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FAAH

FAAH

货号 产品名 CAS号 信息
CSN25682 VDM 11 313998-81-1 VDM 11 is a selective inhibitor of the anandamide membrane transporter (AMT) with IC50 values of 4 - 11 μM.
CSN27279 URB937 1357160-72-5 URB937 is a FAAH inhibitor and increases anandamide levels, with an IC50 of 26.8 nM. URB937 fails to affect FAAH activity in the brain .
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.
CSN23139 FAAH-IN-6 1143578-94-2 TAK-21d is a potent FAAH Inhibitor.
CSN29449 SSR411298 666860-59-9 SSR411298 is a highly selective, brain penetrant and orally-active inhibitor of FAAH with IC50 of 62.5 nM (mouse brain FAAH).
CSN23087 SA 47 792236-07-8 SA 47 is a selective and potent inhibitor of fatty acid amide hydrolase (FAAH) and carbamate[1].
CSN23088 SA57 1346169-63-8 Potent FAAH inhibitor
CSN23040 PF 750 959151-50-9 PF-750 is an irreversible fatty acid amide hydrolase (FAAH) inhibitor with IC50 of 16.2 nM.
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 N-(Pyridazin-3-yl)-4-(3-((5-(trifluoromethyl)pyridin-2-yl)oxy)benzylidene)piperidine-1-carboxamide 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.
CSN23028 PDP-EA 861891-72-7 PDP-EA is an activator at FAAH.
CSN23022 Palmitoylisopropylamide 189939-61-5 Palmitoylisopropylamide is an inhibitor of fatty acid amide hydrolase (FAAH).
CSN29523 (9Z,12Z,15Z)-N-Benzyloctadeca-9,12,15-trienamide 883715-18-2 N-​Benzyllinolenamide is a natural macamide isolated from Lepidium meyenii, acts as an inhibitor of fatty acid amide hydrolase (FAAH) with an IC50 of 41.8 μM.
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.
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 4-((3-Chloro-4-fluorophenyl)amino)-7-methoxyquinazolin-6-ol 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 5,7-Dihydroxy-3-(4-methoxyphenyl)-4H-chromen-4-one 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.
CSN20266 BIA 10-2474 1233855-46-3 BIA10-2474 is an inhibitor of fatty acid amide hydrolase (FAAH) with IC50 of 4.9 nM.
CSN62693 FP-Biotin 259270-28-5
CSN68154 AA38-3 65815-76-1
CSN81205 N-Arachidonoylserotonin 187947-37-1
CSN108142 UCM710 213738-77-3
CSN102911 4-(4,4-Bis(4-fluorophenyl)butyl)-N-ethylpiperazine-1-carboxamide 75529-73-6
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