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Chemical compound
MK-4409
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2-[5-[5-(5-Chloropyridin-2-yl)sulfanyl-2-(4-fluorophenyl)-1,3-oxazol-4-yl]pyridin-2-yl]propan-2-ol
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Formula | C22H17FN3O2S |
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Molar mass | 406.46 g·mol−1 |
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3D model (
JSmol) | |
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c3nc(C(O)(C)C)ccc3-c1nc(-c4ccc(F)cc4)oc1Sc(nc2)ccc2Cl
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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
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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.
[1]
[2]
See also
References
External links
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"MK 4409". Adis Insight. Springer Nature Switzerland AG.
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