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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) Select Batch:

    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.
    MK-6169 shows <10X shift on a majority of the genotypes and mutants tested, other than several mutants, such as GT3a Y93H and GT3a L31V.
    MK-6169 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.
    MK-6169 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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