BindingDB logo
myBDB logout
Compile Data Set for Download or QSAR

Found 47 hits Enz. Inhib. hit(s) with all data for entry = 50039907   
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))
BDBM50386165
PNG
(CHEMBL2042365)
Show SMILES Nc1cc(ccc1Cn1cc(nn1)-c1ccc(cc1)-c1ccccc1COc1cc(ccc1Cl)C(F)(F)F)C(O)=O
Show InChI InChI=1S/C30H22ClF3N4O3/c31-25-12-11-23(30(32,33)34)14-28(25)41-17-22-3-1-2-4-24(22)18-5-7-19(8-6-18)27-16-38(37-36-27)15-21-10-9-20(29(39)40)13-26(21)35/h1-14,16H,15,17,35H2,(H,39,40)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 680n/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of mPGES1 in IL-1beta-stimulated human A549 cell assessed as inhibition of PGE2 production preincubated for 15 mins before substrate addit...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50386165
PNG
(CHEMBL2042365)
Show SMILES Nc1cc(ccc1Cn1cc(nn1)-c1ccc(cc1)-c1ccccc1COc1cc(ccc1Cl)C(F)(F)F)C(O)=O
Show InChI InChI=1S/C30H22ClF3N4O3/c31-25-12-11-23(30(32,33)34)14-28(25)41-17-22-3-1-2-4-24(22)18-5-7-19(8-6-18)27-16-38(37-36-27)15-21-10-9-20(29(39)40)13-26(21)35/h1-14,16H,15,17,35H2,(H,39,40)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 900n/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of human recombinant 5-lipoxygenase in cell-free system preincubated for 10 mins before substrate arachidonic acid addition measured after...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Prostaglandin E synthase


(Homo sapiens (Human))
BDBM50386164
PNG
(CHEMBL2042366)
Show SMILES OC(=O)c1ccc(Cn2cc(nn2)-c2ccc(cc2)-c2ccccc2COc2cc(ccc2Cl)C(F)(F)F)cc1
Show InChI InChI=1S/C30H21ClF3N3O3/c31-26-14-13-24(30(32,33)34)15-28(26)40-18-23-3-1-2-4-25(23)20-9-11-21(12-10-20)27-17-37(36-35-27)16-19-5-7-22(8-6-19)29(38)39/h1-15,17H,16,18H2,(H,38,39)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 1.00E+3n/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of mPGES1 in IL-1beta-stimulated human A549 cell assessed as inhibition of PGE2 production preincubated for 15 mins before substrate addit...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50386163
PNG
(CHEMBL2042367)
Show SMILES OC(=O)c1ccc(cc1)S(=O)(=O)n1cc(nn1)-c1ccc(cc1)-c1ccccc1COc1cc(ccc1Cl)C(F)(F)F
Show InChI InChI=1S/C29H19ClF3N3O5S/c30-25-14-11-22(29(31,32)33)15-27(25)41-17-21-3-1-2-4-24(21)18-5-7-19(8-6-18)26-16-36(35-34-26)42(39,40)23-12-9-20(10-13-23)28(37)38/h1-16H,17H2,(H,37,38)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 1.20E+3n/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of 5-lipoxygenase in human neutrophil preincubated for 15 mins before substrate arachidonic acid addition measured after 10 mins by HPLC m...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Prostaglandin E synthase


