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MK-6169

Chemical Structure : MK-6169

CAS No.: 1620479-63-1

MK-6169 (MK6169;MK 6169)

Catalog No.: PC-63367Not For Human Use, Lab Use Only.

MK-6169 is a potent, pan-genotype HCV NS5A inhibitor with replicon EC90 of 1-33 nM, retains potency against common resistance-associated substitutions in the major genotypes.

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Purity & Documentation Purity: >98% (HPLC)

Biological Activity

MK-6169 is a potent, pan-genotype HCV NS5A inhibitor with replicon EC90 of 1-33 nM, retains potency against common resistance-associated substitutions in the major genotypes; shows <10X shift on a majority of the genotypes and mutants tested, other than several mutants, such as GT3a Y93H and GT3a L31V, also show good potency on prototypical GT1a NS3 RASs such as GT1a R155K and GT1a V36M+R155K double substitution, as well as prototypical GT1b NS3 RASs such as GT1b A156T and GT1b D168Y; exhibits good pharmacokinetics in both rat and dog.

Physicochemical Properties

M.Wt 1016.203
Formula C54H62FN9O8S
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

Methyl ((S)-2-((S)-2-(5-((S)-6-(5-cyclopropylthiophen-2-yl)-1-fluoro-3-(2-((S)-1-((methoxycarbonyl)-L-valyl)pyrrolidin-2-yl)-1H-imidazol-5-yl)-6H-benzo[5,6][1,3]oxazino[3,4-a]indol-10-yl)-1H-imidazol-2-yl)pyrrolidin-1-yl)-1-((R)-2,2-dimethyltetrahydro-2H-

References

1. Yu W, et al. J Med Chem. 2018 Apr 21. doi: 10.1021/acs.jmedchem.7b01927.

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