Chemical structure
Cat.No.
Product Name
CAS no.
Target
Biochanin A, an O-methylated isoflavone from Trifolium pratense, inhibits protein tyrosine kinase (PTK) of epidermal growth factor receptor with IC50 values of 91.5 &muM.
YN373282 N-Benzylpalmitamide 74058-71-2
N-Benzylpalmitamide is a macamide isolated fromLepidium meyenii, acts as an inhibitor offatty acid amide hydrolase (FAAH).
YN370227 Acetylhydrolase-IN-1 79637-91-5
Acetylhydrolase-IN-1 is a 1-Alkyl-2-acetylglycerophosphocholine esterase (Alkylacetyl-GPC: acetylhydrolase) inhibtor.
YN372695 FAAH-IN-2 184475-71-6
FAAH-IN-2 is an inhibitor of fatty acid amide hydrolase (FAAH).
YN370424 FAAH inhibitor 1 326866-17-5
FAAH inhibitor 1 (Benzothiazole analog 3) is a potentfatty acid amide hydrolase (FAAH)inhibitor with an IC50 of 18±8nM.
URB597 is a potent, orally bioavailable FAAH inhibitor with IC50 of 4.6 nM, with no activity on other cannabinoid-related targets. Phase 1.
YN373392 JNJ-1661010 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.
SA 47 is a selective and potent inhibitor offatty acid amide hydrolase (FAAH) and carbamate.
YN373289 N-(3-Methoxybenzyl)Palmitam... 847361-96-0
N-(3-Methoxybenzyl)Palmitamide is a promising inhibitor ofFAAHfor the treatment of pain, inflammation and CNS degenerative disorders.
YN370429 LY2183240 874902-19-9
LY-2183240 is a potent, covalent inhibitor of the EC-degrading enzyme fatty acid amide hydrolase (FAAH). LY-2183240 disrupts the cellular uptake of the lipid endocannabinoid (EC) anandamide and promote analgesia in vivo. ...
YN373313 N-Benzyllinolenamide 883715-18-2
N-Benzyllinolenamide is a natural macamide isolated fromLepidium meyenii, acts as an inhibitor of fatty acid amide hydrolase (FAAH) with an IC50 of 41.8μM.
YN373381 N-Benzyloleamide 883715-21-7
N-Benzyloleamide is a maccamide isolated fromLepidium meyenii(Maca). N-Benzyloleamide irreversibly inhibits fatty acid amide hydrolase(FAAH). N-benzyloleamide influences the energy metabolism and reveals antioxidant and antif...
PF 750 is a selective and covalentfatty acid amide hydrolase (FAAH)inhibitor, with IC50 svaried from 16.2-595nM in different pre-incubation times. Covalently modifies the enzyme’s active site serine nucleophile.
YN372200 PF-04457845 1020315-31-4
PF-04457845 is a potent, favorable selective inhibitor of Fatty acid amide hydrolase (FAAH) with IC50 of 7.2 nM and 7.4 nM for hFAAH and rFAAH, respectively. PF-04457845 covalently modifies the active-site serine...
PF-3845 is a potent, selective and irreversible FAAH inhibitor with Ki of 230 nM, showing negligible activity against FAAH2.
JZL195 is a potent inhibitor of both FAAH and MAGL with IC50s of 2 and 4 nM respectively.
YN372572 BIA 10-2474 1233855-46-3
BIA 10-2474 is a novel fatty acid amide hydrolase (FAAH) inhibitor, with a potent inhibitory effect upon FAAH and prolonged action in vivo.
SA57 is a potent, selectiveFAAHinhibitor with IC50s of 3.2nM and 1.9nM formouse and human FAAH. SA57 also inhibits the 2-arachidonoylglycerol hydrolasesMAGL(IC50s of 410nM and 1.4μM formouse and human MAG...
YN372561 JNJ-42165279 1346528-50-4
JNJ-42165279 (JNJ-5279) is an inhibitor of fatty acid amide hydrolase (FAAH) that inhibits recombinant human and rat FAAH with IC50 of 70 nM and 313 nM, respectively.
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