(Homo sapiens (Human))
BDBM50386154
PNG
(CHEMBL2042361)
Show SMILES OC(=O)c1ccc(Cn2cc(nn2)-c2ccc(cc2)-c2ccccc2COc2cc(ccc2Cl)C(F)(F)F)c(c1)[N+]([O-])=O
Show InChI InChI=1S/C30H20ClF3N4O5/c31-25-12-11-23(30(32,33)34)14-28(25)43-17-22-3-1-2-4-24(22)18-5-7-19(8-6-18)26-16-37(36-35-26)15-21-10-9-20(29(39)40)13-27(21)38(41)42/h1-14,16H,15,17H2,(H,39,40)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 1.20E+3n/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of mPGES1 in IL-1beta-stimulated human A549 cell assessed as inhibition of PGE2 production preincubated for 15 mins before substrate addit...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50386164
PNG
(CHEMBL2042366)
Show SMILES OC(=O)c1ccc(Cn2cc(nn2)-c2ccc(cc2)-c2ccccc2COc2cc(ccc2Cl)C(F)(F)F)cc1
Show InChI InChI=1S/C30H21ClF3N3O3/c31-26-14-13-24(30(32,33)34)15-28(26)40-18-23-3-1-2-4-25(23)20-9-11-21(12-10-20)27-17-37(36-35-27)16-19-5-7-22(8-6-19)29(38)39/h1-15,17H,16,18H2,(H,38,39)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 1.47E+3n/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of human recombinant 5-lipoxygenase in cell-free system preincubated for 10 mins before substrate arachidonic acid addition measured after...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50386163
PNG
(CHEMBL2042367)
Show SMILES OC(=O)c1ccc(cc1)S(=O)(=O)n1cc(nn1)-c1ccc(cc1)-c1ccccc1COc1cc(ccc1Cl)C(F)(F)F
Show InChI InChI=1S/C29H19ClF3N3O5S/c30-25-14-11-22(29(31,32)33)15-27(25)41-17-21-3-1-2-4-24(21)18-5-7-19(8-6-18)26-16-36(35-34-26)42(39,40)23-12-9-20(10-13-23)28(37)38/h1-16H,17H2,(H,37,38)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 1.96E+3n/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of human recombinant 5-lipoxygenase in cell-free system preincubated for 10 mins before substrate arachidonic acid addition measured after...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50386164
PNG
(CHEMBL2042366)
Show SMILES OC(=O)c1ccc(Cn2cc(nn2)-c2ccc(cc2)-c2ccccc2COc2cc(ccc2Cl)C(F)(F)F)cc1
Show InChI InChI=1S/C30H21ClF3N3O3/c31-26-14-13-24(30(32,33)34)15-28(26)40-18-23-3-1-2-4-25(23)20-9-11-21(12-10-20)27-17-37(36-35-27)16-19-5-7-22(8-6-19)29(38)39/h1-15,17H,16,18H2,(H,38,39)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 2.00E+3n/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of 5-lipoxygenase in human neutrophil preincubated for 15 mins before substrate arachidonic acid addition measured after 10 mins by HPLC m...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50386154
PNG
(CHEMBL2042361)
Show SMILES OC(=O)c1ccc(Cn2cc(nn2)-c2ccc(cc2)-c2ccccc2COc2cc(ccc2Cl)C(F)(F)F)c(c1)[N+]([O-])=O
Show InChI InChI=1S/C30H20ClF3N4O5/c31-25-12-11-23(30(32,33)34)14-28(25)43-17-22-3-1-2-4-24(22)18-5-7-19(8-6-18)26-16-37(36-35-26)15-21-10-9-20(29(39)40)13-27(21)38(41)42/h1-14,16H,15,17H2,(H,39,40)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 2.00E+3n/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of human recombinant 5-lipoxygenase in cell-free system preincubated for 10 mins before substrate arachidonic acid addition measured after...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50386165
PNG
(CHEMBL2042365)
Show SMILES Nc1cc(ccc1Cn1cc(nn1)-c1ccc(cc1)-c1ccccc1COc1cc(ccc1Cl)C(F)(F)F)C(O)=O
Show InChI InChI=1S/C30H22ClF3N4O3/c31-25-12-11-23(30(32,33)34)14-28(25)41-17-22-3-1-2-4-24(22)18-5-7-19(8-6-18)27-16-38(37-36-27)15-21-10-9-20(29(39)40)13-26(21)35/h1-14,16H,15,17,35H2,(H,39,40)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 2.10E+3n/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of 5-lipoxygenase in human neutrophil preincubated for 15 mins before substrate arachidonic acid addition measured after 10 mins by HPLC m...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50386166
PNG
(CHEMBL2042364)
Show SMILES OC(=O)c1ccc(cc1)-c1ccc(cc1)-c1cn(Cc2ccc(cc2[N+]([O-])=O)C(O)=O)nn1
Show InChI InChI=1S/C23H16N4O6/c28-22(29)17-7-3-15(4-8-17)14-1-5-16(6-2-14)20-13-26(25-24-20)12-19-10-9-18(23(30)31)11-21(19)27(32)33/h1-11,13H,12H2,(H,28,29)(H,30,31)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a>5.00E+3n/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of 5-lipoxygenase in human neutrophil preincubated for 15 mins before substrate arachidonic acid addition measured after 10 mins by HPLC m...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50386166
PNG
(CHEMBL2042364)
Show SMILES OC(=O)c1ccc(cc1)-c1ccc(cc1)-c1cn(Cc2ccc(cc2[N+]([O-])=O)C(O)=O)nn1
Show InChI InChI=1S/C23H16N4O6/c28-22(29)17-7-3-15(4-8-17)14-1-5-16(6-2-14)20-13-26(25-24-20)12-19-10-9-18(23(30)31)11-21(19)27(32)33/h1-11,13H,12H2,(H,28,29)(H,30,31)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a>5.00E+3n/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of human recombinant 5-lipoxygenase in cell-free system preincubated for 10 mins before substrate arachidonic acid addition measured after...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50386154
PNG
(CHEMBL2042361)
Show SMILES OC(=O)c1ccc(Cn2cc(nn2)-c2ccc(cc2)-c2ccccc2COc2cc(ccc2Cl)C(F)(F)F)c(c1)[N+]([O-])=O
Show InChI InChI=1S/C30H20ClF3N4O5/c31-25-12-11-23(30(32,33)34)14-28(25)43-17-22-3-1-2-4-24(22)18-5-7-19(8-6-18)26-16-37(36-35-26)15-21-10-9-20(29(39)40)13-27(21)38(41)42/h1-14,16H,15,17H2,(H,39,40)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 5.30E+3n/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of 5-lipoxygenase in human neutrophil preincubated for 15 mins before substrate arachidonic acid addition measured after 10 mins by HPLC m...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Prostaglandin E synthase


