Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Melanocortin receptor 4' and Ligand = 'BDBM50136365'   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Melanocortin receptor 4 (Homo sapiens (Human))	BDBM50136365 (CHEMBL337571 | N-[(R)-1-(4-Chloro-benzyl)-2-(4-cyc...) Show SMILES CNCCC(=O)N[C@H](Cc1ccc(Cl)cc1)C(=O)N1CCC(Cn2cncn2)(CC1)C1CCCCC1 Show InChI InChI=1S/C27H39ClN6O2/c1-29-14-11-25(35)32-24(17-21-7-9-23(28)10-8-21)26(36)33-15-12-27(13-16-33,18-34-20-30-19-31-34)22-5-3-2-4-6-22/h7-10,19-20,22,24,29H,2-6,11-18H2,1H3,(H,32,35)/t24-/m1/s1	PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	10	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Pharmaceutical Research Institute Curated by ChEMBL					Assay Description Binding activity was measured using membranes of Hi5 cells expressing the human MC4R receptors				Bioorg Med Chem Lett 13: 4341-4 (2003) BindingDB Entry DOI: 10.7270/Q2F18Z4D
					More data for this Ligand-Target Pair
Melanocortin receptor 4 (Homo sapiens (Human))	BDBM50136365 (CHEMBL337571 | N-[(R)-1-(4-Chloro-benzyl)-2-(4-cyc...) Show SMILES CNCCC(=O)N[C@H](Cc1ccc(Cl)cc1)C(=O)N1CCC(Cn2cncn2)(CC1)C1CCCCC1 Show InChI InChI=1S/C27H39ClN6O2/c1-29-14-11-25(35)32-24(17-21-7-9-23(28)10-8-21)26(36)33-15-12-27(13-16-33,18-34-20-30-19-31-34)22-5-3-2-4-6-22/h7-10,19-20,22,24,29H,2-6,11-18H2,1H3,(H,32,35)/t24-/m1/s1	PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	n/a	n/a	70	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Pharmaceutical Research Institute Curated by ChEMBL					Assay Description Binding activity was measured using membranes of Hi5 cells expressing the human MC4R receptors				Bioorg Med Chem Lett 13: 4341-4 (2003) BindingDB Entry DOI: 10.7270/Q2F18Z4D
					More data for this Ligand-Target Pair