L742791 [Ligand Id: 3467] activity data from GtoPdb and ChEMBL

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ChEMBL ligand: CHEMBL276257
  • β1-adrenoceptor/Beta-1 adrenergic receptor in Human [ChEMBL: CHEMBL213] [GtoPdb: 28] [UniProtKB: P08588]
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  • β2-adrenoceptor/Beta-2 adrenergic receptor in Human [ChEMBL: CHEMBL210] [GtoPdb: 29] [UniProtKB: P07550]
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  • β3-adrenoceptor/Beta-3 adrenergic receptor in Human [ChEMBL: CHEMBL246] [GtoPdb: 30] [UniProtKB: P13945]
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DB Assay description Assay Type Standard value Standard parameter Original value Original units Original parameter Reference
β1-adrenoceptor/Beta-1 adrenergic receptor in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL213] [GtoPdb: 28] [UniProtKB: P08588]
ChEMBL Evaluated for its agonist activity and the binding affinity against human Beta-1 adrenergic receptor in membranes from chinese hamster ovary cell B 6.77 pIC50 170 nM IC50 Bioorg Med Chem Lett (1998) 8: 2111-2116 [PMID:9873496]
ChEMBL Tested for binding affinity against cloned human beta-1 adrenergic receptor from CHO cells using [125I]iodocyanopindolol as the radioligand B 6.77 pIC50 170 nM IC50 Bioorg Med Chem Lett (1998) 8: 1101-1106 [PMID:9871716]
ChEMBL Compound was tested for agonist activity against cloned human beta-1 adrenergic receptor F 6.49 pEC50 320 nM EC50 Bioorg Med Chem Lett (1998) 8: 1101-1106 [PMID:9871716]
β2-adrenoceptor/Beta-2 adrenergic receptor in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL210] [GtoPdb: 29] [UniProtKB: P07550]
ChEMBL Evaluated for its agonist activity and the binding affinity against human Beta-2 adrenergic receptor in membranes from chinese hamster ovary cell B 6.92 pIC50 120 nM IC50 Bioorg Med Chem Lett (1998) 8: 2111-2116 [PMID:9873496]
ChEMBL Binding affinity against cloned human beta-2 adrenergic receptor from CHO cells using [125I]iodocyanopindolol as the radioligand B 6.92 pIC50 120 nM IC50 Bioorg Med Chem Lett (1998) 8: 1101-1106 [PMID:9871716]
β3-adrenoceptor/Beta-3 adrenergic receptor in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL246] [GtoPdb: 30] [UniProtKB: P13945]
ChEMBL Evaluated for its agonist activity against human Beta-3 adrenergic receptor F 8.8 pEC50 1.6 nM EC50 Bioorg Med Chem Lett (1998) 8: 2111-2116 [PMID:9873496]
ChEMBL Agonist activity against cloned human beta-3 adrenergic receptor F 8.8 pEC50 1.6 nM EC50 Bioorg Med Chem Lett (1998) 8: 1101-1106 [PMID:9871716]
GtoPdb - - 8.8 pEC50 1.6 nM EC50 Bioorg Med Chem Lett (1998) 8: 2111-6 [PMID:9873496]

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]