Reaction Details | |||
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Target | Mu-type opioid receptor | ||
Ligand | BDBM50375376 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | ChEMBL_471597 (CHEMBL940228) | ||
Ki | 6800±n/a nM | ||
Citation | Jung, B; Englberger, W; Fröhlich, R; Schepmann, D; Lehmkuhl, K; Wünsch, B Synthesis and pharmacological evaluation of bicyclic SNC80 analogues with separated benzhydryl moiety. Bioorg Med Chem16:2870-85 (2008) [PubMed] Article | ||
More Info.: | Get all data from this article, Assay Method | ||
Mu-type opioid receptor | |||
Name: | Mu-type opioid receptor | ||
Synonyms: | M-OR-1 | MOP | MOR-1 | MOR1 | MUOR1 | Mu Opioid Receptor | Mu opiate receptor | OPIATE Mu | OPRM1 | OPRM_HUMAN | hMOP | mu-type opioid receptor isoform MOR-1 | ||
Type: | G Protein-Coupled Receptor (GPCR) | ||
Mol. Mass.: | 44789.51 | ||
Organism: | Homo sapiens (Human) | ||
Description: | P35372 | ||
Residue: | 400 | ||
Sequence: |
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BDBM50375376 | |||
n/a | |||
Name | BDBM50375376 | ||
Synonyms: | CHEMBL260521 | ||
Type | Small organic molecule | ||
Emp. Form. | C28H35N3O | ||
Mol. Mass. | 429.597 | ||
SMILES | CCN(CC)C(=O)c1ccc(CN2C[C@@H]3CC=C([C@H]2CN3CC=C)c2ccccc2)cc1 |wU:14.21,wD:18.18,c:16,TLB:24:17:20.19:13.12,11:12:20.19:15.16.17,THB:21:20:13.12:15.16.17,(-6.25,1.75,;-4.91,2.52,;-3.58,1.75,;-3.58,.21,;-4.91,-.56,;-2.25,2.51,;-2.25,4.06,;-.92,1.75,;-.92,.2,;.41,-.57,;1.74,.2,;3.07,-.57,;4.45,.13,;5.5,1.31,;7.09,1.26,;8.07,-.07,;7.61,-1.64,;7.04,-.4,;5.74,.25,;6.58,1.88,;7.78,2.62,;8.82,3.74,;10.33,3.41,;11.37,4.53,;5.95,-1.5,;4.45,-1.04,;3.37,-2.13,;3.72,-3.61,;5.21,-4.05,;6.3,-2.97,;1.74,1.75,;.41,2.51,)| | ||
Structure |