->870005-19-9

870005-19-9

870005-19-9 Structure

870005-19-9 Structure
IdentificationBack Directory
[Name]

MK-2048
[CAS]

870005-19-9
[Synonyms]

CS-235
MK-2048
(6S)-2-[(3-Chloro-4-fluorophenyl)methyl]-N,8-diethyl-1,2,6,7,8,9-hexahydro-10-hydroxy-6-methyl
(6S)-2-[(3-chloro-4-fluorophenyl)Methyl]-N,8-diethyl-1,2,6,7,8,9-hexahydro-10-hydroxy-6-Methyl-1,9-dioxo-
(6S)-2-[(3-Chloro-4-fluorophenyl)methyl]-N,8-diethyl-1,2,6,7,8,9-hexahydro-10-hydroxy-6-methyl-1,9-dioxo-pyrazino[1',2':1,5]pyrrolo[2,3-d]pyridazine-4-carboxam
(6S)-2-[(3-chloro-4-fluorophenyl)methyl]-N,8-diethyl-1,2,6,7,8,9-hexahydro-10-hydroxy-6-methyl-1,9-dioxo-pyrazino[1',2':1,5]pyrrolo[2,3-d]pyridazine-4-carboxamide
Pyrazino[1',2':1,5]pyrrolo[2,3-d]pyridazine-4-carboxamide, 2-[(3-chloro-4-fluorophenyl)methyl]-N,8-diethyl-1,2,6,7,8,9-hexahydro-10-hydroxy-6-methyl-1,9-dioxo-, (6S)-
[Molecular Formula]

C22H23ClFN5O4
[MOL File]

870005-19-9.mol
[Molecular Weight]

475.9
Chemical PropertiesBack Directory
[Melting point ]

>240°C (dec.)
[density ]

1.52±0.1 g/cm3(Predicted)
[storage temp. ]

-20°C Freezer
[solubility ]

DMSO (Slightly), Methanol (Slightly)
[form ]

Solid
[pka]

6.52±0.40(Predicted)
[color ]

Yellow
Hazard InformationBack Directory
[Uses]

MK-2048 represents a prototype second generation integrase strand transfer inhibitor (INSTI), it was developed with the goal of retaining activity against viruses containing mutations assiciated with resistance of first-generation INSTIs, raltegravir (R100312). MK-2048 exhibits inhibitory activity towards HIV integrase and towards HIV replication. It is four times more effective in inhibiting HIV enzyme integrase than the first generation inhibitor, raltegravir.
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