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BDBM28693 2-({3-[(7-methoxy-1H-indole-1-)sulfonyl]benzene}amido)-5-methylbenzoic acid::Anthranilic acid deriv., 31

SMILES: COc1cccc2ccn(c12)S(=O)(=O)c1cccc(c1)C(=O)Nc1ccc(C)cc1C(O)=O

InChI Key: InChIKey=DHVJWXQNKUKRQP-UHFFFAOYSA-N

Data: 3 IC50  1 EC50

Find this compound or compounds like it in BindingDB or PDB:
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 28693   
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
Peroxisome proliferator-activated receptor delta


(Homo sapiens (Human))
BDBM28693
PNG
(2-({3-[(7-methoxy-1H-indole-1-)sulfonyl]benzene}am...)
Show SMILES COc1cccc2ccn(c12)S(=O)(=O)c1cccc(c1)C(=O)Nc1ccc(C)cc1C(O)=O
Show InChI InChI=1S/C24H20N2O6S/c1-15-9-10-20(19(13-15)24(28)29)25-23(27)17-6-3-7-18(14-17)33(30,31)26-12-11-16-5-4-8-21(32-2)22(16)26/h3-14H,1-2H3,(H,25,27)(H,28,29)
PDB

UniProtKB/SwissProt
UniProtKB/TrEMBL

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 50n/a 631n/an/an/an/a



GSK



Assay Description
Competition-binding curves for test compounds were determined with expressed human PPAR LBD. Plots of inhibitor concentration versus cpm of radioliga...


Bioorg Med Chem Lett 18: 5018-22 (2008)


Article DOI: 10.1016/j.bmcl.2008.08.011
BindingDB Entry DOI: 10.7270/Q2WD3XWS
More data for this
Ligand-Target Pair
Peroxisome proliferator-activated receptor


(Homo sapiens (Human))
BDBM28693
PNG
(2-({3-[(7-methoxy-1H-indole-1-)sulfonyl]benzene}am...)
Show SMILES COc1cccc2ccn(c12)S(=O)(=O)c1cccc(c1)C(=O)Nc1ccc(C)cc1C(O)=O
Show InChI InChI=1S/C24H20N2O6S/c1-15-9-10-20(19(13-15)24(28)29)25-23(27)17-6-3-7-18(14-17)33(30,31)26-12-11-16-5-4-8-21(32-2)22(16)26/h3-14H,1-2H3,(H,25,27)(H,28,29)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 5.01E+3n/an/an/an/an/an/a



GSK



Assay Description
Competition-binding curves for test compounds were determined with expressed human PPAR LBD. Plots of inhibitor concentration versus cpm of radioliga...


Bioorg Med Chem Lett 18: 5018-22 (2008)


Article DOI: 10.1016/j.bmcl.2008.08.011
BindingDB Entry DOI: 10.7270/Q2WD3XWS
More data for this
Ligand-Target Pair
Peroxisome proliferator-activated receptor alpha (PPAR alpha)


(Homo sapiens (Human))
BDBM28693
PNG
(2-({3-[(7-methoxy-1H-indole-1-)sulfonyl]benzene}am...)
Show SMILES COc1cccc2ccn(c12)S(=O)(=O)c1cccc(c1)C(=O)Nc1ccc(C)cc1C(O)=O
Show InChI InChI=1S/C24H20N2O6S/c1-15-9-10-20(19(13-15)24(28)29)25-23(27)17-6-3-7-18(14-17)33(30,31)26-12-11-16-5-4-8-21(32-2)22(16)26/h3-14H,1-2H3,(H,25,27)(H,28,29)
PDB

UniProtKB/SwissProt
UniProtKB/TrEMBL

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

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



GSK



Assay Description
Competition-binding curves for test compounds were determined with expressed human PPAR LBD. Plots of inhibitor concentration versus cpm of radioliga...


Bioorg Med Chem Lett 18: 5018-22 (2008)


Article DOI: 10.1016/j.bmcl.2008.08.011
BindingDB Entry DOI: 10.7270/Q2WD3XWS
More data for this
Ligand-Target Pair