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FAAH

FAAH

货号 产品名 CAS号 信息
CSN12175 URB-597 546141-08-6 URB-597 is fatty acid amide hydrolase (FAAH, IC50 = 4.6 nM) inhibitor without effect on other cannabinoid-related targets.
CSN23087 SA 47 792236-07-8 SA 47 is a selective and potent inhibitor of fatty acid amide hydrolase (FAAH) and carbamate[1].
CSN23088 SA 57 1346169-63-8 Potent FAAH inhibitor
CSN12801 PF-3845 1196109-52-0 PF-3845 is a potent, selective and irreversible FAAH inhibitor with Ki of 230 nM, showing negligible activity against FAAH2.
CSN23022 Palmitoylisopropylamide 189939-61-5 Palmitoylisopropylamide is an inhibitor of fatty acid amide hydrolase (FAAH).
CSN25339 MAFP 188404-10-6 MAFP is a potent, irreversible inhibitor of fatty acid amide hydrolase (FAAH, anandamide amidase), the enzyme responsible for anandamide hydrolysis (IC50 = 2.5 nM). MAFP also binds irreversibly to CB1 receptors with IC50 of 20 nM.
CSN16816 LY2183240 874902-19-9 LY2183240 is a highly potent blocker of anandamide uptake (IC50 = 270 pM).
CSN17567 JZL 195 1210004-12-8 JZL195 functions as a dual inhibitor of FAAH and MAGL with IC50 of 13 nM and 19 nM respectively in brain of mouse.
CSN16558 JNJ-1661010 681136-29-8 JNJ-1661010 is a selective inhibitor of FAAH with IC50 of 10 nM (rat) and 12 nM (human).
CSN11599 FAAH-IN-2 184475-71-6 FAAH-IN-2 is an inhibitor of fatty acid amide hydrolase (FAAH).
CSN16758 FAAH Inhibitor 1 326866-17-5 FAAH inhibitor 1 is a potent fatty acid amide hydrolase (FAAH) inhibitor with an IC50 of 18±8 nM.
CSN12351 Biochanin A 491-80-5 Biochanin A, a phytoestrogen from Trifolium pratense, is an inhibitor of PTK with IC50 of 91.5 μM. It also can be metabolized in vivo to genistein.
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