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 64 products of "FAAH"
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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:250.25JZL195
CAS:JZL195 is a selective and efficacious dual FAAH/MAGL inhibitor.Formula:C24H23N3O5Purity:99.81%Color and Shape:SolidMolecular weight:433.46Biochanin A
CAS:Biochanin A: an isoflavone from red clover with anticancer properties and inhibits FAAH.Formula:C16H12O5Purity:97.1% - 98.97%Color and Shape:SolidMolecular weight:284.26PF-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:>99.99%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€MAGL-IN-4
CAS:MAGL-IN-4 (His121 ARG57) is one of the monoacylglycerol lipase (MAGL) inhibitors in central nervous system-related diseases.Formula:C18H21ClN2O4Purity:99.79%Color and Shape:SolidMolecular weight:364.82Ref: TM-T9687
1mg133.00€5mg326.00€1mL*10mM (DMSO)353.00€10mg485.00€25mg803.00€50mg1,063.00€100mg1,431.00€URB-597
CAS:URB-597 (FAAH Inhibitor II) is an effective, orally bioavailable FAAH inhibitor (IC50: 4.6 nM), and no effect on other cannabinoid-related targets.Formula:C20H22N2O3Purity:97.20% - 98.24%Color and Shape:SolidMolecular weight:338.4FAAH-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:393.79SA57
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:338.83Acetylhydrolase-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:481.6OL-135
CAS:OL-135: CNS-accessible, potent, selective FAAH inhibitor with analgesic effects in animals, no motor impairment.Formula:C21H22N2O2Color and Shape:SolidMolecular weight:334.41FAAH-IN-7
FAAH-IN-7: Reversible FAAH inhibitor, IC50=8.29 nM, reduces oxidative stress, neuroprotective in neuroinflammation.Formula:C26H29N3O4Color and Shape:SolidMolecular weight:447.53FAAH-IN-5
CAS:FAAH-IN-5 (Compound 7) selectively, irreversibly inhibits FAAH (IC50: 10.5 nM) with low PAMPA permeability.Formula:C21H19N3O6SColor and Shape:SolidMolecular weight:441.46URB-694
CAS:URB-694 is a fatty acid amide hydrolase (FAAH) inhibitor.Formula:C19H21NO3Color and Shape:SolidMolecular weight:311.37MDPD
CAS:MDPD boosts AtFAAH, the enzyme degrading NAEs in Arabidopsis, reducing NAE 12:0's growth inhibition.Formula:C21H19N3O3Color and Shape:SolidMolecular weight:361.39TAK 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:299.36FAAH 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: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€
