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BDBM50437381 CHEMBL2408625

SMILES: CS(=O)(=O)c1ccc2nc([nH]c2c1)-c1ccc(nc1)-c1ccc(O[C@H]2CC[C@@H](CC2)C(O)=O)nc1

InChI Key: InChIKey=BKAFEPXXRGNENW-RZDIXWSQSA-N

Data: 3 IC50

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 3 hits for monomerid = 50437381   
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
Diacylglycerol O-acyltransferase 1


(Mus musculus (mouse))
BDBM50437381
PNG
(CHEMBL2408625)
Show SMILES CS(=O)(=O)c1ccc2nc([nH]c2c1)-c1ccc(nc1)-c1ccc(O[C@H]2CC[C@@H](CC2)C(O)=O)nc1 |r,wU:24.26,wD:27.33,(48.42,-30.59,;48.42,-32.13,;47.64,-33.46,;46.88,-32.12,;49.76,-32.9,;49.76,-34.44,;51.08,-35.2,;52.41,-34.44,;53.88,-34.92,;54.79,-33.67,;53.88,-32.42,;52.41,-32.9,;51.08,-32.12,;56.32,-33.67,;57.09,-32.34,;58.63,-32.34,;59.4,-33.67,;58.63,-35.01,;57.09,-35.01,;60.94,-33.67,;61.7,-32.34,;63.24,-32.34,;64.02,-33.67,;65.56,-33.67,;66.33,-35,;67.86,-34.98,;68.63,-36.32,;67.86,-37.66,;66.32,-37.65,;65.56,-36.32,;68.64,-39,;67.87,-40.33,;70.18,-39,;63.25,-35.01,;61.71,-35.01,)|
Show InChI InChI=1S/C25H24N4O5S/c1-35(32,33)19-8-10-21-22(12-19)29-24(28-21)17-4-9-20(26-14-17)16-5-11-23(27-13-16)34-18-6-2-15(3-7-18)25(30)31/h4-5,8-15,18H,2-3,6-7H2,1H3,(H,28,29)(H,30,31)/t15-,18-
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Similars

Article
PubMed
n/an/a 727n/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of mouse DGAT1


ACS Med Chem Lett 4: 773-8 (2013)


Article DOI: 10.1021/ml400168h
BindingDB Entry DOI: 10.7270/Q2NG4S28
More data for this
Ligand-Target Pair
Diacylglycerol O-acyltransferase 1 (DGAT1)


(Homo sapiens (Human))
BDBM50437381
PNG
(CHEMBL2408625)
Show SMILES CS(=O)(=O)c1ccc2nc([nH]c2c1)-c1ccc(nc1)-c1ccc(O[C@H]2CC[C@@H](CC2)C(O)=O)nc1 |r,wU:24.26,wD:27.33,(48.42,-30.59,;48.42,-32.13,;47.64,-33.46,;46.88,-32.12,;49.76,-32.9,;49.76,-34.44,;51.08,-35.2,;52.41,-34.44,;53.88,-34.92,;54.79,-33.67,;53.88,-32.42,;52.41,-32.9,;51.08,-32.12,;56.32,-33.67,;57.09,-32.34,;58.63,-32.34,;59.4,-33.67,;58.63,-35.01,;57.09,-35.01,;60.94,-33.67,;61.7,-32.34,;63.24,-32.34,;64.02,-33.67,;65.56,-33.67,;66.33,-35,;67.86,-34.98,;68.63,-36.32,;67.86,-37.66,;66.32,-37.65,;65.56,-36.32,;68.64,-39,;67.87,-40.33,;70.18,-39,;63.25,-35.01,;61.71,-35.01,)|
Show InChI InChI=1S/C25H24N4O5S/c1-35(32,33)19-8-10-21-22(12-19)29-24(28-21)17-4-9-20(26-14-17)16-5-11-23(27-13-16)34-18-6-2-15(3-7-18)25(30)31/h4-5,8-15,18H,2-3,6-7H2,1H3,(H,28,29)(H,30,31)/t15-,18-
PDB

UniProtKB/SwissProt

antibodypedia
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AffyNet 
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PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 137n/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of human DGAT1


ACS Med Chem Lett 4: 773-8 (2013)


Article DOI: 10.1021/ml400168h
BindingDB Entry DOI: 10.7270/Q2NG4S28
More data for this
Ligand-Target Pair
Diacylglycerol O-acyltransferase 1 (DGAT1)


(Homo sapiens (Human))
BDBM50437381
PNG
(CHEMBL2408625)
Show SMILES CS(=O)(=O)c1ccc2nc([nH]c2c1)-c1ccc(nc1)-c1ccc(O[C@H]2CC[C@@H](CC2)C(O)=O)nc1 |r,wU:24.26,wD:27.33,(48.42,-30.59,;48.42,-32.13,;47.64,-33.46,;46.88,-32.12,;49.76,-32.9,;49.76,-34.44,;51.08,-35.2,;52.41,-34.44,;53.88,-34.92,;54.79,-33.67,;53.88,-32.42,;52.41,-32.9,;51.08,-32.12,;56.32,-33.67,;57.09,-32.34,;58.63,-32.34,;59.4,-33.67,;58.63,-35.01,;57.09,-35.01,;60.94,-33.67,;61.7,-32.34,;63.24,-32.34,;64.02,-33.67,;65.56,-33.67,;66.33,-35,;67.86,-34.98,;68.63,-36.32,;67.86,-37.66,;66.32,-37.65,;65.56,-36.32,;68.64,-39,;67.87,-40.33,;70.18,-39,;63.25,-35.01,;61.71,-35.01,)|
Show InChI InChI=1S/C25H24N4O5S/c1-35(32,33)19-8-10-21-22(12-19)29-24(28-21)17-4-9-20(26-14-17)16-5-11-23(27-13-16)34-18-6-2-15(3-7-18)25(30)31/h4-5,8-15,18H,2-3,6-7H2,1H3,(H,28,29)(H,30,31)/t15-,18-
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>1.00E+4n/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of human ACAT1


ACS Med Chem Lett 4: 773-8 (2013)


Article DOI: 10.1021/ml400168h
BindingDB Entry DOI: 10.7270/Q2NG4S28
More data for this
Ligand-Target Pair