(Homo sapiens (Human))
BDBM50386153
PNG
(CHEMBL2042362)
Show SMILES OC(=O)c1ccc(Cn2cc(nn2)-c2ccc(cc2)-c2cccs2)c(c1)[N+]([O-])=O
Show InChI InChI=1S/C20H14N4O4S/c25-20(26)15-7-8-16(18(10-15)24(27)28)11-23-12-17(21-22-23)13-3-5-14(6-4-13)19-2-1-9-29-19/h1-10,12H,11H2,(H,25,26)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 5.50E+3n/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of mPGES1 in IL-1beta-stimulated human A549 cell assessed as inhibition of PGE2 production preincubated for 15 mins before substrate addit...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50386159
PNG
(CHEMBL2042356)
Show SMILES CN(C)c1ccc2cc(ccc2c1)S(=O)(=O)Nc1ccc(cc1)-c1ccc(cc1)-c1cn(Cc2ccc(cc2[N+]([O-])=O)C(O)=O)nn1
Show InChI InChI=1S/C34H28N6O6S/c1-38(2)30-15-11-26-18-31(16-12-25(26)17-30)47(45,46)36-29-13-9-23(10-14-29)22-3-5-24(6-4-22)32-21-39(37-35-32)20-28-8-7-27(34(41)42)19-33(28)40(43)44/h3-19,21,36H,20H2,1-2H3,(H,41,42)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 6.10E+3n/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of human recombinant 5-lipoxygenase in cell-free system preincubated for 10 mins before substrate arachidonic acid addition measured after...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50339575
PNG
(4-(4-Biphenyl-4-yl-[1,2,3]triazol-1-ylmethyl)-3-ni...)
Show SMILES OC(=O)c1ccc(Cn2cc(nn2)-c2ccc(cc2)-c2ccccc2)c(c1)[N+]([O-])=O
Show InChI InChI=1S/C22H16N4O4/c27-22(28)18-10-11-19(21(12-18)26(29)30)13-25-14-20(23-24-25)17-8-6-16(7-9-17)15-4-2-1-3-5-15/h1-12,14H,13H2,(H,27,28)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 6.70E+3n/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of human recombinant 5-lipoxygenase in cell-free system preincubated for 10 mins before substrate arachidonic acid addition measured after...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50386162
PNG
(CHEMBL2042363)
Show SMILES OC(=O)c1ccc(Cn2cc(nn2)-c2ccc(cc2)-c2ccc(O)cc2)c(c1)[N+]([O-])=O
Show InChI InChI=1S/C22H16N4O5/c27-19-9-7-15(8-10-19)14-1-3-16(4-2-14)20-13-25(24-23-20)12-18-6-5-17(22(28)29)11-21(18)26(30)31/h1-11,13,27H,12H2,(H,28,29)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 6.80E+3n/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of human recombinant 5-lipoxygenase in cell-free system preincubated for 10 mins before substrate arachidonic acid addition measured after...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50339575
PNG
(4-(4-Biphenyl-4-yl-[1,2,3]triazol-1-ylmethyl)-3-ni...)
Show SMILES OC(=O)c1ccc(Cn2cc(nn2)-c2ccc(cc2)-c2ccccc2)c(c1)[N+]([O-])=O
Show InChI InChI=1S/C22H16N4O4/c27-22(28)18-10-11-19(21(12-18)26(29)30)13-25-14-20(23-24-25)17-8-6-16(7-9-17)15-4-2-1-3-5-15/h1-12,14H,13H2,(H,27,28)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 9.20E+3n/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of 5-lipoxygenase in human neutrophil preincubated for 15 mins before substrate arachidonic acid addition measured after 10 mins by HPLC m...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50386159
PNG
(CHEMBL2042356)
Show SMILES CN(C)c1ccc2cc(ccc2c1)S(=O)(=O)Nc1ccc(cc1)-c1ccc(cc1)-c1cn(Cc2ccc(cc2[N+]([O-])=O)C(O)=O)nn1
Show InChI InChI=1S/C34H28N6O6S/c1-38(2)30-15-11-26-18-31(16-12-25(26)17-30)47(45,46)36-29-13-9-23(10-14-29)22-3-5-24(6-4-22)32-21-39(37-35-32)20-28-8-7-27(34(41)42)19-33(28)40(43)44/h3-19,21,36H,20H2,1-2H3,(H,41,42)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a>1.00E+4n/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of 5-lipoxygenase in human neutrophil preincubated for 15 mins before substrate arachidonic acid addition measured after 10 mins by HPLC m...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50386160
PNG
(CHEMBL2042355)
Show SMILES Nc1ccc(cc1)-c1ccc(cc1)-c1cn(Cc2ccc(cc2[N+]([O-])=O)C(O)=O)nn1
Show InChI InChI=1S/C22H17N5O4/c23-19-9-7-15(8-10-19)14-1-3-16(4-2-14)20-13-26(25-24-20)12-18-6-5-17(22(28)29)11-21(18)27(30)31/h1-11,13H,12,23H2,(H,28,29)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of 5-lipoxygenase in human neutrophil preincubated for 15 mins before substrate arachidonic acid addition measured after 10 mins by HPLC m...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50386161
PNG
(CHEMBL2042354)
Show SMILES OC(=O)c1ccc(Cn2cc(nn2)-c2ccc(cc2)-c2cccc(c2)C(=O)N2CCOCC2)c(c1)[N+]([O-])=O
Show InChI InChI=1S/C27H23N5O6/c33-26(30-10-12-38-13-11-30)21-3-1-2-20(14-21)18-4-6-19(7-5-18)24-17-31(29-28-24)16-23-9-8-22(27(34)35)15-25(23)32(36)37/h1-9,14-15,17H,10-13,16H2,(H,34,35)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of 5-lipoxygenase in human neutrophil preincubated for 15 mins before substrate arachidonic acid addition measured after 10 mins by HPLC m...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Prostaglandin E synthase


