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Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Melanocortin receptor 4' and Ligand = 'BDBM50263838'   
Target/Host
(Institution)
LigandTarget/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
pHTemp
°C
Melanocortin receptor 4


(Homo sapiens (Human))
BDBM50263838
PNG
(CHEMBL4092141)
Show SMILES CC[C@H](C)[C@@H]1NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2c[nH]c3ccccc23)N(C)C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@H](Cc2cnc[nH]2)N(C)C(=O)[C@@H](NC(=O)[C@@H]2CSSC[C@H](NC1=O)C(=O)N[C@@H](Cc1ccccc1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(O)=O)C(=O)NCC(=O)N[C@@H](CCCNC(N)=N)C(=O)N2)[C@@H](C)O |r|
Show InChI InChI=1S/C81H111N23O17S2/c1-6-44(2)65-75(117)98-57-41-122-123-42-58(97-68(110)52(25-15-29-87-80(82)83)92-63(106)40-90-67(109)55(37-64(107)108)95-72(114)59-27-17-31-103(59)77(119)56(96-70(57)112)34-47-21-11-8-12-22-47)71(113)100-66(45(3)105)79(121)101(4)61(36-49-39-86-43-91-49)74(116)94-54(33-46-19-9-7-10-20-46)69(111)93-53(26-16-30-88-81(84)85)76(118)102(5)62(35-48-38-89-51-24-14-13-23-50(48)51)78(120)104-32-18-28-60(104)73(115)99-65/h7-14,19-24,38-39,43-45,52-62,65-66,89,105H,6,15-18,25-37,40-42H2,1-5H3,(H,86,91)(H,90,109)(H,92,106)(H,93,111)(H,94,116)(H,95,114)(H,96,112)(H,97,110)(H,98,117)(H,99,115)(H,100,113)(H,107,108)(H4,82,83,87)(H4,84,85,88)/t44-,45+,52-,53-,54+,55-,56-,57-,58-,59-,60-,61-,62-,65-,66-/m0/s1
PDB

KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
3.09E+3n/an/an/an/an/an/an/an/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))
BDBM50263838
PNG
(CHEMBL4092141)
Show SMILES CC[C@H](C)[C@@H]1NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2c[nH]c3ccccc23)N(C)C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@H](Cc2cnc[nH]2)N(C)C(=O)[C@@H](NC(=O)[C@@H]2CSSC[C@H](NC1=O)C(=O)N[C@@H](Cc1ccccc1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(O)=O)C(=O)NCC(=O)N[C@@H](CCCNC(N)=N)C(=O)N2)[C@@H](C)O |r|
Show InChI InChI=1S/C81H111N23O17S2/c1-6-44(2)65-75(117)98-57-41-122-123-42-58(97-68(110)52(25-15-29-87-80(82)83)92-63(106)40-90-67(109)55(37-64(107)108)95-72(114)59-27-17-31-103(59)77(119)56(96-70(57)112)34-47-21-11-8-12-22-47)71(113)100-66(45(3)105)79(121)101(4)61(36-49-39-86-43-91-49)74(116)94-54(33-46-19-9-7-10-20-46)69(111)93-53(26-16-30-88-81(84)85)76(118)102(5)62(35-48-38-89-51-24-14-13-23-50(48)51)78(120)104-32-18-28-60(104)73(115)99-65/h7-14,19-24,38-39,43-45,52-62,65-66,89,105H,6,15-18,25-37,40-42H2,1-5H3,(H,86,91)(H,90,109)(H,92,106)(H,93,111)(H,94,116)(H,95,114)(H,96,112)(H,97,110)(H,98,117)(H,99,115)(H,100,113)(H,107,108)(H4,82,83,87)(H4,84,85,88)/t44-,45+,52-,53-,54+,55-,56-,57-,58-,59-,60-,61-,62-,65-,66-/m0/s1
PDB

KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 1.74E+3n/an/an/an/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