Found 120 hits with Last Name = 'thérien' and Initial = 'm' Target/Host
(Institution) | Ligand | Target/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 | pH | Temp
°C |
|---|
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50029600
(5-Bromo-2-(4-fluoro-phenyl)-3-(4-methanesulfonyl-p...)Show SMILES CS(=O)(=O)c1ccc(cc1)-c1cc(Br)sc1-c1ccc(F)cc1 Show InChI InChI=1S/C17H12BrFO2S2/c1-23(20,21)14-8-4-11(5-9-14)15-10-16(18)22-17(15)12-2-6-13(19)7-3-12/h2-10H,1H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
| Purchase
CHEMBL
MCE
KEGG
PC cid
PC sid
UniChem
Patents
Similars
| Article
| n/a | n/a | 2 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
In vitro inhibition of the production of PGE-2 in arachidonic acid stimulated chinese hamster ovary (CHO) cellstransfected with human cyclooxygenase-... |
Bioorg Med Chem Lett 7: 47-52 (1997)
Article DOI: 10.1016/S0960-894X(96)00580-X
BindingDB Entry DOI: 10.7270/Q2FN166R |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50029600
(5-Bromo-2-(4-fluoro-phenyl)-3-(4-methanesulfonyl-p...)Show SMILES CS(=O)(=O)c1ccc(cc1)-c1cc(Br)sc1-c1ccc(F)cc1 Show InChI InChI=1S/C17H12BrFO2S2/c1-23(20,21)14-8-4-11(5-9-14)15-10-16(18)22-17(15)12-2-6-13(19)7-3-12/h2-10H,1H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
MCE
KEGG
PC cid
PC sid
UniChem
Patents
Similars
| Article
| n/a | n/a | 2 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Tested in vitro for the ability to inhibit Prostaglandin G/H synthase 2 in chinese hamster ovary (CHO) cells |
Bioorg Med Chem Lett 7: 57-62 (1997)
Article DOI: 10.1016/S0960-894X(96)00582-3
BindingDB Entry DOI: 10.7270/Q29W0FG1 |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50289328
(5-(4-Methanesulfonyl-phenyl)-6-phenyl-2-trifluorom...)Show SMILES CS(=O)(=O)c1ccc(cc1)-c1sc2nc(nn2c1-c1ccccc1)C(F)(F)F Show InChI InChI=1S/C18H12F3N3O2S2/c1-28(25,26)13-9-7-12(8-10-13)15-14(11-5-3-2-4-6-11)24-17(27-15)22-16(23-24)18(19,20)21/h2-10H,1H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
| n/a | n/a | 3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Tested in vitro for the ability to inhibit Prostaglandin G/H synthase 2 in chinese hamster ovary (CHO) cells |
Bioorg Med Chem Lett 7: 57-62 (1997)
Article DOI: 10.1016/S0960-894X(96)00582-3
BindingDB Entry DOI: 10.7270/Q29W0FG1 |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50289327
(5-(4-Methanesulfonyl-phenyl)-6-m-tolyl-2-trifluoro...)Show SMILES Cc1cccc(c1)-c1c(sc2nc(nn12)C(F)(F)F)-c1ccc(cc1)S(C)(=O)=O Show InChI InChI=1S/C19H14F3N3O2S2/c1-11-4-3-5-13(10-11)15-16(12-6-8-14(9-7-12)29(2,26)27)28-18-23-17(19(20,21)22)24-25(15)18/h3-10H,1-2H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
| n/a | n/a | 3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Tested in vitro for the ability to inhibit Prostaglandin G/H synthase 2 in chinese hamster ovary (CHO) cells |
Bioorg Med Chem Lett 7: 57-62 (1997)
Article DOI: 10.1016/S0960-894X(96)00582-3
BindingDB Entry DOI: 10.7270/Q29W0FG1 |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50289321