(Homo sapiens (Human))
BDBM50386157
PNG
(CHEMBL2042358)
Show SMILES OC(=O)c1cccc(c1)-c1ccc(cc1)-c1cn(Cc2ccc(cc2[N+]([O-])=O)C(O)=O)nn1
Show InChI InChI=1S/C23H16N4O6/c28-22(29)17-3-1-2-16(10-17)14-4-6-15(7-5-14)20-13-26(25-24-20)12-19-9-8-18(23(30)31)11-21(19)27(32)33/h1-11,13H,12H2,(H,28,29)(H,30,31)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of mPGES1 in IL-1beta-stimulated human A549 cell assessed as inhibition of PGE2 production preincubated for 15 mins before substrate addit...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Prostaglandin E synthase


(Homo sapiens (Human))
BDBM50386156
PNG
(CHEMBL2042359)
Show SMILES OC(=O)c1ccc(Cn2cc(nn2)-c2ccc(cc2)-c2cccc(O)c2)c(c1)[N+]([O-])=O
Show InChI InChI=1S/C22H16N4O5/c27-19-3-1-2-16(10-19)14-4-6-15(7-5-14)20-13-25(24-23-20)12-18-9-8-17(22(28)29)11-21(18)26(30)31/h1-11,13,27H,12H2,(H,28,29)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of mPGES1 in IL-1beta-stimulated human A549 cell assessed as inhibition of PGE2 production preincubated for 15 mins before substrate addit...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Prostaglandin E synthase


