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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. |