(5-(4-Methanesulfonyl-phenyl)-6-phenyl-2-vinyl-thia...)Show SMILES CS(=O)(=O)c1ccc(cc1)-c1sc2nc(C=C)nn2c1-c1ccccc1 Show InChI InChI=1S/C19H15N3O2S2/c1-3-16-20-19-22(21-16)17(13-7-5-4-6-8-13)18(25-19)14-9-11-15(12-10-14)26(2,23)24/h3-12H,1H2,2H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
| n/a | n/a | 6 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
In vivo ability to inhibit Prostaglandin G/H synthase 2 in human whole blood assay |
Bioorg Med Chem Lett 7: 57-62 (1997)
Article DOI: 10.1016/S0960-894X(96)00582-3
BindingDB Entry DOI: 10.7270/Q29W0FG1 |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50289323
(5-(4-Methanesulfonyl-phenyl)-6-phenyl-thiazolo[3,2...)Show InChI InChI=1S/C17H13N3O2S2/c1-24(21,22)14-9-7-13(8-10-14)16-15(12-5-3-2-4-6-12)20-17(23-16)18-11-19-20/h2-11H,1H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
| n/a | n/a | 10 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
In vivo ability to inhibit Prostaglandin G/H synthase 2 in human whole blood assay |
Bioorg Med Chem Lett 7: 57-62 (1997)
Article DOI: 10.1016/S0960-894X(96)00582-3
BindingDB Entry DOI: 10.7270/Q29W0FG1 |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50289324
(2-Isopropyl-5-(4-methanesulfonyl-phenyl)-6-phenyl-...)Show SMILES CC(C)c1nc2sc(c(-c3ccccc3)n2n1)-c1ccc(cc1)S(C)(=O)=O Show InChI InChI=1S/C20H19N3O2S2/c1-13(2)19-21-20-23(22-19)17(14-7-5-4-6-8-14)18(26-20)15-9-11-16(12-10-15)27(3,24)25/h4-13H,1-3H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
| n/a | n/a | 11 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Tested in vitro for the ability to inhibit Prostaglandin G/H synthase 2 in chinese hamster ovary (CHO) cells |
Bioorg Med Chem Lett 7: 57-62 (1997)
Article DOI: 10.1016/S0960-894X(96)00582-3
BindingDB Entry DOI: 10.7270/Q29W0FG1 |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50289302
(5-(4-Methanesulfonyl-phenyl)-2-methyl-6-phenyl-imi...)Show SMILES Cc1cn2c(c(nc2s1)-c1ccccc1)-c1ccc(cc1)S(C)(=O)=O Show InChI InChI=1S/C19H16N2O2S2/c1-13-12-21-18(15-8-10-16(11-9-15)25(2,22)23)17(20-19(21)24-13)14-6-4-3-5-7-14/h3-12H,1-2H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
| n/a | n/a | 12 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
In vitro inhibition of the production of PGE-2 in arachidonic acid stimulated chinese hamster ovary (CHO) cellstransfected with human cyclooxygenase-... |
Bioorg Med Chem Lett 7: 47-52 (1997)
Article DOI: 10.1016/S0960-894X(96)00580-X
BindingDB Entry DOI: 10.7270/Q2FN166R |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50289297
(6-(3,4-Difluoro-phenyl)-5-(4-methanesulfonyl-pheny...)Show SMILES CS(=O)(=O)c1ccc(cc1)-c1c(nc2sccn12)-c1ccc(F)c(F)c1 Show InChI InChI=1S/C18H12F2N2O2S2/c1-26(23,24)13-5-2-11(3-6-13)17-16(21-18-22(17)8-9-25-18)12-4-7-14(19)15(20)10-12/h2-10H,1H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
| n/a | n/a | 12 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
