BindingDB logo
myBDB logout

BDBM50467131 CHEMBL4288964

SMILES: CCCCc1nc(C(C)C)c(CC(=S)N2CCCC2)c(=O)n1Cc1ccc(cc1)-c1ccccc1-c1noc(=O)[nH]1

InChI Key: InChIKey=CCPJHWPUGFTSMB-UHFFFAOYSA-N

Data: 3 IC50  1 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 4 hits for monomerid = 50467131   
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
1,3-beta-glucan synthase component GLS2


(Saccharomyces cerevisiae)
BDBM50467131
PNG
(CHEMBL4288964)
Show SMILES CCCCc1nc(C(C)C)c(CC(=S)N2CCCC2)c(=O)n1Cc1ccc(cc1)-c1ccccc1-c1noc(=O)[nH]1
Show InChI InChI=1S/C32H37N5O3S/c1-4-5-12-27-33-29(21(2)3)26(19-28(41)36-17-8-9-18-36)31(38)37(27)20-22-13-15-23(16-14-22)24-10-6-7-11-25(24)30-34-32(39)40-35-30/h6-7,10-11,13-16,21H,4-5,8-9,12,17-20H2,1-3H3,(H,34,35,39)
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 7.00E+3n/an/an/an/an/an/a



Boryung Pharmaceuticals Co. Ltd.

Curated by ChEMBL


Assay Description
Inhibition of human ERG


Bioorg Med Chem Lett 28: 3155-3160 (2018)


Article DOI: 10.1016/j.bmcl.2018.08.036
BindingDB Entry DOI: 10.7270/Q2X63QMZ
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM50467131
PNG
(CHEMBL4288964)
Show SMILES CCCCc1nc(C(C)C)c(CC(=S)N2CCCC2)c(=O)n1Cc1ccc(cc1)-c1ccccc1-c1noc(=O)[nH]1
Show InChI InChI=1S/C32H37N5O3S/c1-4-5-12-27-33-29(21(2)3)26(19-28(41)36-17-8-9-18-36)31(38)37(27)20-22-13-15-23(16-14-22)24-10-6-7-11-25(24)30-34-32(39)40-35-30/h6-7,10-11,13-16,21H,4-5,8-9,12,17-20H2,1-3H3,(H,34,35,39)
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 2.20n/an/an/an/an/an/a



Boryung Pharmaceuticals Co. Ltd.

Curated by ChEMBL


Assay Description
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by calcium mobilizing assay


Bioorg Med Chem Lett 28: 3155-3160 (2018)


Article DOI: 10.1016/j.bmcl.2018.08.036
BindingDB Entry DOI: 10.7270/Q2X63QMZ
More data for this
Ligand-Target Pair
Peroxisome proliferator-activated receptor


(Homo sapiens (Human))
BDBM50467131
PNG
(CHEMBL4288964)
Show SMILES CCCCc1nc(C(C)C)c(CC(=S)N2CCCC2)c(=O)n1Cc1ccc(cc1)-c1ccccc1-c1noc(=O)[nH]1
Show InChI InChI=1S/C32H37N5O3S/c1-4-5-12-27-33-29(21(2)3)26(19-28(41)36-17-8-9-18-36)31(38)37(27)20-22-13-15-23(16-14-22)24-10-6-7-11-25(24)30-34-32(39)40-35-30/h6-7,10-11,13-16,21H,4-5,8-9,12,17-20H2,1-3H3,(H,34,35,39)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/an/an/a 3.10E+3n/an/an/an/a



Boryung Pharmaceuticals Co. Ltd.

Curated by ChEMBL


Assay Description
Agonist activity at PPARgamma (unknown origin)


Bioorg Med Chem Lett 28: 3155-3160 (2018)


Article DOI: 10.1016/j.bmcl.2018.08.036
BindingDB Entry DOI: 10.7270/Q2X63QMZ
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM50467131
PNG
(CHEMBL4288964)
Show SMILES CCCCc1nc(C(C)C)c(CC(=S)N2CCCC2)c(=O)n1Cc1ccc(cc1)-c1ccccc1-c1noc(=O)[nH]1
Show InChI InChI=1S/C32H37N5O3S/c1-4-5-12-27-33-29(21(2)3)26(19-28(41)36-17-8-9-18-36)31(38)37(27)20-22-13-15-23(16-14-22)24-10-6-7-11-25(24)30-34-32(39)40-35-30/h6-7,10-11,13-16,21H,4-5,8-9,12,17-20H2,1-3H3,(H,34,35,39)
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 11n/an/an/an/an/an/a



Boryung Pharmaceuticals Co. Ltd.

Curated by ChEMBL


Assay Description
Antagonist activity at type-1 angiotensin 2 receptor (unknown origin) by beta-arrestin recruitment assay


Bioorg Med Chem Lett 28: 3155-3160 (2018)


Article DOI: 10.1016/j.bmcl.2018.08.036
BindingDB Entry DOI: 10.7270/Q2X63QMZ
More data for this
Ligand-Target Pair