BDBM50263814 CHEMBL4101216

SMILES: CC[C@H](C)[C@@H]1NC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](C)NC(=O)[C@@H](NC(=O)[C@@H]2CSSC[C@H](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)[C@@H](Cc1c[nH]c3ccccc13)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N2)[C@H](C)O)[C@@H](C)CC

InChI Key: InChIKey=WQIHSOXKRYCWEW-RMGWGXNZSA-N

Data: 3 KI  1 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 = 50263814   

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))	BDBM50263814 (CHEMBL4101216) Show SMILES CC[C@H](C)[C@@H]1NC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](C)NC(=O)[C@@H](NC(=O)[C@@H]2CSSC[C@H](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)[C@@H](Cc1c[nH]c3ccccc13)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N2)[C@H](C)O)[C@@H](C)CC |r| Show InChI InChI=1S/C77H113N23O16S2/c1-8-40(3)59-71(112)94-54-37-117-118-38-55(68(109)97-61(43(6)102)72(113)87-42(5)62(103)92-53(36-101)66(107)96-60(41(4)9-2)75(116)100-30-18-26-57(100)74(115)99-29-17-25-56(99)69(110)95-59)93-63(104)49(23-15-27-83-76(78)79)88-70(111)58(32-45-34-85-48-22-14-13-21-47(45)48)98(7)73(114)50(24-16-28-84-77(80)81)89-64(105)51(31-44-19-11-10-12-20-44)90-65(106)52(91-67(54)108)33-46-35-82-39-86-46/h10-14,19-22,34-35,39-43,49-61,85,101-102H,8-9,15-18,23-33,36-38H2,1-7H3,(H,82,86)(H,87,113)(H,88,111)(H,89,105)(H,90,106)(H,91,108)(H,92,103)(H,93,104)(H,94,112)(H,95,110)(H,96,107)(H,97,109)(H4,78,79,83)(H4,80,81,84)/t40-,41-,42-,43-,49-,50-,51+,52-,53-,54-,55-,56-,57-,58-,59-,60-,61-/m0/s1	PDB KEGG UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	3.90	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Queensland Curated by ChEMBL					Assay Description Displacement of [125I]-NDP-alpha-MSH from human MC1R LBD expressed in HEK293 cell membranes incubated for 16 to 23 hrs in dark by scintillation proxi...				J Med Chem 61: 3674-3684 (2018) Article DOI: 10.1021/acs.jmedchem.8b00170 BindingDB Entry DOI: 10.7270/Q2736TCZ
					More data for this Ligand-Target Pair
Melanocortin receptor 3 (Homo sapiens (Human))	BDBM50263814 (CHEMBL4101216) Show SMILES CC[C@H](C)[C@@H]1NC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](C)NC(=O)[C@@H](NC(=O)[C@@H]2CSSC[C@H](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)[C@@H](Cc1c[nH]c3ccccc13)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N2)[C@H](C)O)[C@@H](C)CC |r| Show InChI InChI=1S/C77H113N23O16S2/c1-8-40(3)59-71(112)94-54-37-117-118-38-55(68(109)97-61(43(6)102)72(113)87-42(5)62(103)92-53(36-101)66(107)96-60(41(4)9-2)75(116)100-30-18-26-57(100)74(115)99-29-17-25-56(99)69(110)95-59)93-63(104)49(23-15-27-83-76(78)79)88-70(111)58(32-45-34-85-48-22-14-13-21-47(45)48)98(7)73(114)50(24-16-28-84-77(80)81)89-64(105)51(31-44-19-11-10-12-20-44)90-65(106)52(91-67(54)108)33-46-35-82-39-86-46/h10-14,19-22,34-35,39-43,49-61,85,101-102H,8-9,15-18,23-33,36-38H2,1-7H3,(H,82,86)(H,87,113)(H,88,111)(H,89,105)(H,90,106)(H,91,108)(H,92,103)(H,93,104)(H,94,112)(H,95,110)(H,96,107)(H,97,109)(H4,78,79,83)(H4,80,81,84)/t40-,41-,42-,43-,49-,50-,51+,52-,53-,54-,55-,56-,57-,58-,59-,60-,61-/m0/s1	UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	324	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Queensland Curated by ChEMBL					Assay Description Displacement of [125I]-NDP-alpha-MSH from human MC3R LBD expressed in HEK293 cell membranes incubated for 16 to 23 hrs in dark by scintillation proxi...				J Med Chem 61: 3674-3684 (2018) Article DOI: 10.1021/acs.jmedchem.8b00170 BindingDB Entry DOI: 10.7270/Q2736TCZ
