Reaction Details |
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Target | Melanocortin receptor 5 |
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Ligand | BDBM50179138 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_335080 (CHEMBL859197) |
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IC50 | 630±n/a nM |
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Citation | Bakshi, RK; Hong, Q; Tang, R; Kalyani, RN; Macneil, T; Weinberg, DH; Van der Ploeg, LH; Patchett, AA; Nargund, RP Optimization of a privileged structure leading to potent and selective human melanocortin subtype-4 receptor ligands. Bioorg Med Chem Lett16:1130-3 (2006) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Melanocortin receptor 5 |
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Name: | Melanocortin receptor 5 |
Synonyms: | MC-2 | MC5-R | MC5R | MC5R_HUMAN | Melanocortin MC5 | Melanocortin receptor (M4 and M5) | Melanocortin receptor 5 | Melanocortin receptor 5 (MC5R) |
Type: | Enzyme |
Mol. Mass.: | 36612.92 |
Organism: | Homo sapiens (Human) |
Description: | P33032 |
Residue: | 325 |
Sequence: | MNSSFHLHFLDLNLNATEGNLSGPNVKNKSSPCEDMGIAVEVFLTLGVISLLENILVIGA
IVKNKNLHSPMYFFVCSLAVADMLVSMSSAWETITIYLLNNKHLVIADAFVRHIDNVFDS
MICISVVASMCSLLAIAVDRYVTIFYALRYHHIMTARRSGAIIAGIWAFCTGCGIVFILY
SESTYVILCLISMFFAMLFLLVSLYIHMFLLARTHVKRIAALPGASSARQRTSMQGAVTV
TMLLGVFTVCWAPFFLHLTLMLSCPQNLYCSRFMSHFNMYLILIMCNSVMDPLIYAFRSQ
EMRKTFKEIICCRGFRIACSFPRRD
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BDBM50179138 |
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n/a |
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Name | BDBM50179138 |
Synonyms: | CHEMBL380727 | ethyl (1-((R)-3-(4-chlorophenyl)-2-((R)-1,2,3,4-tetrahydroisoquinoline-3-carboxamido)propanoyl)-4-cyclohexylpiperidin-4-yl)methyl(isopropyl)carbamate |
Type | Small organic molecule |
Emp. Form. | C37H51ClN4O4 |
Mol. Mass. | 651.278 |
SMILES | CCOC(=O)N(CC1(CCN(CC1)C(=O)[C@@H](Cc1ccc(Cl)cc1)NC(=O)[C@H]1Cc2ccccc2CN1)C1CCCCC1)C(C)C |
Structure |
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