Reaction Details |
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Target | Melanocortin receptor 3 |
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Ligand | BDBM50034910 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1498848 (CHEMBL3583822) |
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EC50 | 960±n/a nM |
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Citation | Singh, A; Tala, SR; Flores, V; Freeman, K; Haskell-Luevano, C Synthesis and Pharmacology ofa/ß(3)-Peptides Based on the Melanocortin Agonist Ac-His-dPhe-Arg-Trp-NH2 Sequence. ACS Med Chem Lett6:568-72 (2015) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Melanocortin receptor 3 |
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Name: | Melanocortin receptor 3 |
Synonyms: | MC3-R | MC3R_MOUSE | Mc3r |
Type: | PROTEIN |
Mol. Mass.: | 35808.24 |
Organism: | Mus musculus |
Description: | ChEMBL_1498848 |
Residue: | 323 |
Sequence: | MNSSCCLSSVSPMLPNLSEHPAAPPASNRSGSGFCEQVFIKPEVFLALGIVSLMENILVI
LAVVRNGNLHSPMYFFLCSLAAADMLVSLSNSLETIMIAVINSDSLTLEDQFIQHMDNIF
DSMICISLVASICNLLAIAIDRYVTIFYALRYHSIMTVRKALTLIGVIWVCCGICGVMFI
IYSESKMVIVCLITMFFAMVLLMGTLYIHMFLFARLHVQRIAVLPPAGVVAPQQHSCMKG
AVTITILLGVFIFCWAPFFLHLVLIITCPTNPYCICYTAHFNTYLVLIMCNSVIDPLIYA
FRSLELRNTFKEILCGCNSMNLG
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BDBM50034910 |
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n/a |
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Name | BDBM50034910 |
Synonyms: | (S)-2-{(S)-2-[(S)-2-acetylamino-3-(3H-imidazol-4-yl)-propionylamino]-3-phenyl-propionylamino}-5-guanidino-pentanoic acid [(S)-1-carbamoyl-2-(1H-indol-3-yl)-ethyl]-amide | 2-{2-[2-Acetylamino-3-(1H-imidazol-4-yl)-propionylamino]-3-phenyl-propionylamino}-5-guanidino-pentanoic acid [1-carbamoyl-2-(1H-indol-3-yl)-ethyl]-amideAc-His-DPhe-DArg-Trp-NH2 | 2-{2-[2-Acetylamino-3-(3H-imidazol-4-yl)-propionylamino]-3-phenyl-propionylamino}-5-guanidino-pentanoic acid [1-carbamoyl-2-(1H-indol-3-yl)-ethyl]-amide | 2-{2-[2-Acetylamino-3-(3H-imidazol-4-yl)-propionylamino]-3-phenyl-propionylamino}-5-guanidino-pentanoic acid [1-carbamoyl-2-(1H-indol-3-yl)-ethyl]-amide(Ac-His-Phe-Arg-Trp-NH2) | Ac-His-D-Phe-Arg-D-Trp-NH2 | Ac-His-DPhe-Arg-Trp-NH2 | Ac-His-Phe-Arg-Trp-NH2 | CHEMBL50056 |
Type | Small organic molecule |
Emp. Form. | C34H43N11O5 |
Mol. Mass. | 685.7759 |
SMILES | CC(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(N)=O |
Structure |
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