					More data for this Ligand-Target Pair
Melanocortin receptor 4 (Homo sapiens (Human))	BDBM50263814 (CHEMBL4101216) Show SMILES CC[C@H](C)[C@@H]1NC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](C)NC(=O)[C@@H](NC(=O)[C@@H]2CSSC[C@H](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)[C@@H](Cc1c[nH]c3ccccc13)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N2)[C@H](C)O)[C@@H](C)CC |r| Show InChI InChI=1S/C77H113N23O16S2/c1-8-40(3)59-71(112)94-54-37-117-118-38-55(68(109)97-61(43(6)102)72(113)87-42(5)62(103)92-53(36-101)66(107)96-60(41(4)9-2)75(116)100-30-18-26-57(100)74(115)99-29-17-25-56(99)69(110)95-59)93-63(104)49(23-15-27-83-76(78)79)88-70(111)58(32-45-34-85-48-22-14-13-21-47(45)48)98(7)73(114)50(24-16-28-84-77(80)81)89-64(105)51(31-44-19-11-10-12-20-44)90-65(106)52(91-67(54)108)33-46-35-82-39-86-46/h10-14,19-22,34-35,39-43,49-61,85,101-102H,8-9,15-18,23-33,36-38H2,1-7H3,(H,82,86)(H,87,113)(H,88,111)(H,89,105)(H,90,106)(H,91,108)(H,92,103)(H,93,104)(H,94,112)(H,95,110)(H,96,107)(H,97,109)(H4,78,79,83)(H4,80,81,84)/t40-,41-,42-,43-,49-,50-,51+,52-,53-,54-,55-,56-,57-,58-,59-,60-,61-/m0/s1	PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	832	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Queensland Curated by ChEMBL					Assay Description Displacement of [125I]-NDP-alpha-MSH from human MC4R LBD expressed in HEK293 cell membranes incubated for 16 to 23 hrs in dark by scintillation proxi...				J Med Chem 61: 3674-3684 (2018) Article DOI: 10.1021/acs.jmedchem.8b00170 BindingDB Entry DOI: 10.7270/Q2736TCZ
					More data for this Ligand-Target Pair
Melanocortin receptor 4 (Homo sapiens (Human))	BDBM50263814 (CHEMBL4101216) Show SMILES CC[C@H](C)[C@@H]1NC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](C)NC(=O)[C@@H](NC(=O)[C@@H]2CSSC[C@H](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)[C@@H](Cc1c[nH]c3ccccc13)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N2)[C@H](C)O)[C@@H](C)CC |r| Show InChI InChI=1S/C77H113N23O16S2/c1-8-40(3)59-71(112)94-54-37-117-118-38-55(68(109)97-61(43(6)102)72(113)87-42(5)62(103)92-53(36-101)66(107)96-60(41(4)9-2)75(116)100-30-18-26-57(100)74(115)99-29-17-25-56(99)69(110)95-59)93-63(104)49(23-15-27-83-76(78)79)88-70(111)58(32-45-34-85-48-22-14-13-21-47(45)48)98(7)73(114)50(24-16-28-84-77(80)81)89-64(105)51(31-44-19-11-10-12-20-44)90-65(106)52(91-67(54)108)33-46-35-82-39-86-46/h10-14,19-22,34-35,39-43,49-61,85,101-102H,8-9,15-18,23-33,36-38H2,1-7H3,(H,82,86)(H,87,113)(H,88,111)(H,89,105)(H,90,106)(H,91,108)(H,92,103)(H,93,104)(H,94,112)(H,95,110)(H,96,107)(H,97,109)(H4,78,79,83)(H4,80,81,84)/t40-,41-,42-,43-,49-,50-,51+,52-,53-,54-,55-,56-,57-,58-,59-,60-,61-/m0/s1	PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	331	n/a	n/a	n/a	n/a
