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Compile Data Set for Download or QSAR

Marvin 2D Structure

The following exact ligands are found in BindingDB

Wt: 446.5
BDBM50351422

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB (change energy unit to kcal/mol)

Found 4 hits in this display   
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
Prostaglandin E synthase


(Homo sapiens (Human))
BDBM50351422
PNG
(CHEMBL1819394)
Show SMILES CCCCC(Cc1ccc(OCCc2ccccc2)c(OCCc2ccccc2)c1)C(O)=O
Show InChI InChI=1S/C29H34O4/c1-2-3-14-26(29(30)31)21-25-15-16-27(32-19-17-23-10-6-4-7-11-23)28(22-25)33-20-18-24-12-8-5-9-13-24/h4-13,15-16,22,26H,2-3,14,17-21H2,1H3,(H,30,31)
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Article
PubMed
n/an/a 2.70E+3n/an/an/an/an/an/a



ZAFES/LiFF/Goethe-University Frankfurt

Curated by ChEMBL


Assay Description
Inhibition of mPGES-1 in human IL-1beta-stimulated A549 cell microsomes assessed as reduction of PGE2 formation from PGH2 after 15 mins by RP-HPLC an...


J Med Chem 54: 4490-507 (2011)


Article DOI: 10.1021/jm200092b
BindingDB Entry DOI: 10.7270/Q2XG9S8B
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50351422
PNG
(CHEMBL1819394)
Show SMILES CCCCC(Cc1ccc(OCCc2ccccc2)c(OCCc2ccccc2)c1)C(O)=O
Show InChI InChI=1S/C29H34O4/c1-2-3-14-26(29(30)31)21-25-15-16-27(32-19-17-23-10-6-4-7-11-23)28(22-25)33-20-18-24-12-8-5-9-13-24/h4-13,15-16,22,26H,2-3,14,17-21H2,1H3,(H,30,31)
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n/an/a 6.00E+3n/an/an/an/an/an/a



ZAFES/LiFF/Goethe-University Frankfurt

Curated by ChEMBL


Assay Description
Inhibition of 5-lipoxygenase-mediated 5(S)-H(p)ETE formation in fMLP-stimulated human PMNL incubated 10 mins prior to fMLP challenge


J Med Chem 54: 4490-507 (2011)


Article DOI: 10.1021/jm200092b
BindingDB Entry DOI: 10.7270/Q2XG9S8B
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50351422
PNG
(CHEMBL1819394)
Show SMILES CCCCC(Cc1ccc(OCCc2ccccc2)c(OCCc2ccccc2)c1)C(O)=O
Show InChI InChI=1S/C29H34O4/c1-2-3-14-26(29(30)31)21-25-15-16-27(32-19-17-23-10-6-4-7-11-23)28(22-25)33-20-18-24-12-8-5-9-13-24/h4-13,15-16,22,26H,2-3,14,17-21H2,1H3,(H,30,31)
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n/an/a>1.00E+4n/an/an/an/an/an/a



ZAFES/LiFF/Goethe-University Frankfurt

Curated by ChEMBL


Assay Description
Inhibition of human recombinant 5-lipoxygenase-mediated product formation from arachidonic acid after 5 to 10 mins by HPLC analysis


J Med Chem 54: 4490-507 (2011)


Article DOI: 10.1021/jm200092b
BindingDB Entry DOI: 10.7270/Q2XG9S8B
More data for this
Ligand-Target Pair
Peroxisome proliferator-activated receptor gamma


(Homo sapiens (Human))
BDBM50351422
PNG
(CHEMBL1819394)
Show SMILES CCCCC(Cc1ccc(OCCc2ccccc2)c(OCCc2ccccc2)c1)C(O)=O
Show InChI InChI=1S/C29H34O4/c1-2-3-14-26(29(30)31)21-25-15-16-27(32-19-17-23-10-6-4-7-11-23)28(22-25)33-20-18-24-12-8-5-9-13-24/h4-13,15-16,22,26H,2-3,14,17-21H2,1H3,(H,30,31)
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n/an/an/an/a 2.20E+3n/an/an/an/a



Goethe-University Frankfurt

Curated by ChEMBL


Assay Description
Modulation of human PPARgamma-LBD expressed in african green monkey COS7 cells co-transfected with Gal4 assessed as activation of transactivation act...


Bioorg Med Chem 19: 5372-82 (2011)


Article DOI: 10.1016/j.bmc.2011.08.003
BindingDB Entry DOI: 10.7270/Q2JQ11D0
More data for this
Ligand-Target Pair