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FAAH

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FAAH

Chemical Structure Cat. No. Product Name CAS No.
CAY10499 Chemical Structure
 BCP46929 CAY10499 359714-55-9
CAY10499 is a potent and selective monoglyceride lipase inhibitor exhibiting an IC50 of 90 nM for the recombinant enzyme.
AA38-3 Chemical Structure
 BCP46457 AA38-3 65815-76-1
AA38-3 inhibites three SHs (ABHD6, ABHD11, and FAAH).
FAA1 agonist-1 Chemical Structure
 BCP39847 FAA1 agonist-1 2102196-57-4
FAA1 agonist-1, also known as MDK6574, is a FAA1 agonist.
4-Nonylphenylboronic acid Chemical Structure
 BCP36136 4-Nonylphenylboronic acid 256383-45-6
4-(n-nonyl) benzeneboronic acid is a potent inhibitor of FAAH, with an IC50 of 9.1 nM.
URB 937 Chemical Structure
 BCP35209 URB 937 1357160-72-5
URB 937 is a FAAH inhibitor and increases anandamide levels.
LY2183240 Chemical Structure
 BCP22610 LY2183240 874902-19-9
LY2183240 is a novel and highly potent blocker of anandamide uptake (IC50 = 270 pM).
ARN272 Chemical Structure
 BCP17386 ARN272 488793-85-7
ARN 272 is a FAAH-like anandamide transporter (FLAT) inhibitor (IC50 = 1.8 μM); cytosolic variant of FAAH-1 that binds anandamide.
JZL195 Chemical Structure
 BCP23894 JZL195 1210004-12-8
JZL195 is a selective and efficacious dual FAAH/MAGL inhibitor with IC50 of 13 nM and 19 nM for mouse brain FAAH and MAGL respectively.
BIA10-2474 Chemical Structure
 BCP29970 BIA10-2474 1233855-46-3
BIA 10-2474 is an inhibitor of fatty acid amide hydrolase (FAAH) with IC50 values of 50 to 70mg/kg in various rat brain regions.
JNJ1661010 Chemical Structure
 BCP06935 JNJ1661010 681136-29-8
JNJ-1661010 is a potent and selective FAAH inhibitor with IC50 of 10 nM (rat) and 12 nM (human), exhibits >100-fold selectivity for FAAH-1 when compared to FAAH-2.
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