URB-597

  Cat. No.:  DC7335   Featured
Chemical Structure
546141-08-6
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More than 5000 active chemicals with high quality for research!
Field of application
URB597 is a potent, orally bioavailable FAAH inhibitor with IC50 of 4.6 nM, with no activity on other cannabinoid-related targets.
Cas No.: 546141-08-6
Chemical Name: URB-597
Synonyms: 3'-Carbamoyl-[1,1'-biphenyl]-3-yl cyclohexylcarbamate;URB597;[3-(3-Carbamoylphenyl)phenyl] N-cyclohexylcarbamate;3'-carbamoylbiphenyl-3-yl cyclohexylcarbamate;Carbamic acid,N-cyclohexyl-, 3'-(aminocarbonyl)[1,1'-biphenyl]-3-yl ester;FAAH Inhibitor II;KDS4103;URB-597;KDS-4103;N-Cyclohexylcarbamic acid 3'-(aminocarbonyl)[1,1'-biphenyl]-3-yl ester;URB 597;3-(3-carbamoylphenyl)phenyl N-cyclohexylcarbamate;PX47LB88FO;Carbamic acid, N-cyclohexyl-, 3'-(aminocarbonyl)[1,1'-biphenyl]-3-yl ester;3′-Carbamoyl-biphenyl-3-yl-cyclohexylcarbamate;Cyclohexyl-carbamic acid 3'-carbamoyl-biphenyl-3-yl;Q7865591;SR-01000342602;CARBAMIC ACID, N-CYCLOHEXYL-, 3'-(AMINOCARBONYL)(1,1'-BIPHENYL)-3-YL ESTER;SCHEMBL93842;C16H23N5O.C4H4O4;HMS3648C09;HB2365;Cyclohexylcarbamic acid 3'-(Aminocarbonyl)-[1,1'-biphenyl]-3- yl ester;HMS3884N12;J-523541;HMS3656B07;EX-A769;SR-01000342602-3;3'-(aminocarbonyl)-[1,1'-biphenyl]-3-yl cyclohexylcarbamate;Org-231295;BDBM26739;NCGC00165915-01;ZINC01238258;AS-18410;3'-CARBAMOYL-BIPHENYL-3-YL-CYCLOHEXYLCARBAMATE;Cyclohexylcarbamic acid 3'-(Aminocarbonyl)-[1,1'-biphenyl]-3-yl ester;s2631;MLS001210199;DTXSID70203046;AC-26873;Cyclohexylcarbamic acid 3 -carbamoyl-biphenyl-3-yl ester;AKOS000674060;2-[(5-Methoxy-1H-indol-3-yl)methyle ne]-N-pentyl-hydrazinecarboximidamide maleate;NCGC00165915-03;3'-carbamoylbiphenyl 3-ylcyclohexylcarbamate;CHEBI:188061;SMR000524783;HMS2844K18;BU140504;BCP27727;3'-(3-aminocarbonyl)[1,1'-biphenyl]-3-yl)-cyclohexylcarbamat;3'-CarbaMoyl-biphenyl-3-yl cyclohexylcarbaMate;cyclohexyl carbamic acid 3'-carbamoylbiphenyl-3-yl ester;MLS006012031;CS-0266;SW219633-1;FT-0700483;HY-10864;Cyclohexyl-carbamic acid 3'-carbamoyl-biphenyl-3-yl ester;UNII-PX47LB88FO;URB597 (KDS-4103);CCG-207886;ROFVXGGUISEHAM-UHFFFAOYSA-N;CHEMBL184238;GTPL4339;NS00017274;A830267;FAAH Inhibitor II - CAS 546141-08-6;3'-(AMINOCARBONYL)(1,1'-BIPHENYL)-3-YL N-CYCLOHEXYLCARBAMATE;N-Cyclohexylcarbamc acd 3'-(amnocarbonyl)[1,1'-bphenyl]-3-yl ester;546141-08-6;URB597, >=98% (HPLC), powder;MFCD05863934;C20H22N2O3;CARBAMIC ACID, CYCLOHEXYL-, 3'-(AMINOCARBONYL)[1,1'-BIPHENYL]-3-YL ESTER;SR-01000342602-1;HB1800;3\\'-Carbamoyl-[1,1\\'-biphenyl]-3-yl cyclohexylcarbamate;3\\'-Carbamoyl-[1,1\\'-biphenyl]-3-yl cyclohexylcarbamate;3\\'-Carbamoyl-[1,1\\'-biphenyl]-3-yl cyclohexylcarbamate;3\\'-Carbamoyl-[1,1\\'-biphenyl]-3-yl