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FAAH

Chemical structure

Cat.No.

Product Name

CAS no.

Target

  • YN372213 Biochanin A 491-80-5

    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.

  • YN370427 URB-597 546141-08-6

    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.

  • YN372469 SA 47 792236-07-8

    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...

  • YN372470 PF 750 959151-50-9

    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...

  • YN372201 PF-3845 1196109-52-0

    PF-3845 is a potent, selective and irreversible FAAH inhibitor with Ki of 230 nM, showing negligible activity against FAAH2.

  • YN372273 JZL195 1210004-12-8

    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.

  • YN370275 SA57 1346169-63-8

    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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