The University of Queensland Curated by ChEMBL					Assay Description Agonist activity at human MC4R expressed in low doxycyclin-treated HEK293 cell membranes assessed as increase in cAMP production after 45 mins by HTR...				J Med Chem 61: 3674-3684 (2018) Article DOI: 10.1021/acs.jmedchem.8b00170 BindingDB Entry DOI: 10.7270/Q2736TCZ
					More data for this Ligand-Target Pair
Melanocortin receptor 4 (Homo sapiens (Human))	BDBM50263814 (CHEMBL4101216) Show SMILES CC[C@H](C)[C@@H]1NC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](C)NC(=O)[C@@H](NC(=O)[C@@H]2CSSC[C@H](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)[C@@H](Cc1c[nH]c3ccccc13)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N2)[C@H](C)O)[C@@H](C)CC |r| Show InChI InChI=1S/C77H113N23O16S2/c1-8-40(3)59-71(112)94-54-37-117-118-38-55(68(109)97-61(43(6)102)72(113)87-42(5)62(103)92-53(36-101)66(107)96-60(41(4)9-2)75(116)100-30-18-26-57(100)74(115)99-29-17-25-56(99)69(110)95-59)93-63(104)49(23-15-27-83-76(78)79)88-70(111)58(32-45-34-85-48-22-14-13-21-47(45)48)98(7)73(114)50(24-16-28-84-77(80)81)89-64(105)51(31-44-19-11-10-12-20-44)90-65(106)52(91-67(54)108)33-46-35-82-39-86-46/h10-14,19-22,34-35,39-43,49-61,85,101-102H,8-9,15-18,23-33,36-38H2,1-7H3,(H,82,86)(H,87,113)(H,88,111)(H,89,105)(H,90,106)(H,91,108)(H,92,103)(H,93,104)(H,94,112)(H,95,110)(H,96,107)(H,97,109)(H4,78,79,83)(H4,80,81,84)/t40-,41-,42-,43-,49-,50-,51+,52-,53-,54-,55-,56-,57-,58-,59-,60-,61-/m0/s1	PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	28	n/a	n/a	n/a	n/a
The University of Queensland Curated by ChEMBL					Assay Description Agonist activity at human MC4R expressed in high doxycyclin-treated HEK293 cell membranes assessed as increase in cAMP production after 15 mins by HT...				J Med Chem 61: 3674-3684 (2018) Article DOI: 10.1021/acs.jmedchem.8b00170 BindingDB Entry DOI: 10.7270/Q2736TCZ
					More data for this Ligand-Target Pair
Melanocortin receptor (M4 and M5) (Homo sapiens (Human))	BDBM50263814 (CHEMBL4101216) Show SMILES CC[C@H](C)[C@@H]1NC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](C)NC(=O)[C@@H](NC(=O)[C@@H]2CSSC[C@H](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)[C@@H](Cc1c[nH]c3ccccc13)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N2)[C@H](C)O)[C@@H](C)CC |r| Show InChI InChI=1S/C77H113N23O16S2/c1-8-40(3)59-71(112)94-54-37-117-118-38-55(68(109)97-61(43(6)102)72(113)87-42(5)62(103)92-53(36-101)66(107)96-60(41(4)9-2)75(116)100-30-18-26-57(100)74(115)99-29-17-25-56(99)69(110)95-59)93-63(104)49(23-15-27-83-76(78)79)88-70(111)58(32-45-34-85-48-22-14-13-21-47(45)48)98(7)73(114)50(24-16-28-84-77(80)81)89-64(105)51(31-44-19-11-10-12-20-44)90-65(106)52(91-67(54)108)33-46-35-82-39-86-46/h10-14,19-22,34-35,39-43,49-61,85,101-102H,8-9,15-18,23-33,36-38H2,1-7H3,(H,82,86)(H,87,113)(H,88,111)(H,89,105)(H,90,106)(H,91,108)(H,92,103)(H,93,104)(H,94,112)(H,95,110)(H,96,107)(H,97,109)(H4,78,79,83)(H4,80,81,84)/t40-,41-,42-,43-,49-,50-,51+,52-,53-,54-,55-,56-,57-,58-,59-,60-,61-/m0/s1	UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	59	n/a	n/a	n/a	n/a	n/a	n/a
The University of Queensland Curated by ChEMBL					Assay Description Displacement of [125I]-NDP-alpha-MSH from human MC5R LBD expressed in HEK293 cell membranes incubated for 16 to 23 hrs in dark by scintillation proxi...				J Med Chem 61: 3674-3684 (2018) Article DOI: 10.1021/acs.jmedchem.8b00170 BindingDB Entry DOI: 10.7270/Q2736TCZ
