BDBM50112905 CHEMBL3600916

SMILES: CCCC[C@@H](NC(C)=O)C(=O)N[C@H]1CC(=O)NCCCC[C@H](N(C)C(=O)[C@H](Cc2c[nH]c3ccccc23)N(C)C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](Cc2cnc[nH]2)N(C)C1=O)C(N)=O

InChI Key: InChIKey=WCVJJQCPIDBNFM-HEKKFFGGSA-N

Data: 4 IC50  4 EC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 8 hits for monomerid = 50112905   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Melanocyte-stimulating hormone receptor (Homo sapiens (Human))	BDBM50112905 (CHEMBL3600916) Show SMILES CCCC[C@@H](NC(C)=O)C(=O)N[C@H]1CC(=O)NCCCC[C@H](N(C)C(=O)[C@H](Cc2c[nH]c3ccccc23)N(C)C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](Cc2cnc[nH]2)N(C)C1=O)C(N)=O |r| Show InChI InChI=1S/C57H77N15O9/c1-6-7-18-42(66-34(2)73)51(76)69-45-30-49(74)62-24-13-12-21-46(50(58)75)70(3)56(81)48(28-38-31-64-41-19-11-10-17-40(38)41)72(5)54(79)43(20-14-25-63-57(59)60)67-52(77)44(27-35-22-23-36-15-8-9-16-37(36)26-35)68-53(78)47(71(4)55(45)80)29-39-32-61-33-65-39/h8-11,15-17,19,22-23,26,31-33,42-48,64H,6-7,12-14,18,20-21,24-25,27-30H2,1-5H3,(H2,58,75)(H,61,65)(H,62,74)(H,66,73)(H,67,77)(H,68,78)(H,69,76)(H4,59,60,63)/t42-,43+,44-,45+,46+,47+,48+/m1/s1	PDB KEGG UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	242	n/a	n/a	n/a	n/a	n/a	n/a
University of Arizona Curated by ChEMBL					Assay Description Displacement of [125I]-[Nle4,D-Phe7]-alpha-MSH from human MC1 receptor expressed in HEK293 cells after 40 mins by luminescence counting				J Med Chem 58: 6359-67 (2015) BindingDB Entry DOI: 10.7270/Q251410F
					More data for this Ligand-Target Pair
Melanocortin receptor 3 (Homo sapiens (Human))	BDBM50112905 (CHEMBL3600916) Show SMILES CCCC[C@@H](NC(C)=O)C(=O)N[C@H]1CC(=O)NCCCC[C@H](N(C)C(=O)[C@H](Cc2c[nH]c3ccccc23)N(C)C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](Cc2cnc[nH]2)N(C)C1=O)C(N)=O |r| Show InChI InChI=1S/C57H77N15O9/c1-6-7-18-42(66-34(2)73)51(76)69-45-30-49(74)62-24-13-12-21-46(50(58)75)70(3)56(81)48(28-38-31-64-41-19-11-10-17-40(38)41)72(5)54(79)43(20-14-25-63-57(59)60)67-52(77)44(27-35-22-23-36-15-8-9-16-37(36)26-35)68-53(78)47(71(4)55(45)80)29-39-32-61-33-65-39/h8-11,15-17,19,22-23,26,31-33,42-48,64H,6-7,12-14,18,20-21,24-25,27-30H2,1-5H3,(H2,58,75)(H,61,65)(H,62,74)(H,66,73)(H,67,77)(H,68,78)(H,69,76)(H4,59,60,63)/t42-,43+,44-,45+,46+,47+,48+/m1/s1	UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	11	n/a	n/a	n/a	n/a
University of Arizona Curated by ChEMBL					Assay Description Agonist activity at human MC3 receptor expressed in HEK293 cells assessed as intracellular cAMP accumulation using [3H]-cAMP by luminescence counting				J Med Chem 58: 6359-67 (2015) BindingDB Entry DOI: 10.7270/Q251410F
					More data for this Ligand-Target Pair
Melanocortin receptor 4 (Homo sapiens (Human))	BDBM50112905 (CHEMBL3600916) Show SMILES CCCC[C@@H](NC(C)=O)C(=O)N[C@H]1CC(=O)NCCCC[C@H](N(C)C(=O)[C@H](Cc2c[nH]c3ccccc23)N(C)C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](Cc2cnc[nH]2)N(C)C1=O)C(N)=O |r| Show InChI InChI=1S/C57H77N15O9/c1-6-7-18-42(66-34(2)73)51(76)69-45-30-49(74)62-24-13-12-21-46(50(58)75)70(3)56(81)48(28-38-31-64-41-19-11-10-17-40(38)41)72(5)54(79)43(20-14-25-63-57(59)60)67-52(77)44(27-35-22-23-36-15-8-9-16-37(36)26-35)68-53(78)47(71(4)55(45)80)29-39-32-61-33-65-39/h8-11,15-17,19,22-23,26,31-33,42-48,64H,6-7,12-14,18,20-21,24-25,27-30H2,1-5H3,(H2,58,75)(H,61,65)(H,62,74)(H,66,73)(H,67,77)(H,68,78)(H,69,76)(H4,59,60,63)/t42-,43+,44-,45+,46+,47+,48+/m1/s1	PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	9.06E+3	n/a	n/a	n/a	n/a
