Reaction Details |
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Target | Beta-2 adrenergic receptor |
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Ligand | BDBM50318160 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_632382 (CHEMBL1115587) |
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IC50 | 48±n/a nM |
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Citation | Baur, F; Beattie, D; Beer, D; Bentley, D; Bradley, M; Bruce, I; Charlton, SJ; Cuenoud, B; Ernst, R; Fairhurst, RA; Faller, B; Farr, D; Keller, T; Fozard, JR; Fullerton, J; Garman, S; Hatto, J; Hayden, C; He, H; Howes, C; Janus, D; Jiang, Z; Lewis, C; Loeuillet-Ritzler, F; Moser, H; Reilly, J; Steward, A; Sykes, D; Tedaldi, L; Trifilieff, A; Tweed, M; Watson, S; Wissler, E; Wyss, D The identification of indacaterol as an ultralong-acting inhaled beta2-adrenoceptor agonist. J Med Chem53:3675-84 (2010) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Beta-2 adrenergic receptor |
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Name: | Beta-2 adrenergic receptor |
Synonyms: | ADRB2_CAVPO | Adrb2 | adrenergic Beta2 |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 46993.24 |
Organism: | GUINEA PIG |
Description: | adrenergic Beta2 ADRB2 GUINEA PIG::Q8K4Z4 |
Residue: | 418 |
Sequence: | MGHLGNGSDFLLAPNASHAPDHNVTRERDEAWVVGMAIVMSLIVLAIVFGNVLVITAIAK
FERLQTVTNYFITSLACADLVMGLAVVPFGASHILMNMWTFGNFWCEFWTSIDVLCVTAS
IETLCVIAVDRYFAITSPFKYQSLLTKNKARVVILMVWVVSGLTSFLPIQMHWYRATHKD
AINCYAEETCCDFFTNQAYAIASSIVSFYLPLVVMVFVYSRVFQVAKKQLQKIDRSEGRF
HTQNLSQVEQDGRSGHGLRRSSKFYLKEHKALKTLGIIMGTFTLCWLPFFIVNIVHVIQD
NLIPKEVYILLNWVGYVNSAFNPLIYCRSPDFRIAFQELLCLRRSALKAYGNDCSSNSNG
KTDYTGEPNVCHQGQEKERELLCEDPPGTEDLVSCPGTVPSDSIDSQGRNYSTNDSLL
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BDBM50318160 |
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n/a |
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Name | BDBM50318160 |
Synonyms: | 8-Hydroxy-5-[(R)-1-hydroxy-2-(5,6-dimethylindan-2-ylamino)-ethyl]-1H-quinolin-2-one | CHEMBL1094483 |
Type | Small organic molecule |
Emp. Form. | C22H24N2O3 |
Mol. Mass. | 364.4376 |
SMILES | Cc1cc2CC(Cc2cc1C)NC[C@H](O)c1ccc(O)c2[nH]c(=O)ccc12 |r| |
Structure |
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