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.
Products of "FAAH"
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AM 374
CAS:AM 374 (HDSF), a fatty acid amide hydrolase (FAAH) inhibitor, demonstrates the capacity to inhibit amidase activity, boasting an IC50 value of 13 nM.Formula:C16H33FO2SPurity:98.39%Color and Shape:SolidMolecular weight:308.5FAAH-IN-1
CAS:FAAH-IN-1 is a fatty acid amide hydrolase (FAAH) inhibitor, with IC50s of 145 nM and 650 nM for rat and human FAAH, respectively.Formula:C20H19ClN4OSPurity:98%Color and Shape:SolidMolecular weight:398.91N-Benzylpalmitamide
CAS:N-Benzylpalmitamide (Macamide 1) inhibits fatty acid amide hydrolase (FAAH) in a time-dependent manner and could potentially offer a good alternative for theFormula:C23H39NOPurity:97.08% - 99.77%Color and Shape:SolidMolecular weight:345.56PF-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:100%Color and Shape:SolidMolecular weight:455.43Ref: TM-T4323
2mg35.00€5mg52.00€10mg88.00€25mg163.00€50mg235.00€100mg419.00€200mg545.00€1mL*10mM (DMSO)58.00€LY2183240
CAS:LY2183240 inhibits fatty acid amide hydrolase (FAAH) activity (IC50 = 12.4 nM).Formula:C17H17N5OPurity:99.26%Color and Shape:SolidMolecular weight:307.35JP104
CAS:JP104 is an aryl carbamate that irreversibly inhibits fatty acid amide hydrolase (FAAH) with a pIC50 value of approximately 8 [1].Formula:C25H30N2O3Purity:98%Color and Shape:SolidMolecular weight:406.52AA38-3
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:250.25URB-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:98.24%Color and Shape:SolidMolecular weight:338.4N-(3-Methoxybenzyl)Palmitamide
CAS:N-(3-Methoxybenzyl)Palmitamide is a promising FAAH inhibitor, treatment of pain, inflammation and CNS degenerative disorders.Formula:C24H41NO2Purity:99.89%Color and Shape:SolidMolecular weight:375.59MAGL-IN-5
CAS:MAGL-IN-5 is a non-selective lipase inhibitor.Formula:C18H17N3O5Purity:99.9%Color and Shape:SolidMolecular weight:355.34Ref: TM-T9967
1mg35.00€5mg70.00€10mg96.00€25mg202.00€50mg323.00€100mg512.00€200mg738.00€1mL*10mM (DMSO)81.00€OMDM-1
CAS:OMDM-1 ((Z)-N-[(2S)-1-hydroxy-3-(4-hydroxyphenyl)propan-2-yl]octadec-9-enamide) is a selective and metabolically stable anandamide cellular uptake (ACU)Formula:C27H45NO3Purity:97.88%Color and Shape:SolidMolecular weight:431.65PF 750
CAS:PF 750 (ZINC27647189) is a selective and covalent inhibitor of FAAH. PF 750 shows IC50s varying from 16.2 to 595 nM in different incubation times.Formula:C22H23N3OPurity:98.83%Color and Shape:SolidMolecular weight:345.44Ref: TM-T16515
2mg39.00€5mg62.00€10mg87.00€25mg187.00€50mg298.00€100mg444.00€200mg635.00€500mg938.00€1mL*10mM (DMSO)67.00€URB937
CAS:URB937 is an inhibitor of FAAH and increases anandamide levels(IC50 : 26.8 nM).Formula:C20H22N2O4Purity:99.55%Color and Shape:SolidMolecular weight:354.4FAAH-IN-2
CAS:FAAH-IN-2 (O-Desmorpholinopropyl Gefitinib) is a potent inhibitor of FAAH(fatty acid amide hydrolase).Formula:C15H11ClFN3O2Purity:99.18%Color and Shape:Tan SolidMolecular weight:319.72MK-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:99.70% - 99.81%Color and Shape:SolidMolecular weight:441.911-Monomyristin
CAS:1-Monomyristin (2,3-Dihydroxypropyl tetradecanoate) , a 1-monoglyceride of myristic acid, has antibacterial activity against several Gram-positive bacterialFormula:C17H34O4Purity:99.58%Color and Shape:SolidMolecular weight:302.45JZL195
CAS:JZL195 is a selective and efficacious dual FAAH/MAGL inhibitor.Formula:C24H23N3O5Purity:99.81%Color and Shape:SolidMolecular weight:433.46SA57
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:338.83Isopropyl dodec-11-enylfluorophosphonate
CAS:Isopropyl dodec-11-enylfluorophosphonate (IDEFP) is an organophosphorus ester functioning as a central cannabinoid receptor (CB1) antagonist and exhibitsFormula:C15H30FO2PPurity:98%Color and Shape:SolidMolecular weight:292.37BIA 10-2474
CAS:BIA 10-2474 is a long-acting reversible inhibitor of FAAH that increases levels of the neurotransmitter anandamide in the nervous system.Formula:C16H20N4O2Purity:99.27%Color and Shape:SolidMolecular weight:300.36
