Target
Melanocortin receptor 5
Ligand
BDBM50358564
Substrate
n/a
Meas. Tech.
ChEMBL_790330 (CHEMBL1925783)
Ki
0.71±n/a nM
Citation
 Barkey, NMTafreshi, NKJosan, JSDe Silva, CRSill, KNHruby, VJGillies, RJMorse, DLVagner, J Development of melanoma-targeted polymer micelles by conjugation of a melanocortin 1 receptor (MC1R) specific ligand. J Med Chem 54:8078-84 (2011) [PubMed]  Article 
Target
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:
MNSSFHLHFLDLNLNATEGNLSGPNVKNKSSPCEDMGIAVEVFLTLGVISLLENILVIGAIVKNKNLHSPMYFFVCSLAVADMLVSMSSAWETITIYLLNNKHLVIADAFVRHIDNVFDSMICISVVASMCSLLAIAVDRYVTIFYALRYHHIMTARRSGAIIAGIWAFCTGCGIVFILYSESTYVILCLISMFFAMLFLLVSLYIHMFLLARTHVKRIAALPGASSARQRTSMQGAVTVTMLLGVFTVCWAPFFLHLTLMLSCPQNLYCSRFMSHFNMYLILIMCNSVMDPLIYAFRSQEMRKTFKEIICCRGFRIACSFPRRD
  
Inhibitor
Name:
BDBM50358564
Synonyms:
CHEMBL1923667
Type:
Small organic molecule
Emp. Form.:
C77H103N21O15
Mol. Mass.:
1562.7734
SMILES:
CCCC[C@H](NC(=O)[C@@H](NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(C)C)C(=O)NCC(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@H](Cc1ccc2ccccc2c1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](Cc1ccccc1)C(=O)NCC(N)=O |r,wU:12.12,4.4,32.32,42.43,57.60,68.71,79.83,98.102,wD:8.8,87.91,(2.8,4.52,;1.47,3.75,;1.47,2.22,;.14,1.44,;.14,-.09,;-1.2,-.87,;-2.53,-.09,;-2.53,1.44,;-3.86,-.87,;-5.19,-.09,;-6.53,-.87,;-6.53,-2.4,;-7.86,-.09,;-9.2,-.87,;-7.86,1.44,;-6.53,2.22,;-5.19,1.44,;-3.86,2.22,;-3.86,3.75,;-2.53,4.53,;-5.19,4.53,;-6.53,3.75,;-3.86,-2.4,;-2.53,-3.18,;-5.19,-3.18,;1.47,-.87,;1.47,-2.4,;2.8,-.09,;4.13,-.87,;5.46,-.09,;5.46,1.44,;6.8,-.87,;8.13,-.09,;8.13,1.44,;9.46,2.22,;10.94,1.76,;11.83,3.01,;10.9,4.25,;9.45,3.76,;9.46,-.87,;9.46,-2.4,;10.79,-.09,;12.13,-.87,;12.13,-2.4,;11.36,-3.72,;9.83,-3.7,;9.05,-5.02,;9.81,-6.35,;9.03,-7.67,;9.79,-9.01,;11.34,-9.01,;12.1,-7.68,;11.34,-6.36,;12.11,-5.04,;13.47,-.09,;13.47,1.44,;14.8,-.87,;16.13,-.09,;16.13,1.44,;17.47,2.22,;17.47,3.75,;18.8,4.53,;18.8,6.06,;17.47,6.83,;20.13,6.83,;17.47,-.87,;17.47,-2.4,;18.8,-.09,;20.13,-.87,;20.13,-2.4,;21.46,-3.18,;22.8,-2.4,;24.13,-3.18,;24.13,-4.71,;22.8,-5.48,;21.46,-4.71,;21.46,-.09,;21.46,1.44,;22.8,-.87,;24.13,-.09,;24.13,1.44,;25.46,2.22,;26.79,1.44,;25.46,3.75,;25.46,-.87,;25.46,-2.4,;26.79,-.09,;28.13,-.87,;28.13,-2.4,;29.46,-3.18,;29.46,-4.71,;30.79,-5.48,;30.79,-7.02,;29.46,-7.79,;32.12,-7.79,;29.46,-.09,;29.46,1.44,;30.79,-.87,;32.12,-.09,;32.12,1.44,;33.45,2.22,;34.79,1.44,;36.12,2.22,;36.12,3.75,;34.79,4.53,;33.45,3.75,;33.45,-.87,;33.45,-2.4,;34.79,-.09,;36.12,-.87,;37.46,-.09,;38.79,-.87,;37.46,1.44,)|
Structure:
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