University of Arizona Curated by ChEMBL					Assay Description Agonist activity at human MC4 receptor expressed in HEK293 cells assessed as intracellular cAMP accumulation using [3H]-cAMP by luminescence counting				J Med Chem 58: 6359-67 (2015) BindingDB Entry DOI: 10.7270/Q251410F
					More data for this Ligand-Target Pair
Melanocyte-stimulating hormone receptor (Homo sapiens (Human))	BDBM50112905 (CHEMBL3600916) Show SMILES CCCC[C@@H](NC(C)=O)C(=O)N[C@H]1CC(=O)NCCCC[C@H](N(C)C(=O)[C@H](Cc2c[nH]c3ccccc23)N(C)C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](Cc2cnc[nH]2)N(C)C1=O)C(N)=O |r| Show InChI InChI=1S/C57H77N15O9/c1-6-7-18-42(66-34(2)73)51(76)69-45-30-49(74)62-24-13-12-21-46(50(58)75)70(3)56(81)48(28-38-31-64-41-19-11-10-17-40(38)41)72(5)54(79)43(20-14-25-63-57(59)60)67-52(77)44(27-35-22-23-36-15-8-9-16-37(36)26-35)68-53(78)47(71(4)55(45)80)29-39-32-61-33-65-39/h8-11,15-17,19,22-23,26,31-33,42-48,64H,6-7,12-14,18,20-21,24-25,27-30H2,1-5H3,(H2,58,75)(H,61,65)(H,62,74)(H,66,73)(H,67,77)(H,68,78)(H,69,76)(H4,59,60,63)/t42-,43+,44-,45+,46+,47+,48+/m1/s1	PDB KEGG UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	>3.00E+3	n/a	n/a	n/a	n/a
University of Arizona Curated by ChEMBL					Assay Description Agonist activity at human MC1 receptor expressed in HEK293 cells assessed as intracellular cAMP accumulation using [3H]-cAMP by luminescence counting				J Med Chem 58: 6359-67 (2015) BindingDB Entry DOI: 10.7270/Q251410F
					More data for this Ligand-Target Pair
Melanocortin receptor 5 (MC5R) (Homo sapiens (Human))	BDBM50112905 (CHEMBL3600916) Show SMILES CCCC[C@@H](NC(C)=O)C(=O)N[C@H]1CC(=O)NCCCC[C@H](N(C)C(=O)[C@H](Cc2c[nH]c3ccccc23)N(C)C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](Cc2cnc[nH]2)N(C)C1=O)C(N)=O |r| Show InChI InChI=1S/C57H77N15O9/c1-6-7-18-42(66-34(2)73)51(76)69-45-30-49(74)62-24-13-12-21-46(50(58)75)70(3)56(81)48(28-38-31-64-41-19-11-10-17-40(38)41)72(5)54(79)43(20-14-25-63-57(59)60)67-52(77)44(27-35-22-23-36-15-8-9-16-37(36)26-35)68-53(78)47(71(4)55(45)80)29-39-32-61-33-65-39/h8-11,15-17,19,22-23,26,31-33,42-48,64H,6-7,12-14,18,20-21,24-25,27-30H2,1-5H3,(H2,58,75)(H,61,65)(H,62,74)(H,66,73)(H,67,77)(H,68,78)(H,69,76)(H4,59,60,63)/t42-,43+,44-,45+,46+,47+,48+/m1/s1	UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	268	n/a	n/a	n/a	n/a	n/a	n/a
University of Arizona Curated by ChEMBL					Assay Description Displacement of [125I]-[Nle4,D-Phe7]-alpha-MSH from human MC5 receptor expressed in HEK293 cells after 40 mins by luminescence counting				J Med Chem 58: 6359-67 (2015) BindingDB Entry DOI: 10.7270/Q251410F
					More data for this Ligand-Target Pair