(Homo sapiens (Human))
BDBM50386155
PNG
(CHEMBL2042360)
Show SMILES COc1cc(cc(OC)c1OC)-c1ccc(cc1)-c1cn(Cc2ccc(cc2[N+]([O-])=O)C(O)=O)nn1
Show InChI InChI=1S/C25H22N4O7/c1-34-22-11-19(12-23(35-2)24(22)36-3)15-4-6-16(7-5-15)20-14-28(27-26-20)13-18-9-8-17(25(30)31)10-21(18)29(32)33/h4-12,14H,13H2,1-3H3,(H,30,31)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of mPGES1 in IL-1beta-stimulated human A549 cell assessed as inhibition of PGE2 production preincubated for 15 mins before substrate addit...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50386153
PNG
(CHEMBL2042362)
Show SMILES OC(=O)c1ccc(Cn2cc(nn2)-c2ccc(cc2)-c2cccs2)c(c1)[N+]([O-])=O
Show InChI InChI=1S/C20H14N4O4S/c25-20(26)15-7-8-16(18(10-15)24(27)28)11-23-12-17(21-22-23)13-3-5-14(6-4-13)19-2-1-9-29-19/h1-10,12H,11H2,(H,25,26)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of human recombinant 5-lipoxygenase in cell-free system preincubated for 10 mins before substrate arachidonic acid addition measured after...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50386155
PNG
(CHEMBL2042360)
Show SMILES COc1cc(cc(OC)c1OC)-c1ccc(cc1)-c1cn(Cc2ccc(cc2[N+]([O-])=O)C(O)=O)nn1
Show InChI InChI=1S/C25H22N4O7/c1-34-22-11-19(12-23(35-2)24(22)36-3)15-4-6-16(7-5-15)20-14-28(27-26-20)13-18-9-8-17(25(30)31)10-21(18)29(32)33/h4-12,14H,13H2,1-3H3,(H,30,31)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of human recombinant 5-lipoxygenase in cell-free system preincubated for 10 mins before substrate arachidonic acid addition measured after...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50386156
PNG
(CHEMBL2042359)
Show SMILES OC(=O)c1ccc(Cn2cc(nn2)-c2ccc(cc2)-c2cccc(O)c2)c(c1)[N+]([O-])=O
Show InChI InChI=1S/C22H16N4O5/c27-19-3-1-2-16(10-19)14-4-6-15(7-5-14)20-13-25(24-23-20)12-18-9-8-17(22(28)29)11-21(18)26(30)31/h1-11,13,27H,12H2,(H,28,29)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of human recombinant 5-lipoxygenase in cell-free system preincubated for 10 mins before substrate arachidonic acid addition measured after...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50386157
PNG
(CHEMBL2042358)
Show SMILES OC(=O)c1cccc(c1)-c1ccc(cc1)-c1cn(Cc2ccc(cc2[N+]([O-])=O)C(O)=O)nn1
Show InChI InChI=1S/C23H16N4O6/c28-22(29)17-3-1-2-16(10-17)14-4-6-15(7-5-14)20-13-26(25-24-20)12-19-9-8-18(23(30)31)11-21(19)27(32)33/h1-11,13H,12H2,(H,28,29)(H,30,31)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of human recombinant 5-lipoxygenase in cell-free system preincubated for 10 mins before substrate arachidonic acid addition measured after...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50386158
PNG
(CHEMBL2042357)
Show SMILES OC(=O)c1ccc(Cn2cc(nn2)-c2ccc(cc2)-c2ccccc2C(O)=O)c(c1)[N+]([O-])=O
Show InChI InChI=1S/C23H16N4O6/c28-22(29)16-9-10-17(21(11-16)27(32)33)12-26-13-20(24-25-26)15-7-5-14(6-8-15)18-3-1-2-4-19(18)23(30)31/h1-11,13H,12H2,(H,28,29)(H,30,31)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of human recombinant 5-lipoxygenase in cell-free system preincubated for 10 mins before substrate arachidonic acid addition measured after...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50386160
PNG
(CHEMBL2042355)
Show SMILES Nc1ccc(cc1)-c1ccc(cc1)-c1cn(Cc2ccc(cc2[N+]([O-])=O)C(O)=O)nn1
Show InChI InChI=1S/C22H17N5O4/c23-19-9-7-15(8-10-19)14-1-3-16(4-2-14)20-13-26(25-24-20)12-18-6-5-17(22(28)29)11-21(18)27(30)31/h1-11,13H,12,23H2,(H,28,29)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of human recombinant 5-lipoxygenase in cell-free system preincubated for 10 mins before substrate arachidonic acid addition measured after...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50386161
PNG
(CHEMBL2042354)
Show SMILES OC(=O)c1ccc(Cn2cc(nn2)-c2ccc(cc2)-c2cccc(c2)C(=O)N2CCOCC2)c(c1)[N+]([O-])=O
Show InChI InChI=1S/C27H23N5O6/c33-26(30-10-12-38-13-11-30)21-3-1-2-20(14-21)18-4-6-19(7-5-18)24-17-31(29-28-24)16-23-9-8-22(27(34)35)15-25(23)32(36)37/h1-9,14-15,17H,10-13,16H2,(H,34,35)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of human recombinant 5-lipoxygenase in cell-free system preincubated for 10 mins before substrate arachidonic acid addition measured after...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Prostaglandin E synthase


