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SA57
CAS No. : 1346169-63-8
Biological Activity：SA57 is a potent, selective FAAH inhibitor with IC50s of 3.2 nM and 1.9 nM for mouse and human FAAH. SA57 also inhibits the 2-arachidonoylglycerol hydrolases MAGL (IC50s of 410 nM and 1.4 μM for mouse and human MAGL) and mouse α/β-hydrolase domain-containing protein 6 (mABHD6; IC50 of 850 nM), but not other brain serine hydrolases[2].
Research Area：Neurological Disease
Targets：MAGL|FAAH
Related Small Molecules:JNJ-1661010;MAGL-IN-6;MK-4409;PF-06795071;JZL195;Carpro-AM1;N-Arachidonyl maleimide;FAAH-IN-6;ML-226;JW 642;WWL123;Euphol;SSR411298;FAAH inhibitor 1;N-Arachidonoylserotonin;Biochanin A;WWL154;JNJ-42165279;ABX-1431;JJKK 048;LEI-106;SAR629;PF-3845;DO-264;SA72;N-Benzyllinolenamide;FAAH-IN-2;FP-Biotin;FAAH-IN-5;LY2183240
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