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FAAH
| Cat. No. | Product Name | CAS No. | Information |
|---|---|---|---|
| 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. |
| CSN16926 | PF-04457845 | 1020315-31-4 | PF-04457845 selectively inhibits FAAH with an IC50 of 7.2 nM. It has anti-inflammatory effects and is used as analgesic. |
| 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. |
| CSN17723 | JNJ-42165279 | 1346528-50-4 | JNJ-42165279 inhibits hFAAH and rFAAH with IC50 of 70 8 nM and 313 28 nM respectively. |
| 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 188 nM |
| CSN12351 | Biochanin A | 491-80-5 | Biochanin A, a phytoestrogen from Trifolium pratense, is an inhibitor of PTK with IC50 of 91.5 M. It also can be metabolized in vivo to genistein. |
| CSN20266 | BIA 10-2474 | 1233855-46-3 | BIA10-2474 is an inhibitor of fatty acid amide hydrolase FAAH with IC50 of 49 nM |
| CSN22677 | AM 1172 | 251908-92-6 | |
| CSN23040 | PF-750 | 959151-50-9 | |
| CSN23022 | Palmitoylisopropylamide | 189939-61-5 | |
| CSN23028 | PDP-EA | 861891-72-7 | |
| CSN23088 | SA 57 | 1346169-63-8 | |
| CSN23087 | SA 47 | 792236-07-8 | |
| CSN23139 | TAK 21d | 1143578-94-2 | |
| CSN23152 | TC-F 2 | 1304778-15-1 |
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