(Homo sapiens (Human))
BDBM50386163
PNG
(CHEMBL2042367)
Show SMILES OC(=O)c1ccc(cc1)S(=O)(=O)n1cc(nn1)-c1ccc(cc1)-c1ccccc1COc1cc(ccc1Cl)C(F)(F)F
Show InChI InChI=1S/C29H19ClF3N3O5S/c30-25-14-11-22(29(31,32)33)15-27(25)41-17-21-3-1-2-4-24(21)18-5-7-19(8-6-18)26-16-36(35-34-26)42(39,40)23-12-9-20(10-13-23)28(37)38/h1-16H,17H2,(H,37,38)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of mPGES1 in IL-1beta-stimulated human A549 cell assessed as inhibition of PGE2 production preincubated for 15 mins before substrate addit...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50386152
PNG
(CHEMBL2042353)
Show SMILES COc1ccc(cc1CN1CCOCC1)-c1ccc(cc1)-c1cn(Cc2ccc(cc2[N+]([O-])=O)C(O)=O)nn1
Show InChI InChI=1S/C28H27N5O6/c1-38-27-9-8-21(14-24(27)16-31-10-12-39-13-11-31)19-2-4-20(5-3-19)25-18-32(30-29-25)17-23-7-6-22(28(34)35)15-26(23)33(36)37/h2-9,14-15,18H,10-13,16-17H2,1H3,(H,34,35)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of 5-lipoxygenase in human neutrophil preincubated for 15 mins before substrate arachidonic acid addition measured after 10 mins by HPLC m...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Prostaglandin E synthase


(Homo sapiens (Human))
BDBM50386166
PNG
(CHEMBL2042364)
Show SMILES OC(=O)c1ccc(cc1)-c1ccc(cc1)-c1cn(Cc2ccc(cc2[N+]([O-])=O)C(O)=O)nn1
Show InChI InChI=1S/C23H16N4O6/c28-22(29)17-7-3-15(4-8-17)14-1-5-16(6-2-14)20-13-26(25-24-20)12-19-10-9-18(23(30)31)11-21(19)27(32)33/h1-11,13H,12H2,(H,28,29)(H,30,31)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of mPGES1 in IL-1beta-stimulated human A549 cell assessed as inhibition of PGE2 production preincubated for 15 mins before substrate addit...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Prostaglandin E synthase


(Homo sapiens (Human))
BDBM50386162
PNG
(CHEMBL2042363)
Show SMILES OC(=O)c1ccc(Cn2cc(nn2)-c2ccc(cc2)-c2ccc(O)cc2)c(c1)[N+]([O-])=O
Show InChI InChI=1S/C22H16N4O5/c27-19-9-7-15(8-10-19)14-1-3-16(4-2-14)20-13-25(24-23-20)12-18-6-5-17(22(28)29)11-21(18)26(30)31/h1-11,13,27H,12H2,(H,28,29)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of mPGES1 in IL-1beta-stimulated human A549 cell assessed as inhibition of PGE2 production preincubated for 15 mins before substrate addit...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Prostaglandin E synthase


