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TargetMelanocortin receptor 5
LigandBDBM50121258
Substrate/Competitorn/a
Meas. Tech.ChEMBL_106526 (CHEMBL713030)
IC50 4.6±n/a nM
Citation Grieco, PLavecchia, ACai, MTrivedi, DWeinberg, DMacNeil, TVan der Ploeg, LHHruby, VJ Structure-activity studies of the melanocortin peptides: discovery of potent and selective affinity antagonists for the hMC3 and hMC4 receptors. J Med Chem45:5287-94 (2002) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Melanocortin receptor 5
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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  Blast E-value cutoff:
BDBM50121258
n/a
NameBDBM50121258
Synonyms:9-(2-Acetylamino-hexanoylamino)-23-[3-(diaminomethaniminium)-propyl]-20-(1H-indol-3-ylmethyl)-26-naphthalen-2-ylmethyl-8,11,19,22,25,28-hexaoxo-7,12,18,21,24,27-hexaaza-spiro[5.22]octacosane-17-carboxylic acid amide | CID44366181 | PG-914
TypeSmall organic molecule
Emp. Form.C55H76N13O9
Mol. Mass.1063.2731
SMILESCCCC[C@@H](NC(C)=O)C(=O)N[C@@H]1CC(=O)NCCCC[C@H](NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@@H](CCCNC(N)=[NH2+])NC(=O)[C@H](Cc2ccc3ccccc3c2)NC(=O)C2(CCCCC2)NC1=O)C(N)=O
Structure
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