					More data for this Ligand-Target Pair
Melanocortin receptor 3 (Homo sapiens (Human))	BDBM50263814 (CHEMBL4101216) Show SMILES CC[C@H](C)[C@@H]1NC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](C)NC(=O)[C@@H](NC(=O)[C@@H]2CSSC[C@H](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)[C@@H](Cc1c[nH]c3ccccc13)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N2)[C@H](C)O)[C@@H](C)CC |r| Show InChI InChI=1S/C77H113N23O16S2/c1-8-40(3)59-71(112)94-54-37-117-118-38-55(68(109)97-61(43(6)102)72(113)87-42(5)62(103)92-53(36-101)66(107)96-60(41(4)9-2)75(116)100-30-18-26-57(100)74(115)99-29-17-25-56(99)69(110)95-59)93-63(104)49(23-15-27-83-76(78)79)88-70(111)58(32-45-34-85-48-22-14-13-21-47(45)48)98(7)73(114)50(24-16-28-84-77(80)81)89-64(105)51(31-44-19-11-10-12-20-44)90-65(106)52(91-67(54)108)33-46-35-82-39-86-46/h10-14,19-22,34-35,39-43,49-61,85,101-102H,8-9,15-18,23-33,36-38H2,1-7H3,(H,82,86)(H,87,113)(H,88,111)(H,89,105)(H,90,106)(H,91,108)(H,92,103)(H,93,104)(H,94,112)(H,95,110)(H,96,107)(H,97,109)(H4,78,79,83)(H4,80,81,84)/t40-,41-,42-,43-,49-,50-,51+,52-,53-,54-,55-,56-,57-,58-,59-,60-,61-/m0/s1	UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	20	n/a	n/a	n/a	n/a
The University of Queensland Curated by ChEMBL					Assay Description Agonist activity at human MC3R expressed in low doxycyclin-treated HEK293 cell membranes assessed as increase in cAMP production after 45 mins by HTR...				J Med Chem 61: 3674-3684 (2018) Article DOI: 10.1021/acs.jmedchem.8b00170 BindingDB Entry DOI: 10.7270/Q2736TCZ
					More data for this Ligand-Target Pair
Melanocyte-stimulating hormone receptor (Homo sapiens (Human))	BDBM50263814 (CHEMBL4101216) Show SMILES CC[C@H](C)[C@@H]1NC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](C)NC(=O)[C@@H](NC(=O)[C@@H]2CSSC[C@H](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)[C@@H](Cc1c[nH]c3ccccc13)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N2)[C@H](C)O)[C@@H](C)CC |r| Show InChI InChI=1S/C77H113N23O16S2/c1-8-40(3)59-71(112)94-54-37-117-118-38-55(68(109)97-61(43(6)102)72(113)87-42(5)62(103)92-53(36-101)66(107)96-60(41(4)9-2)75(116)100-30-18-26-57(100)74(115)99-29-17-25-56(99)69(110)95-59)93-63(104)49(23-15-27-83-76(78)79)88-70(111)58(32-45-34-85-48-22-14-13-21-47(45)48)98(7)73(114)50(24-16-28-84-77(80)81)89-64(105)51(31-44-19-11-10-12-20-44)90-65(106)52(91-67(54)108)33-46-35-82-39-86-46/h10-14,19-22,34-35,39-43,49-61,85,101-102H,8-9,15-18,23-33,36-38H2,1-7H3,(H,82,86)(H,87,113)(H,88,111)(H,89,105)(H,90,106)(H,91,108)(H,92,103)(H,93,104)(H,94,112)(H,95,110)(H,96,107)(H,97,109)(H4,78,79,83)(H4,80,81,84)/t40-,41-,42-,43-,49-,50-,51+,52-,53-,54-,55-,56-,57-,58-,59-,60-,61-/m0/s1	PDB KEGG UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	1.5	n/a	n/a	n/a	n/a
The University of Queensland Curated by ChEMBL					Assay Description Agonist activity at human MC1R expressed in low doxycyclin-treated HEK293 cell membranes assessed as increase in cAMP production after 45 mins by HTR...				J Med Chem 61: 3674-3684 (2018) Article DOI: 10.1021/acs.jmedchem.8b00170 BindingDB Entry DOI: 10.7270/Q2736TCZ
					More data for this Ligand-Target Pair