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ChEMBL ligand: CHEMBL14227 (Butanoic acid) |
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DB | Assay description | Assay Type | Standard value | Standard parameter | Original value | Original units | Original parameter | Reference |
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FFA3 receptor/Free fatty acid receptor 3 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL5201] [GtoPdb: 227] [UniProtKB: O14843] | ||||||||
GtoPdb | - | - | 4.9 | pEC50 | - | - | - |
J Biol Chem (2003) 278: 11312-9 [PMID:12496283]; J Biol Chem (2003) 278: 25481-9 [PMID:12711604]; Proc Natl Acad Sci USA (2004) 101: 1045-50 [PMID:14722361]; J Biol Chem (2011) 286: 10628-40 [PMID:21220428] |
ChEMBL | Agonist activity at human GPCR41 transfected in HEK293 cells assessed as [35S]GTPgammaS binding by scintillation counting method | F | 4.92 | pEC50 | 12000 | nM | EC50 | J Med Chem (2018) 61: 47-61 [PMID:28745893] |
histone deacetylase 1/Histone deacetylase 1 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL325] [GtoPdb: 2658] [UniProtKB: Q13547] | ||||||||
ChEMBL | Inhibition of human recombinant HDAC1 | B | 4.8 | pIC50 | 16000 | nM | IC50 | ACS Med. Chem. Lett. (2011) 2: 39-42 [PMID:21874153] |
GtoPdb | - | - | 4.8 | pIC50 | 16000 | nM | IC50 | ACS Med Chem Lett (2010) 2: 39-42 [PMID:21874153] |
histone deacetylase 2/Histone deacetylase 2 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL1937] [GtoPdb: 2616] [UniProtKB: Q92769] | ||||||||
GtoPdb | - | - | 4.92 | pIC50 | 12000 | nM | IC50 | ACS Med Chem Lett (2010) 2: 39-42 [PMID:21874153] |
ChEMBL | Inhibition of human recombinant HDAC2 | B | 4.92 | pIC50 | 12000 | nM | IC50 | ACS Med. Chem. Lett. (2011) 2: 39-42 [PMID:21874153] |
histone deacetylase 3/Histone deacetylase 3 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL1829] [GtoPdb: 2617] [UniProtKB: O15379] | ||||||||
ChEMBL | Inhibition of human recombinant HDAC3 | B | 5.05 | pIC50 | 9000 | nM | IC50 | ACS Med. Chem. Lett. (2011) 2: 39-42 [PMID:21874153] |
GtoPdb | - | - | 5.05 | pIC50 | 9000 | nM | IC50 | ACS Med Chem Lett (2010) 2: 39-42 [PMID:21874153] |
histone deacetylase 8/Histone deacetylase 8 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3192] [GtoPdb: 2619] [UniProtKB: Q9BY41] | ||||||||
GtoPdb | - | - | 4.82 | pIC50 | 15000 | nM | IC50 | ACS Med Chem Lett (2010) 2: 39-42 [PMID:21874153] |
ChEMBL | Inhibition of human recombinant HDAC8 | B | 4.82 | pIC50 | 15000 | nM | IC50 | ACS Med. Chem. Lett. (2011) 2: 39-42 [PMID:21874153] |
OAT6/Solute carrier family 22 member 20 in Mouse (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL5269] [GtoPdb: 1037] [UniProtKB: Q80UJ1] | ||||||||
ChEMBL | Inhibition of mouse Oat6-mediated [3H]ES uptake in Xenopus oocytes after 1 hr | B | 4.09 | pKi | 82000 | nM | Ki | J. Biol. Chem. (2007) 282: 23841-23853 [PMID:17553798] |
ChEMBL | Inhibition of mouse Oat6-mediated [3H]ES uptake in Xenopus oocytes after 1 hr | B | 4.09 | pKi | 81283.05 | nM | Ki | J. Biol. Chem. (2007) 282: 23841-23853 [PMID:17553798] |
FFA2 receptor in Human [GtoPdb: 226] [UniProtKB: O15552] | ||||||||
GtoPdb | - | - | 4.6 | pEC50 | - | - | - |
J Biol Chem (2003) 278: 11312-9 [PMID:12496283]; Biochem Biophys Res Commun (2003) 303: 1047-52 [PMID:12684041]; J Biol Chem (2003) 278: 25481-9 [PMID:12711604]; J Biol Chem (2011) 286: 10628-40 [PMID:21220428] |
HCA2 receptor in Human [GtoPdb: 312] [UniProtKB: Q8TDS4] | ||||||||
GtoPdb | - | - | 2.8 | pEC50 | - | - | - |
ChEMBL data shown on this page come from version 31:
Gaulton A, Hersey A, Nowotka M, Bento AP, Chambers J, Mendez D, Mutowo P, Atkinson F, Bellis LJ, CibriƔn-Uhalte E, Davies M, Dedman N, Karlsson A, MagariƱos MP, Overington JP, Papadatos G, Smit I, Leach AR. (2017) 'The ChEMBL database in 2017.' Nucleic Acids Res., 45(D1). DOI: 10.1093/nar/gkw1074. [PMCID:5210557]