Fatty Acid Amide Hydrolase

Fatty acid amide hydrolase, (FAAH, Oleamide hydrolase, Anandamide amidohydrolase), is an integral membrane protein that hydrolyzes bioactive amides, including anandamide, to free fatty acid and ethanolamine. FAAH belongs to the serine hydrolase enzyme family.

Products for Fatty Acid Amide Hydrolase

  1. Cat.No. Product Name Information/Activity
  2. BCC7075 AACOCF3 Phospholipase A<sub>2</sub> inhibitor AACOCF3 chemical structure
  3. BCC7675 AM 1172 FAAH inhibitor; also anandamide uptake inhibitor and CB receptor partial agonist AM 1172 chemical structure
  4. BCC7500 Arachidonyl serotonin 187947-37-1 Arachidonyl serotonin chemical structure
  5. BCC2315 JNJ-1661010 JNJ-1661010 (Takeda-25) a potent and selective fatty acid amide hydrolase (FAAH) inhibitor with IC50s of 34 and 33 nM for rat FAAH and human FAAH, respectively. JNJ-1661010 can cross the blood-brain barrier and used as broad-spectrum analgesics. JNJ-1661010 chemical structure
  6. BCC7966 JZL 195 JZL195 is a selective and efficacious dual fatty acid amide hydrolase (FAAH) and monoacylglycerol lipase (MAGL) inhibitor with IC50s of 2 and 4 nM, respectively. JZL 195 chemical structure
  7. BCC1718 LY2183240 LY2183240 is a novel and highly potent blocker of anandamide uptake (IC50 = 270 pM). LY2183240 chemical structure
  8. BCC7187 Palmitoylisopropylamide 189939-61-5 Palmitoylisopropylamide chemical structure
  9. BCC2326 PF-3845 PF-3845 is a selective fatty acid amide hydrolase (FAAH) inhibitor (Ki = 0.23 μM); showing negligible activity against FAAH2. PF-3845 chemical structure
  10. BCC7641 PF 750 PF 750 is a selective and covalent fatty acid amide hydrolase (FAAH) inhibitor, with IC50s varied from 16.2-595 nM in different pre-incubation times. Covalently modifies the enzyme’s active site serine nucleophile. PF 750 chemical structure
  11. BCC6289 SA 47 SA 47 is a selective and potent inhibitor of fatty acid amide hydrolase (FAAH) and carbamate. SA 47 chemical structure

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