Reaction Details |
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Target | Mu-type opioid receptor |
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Ligand | BDBM50010703 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_146979 |
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IC50 | 0.986000±n/a nM |
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Citation | Kawasaki, AM; Knapp, RJ; Kramer, TH; Wire, WS; Vasquez, OS; Yamamura, HI; Burks, TF; Hruby, VJ Design and synthesis of highly potent and selective cyclic dynorphin A analogues. J Med Chem33:1874-9 (1990) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Mu-type opioid receptor |
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Name: | Mu-type opioid receptor |
Synonyms: | M-OR-1 | MOR-1 | Mu opioid receptor | Mu-type opioid receptor (Mu) | OPIATE Mu | OPRM1 | OPRM_CAVPO |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 11165.58 |
Organism: | GUINEA PIG |
Description: | P97266 |
Residue: | 98 |
Sequence: | YTKMKTATNIYIFNLALADALATSTLPFQSVNYLMGTWPFGTILCKIVISIDYYNMFTSI
FTLCTMSVDRYIAVCHPVKALDFRTPRNAKTVNVCNWI
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BDBM50010703 |
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n/a |
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Name | BDBM50010703 |
Synonyms: | CHEMBL443068 | H-Tyr-Gly-Gly-Phe-Leu-Arg-Arg-Cys-Arg-Pro-Lys-Leu-Cys-NH2 |
Type | Small organic molecule |
Emp. Form. | C69H112N24O14S2 |
Mol. Mass. | 1565.91 |
SMILES | CC(C)C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@H]1CSSC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@@H]2CCCN2C(=O)[C@H](CCCNC(N)=N)NC1=O)C(N)=O |
Structure |
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