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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PDP-EA
CAS:PDP-EA is an activator of fatty acid amide hydrolase(FAAH) and enhances the amidohydrolase activity of FAAH.Formula:C25H43NO3Purity:98.06%Color and Shape:SolidMolecular weight:405.61OMDM-5
CAS:OMDM-5 is a potent vanilloid receptor type 1 (TRPV1, EC50 = 75 nM) agonist, showing weak ligand activity at cannabinoid type 1 receptor (CB1, Ki=4.9 μM).Formula:C26H44N2O3Purity:99.72%Color and Shape:SolidMolecular weight:432.64Ref: TM-T12306
1mg87.00€5mg187.00€10mg284.00€25mg452.00€50mg645.00€100mg867.00€200mg1,130.00€1mL*10mM (DMSO)221.00€FAAH inhibitor 1
CAS:FAAH inhibitor 1 (Benzothiazole analog 3) is an effective FAAH inhibitor with an IC50 of 18 nM.Formula:C24H23N3O3S3Purity:98.05%Color and Shape:SolidMolecular weight:497.65Ref: TM-T11256
1mg52.00€5mg116.00€10mg182.00€25mg306.00€50mg442.00€100mg620.00€200mg835.00€1mL*10mM (DMSO)128.00€ARN272
CAS:ARN272 is a FAAH-like anandamide transporter (FLAT) inhibitor (IC50: 1.8 μM).Formula:C27H20N4O2Purity:98.23%Color and Shape:SolidMolecular weight:432.47MAGL-IN-4
CAS:MAGL-IN-4 (His121 ARG57) is one of the monoacylglycerol lipase (MAGL) inhibitors in central nervous system-related diseases.Formula:C18H21ClN2O4Purity:≥98%Color and Shape:SolidMolecular weight:364.82Ref: TM-T9687
1mg140.00€5mg344.00€10mg512.00€25mg848.00€50mg1,121.00€100mg1,510.00€1mL*10mM (DMSO)373.00€VU534
CAS:VU534 is a NAPE-PLD agonist with an EC50 of 0.30 μM.VU534 is a dual inhibitor of FAAH and sEH, with an IC50 of 1.2 μM for sEH.VU534 is used in diseases relatedFormula:C21H22FN3O3S2Purity:99.22%Color and Shape:SolidMolecular weight:447.55Sob-AM2
CAS:Sob-AM2 is an effective substrate targeting the fatty acid amide hydrolase (FAAH) expressed in the brain, with a Km of 1.3 μM. It delivers higher concentrations of Sobetirome to the central nervous system at minimal peripheral systemic doses, thereby activating the central thyroid hormone receptor β (TRβ).Formula:C21H27NO3Color and Shape:SolidMolecular weight:341.44JNJ-1661010
CAS:JNJ-1661010 (Takeda-25) is an effective and specific FAAH inhibitor (IC50: 10/ 12 nM for rat/human), shows >100-fold selectivity for FAAH-1 than FAAH-2.Formula:C19H19N5OSPurity:99.79% - 99.97%Color and Shape:SolidMolecular weight:365.454-Nonylphenylboronic acid
CAS:4-Nonylphenylboronic acid is a inhibitor of FAAH.Formula:C15H25BO2Purity:97.63%Color and Shape:SolidMolecular weight:248.17Biochanin 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:284.26N-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:98.00% - 99.92%Color and Shape:SolidMolecular weight:367.57Ref: TM-TN1965
1mg88.00€5mg187.00€10mg281.00€25mg475.00€50mg692.00€100mg935.00€200mg1,264.00€1mL*10mM (DMSO)188.00€JNJ-40355003
CAS:JNJ-40355003 is a FAAH inhibitor that increases plasma levels of fatty acid amides in rats, dogs, and crabs.Formula:C23H23ClN4O2Purity:99.32%Color and Shape:SolidMolecular weight:422.91MK-3168 (12C)
CAS:MK-3168 (12C) functions as a FAAH inhibitor, exhibiting IC50 values of 1.0 nM, 5.5 nM, and 1.7 nM for human, rhesus, and rat respectively. It demonstrates effective brain uptake and FAAH-specific signaling. Additionally, 11 C MK-3168 is applicable as a FAAH PET tracer.Formula:C21H21ClN4OSColor and Shape:SolidMolecular weight:412.94Palmitoylisopropylamide
CAS:Palmitoylisopropylamide is a selective FAAH inhibitor that inhibits [H]-AEA uptake and cell proliferation at low concentrations.Formula:C19H39NOPurity:100%Color and Shape:SolidMolecular weight:297.52WWL 154
CAS:WWL 154 is an serine hydrolase (SH) and fatty acid amide hydrolase FAAH-4 inhibitor.Formula:C18H19N3O5Purity:99.22%Color and Shape:SolidMolecular weight:357.36Ref: TM-T8927
1mg46.00€5mg84.00€10mg106.00€25mg150.00€50mg207.00€100mg311.00€200mg444.00€1mL*10mM (DMSO)85.00€BuChE-IN-15
BuChE-IN-15, a chemical compound, exhibits potent inhibitory activity with IC50 values of 81 nM and 400 nM, respectively. It also demonstrates good blood-brain barrier permeability and neuroprotective properties, making it suitable for research in Alzheimer's disease.Formula:C18H18FNO4Color and Shape:SolidMolecular weight:331.34PF-3845
CAS:PF-3845 is a potent, selective and irreversible FAAH inhibitor with Ki of 230 nM, showing negligible activity against FAAH2.Formula:C24H23F3N4O2Purity:99.54% - 99.58%Color and Shape:SolidMolecular weight:456.46Ref: TM-T6043
2mg42.00€5mg59.00€10mg97.00€25mg205.00€50mg354.00€100mg560.00€200mg800.00€1mL*10mM (DMSO)59.00€SA 47
CAS:SA 47 is a selective and effective inhibitor of fatty acid amide hydrolase and carbamate.Formula:C17H26N4O3Purity:98%Color and Shape:SolidMolecular weight:334.41Carprofen
CAS:Carprofen (Ridamyl) is a propionic acid derivate and nonsteroidal anti-inflammatory drug (NSAID) with anti-inflammatory, analgesic, and antipyretic activities.Formula:C15H12ClNO2Purity:98.99% - 99.65%Color and Shape:SolidMolecular weight:273.71JNJ-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% - 99.89%Color and Shape:SolidMolecular weight:410.8Ref: TM-T3215
2mg46.00€5mg65.00€10mg96.00€25mg170.00€50mg246.00€100mg363.00€200mg512.00€1mL*10mM (DMSO)75.00€
