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BDBM50221137 4-((S)-1-(2-(4-((R)-3-(2,4-dichlorophenyl)-2-(2-oxopyrrolidin-1-yl)propanoyl)piperazin-1-yl)-5-(trifluoromethyl)phenyl)-3-methylbutylamino)butanoic acid::CHEMBL262320

SMILES: CC(C)C[C@H](NCCCC(O)=O)c1cc(ccc1N1CCN(CC1)C(=O)[C@@H](Cc1ccc(Cl)cc1Cl)N1CCCC1=O)C(F)(F)F

InChI Key: InChIKey=XNPVNWIDDNEPTG-LMSSTIIKSA-N

Data: 1 KI  2 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50221137   
Target/Host
(Institution)
LigandTarget/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
pHTemp
°C
Melanocortin receptor 4


(Homo sapiens (Human))
BDBM50221137
PNG
(4-((S)-1-(2-(4-((R)-3-(2,4-dichlorophenyl)-2-(2-ox...)
Show SMILES CC(C)C[C@H](NCCCC(O)=O)c1cc(ccc1N1CCN(CC1)C(=O)[C@@H](Cc1ccc(Cl)cc1Cl)N1CCCC1=O)C(F)(F)F
Show InChI InChI=1S/C33H41Cl2F3N4O4/c1-21(2)17-27(39-11-3-6-31(44)45)25-19-23(33(36,37)38)8-10-28(25)40-13-15-41(16-14-40)32(46)29(42-12-4-5-30(42)43)18-22-7-9-24(34)20-26(22)35/h7-10,19-21,27,29,39H,3-6,11-18H2,1-2H3,(H,44,45)/t27-,29+/m0/s1
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PC cid
PC sid
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Article
PubMed
40n/an/an/an/an/an/an/an/a



Neurocrine Biosciences, Inc.

Curated by ChEMBL


Assay Description
Binding affinity at human MC4R


Bioorg Med Chem Lett 17: 5610-3 (2007)


Article DOI: 10.1016/j.bmcl.2007.07.097
BindingDB Entry DOI: 10.7270/Q2XK8F8V
More data for this
Ligand-Target Pair
Cytochrome P450 3A4


(Homo sapiens (Human))
BDBM50221137
PNG
(4-((S)-1-(2-(4-((R)-3-(2,4-dichlorophenyl)-2-(2-ox...)
Show SMILES CC(C)C[C@H](NCCCC(O)=O)c1cc(ccc1N1CCN(CC1)C(=O)[C@@H](Cc1ccc(Cl)cc1Cl)N1CCCC1=O)C(F)(F)F
Show InChI InChI=1S/C33H41Cl2F3N4O4/c1-21(2)17-27(39-11-3-6-31(44)45)25-19-23(33(36,37)38)8-10-28(25)40-13-15-41(16-14-40)32(46)29(42-12-4-5-30(42)43)18-22-7-9-24(34)20-26(22)35/h7-10,19-21,27,29,39H,3-6,11-18H2,1-2H3,(H,44,45)/t27-,29+/m0/s1
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MMDB

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n/an/a 2.50E+4n/an/an/an/an/an/a



Neurocrine Biosciences, Inc.

Curated by ChEMBL


Assay Description
Inhibition of microsomal CYP3A4


Bioorg Med Chem Lett 17: 5610-3 (2007)


Article DOI: 10.1016/j.bmcl.2007.07.097
BindingDB Entry DOI: 10.7270/Q2XK8F8V
More data for this
Ligand-Target Pair
Melanocortin receptor 4


(Homo sapiens (Human))
BDBM50221137
PNG
(4-((S)-1-(2-(4-((R)-3-(2,4-dichlorophenyl)-2-(2-ox...)
Show SMILES CC(C)C[C@H](NCCCC(O)=O)c1cc(ccc1N1CCN(CC1)C(=O)[C@@H](Cc1ccc(Cl)cc1Cl)N1CCCC1=O)C(F)(F)F
Show InChI InChI=1S/C33H41Cl2F3N4O4/c1-21(2)17-27(39-11-3-6-31(44)45)25-19-23(33(36,37)38)8-10-28(25)40-13-15-41(16-14-40)32(46)29(42-12-4-5-30(42)43)18-22-7-9-24(34)20-26(22)35/h7-10,19-21,27,29,39H,3-6,11-18H2,1-2H3,(H,44,45)/t27-,29+/m0/s1
PDB

KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 340n/an/an/an/an/an/a



Neurocrine Biosciences, Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human MC4R expressed in HEK293 cells by cAMP accumulation assay


Bioorg Med Chem Lett 17: 5610-3 (2007)


Article DOI: 10.1016/j.bmcl.2007.07.097
BindingDB Entry DOI: 10.7270/Q2XK8F8V
More data for this
Ligand-Target Pair