Reaction Details |
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Target | Melanocortin receptor 3 |
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Ligand | BDBM50590042 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_2194697 (CHEMBL5107057) |
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Ki | 0.630957±n/a nM |
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Citation | White, AM; Dellsén, A; Larsson, N; Kaas, Q; Jansen, F; Plowright, AT; Knerr, L; Durek, T; Craik, DJ Late-Stage Functionalization with Cysteine Staples Generates Potent and Selective Melanocortin Receptor-1 Agonists. J Med Chem65:12956-12969 (2022) [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 | MC3R_HUMAN | Melanocortin MC3 | Melanocortin receptor (M3 and M4) |
Type: | Enzyme |
Mol. Mass.: | 36044.86 |
Organism: | Homo sapiens (Human) |
Description: | P41968 |
Residue: | 323 |
Sequence: | MNASCCLPSVQPTLPNGSEHLQAPFFSNQSSSAFCEQVFIKPEVFLSLGIVSLLENILVI
LAVVRNGNLHSPMYFFLCSLAVADMLVSVSNALETIMIAIVHSDYLTFEDQFIQHMDNIF
DSMICISLVASICNLLAIAVDRYVTIFYALRYHSIMTVRKALTLIVAIWVCCGVCGVVFI
VYSESKMVIVCLITMFFAMMLLMGTLYVHMFLFARLHVKRIAALPPADGVAPQQHSCMKG
AVTITILLGVFIFCWAPFFLHLVLIITCPTNPYCICYTAHFNTYLVLIMCNSVIDPLIYA
FRSLELRNTFREILCGCNGMNLG
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BDBM50590042 |
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n/a |
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Name | BDBM50590042 |
Synonyms: | CHEMBL5175981 |
Type | Small organic molecule |
Emp. Form. | C109H147N37O19S2 |
Mol. Mass. | 2343.7 |
SMILES | [H][C@]12CSc3nnc(SC[C@]([H])(NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](Cc4c[nH]c5ccccc45)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc4ccccc4)NC(=O)[C@H](Cc4cnc[nH]4)NC(=O)CNC(=O)[C@H](CCCC)NC1=O)C(=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]c4ccccc14)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N2)c1CCC2C(COC(=O)NCCN)C2CCc31 |r| |
Structure |
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