Reaction Details |
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Target | Beta-1 adrenergic receptor |
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Ligand | BDBM50313929 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_615506 (CHEMBL1105984) |
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IC50 | 3100±n/a nM |
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Citation | Goble, SD; Wang, L; Howell, KL; Bansal, A; Berger, R; Brockunier, L; DiSalvo, J; Feighner, S; Harper, B; He, J; Hurley, A; Hreniuk, D; Parmee, E; Robbins, M; Salituro, G; Sanfiz, A; Streckfuss, E; Watkins, E; Weber, AE; Struthers, M; Edmondson, SD Heterocyclic acetamide and benzamide derivatives as potent and selective beta3-adrenergic receptor agonists with improved rodent pharmacokinetic profiles. Bioorg Med Chem Lett20:1895-9 (2010) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Beta-1 adrenergic receptor |
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Name: | Beta-1 adrenergic receptor |
Synonyms: | ADRB1 | ADRB1R | ADRB1_HUMAN | B1AR | Beta-1 adrenoceptor | Beta-1 adrenoreceptor | adrenergic Beta1 |
Type: | G Protein-Coupled Receptor (GPCR) |
Mol. Mass.: | 51338.40 |
Organism: | Homo sapiens (Human) |
Description: | P08588 |
Residue: | 477 |
Sequence: | MGAGVLVLGASEPGNLSSAAPLPDGAATAARLLVPASPPASLLPPASESPEPLSQQWTAG
MGLLMALIVLLIVAGNVLVIVAIAKTPRLQTLTNLFIMSLASADLVMGLLVVPFGATIVV
WGRWEYGSFFCELWTSVDVLCVTASIETLCVIALDRYLAITSPFRYQSLLTRARARGLVC
TVWAISALVSFLPILMHWWRAESDEARRCYNDPKCCDFVTNRAYAIASSVVSFYVPLCIM
AFVYLRVFREAQKQVKKIDSCERRFLGGPARPPSPSPSPVPAPAPPPGPPRPAAAAATAP
LANGRAGKRRPSRLVALREQKALKTLGIIMGVFTLCWLPFFLANVVKAFHRELVPDRLFV
FFNWLGYANSAFNPIIYCRSPDFRKAFQGLLCCARRAARRRHATHGDRPRASGCLARPGP
PPSPGAASDDDDDDVVGATPPARLLEPWAGCNGGAAADSDSSLDEPCRPGFASESKV
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BDBM50313929 |
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n/a |
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Name | BDBM50313929 |
Synonyms: | (R)-N-(4-(2-(2-hydroxy-2-(pyridin-3-yl)ethylamino)ethyl)phenyl)-2-(2H-indazol-2-yl)acetamide | CHEMBL1089386 |
Type | Small organic molecule |
Emp. Form. | C24H25N5O2 |
Mol. Mass. | 415.4876 |
SMILES | O[C@@H](CNCCc1ccc(NC(=O)Cn2cc3ccccc3n2)cc1)c1cccnc1 |r| |
Structure |
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