In vitro inhibition of the production of PGE-2 in arachidonic acid stimulated chinese hamster ovary (CHO) cellstransfected with human cyclooxygenase-... |
Bioorg Med Chem Lett 7: 47-52 (1997)
Article DOI: 10.1016/S0960-894X(96)00580-X
BindingDB Entry DOI: 10.7270/Q2FN166R |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50289331
(6-(3-Fluoro-phenyl)-5-(4-methanesulfonyl-phenyl)-2...)Show SMILES CS(=O)(=O)c1ccc(cc1)-c1sc2nc(nn2c1-c1cccc(F)c1)C(F)(F)F Show InChI InChI=1S/C18H11F4N3O2S2/c1-29(26,27)13-7-5-10(6-8-13)15-14(11-3-2-4-12(19)9-11)25-17(28-15)23-16(24-25)18(20,21)22/h2-9H,1H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
| n/a | n/a | 13 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Tested in vitro for the ability to inhibit Prostaglandin G/H synthase 2 in chinese hamster ovary (CHO) cells |
Bioorg Med Chem Lett 7: 57-62 (1997)
Article DOI: 10.1016/S0960-894X(96)00582-3
BindingDB Entry DOI: 10.7270/Q29W0FG1 |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50289298
(6-(4-Fluoro-phenyl)-5-(4-methanesulfonyl-phenyl)-i...)Show SMILES CS(=O)(=O)c1ccc(cc1)-c1c(nc2sccn12)-c1ccc(F)cc1 Show InChI InChI=1S/C18H13FN2O2S2/c1-25(22,23)15-8-4-13(5-9-15)17-16(12-2-6-14(19)7-3-12)20-18-21(17)10-11-24-18/h2-11H,1H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
| n/a | n/a | 14 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
In vitro inhibition of the production of PGE-2 in arachidonic acid stimulated chinese hamster ovary (CHO) cellstransfected with human cyclooxygenase-... |
Bioorg Med Chem Lett 7: 47-52 (1997)
Article DOI: 10.1016/S0960-894X(96)00580-X
BindingDB Entry DOI: 10.7270/Q2FN166R |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50289332
(2-Ethyl-5-(4-methanesulfonyl-phenyl)-6-phenyl-thia...)Show SMILES CCc1nc2sc(c(-c3ccccc3)n2n1)-c1ccc(cc1)S(C)(=O)=O Show InChI InChI=1S/C19H17N3O2S2/c1-3-16-20-19-22(21-16)17(13-7-5-4-6-8-13)18(25-19)14-9-11-15(12-10-14)26(2,23)24/h4-12H,3H2,1-2H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
| n/a | n/a | 15 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Tested in vitro for the ability to inhibit Prostaglandin G/H synthase 2 in chinese hamster ovary (CHO) cells |
Bioorg Med Chem Lett 7: 57-62 (1997)
Article DOI: 10.1016/S0960-894X(96)00582-3
BindingDB Entry DOI: 10.7270/Q29W0FG1 |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50289299
(2-Chloro-6-(4-chloro-phenyl)-5-(4-methanesulfonyl-...)Show SMILES CS(=O)(=O)c1ccc(cc1)-c1c(nc2sc(Cl)cn12)-c1ccc(Cl)cc1 Show InChI InChI=1S/C18H12Cl2N2O2S2/c1-26(23,24)14-8-4-12(5-9-14)17-16(11-2-6-13(19)7-3-11)21-18-22(17)10-15(20)25-18/h2-10H,1H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
| n/a | n/a | 16 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
In vitro inhibition of the production of PGE-2 in arachidonic acid stimulated chinese hamster ovary (CHO) cellstransfected with human cyclooxygenase-... |
Bioorg Med Chem Lett 7: 47-52 (1997)
Article DOI: 10.1016/S0960-894X(96)00580-X
BindingDB Entry DOI: 10.7270/Q2FN166R |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50289303
