FAAH
Fatty Acid Amide Hydrolase (FAAH) is an enzyme that breaks down fatty acid amides, including endocannabinoids like anandamide. These compounds are involved in the regulation of pain, mood, appetite, and memory. Inhibition of FAAH can increase the levels of these signaling molecules, offering potential therapeutic benefits for pain, anxiety, and neurodegenerative diseases. At CymitQuimica, we offer a selection of FAAH inhibitors to support your research in neuroscience, pain management, and endocannabinoid signaling.
Found 62 products for "FAAH".
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PF-04457845
CAS:PF-04457845 is a greatly and effctive FAAH inhibitor, and for hFAAH(IC50=7.2±0.63 nM) and rFAAH(IC50=7.4±0.62 nM).Formula:C23H20F3N5O2Purity:99.93%Color and Shape:SolidMolecular weight:455.43Ref: TM-T4323
2mg34.00€5mg50.00€1mL*10mM (DMSO)55.00€10mg84.00€25mg155.00€50mg222.00€100mg396.00€200mg515.00€Biochanin A
CAS:Biochanin A: an isoflavone from red clover with anticancer properties and inhibits FAAH.Formula:C16H12O5Purity:97.59% - 98.97%Color and Shape:SolidMolecular weight:284.26JNJ-42165279
CAS:JNJ-42165279 selectively inactivates FAAH without notably affecting other enzymes, ion channels, receptors, or CYPs/hERG at 10 μM.Formula:C18H17ClF2N4O3Purity:99.88% - 99.95%Color and Shape:SolidMolecular weight:410.8Ref: TM-T3215
2mg43.00€5mg62.00€1mL*10mM (DMSO)72.00€10mg92.00€25mg161.00€50mg234.00€100mg344.00€200mg485.00€4-Nonylphenylboronic acid
CAS:4-Nonylphenylboronic acid is a inhibitor of FAAH.Formula:C15H25BO2Purity:97.63%Color and Shape:SolidMolecular weight:248.17N-Benzyllinolenamide
CAS:N-Benzyllinolenamide is a natural product. It is an inhibitor of fatty acid amide hydrolase (FAAH, IC50 of 41.8 μM).Formula:C25H37NOPurity:98.7% - 99.92%Color and Shape:SolidMolecular weight:367.57Ref: TM-TN1965
1mg81.00€5mg170.00€1mL*10mM (DMSO)177.00€10mg260.00€25mg440.00€50mg628.00€100mg872.00€200mg1,153.00€AA38-3
CAS:AA38-3 (1-Piperidinecarboxylic acid, 4-nitrophenyl ester) inhibites three SHs (ABHD6, ABHD11, and FAAH)Formula:C12H14N2O4Purity:99.56%Color and Shape:SolidMolecular weight:250.25FAAH inhibitor 2
CAS:FAAH Inhibitor 2 (Compound 17b) is an irreversible inhibitor of fatty acid amide hydrolase (FAAH), demonstrating an IC50 value of 0.153 μM [1].Formula:C24H40N2O2Color and Shape:SolidMolecular weight:388.59FAAH-IN-8
CAS:FAAH-IN-8 (compound 11) is a competitive inhibitor of FAAH with an IC50 of 6.7 nM and a Ki of 5 nM. It exhibits high blood-brain permeability and a significant antioxidant profile without neurotoxicity [1].Formula:C18H14N4OColor and Shape:SolidMolecular weight:302.33AKU-005
CAS:AKU-005 is a dual inhibitor of FAAH and MAGL, exhibiting IC50 values of 63 nM and 389 nM against rat and human FAAH, respectively. This compound has potential for researching trigeminal nociceptive hypersensitivity.Formula:C20H21N5OColor and Shape:SolidMolecular weight:347.41JNJ-40413269
CAS:JNJ-40413269 inhibits FAAH, engages central targets, and is effective in rat neuropathic pain.Formula:C19H15ClF3N3OColor and Shape:SolidMolecular weight:393.79TAK 21d
CAS:Potent FAAH inhibitorFormula:C19H17F2N7OPurity:98%Color and Shape:SolidMolecular weight:397.38Arachidonyl serotonin
CAS:Dual FAAH inhibitor/TRPV1 antagonistFormula:C30H42N2O2Purity:98%Color and Shape:SolidMolecular weight:462.67URB532
CAS:URB532 is an irreversible fatty acid amide hydrolase (FAAH) inhibitor.Formula:C18H21NO3Purity:98%Color and Shape:SolidMolecular weight:299.36JNJ-42165279 dihydrochloride
CAS:JNJ-42165279 (dihydrochloride) is an FAAH inhibitor with IC50 values of 70 nM for hFAAH and 313 nM for rFAAH, respectively [1].Formula:C18H19Cl3F2N4O3Color and Shape:SolidMolecular weight:483.72VDM 11
CAS:anandamide transport inhibitorFormula:C27H39NO2Purity:98%Color and Shape:SolidMolecular weight:409.6MK-4409
CAS:MK-4409, a potent and selective fatty acid amide hydrolase (FAAH) inhibitor, is being investigated for the treatment of inflammatory and neuropathic pain.Formula:C22H17ClFN3O2SPurity:99.80% - 99.87%Color and Shape:White SolidMolecular weight:441.91FAAH inhibitor 1
CAS:FAAH inhibitor 1 (Benzothiazole analog 3) is an effective FAAH inhibitor with an IC50 of 18 nM.Formula:C24H23N3O3S3Purity:99.6%Color and Shape:Yellow SolidMolecular weight:497.65Ref: TM-T11256
1mg38.00€5mg86.00€1mL*10mM (DMSO)94.00€10mg124.00€25mg203.00€50mg294.00€100mg411.00€200mg553.00€OL-135
CAS:OL-135: CNS-accessible, potent, selective FAAH inhibitor with analgesic effects in animals, no motor impairment.Formula:C21H22N2O2Color and Shape:SolidMolecular weight:334.41Acetylhydrolase-IN-1
CAS:Acetylhydrolase-IN-1 is an inhibitor of the esterase 1-Alkyl-2-acetylglycerophosphocholine (Alkylacetyl-GPC: acetylhydrolase).Formula:C23H48NO7PPurity:98%Color and Shape:SolidMolecular weight:481.6SA57
CAS:SA57 is a potent, selective inhibitor of FAAH(IC50s of 3.2 nM and 1.9 nM for mouse and human FAAH).Formula:C17H23ClN2O3Purity:98%Color and Shape:SolidMolecular weight:338.83
