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ChEMBL ligand: CHEMBL4297588 (A-4250, A4250, AR-H064974, AZD-8294, AZD8294, Bylvay, Odevixibat, Odevixibat sesquihydrate) |
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DB | Assay description | Assay Type | Standard value | Standard parameter | Original value | Original units | Original parameter | Reference |
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Sodium/bile acid and sulphated solute cotransporter 2 in Human [GtoPdb: 960] [UniProtKB: Q12908] | ||||||||
GtoPdb | Inhibition of glycocholic acid uptake via hASBT in vitro. | - | 9.8 | pIC50 | 0.16 | nM | IC50 | US9694018B1. IBAT inhibitors for the treatment of liver disease (2017) |
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]