(5-(4-Methanesulfonyl-phenyl)-6-phenyl-3,5-dihydro-...)Show SMILES CS(=O)(=O)c1ccc(cc1)-c1c(nc2sccn12)-c1ccccc1 Show InChI InChI=1S/C18H14N2O2S2/c1-24(21,22)15-9-7-14(8-10-15)17-16(13-5-3-2-4-6-13)19-18-20(17)11-12-23-18/h2-12H,1H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
| n/a | n/a | 16 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
In vivo ability of the compound to inhibit cyclooxygenase-1 enzyme in human whole blood was determined |
Bioorg Med Chem Lett 7: 47-52 (1997)
Article DOI: 10.1016/S0960-894X(96)00580-X
BindingDB Entry DOI: 10.7270/Q2FN166R |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 1
(Homo sapiens (Human)) | BDBM17638
(2-{1-[(4-chlorophenyl)carbonyl]-5-methoxy-2-methyl...)Show SMILES COc1ccc2n(C(=O)c3ccc(Cl)cc3)c(C)c(CC(O)=O)c2c1 Show InChI InChI=1S/C19H16ClNO4/c1-11-15(10-18(22)23)16-9-14(25-2)7-8-17(16)21(11)19(24)12-3-5-13(20)6-4-12/h3-9H,10H2,1-2H3,(H,22,23) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| Article
| n/a | n/a | 18 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Tested in vitro for the ability to inhibit Prostaglandin G/H synthase 1 in chinese hamster ovary (CHO) cells |
Bioorg Med Chem Lett 7: 57-62 (1997)
Article DOI: 10.1016/S0960-894X(96)00582-3
BindingDB Entry DOI: 10.7270/Q29W0FG1 |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 1
(Homo sapiens (Human)) | BDBM17638
(2-{1-[(4-chlorophenyl)carbonyl]-5-methoxy-2-methyl...)Show SMILES COc1ccc2n(C(=O)c3ccc(Cl)cc3)c(C)c(CC(O)=O)c2c1 Show InChI InChI=1S/C19H16ClNO4/c1-11-15(10-18(22)23)16-9-14(25-2)7-8-17(16)21(11)19(24)12-3-5-13(20)6-4-12/h3-9H,10H2,1-2H3,(H,22,23) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| Article
| n/a | n/a | 18 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
In vitro inhibition of the production of PGE-2 in arachidonic acid stimulated chinese hamster ovary (CHO) cellstransfected with human cyclooxygenase-... |
Bioorg Med Chem Lett 7: 47-52 (1997)
Article DOI: 10.1016/S0960-894X(96)00580-X
BindingDB Entry DOI: 10.7270/Q2FN166R |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50289319
(5-(4-Methanesulfonyl-phenyl)-2-methyl-6-phenyl-thi...)Show SMILES Cc1nc2sc(c(-c3ccccc3)n2n1)-c1ccc(cc1)S(C)(=O)=O Show InChI InChI=1S/C18H15N3O2S2/c1-12-19-18-21(20-12)16(13-6-4-3-5-7-13)17(24-18)14-8-10-15(11-9-14)25(2,22)23/h3-11H,1-2H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
| n/a | n/a | 20 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Tested in vitro for the ability to inhibit Prostaglandin G/H synthase 2 in chinese hamster ovary (CHO) cells |
Bioorg Med Chem Lett 7: 57-62 (1997)
Article DOI: 10.1016/S0960-894X(96)00582-3
BindingDB Entry DOI: 10.7270/Q29W0FG1 |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50289317
(6-(3-Fluoro-phenyl)-5-(4-methanesulfonyl-phenyl)-t...)Show SMILES CS(=O)(=O)c1ccc(cc1)-c1sc2ncnn2c1-c1cccc(F)c1 Show InChI InChI=1S/C17H12FN3O2S2/c1-25(22,23)14-7-5-11(6-8-14)16-15(12-3-2-4-13(18)9-12)21-17(24-16)19-10-20-21/h2-10H,1H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
