JNJ1661010 [Ligand Id: 5206] activity data from GtoPdb and ChEMBL

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ChEMBL ligand: CHEMBL460273 (JNJ-1661010)
  • Fatty acid amide hydrolase/Anandamide amidohydrolase in Human [ChEMBL: CHEMBL2243] [GtoPdb: 1400] [UniProtKB: O00519]
  • Fatty acid amide hydrolase/Anandamide amidohydrolase in Rat [ChEMBL: CHEMBL3229] [GtoPdb: 1400] [UniProtKB: P97612]
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  • Fatty acid amide hydrolase-2 in Human [GtoPdb: 1401] [UniProtKB: Q6GMR7]
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DB Assay description Assay Type Standard value Standard parameter Original value Original units Original parameter Reference
Fatty acid amide hydrolase/Anandamide amidohydrolase in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2243] [GtoPdb: 1400] [UniProtKB: O00519]
ChEMBL Inhibition of human FAAH preincubated for 10 mins B 7.15 pIC50 70 nM IC50 Bioorg Med Chem Lett (2008) 18: 4838-4843 [PMID:18693015]
ChEMBL Inhibition of human FAAH preincubated for 20 mins B 7.48 pIC50 33 nM IC50 Bioorg Med Chem Lett (2008) 18: 4838-4843 [PMID:18693015]
ChEMBL Inhibition of FAAH B 7.48 pIC50 33 nM IC50 Bioorg Med Chem Lett (2009) 19: 4241-4244 [PMID:19515560]
ChEMBL Inhibition of FAAH B 7.48 pIC50 33 nM IC50 Bioorg Med Chem Lett (2011) 21: 4674-4685 [PMID:21764305]
GtoPdb - - 7.8 pIC50 15.8 nM IC50 Bioorg Med Chem Lett (2008) 18: 4838-43 [PMID:18693015]
ChEMBL Inhibition of human FAAH preincubated for 40 mins B 7.82 pIC50 15 nM IC50 Bioorg Med Chem Lett (2008) 18: 4838-4843 [PMID:18693015]
ChEMBL Inhibition of human FAAH after 60 mins B 7.92 pIC50 12 nM IC50 Bioorg Med Chem Lett (2008) 18: 4838-4843 [PMID:18693015]
ChEMBL Apparent inhibition of human FAAH expressed in CHO-K1 cells using ethanolamine 1-3[H] as substrate after 30 mins by liquid scintillation counting B 7.96 pIC50 11 nM IC50 Bioorg Med Chem (2013) 21: 28-41 [PMID:23218778]
Fatty acid amide hydrolase/Anandamide amidohydrolase in Rat (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3229] [GtoPdb: 1400] [UniProtKB: P97612]
ChEMBL Inhibition of rat FAAH preincubated for 20 mins B 7.47 pIC50 34 nM IC50 Bioorg Med Chem Lett (2008) 18: 4838-4843 [PMID:18693015]
ChEMBL Inhibition of rat FAAH B 7.47 pIC50 34 nM IC50 Bioorg Med Chem Lett (2011) 21: 4674-4685 [PMID:21764305]
ChEMBL Inhibition of rat FAAH assessed as hydrolysis of anandamido-amino-methyl-cumarin B 8 pIC50 10 nM IC50 Bioorg Med Chem Lett (2011) 21: 2492-2496 [PMID:21392988]
Fatty acid amide hydrolase-2 in Human [GtoPdb: 1401] [UniProtKB: Q6GMR7]
GtoPdb 20 min preincubation - 5.24 pIC50 5700 nM IC50 Anesth Analg (2009) 108: 316-29 [PMID:19095868]

ChEMBL data shown on this page come from version 33:

Mendez D, Gaulton A, Bento AP, Chambers J, De Veij M, Félix E, Magariños MP, Mosquera JF, Mutowo P, Nowotka M, Gordillo-Marañón M, Hunter F, Junco L, Mugumbate G, Rodriguez-Lopez M, Atkinson F, Bosc N, Radoux CJ, Segura-Cabrera A, Hersey A, Leach AR. (2019) 'ChEMBL: towards direct deposition of bioassay data' Nucleic Acids Res., 47(D1). DOI: 10.1093/nar/gky1075. [EPMCID:30398643]
Davies M, Nowotka M, Papadatos G, Dedman N, Gaulton A, Atkinson F, Bellis L, Overington JP. (2015) 'ChEMBL web services: streamlining access to drug discovery data and utilities.' Nucleic Acids Res., 43(W1). DOI: 10.1093/nar/gkv352. [EPMCID:25883136]