Reaction Details |
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Target | Mu-type opioid receptor |
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Ligand | BDBM50114010 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1468973 (CHEMBL3412630) |
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Ki | 10.0±n/a nM |
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Citation | Hu, M; Giulianotti, MA; McLaughlin, JP; Shao, J; Debevec, G; Maida, LE; Geer, P; Cazares, M; Misler, J; Li, L; Dooley, C; Ganno, ML; Eans, SO; Mizrachi, E; Santos, RG; Yongye, AB; Houghten, RA; Yu, Y Synthesis and biological evaluations of novel endomorphin analogues containinga-hydroxy-ß-phenylalanine (AHPBA) displaying mixedµ/d opioid receptor agonist andd opioid receptor antagonist activities. Eur J Med Chem92:270-81 (2015) [PubMed] Article |
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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: | MOR-1 | MUOR1 | Mu-type opioid receptor (MOR) | OPIATE Mu | OPRM_RAT | Opiate non-selective | Opioid receptor B | Oprm1 | Ror-b |
Type: | G Protein-Coupled Receptor (GPCR) |
Mol. Mass.: | 44503.11 |
Organism: | Rattus norvegicus (rat) |
Description: | Competition binding assays were carried out using membrane preparations from transfected HN9.10 cells that constitutively expressed the mu opioid receptor. |
Residue: | 398 |
Sequence: | MDSSTGPGNTSDCSDPLAQASCSPAPGSWLNLSHVDGNQSDPCGLNRTGLGGNDSLCPQT
GSPSMVTAITIMALYSIVCVVGLFGNFLVMYVIVRYTKMKTATNIYIFNLALADALATST
LPFQSVNYLMGTWPFGTILCKIVISIDYYNMFTSIFTLCTMSVDRYIAVCHPVKALDFRT
PRNAKIVNVCNWILSSAIGLPVMFMATTKYRQGSIDCTLTFSHPTWYWENLLKICVFIFA
FIMPVLIITVCYGLMILRLKSVRMLSGSKEKDRNLRRITRMVLVVVAVFIVCWTPIHIYV
IIKALITIPETTFQTVSWHFCIALGYTNSCLNPVLYAFLDENFKRCFREFCIPTSSTIEQ
QNSTRVRQNTREHPSTANTVDRTNHQLENLEAETAPLP
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BDBM50114010 |
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n/a |
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Name | BDBM50114010 |
Synonyms: | 1-[2-Amino-3-(4-hydroxy-phenyl)-propionyl]-pyrrolidine-2-carboxylic acid [1-(1-benzyl-2-carbamoyl-ethylcarbamoyl)-2-(1H-indol-3-yl)-ethyl]-amide | CHEMBL430643 |
Type | Small organic molecule |
Emp. Form. | C35H40N6O5 |
Mol. Mass. | 624.7293 |
SMILES | N[C@@H](Cc1ccc(O)cc1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](CC(N)=O)Cc1ccccc1 |
Structure |
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