Melanocortin receptor 3 (Homo sapiens (Human))	BDBM50112905 (CHEMBL3600916) Show SMILES CCCC[C@@H](NC(C)=O)C(=O)N[C@H]1CC(=O)NCCCC[C@H](N(C)C(=O)[C@H](Cc2c[nH]c3ccccc23)N(C)C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](Cc2cnc[nH]2)N(C)C1=O)C(N)=O |r| Show InChI InChI=1S/C57H77N15O9/c1-6-7-18-42(66-34(2)73)51(76)69-45-30-49(74)62-24-13-12-21-46(50(58)75)70(3)56(81)48(28-38-31-64-41-19-11-10-17-40(38)41)72(5)54(79)43(20-14-25-63-57(59)60)67-52(77)44(27-35-22-23-36-15-8-9-16-37(36)26-35)68-53(78)47(71(4)55(45)80)29-39-32-61-33-65-39/h8-11,15-17,19,22-23,26,31-33,42-48,64H,6-7,12-14,18,20-21,24-25,27-30H2,1-5H3,(H2,58,75)(H,61,65)(H,62,74)(H,66,73)(H,67,77)(H,68,78)(H,69,76)(H4,59,60,63)/t42-,43+,44-,45+,46+,47+,48+/m1/s1	UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	106	n/a	n/a	n/a	n/a	n/a	n/a
University of Arizona Curated by ChEMBL					Assay Description Displacement of [125I]-[Nle4,D-Phe7]-alpha-MSH from human MC3 receptor expressed in HEK293 cells after 40 mins by luminescence counting				J Med Chem 58: 6359-67 (2015) BindingDB Entry DOI: 10.7270/Q251410F
					More data for this Ligand-Target Pair
Melanocortin receptor 4 (Homo sapiens (Human))	BDBM50112905 (CHEMBL3600916) Show SMILES CCCC[C@@H](NC(C)=O)C(=O)N[C@H]1CC(=O)NCCCC[C@H](N(C)C(=O)[C@H](Cc2c[nH]c3ccccc23)N(C)C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](Cc2cnc[nH]2)N(C)C1=O)C(N)=O |r| Show InChI InChI=1S/C57H77N15O9/c1-6-7-18-42(66-34(2)73)51(76)69-45-30-49(74)62-24-13-12-21-46(50(58)75)70(3)56(81)48(28-38-31-64-41-19-11-10-17-40(38)41)72(5)54(79)43(20-14-25-63-57(59)60)67-52(77)44(27-35-22-23-36-15-8-9-16-37(36)26-35)68-53(78)47(71(4)55(45)80)29-39-32-61-33-65-39/h8-11,15-17,19,22-23,26,31-33,42-48,64H,6-7,12-14,18,20-21,24-25,27-30H2,1-5H3,(H2,58,75)(H,61,65)(H,62,74)(H,66,73)(H,67,77)(H,68,78)(H,69,76)(H4,59,60,63)/t42-,43+,44-,45+,46+,47+,48+/m1/s1	PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	100	n/a	n/a	n/a	n/a	n/a	n/a
University of Arizona Curated by ChEMBL					Assay Description Displacement of [125I]-[Nle4,D-Phe7]-alpha-MSH from human MC4 receptor expressed in HEK293 cells after 40 mins by luminescence counting				J Med Chem 58: 6359-67 (2015) BindingDB Entry DOI: 10.7270/Q251410F
					More data for this Ligand-Target Pair
Melanocortin receptor 5 (MC5R) (Homo sapiens (Human))	BDBM50112905 (CHEMBL3600916) Show SMILES CCCC[C@@H](NC(C)=O)C(=O)N[C@H]1CC(=O)NCCCC[C@H](N(C)C(=O)[C@H](Cc2c[nH]c3ccccc23)N(C)C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](Cc2cnc[nH]2)N(C)C1=O)C(N)=O |r| Show InChI InChI=1S/C57H77N15O9/c1-6-7-18-42(66-34(2)73)51(76)69-45-30-49(74)62-24-13-12-21-46(50(58)75)70(3)56(81)48(28-38-31-64-41-19-11-10-17-40(38)41)72(5)54(79)43(20-14-25-63-57(59)60)67-52(77)44(27-35-22-23-36-15-8-9-16-37(36)26-35)68-53(78)47(71(4)55(45)80)29-39-32-61-33-65-39/h8-11,15-17,19,22-23,26,31-33,42-48,64H,6-7,12-14,18,20-21,24-25,27-30H2,1-5H3,(H2,58,75)(H,61,65)(H,62,74)(H,66,73)(H,67,77)(H,68,78)(H,69,76)(H4,59,60,63)/t42-,43+,44-,45+,46+,47+,48+/m1/s1	UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	1.10	n/a	n/a	n/a	n/a
University of Arizona Curated by ChEMBL					Assay Description Agonist activity at human MC5 receptor expressed in HEK293 cells assessed as intracellular cAMP accumulation using [3H]-cAMP by luminescence counting				J Med Chem 58: 6359-67 (2015) BindingDB Entry DOI: 10.7270/Q251410F
					More data for this Ligand-Target Pair