(Homo sapiens (Human))
BDBM50386152
PNG
(CHEMBL2042353)
Show SMILES COc1ccc(cc1CN1CCOCC1)-c1ccc(cc1)-c1cn(Cc2ccc(cc2[N+]([O-])=O)C(O)=O)nn1
Show InChI InChI=1S/C28H27N5O6/c1-38-27-9-8-21(14-24(27)16-31-10-12-39-13-11-31)19-2-4-20(5-3-19)25-18-32(30-29-25)17-23-7-6-22(28(34)35)15-26(23)33(36)37/h2-9,14-15,18H,10-13,16-17H2,1H3,(H,34,35)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of mPGES1 in IL-1beta-stimulated human A549 cell assessed as inhibition of PGE2 production preincubated for 15 mins before substrate addit...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Prostaglandin E synthase


(Homo sapiens (Human))
BDBM50386159
PNG
(CHEMBL2042356)
Show SMILES CN(C)c1ccc2cc(ccc2c1)S(=O)(=O)Nc1ccc(cc1)-c1ccc(cc1)-c1cn(Cc2ccc(cc2[N+]([O-])=O)C(O)=O)nn1
Show InChI InChI=1S/C34H28N6O6S/c1-38(2)30-15-11-26-18-31(16-12-25(26)17-30)47(45,46)36-29-13-9-23(10-14-29)22-3-5-24(6-4-22)32-21-39(37-35-32)20-28-8-7-27(34(41)42)19-33(28)40(43)44/h3-19,21,36H,20H2,1-2H3,(H,41,42)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a>1.00E+4n/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of mPGES1 in IL-1beta-stimulated human A549 cell assessed as inhibition of PGE2 production preincubated for 15 mins before substrate addit...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50386158
PNG
(CHEMBL2042357)
Show SMILES OC(=O)c1ccc(Cn2cc(nn2)-c2ccc(cc2)-c2ccccc2C(O)=O)c(c1)[N+]([O-])=O
Show InChI InChI=1S/C23H16N4O6/c28-22(29)16-9-10-17(21(11-16)27(32)33)12-26-13-20(24-25-26)15-7-5-14(6-8-15)18-3-1-2-4-19(18)23(30)31/h1-11,13H,12H2,(H,28,29)(H,30,31)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of 5-lipoxygenase in human neutrophil preincubated for 15 mins before substrate arachidonic acid addition measured after 10 mins by HPLC m...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50386157
PNG
(CHEMBL2042358)
Show SMILES OC(=O)c1cccc(c1)-c1ccc(cc1)-c1cn(Cc2ccc(cc2[N+]([O-])=O)C(O)=O)nn1
Show InChI InChI=1S/C23H16N4O6/c28-22(29)17-3-1-2-16(10-17)14-4-6-15(7-5-14)20-13-26(25-24-20)12-19-9-8-18(23(30)31)11-21(19)27(32)33/h1-11,13H,12H2,(H,28,29)(H,30,31)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of 5-lipoxygenase in human neutrophil preincubated for 15 mins before substrate arachidonic acid addition measured after 10 mins by HPLC m...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50386156
PNG
(CHEMBL2042359)
Show SMILES OC(=O)c1ccc(Cn2cc(nn2)-c2ccc(cc2)-c2cccc(O)c2)c(c1)[N+]([O-])=O
Show InChI InChI=1S/C22H16N4O5/c27-19-3-1-2-16(10-19)14-4-6-15(7-5-14)20-13-25(24-23-20)12-18-9-8-17(22(28)29)11-21(18)26(30)31/h1-11,13,27H,12H2,(H,28,29)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of 5-lipoxygenase in human neutrophil preincubated for 15 mins before substrate arachidonic acid addition measured after 10 mins by HPLC m...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50386155
PNG
(CHEMBL2042360)
Show SMILES COc1cc(cc(OC)c1OC)-c1ccc(cc1)-c1cn(Cc2ccc(cc2[N+]([O-])=O)C(O)=O)nn1
Show InChI InChI=1S/C25H22N4O7/c1-34-22-11-19(12-23(35-2)24(22)36-3)15-4-6-16(7-5-15)20-14-28(27-26-20)13-18-9-8-17(25(30)31)10-21(18)29(32)33/h4-12,14H,13H2,1-3H3,(H,30,31)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of 5-lipoxygenase in human neutrophil preincubated for 15 mins before substrate arachidonic acid addition measured after 10 mins by HPLC m...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50386153
PNG
(CHEMBL2042362)
Show SMILES OC(=O)c1ccc(Cn2cc(nn2)-c2ccc(cc2)-c2cccs2)c(c1)[N+]([O-])=O
Show InChI InChI=1S/C20H14N4O4S/c25-20(26)15-7-8-16(18(10-15)24(27)28)11-23-12-17(21-22-23)13-3-5-14(6-4-13)19-2-1-9-29-19/h1-10,12H,11H2,(H,25,26)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of 5-lipoxygenase in human neutrophil preincubated for 15 mins before substrate arachidonic acid addition measured after 10 mins by HPLC m...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50386162
PNG
(CHEMBL2042363)
Show SMILES OC(=O)c1ccc(Cn2cc(nn2)-c2ccc(cc2)-c2ccc(O)cc2)c(c1)[N+]([O-])=O
Show InChI InChI=1S/C22H16N4O5/c27-19-9-7-15(8-10-19)14-1-3-16(4-2-14)20-13-25(24-23-20)12-18-6-5-17(22(28)29)11-21(18)26(30)31/h1-11,13,27H,12H2,(H,28,29)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of 5-lipoxygenase in human neutrophil preincubated for 15 mins before substrate arachidonic acid addition measured after 10 mins by HPLC m...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase


