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MK-4409
Другие языки:

    MK-4409

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    MK-4409
    MK-4409 structure.svg
    Clinical data
    ATC code
    • None
    Legal status
    Legal status
    Identifiers
    • 2-[5-[5-(5-Chloropyridin-2-yl)sulfanyl-2-(4-fluorophenyl)-1,3-oxazol-4-yl]pyridin-2-yl]propan-2-ol
    CAS Number
    PubChem CID
    ChemSpider
    UNII
    ChEMBL
    Chemical and physical data
    Formula C22H17FN3O2S
    Molar mass 406.46 g·mol−1
    3D model (JSmol)
    • c3nc(C(O)(C)C)ccc3-c1nc(-c4ccc(F)cc4)oc1Sc(nc2)ccc2Cl
    • InChI=1S/C22H17ClFN3O2S/c1-22(2,28)17-9-5-14(11-25-17)19-21(30-18-10-6-15(23)12-26-18)29-20(27-19)13-3-7-16(24)8-4-13/h3-12,28H,1-2H3
    • Key:DBZMCSVIITXLCC-UHFFFAOYSA-N

    MK-4409 is an experimental drug which acts as a potent and selective inhibitor of the enzyme fatty acid amide hydrolase (FAAH), with an IC50 of 11 nM, and both analgesic and antiinflammatory effects in animal studies. It was studied for the treatment of neuropathic pain and progressed to early stage human clinical trials by 2009.

    See also

    External links

    • "MK 4409". Adis Insight. Springer Nature Switzerland AG.

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