Reaction Details |
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Target | Substance-P receptor |
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Ligand | BDBM50290861 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_143042 |
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IC50 | 0.090000±n/a nM |
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Citation | Swain, CJ; Williams, BJ; Baker, R; Cascieri, MA; Chicchi, G; Forrest, M; Herbert, R; Keown, L; Ladduwahetty, T; Luell, S; MacIntyre, DE; Metzger, J; Morton, S; Owens, AP; Sadowski, S; Watt, AP 3-Benzyloxy-2-phenylpiperidine NK1 antagonists: the influence of alpha methyl substitution Bioorg Med Chem Lett7:2959-2962 (1997) Article |
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More Info.: | Get all data from this article, Assay Method |
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Substance-P receptor |
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Name: | Substance-P receptor |
Synonyms: | NK-1 receptor | NK-1R | NK1 Receptor | NK1R_RAT | Neurokinin 1 receptor | Neurokinin NK1 | SPR | Substance-P receptor | Tac1r | Tachykinin receptor 1 | Tacr1 |
Type: | G Protein-Coupled Receptor (GPCR) |
Mol. Mass.: | 46371.54 |
Organism: | Rattus norvegicus (rat) |
Description: | Competition binding assays were carried out using membrane preparations from transfected CHO cells that constitutively expressed the rat NK1 receptor. |
Residue: | 407 |
Sequence: | MDNVLPMDSDLFPNISTNTSESNQFVQPTWQIVLWAAAYTVIVVTSVVGNVVVIWIILAH
KRMRTVTNYFLVNLAFAEACMAAFNTVVNFTYAVHNVWYYGLFYCKFHNFFPIAALFASI
YSMTAVAFDRYMAIIHPLQPRLSATATKVVIFVIWVLALLLAFPQGYYSTTETMPSRVVC
MIEWPEHPNRTYEKAYHICVTVLIYFLPLLVIGYAYTVVGITLWASEIPGDSSDRYHEQV
SAKRKVVKMMIVVVCTFAICWLPFHVFFLLPYINPDLYLKKFIQQVYLASMWLAMSSTMY
NPIIYCCLNDRFRLGFKHAFRCCPFISAGDYEGLEMKSTRYLQTQSSVYKVSRLETTIST
VVGAHEEEPEEGPKATPSSLDLTSNGSSRSNSKTMTESSSFYSNMLA
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BDBM50290861 |
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n/a |
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Name | BDBM50290861 |
Synonyms: | 5-{3-[1-(3,5-Dichloro-phenyl)-ethoxy]-2-phenyl-piperidin-1-ylmethyl}-2,4-dihydro-[1,2,4]triazol-3-one | CHEMBL100636 |
Type | Small organic molecule |
Emp. Form. | C22H24Cl2N4O2 |
Mol. Mass. | 447.358 |
SMILES | C[C@@H](O[C@H]1CCCN(Cc2n[nH]c(=O)[nH]2)[C@H]1c1ccccc1)c1cc(Cl)cc(Cl)c1 |
Structure |
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