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1034474-19-5

1034474-19-5 Structure

1034474-19-5 Structure
IdentificationBack Directory
[Name]

3-(1-((1H-pyrazolo[3,4-b]pyridin-3-yl)Methyl)-5-chloro-1H-indazol-4-yloxy)-5-chlorobenzonitrile
[CAS]

1034474-19-5
[Synonyms]

3-(1-((1H-pyrazolo[3,4-b]pyridin-3-yl)Methyl)-5-chloro-1H-indazol-4-yloxy)-5-chlorobenzonitrile
-((1-((1H-pyrazolo[3,4-b]pyridin-3-yl)Methyl)-5-chloro-1H-indazol-4-yl)oxy)-5-chlorobenzonitrile
[EINECS(EC#)]

680-612-8
[Molecular Formula]

C21H12Cl2N6O
[MOL File]

1034474-19-5.mol
[Molecular Weight]

435.27
Chemical PropertiesBack Directory
[Boiling point ]

656.4±55.0 °C(Predicted)
[density ]

1.55±0.1 g/cm3(Predicted)
[pka]

9.43±0.40(Predicted)
Hazard InformationBack Directory
[Uses]

MK-6186 is a novel non-nucleoside reverse transcriptase inhibitor with sub-nanomolar activity against wild-type viruses and the two most common NNRTI-resistant RT mutants (K103N and Y181C). MK-6186 exhibits excellent antiviral activity against K103N and Y181C mutant viruses. When MK-6186 targets 12 common NNRTI-associated mutant viruses, only two relatively rare mutants (Y188L and V106I/Y188L) show high resistance, with FC values exceeding 100, while the FC values of the remaining viruses are all below 10. In addition, when MK-6186 faces 96 clinical virus isolates carrying NNRTI-resistant mutations, most (70%) viruses show more than 10-fold resistance to efavirenz (EFV), while only 29% of mutant viruses show more than 10-fold resistance to MK-6186[1].
[References]

[1] Antiviral activity and in vitro mutation development pathways of MK-6186, a novel nonnucleoside reverse transcriptase inhibitor
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