cyclohexylcarbamate;BRD-K92169341-001-10-4;BRD-K92169341-001-10-4;BRD-K92169341-001-10-4;BRD-K92169341-001-10-4;DB-366359;DB-366359;DB-366359;3'-CARBAMOYL-[1,1'-BIPHENYL]-3-YL N-CYCLOHEXYLCARBAMATE;3'-CARBAMOYL-[1,1'-BIPHENYL]-3-YL N-CYCLOHEXYLCARBAMATE;3'-CARBAMOYL-[1,1'-BIPHENYL]-3-YL N-CYCLOHEXYLCARBAMATE;DB-366359;3'-Carbamoylbiphenyl-3-yl cyclohexylcarbamate;3'-Carbamoylbiphenyl-3-yl cyclohexylcarbamate;3'-Carbamoylbiphenyl-3-yl cyclohexylcarbamate;3'-CARBAMOYL-[1,1'-BIPHENYL]-3-YL N-CYCLOHEXYLCARBAMATE;BRD-K92169341-001-11-...
SMILES: O(C1=C([H])C([H])=C([H])C(C2C([H])=C([H])C([H])=C(C(N([H])[H])=O)C=2[H])=C1[H])C(N([H])C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H])=O
Formula: C20H22N2O3
M.Wt: 338.4003
Purity: >98%
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description: URB597 binds in the hydrophobic pocket and catalytic core of FAAH that connects the active site residues to the membrane surface of FAAH. URB597 inhibits FAAH activity in human liver microsomes with IC50 of 3 nM. URB597 reduces the expression of the LPS-induced enzymes cyclo-oxygenase 2 (COX-2) and inducible nitric oxide synthase (iNOS; NOS2) in primary rat microglial cell, with a concomitant reduction in the release of the inflammatory mediators prostaglandin E2 (PGE2) and (NO) nitric oxide. URB597 evokes Ca2+ entry in HEK293-F Cells transiently expressing human or rat TRPA1 gene. URB597 also activates Ca2+ entry in rat DRG neurons natively expressed TRPA1 channels. URB597 inhibits [3H]anandamide hydrolysis in rat brain membranes with a parallel increase in brain anandamide, OEA, and PEA content by inhibition of FAAH. URB597 enhances the hypothermia effect induced by ethanolamide by inhibiting FAAH. [5] When delivered intraperitonealy (0.3 mg/kg) URB597 reduces allodynia and hyperalgesia through cannabinoid CB1 and CB2 receptor-mediated analgesia in rats with inflammatory pain. [6] URB597 reduces the reduction in body weight gain and sucrose intake induced by the chronic mild stress in rats through inhibition of brain FAAH activity. [7] URB597 could reverse most depressive-like symptoms induced by adolescent THC exposure in femal rats. [8]For the detailed information of URB-597, the solubility of URB-597 in water, the solubility of URB-597 in DMSO, the solubility of URB-597 in PBS buffer, the animal experiment (test) of URB-597, the cell expriment (test) of URB-597, the in vivo, in vitro and clinical trial test of URB-597, the EC50, IC50,and Affinity of URB-597, Please contact DC Chemicals.
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
Cat. No. Product name Field of application
DC7335 URB-597 URB597 is a potent, orally bioavailable FAAH inhibitor with IC50 of 4.6 nM, with no activity on other cannabinoid-related targets.
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