(Homo sapiens (Human))
BDBM50386152
PNG
(CHEMBL2042353)
Show SMILES COc1ccc(cc1CN1CCOCC1)-c1ccc(cc1)-c1cn(Cc2ccc(cc2[N+]([O-])=O)C(O)=O)nn1
Show InChI InChI=1S/C28H27N5O6/c1-38-27-9-8-21(14-24(27)16-31-10-12-39-13-11-31)19-2-4-20(5-3-19)25-18-32(30-29-25)17-23-7-6-22(28(34)35)15-26(23)33(36)37/h2-9,14-15,18H,10-13,16-17H2,1H3,(H,34,35)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of human recombinant 5-lipoxygenase in cell-free system preincubated for 10 mins before substrate arachidonic acid addition measured after...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Prostaglandin E synthase


(Homo sapiens (Human))
BDBM50386158
PNG
(CHEMBL2042357)
Show SMILES OC(=O)c1ccc(Cn2cc(nn2)-c2ccc(cc2)-c2ccccc2C(O)=O)c(c1)[N+]([O-])=O
Show InChI InChI=1S/C23H16N4O6/c28-22(29)16-9-10-17(21(11-16)27(32)33)12-26-13-20(24-25-26)15-7-5-14(6-8-15)18-3-1-2-4-19(18)23(30)31/h1-11,13H,12H2,(H,28,29)(H,30,31)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of mPGES1 in IL-1beta-stimulated human A549 cell assessed as inhibition of PGE2 production preincubated for 15 mins before substrate addit...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Prostaglandin E synthase


(Homo sapiens (Human))
BDBM50386160
PNG
(CHEMBL2042355)
Show SMILES Nc1ccc(cc1)-c1ccc(cc1)-c1cn(Cc2ccc(cc2[N+]([O-])=O)C(O)=O)nn1
Show InChI InChI=1S/C22H17N5O4/c23-19-9-7-15(8-10-19)14-1-3-16(4-2-14)20-13-26(25-24-20)12-18-6-5-17(22(28)29)11-21(18)27(30)31/h1-11,13H,12,23H2,(H,28,29)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of mPGES1 in IL-1beta-stimulated human A549 cell assessed as inhibition of PGE2 production preincubated for 15 mins before substrate addit...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair
Prostaglandin E synthase


(Homo sapiens (Human))
BDBM50386161
PNG
(CHEMBL2042354)
Show SMILES OC(=O)c1ccc(Cn2cc(nn2)-c2ccc(cc2)-c2cccc(c2)C(=O)N2CCOCC2)c(c1)[N+]([O-])=O
Show InChI InChI=1S/C27H23N5O6/c33-26(30-10-12-38-13-11-30)21-3-1-2-20(14-21)18-4-6-19(7-5-18)24-17-31(29-28-24)16-23-9-8-22(27(34)35)15-25(23)32(36)37/h1-9,14-15,17H,10-13,16H2,(H,34,35)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of mPGES1 in IL-1beta-stimulated human A549 cell assessed as inhibition of PGE2 production preincubated for 15 mins before substrate addit...


Eur J Med Chem 54: 311-23 (2012)


Article DOI: 10.1016/j.ejmech.2012.05.014
BindingDB Entry DOI: 10.7270/Q21J9BTR
More data for this
Ligand-Target Pair