Reaction Details |
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Target | Alpha-1B adrenergic receptor |
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Ligand | BDBM50067212 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_32289 (CHEMBL646236) |
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EC50 | 10965±n/a nM |
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Citation | Meyer, MD; Altenbach, RJ; Hancock, AA; Buckner, SA; Knepper, SM; Kerwin, JF Synthesis and in vitro characterization of N-[5-(4,5-dihydro-1H-imidazol-2-yl)-2-hydroxy-5,6,7,8- tetrahydronaphthalen-1-yl]methanesulfonamide and its enantiomers: a novel selective alpha 1A receptor agonist. J Med Chem39:4116-9 (1996) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Alpha-1B adrenergic receptor |
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Name: | Alpha-1B adrenergic receptor |
Synonyms: | ADA1B_RAT | Adra1b | Alpha 1B-adrenoceptor | Alpha 1B-adrenoreceptor | Alpha adrenergic receptor 1A and 1B | Alpha-1 Adrenergic Receptor | Alpha-1Adrenoceptor | Alpha-1B adrenergic receptor | Alpha-1B adrenoreceptor | adrenergic Alpha1B |
Type: | G Protein-Coupled Receptor (GPCR) |
Mol. Mass.: | 56606.71 |
Organism: | Rattus norvegicus (rat) |
Description: | Receptor binding assays were performed using rat cortical membranes. |
Residue: | 515 |
Sequence: | MNPDLDTGHNTSAPAHWGELKDDNFTGPNQTSSNSTLPQLDVTRAISVGLVLGAFILFAI
VGNILVILSVACNRHLRTPTNYFIVNLAIADLLLSFTVLPFSATLEVLGYWVLGRIFCDI
WAAVDVLCCTASILSLCAISIDRYIGVRYSLQYPTLVTRRKAILALLSVWVLSTVISIGP
LLGWKEPAPNDDKECGVTEEPFYALFSSLGSFYIPLAVILVMYCRVYIVAKRTTKNLEAG
VMKEMSNSKELTLRIHSKNFHEDTLSSTKAKGHNPRSSIAVKLFKFSREKKAAKTLGIVV
GMFILCWLPFFIALPLGSLFSTLKPPDAVFKVVFWLGYFNSCLNPIIYPCSSKEFKRAFM
RILGCQCRGGRRRRRRRRLGACAYTYRPWTRGGSLERSQSRKDSLDDSGSCMSGTQRTLP
SASPSPGYLGRGTQPPVELCAFPEWKPGALLSLPEPPGRRGRLDSGPLFTFKLLGDPESP
GTEGDTSNGGCDTTTDLANGQPGFKSNMPLAPGHF
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BDBM50067212 |
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n/a |
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Name | BDBM50067212 |
Synonyms: | CHEBI:8093 | Cyclomydril | Duo-Medihaler | Phenylephrine |
Type | Small organic molecule |
Emp. Form. | C9H13NO2 |
Mol. Mass. | 167.205 |
SMILES | CNC[C@H](O)c1cccc(O)c1 |r| |
Structure |
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