| n/a | n/a | 22 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Tested in vitro for the ability to inhibit Prostaglandin G/H synthase 2 in chinese hamster ovary (CHO) cells |
Bioorg Med Chem Lett 7: 57-62 (1997)
Article DOI: 10.1016/S0960-894X(96)00582-3
BindingDB Entry DOI: 10.7270/Q29W0FG1 |
More data for this
Ligand-Target Pair | |
Polyunsaturated fatty acid 5-lipoxygenase
(Homo sapiens (Human)) | BDBM50280965
(4-Phenyl-7-(5-phenyl-pyridin-2-ylmethoxy)-3H-napht...)Show SMILES O=C1OCc2c1cc1cc(OCc3ccc(cn3)-c3ccccc3)ccc1c2-c1ccccc1 Show InChI InChI=1S/C30H21NO3/c32-30-27-16-23-15-25(33-18-24-12-11-22(17-31-24)20-7-3-1-4-8-20)13-14-26(23)29(28(27)19-34-30)21-9-5-2-6-10-21/h1-17H,18-19H2 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
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TBA
Curated by ChEMBL
| Assay Description
Compound was evaluated in vitro for inhibition of LTB4 biosynthesis by human leukocytes |
Bioorg Med Chem Lett 3: 2063-2066 (1993)
Article DOI: 10.1016/S0960-894X(01)81016-7
BindingDB Entry DOI: 10.7270/Q2T43T1Z |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM17638
(2-{1-[(4-chlorophenyl)carbonyl]-5-methoxy-2-methyl...)Show SMILES COc1ccc2n(C(=O)c3ccc(Cl)cc3)c(C)c(CC(O)=O)c2c1 Show InChI InChI=1S/C19H16ClNO4/c1-11-15(10-18(22)23)16-9-14(25-2)7-8-17(16)21(11)19(24)12-3-5-13(20)6-4-12/h3-9H,10H2,1-2H3,(H,22,23) | PDB
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| DrugBank
PDB
Article
| n/a | n/a | 26 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
In vitro inhibition of the production of PGE-2 in arachidonic acid stimulated chinese hamster ovary (CHO) cellstransfected with human cyclooxygenase-... |
Bioorg Med Chem Lett 7: 47-52 (1997)
Article DOI: 10.1016/S0960-894X(96)00580-X
BindingDB Entry DOI: 10.7270/Q2FN166R |
More data for this
Ligand-Target Pair | 
3D Structure (crystal) |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM17638
(2-{1-[(4-chlorophenyl)carbonyl]-5-methoxy-2-methyl...)Show SMILES COc1ccc2n(C(=O)c3ccc(Cl)cc3)c(C)c(CC(O)=O)c2c1 Show InChI InChI=1S/C19H16ClNO4/c1-11-15(10-18(22)23)16-9-14(25-2)7-8-17(16)21(11)19(24)12-3-5-13(20)6-4-12/h3-9H,10H2,1-2H3,(H,22,23) | PDB
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PDB
Article
| n/a | n/a | 26 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Tested in vitro for the ability to inhibit Prostaglandin G/H synthase 2 in chinese hamster ovary (CHO) cells |
Bioorg Med Chem Lett 7: 57-62 (1997)
Article DOI: 10.1016/S0960-894X(96)00582-3
BindingDB Entry DOI: 10.7270/Q29W0FG1 |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50289325
(6-(4-Methanesulfonyl-phenyl)-5-phenyl-thiazolo[3,2...)Show SMILES CS(=O)(=O)c1ccc(cc1)-c1c(sc2ncnn12)-c1ccccc1 Show InChI InChI=1S/C17H13N3O2S2/c1-24(21,22)14-9-7-12(8-10-14)15-16(13-5-3-2-4-6-13)23-17-18-11-19-20(15)17/h2-11H,1H3 | PDB
MMDB
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| n/a | n/a | 32 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Tested in vitro for the ability to inhibit Prostaglandin G/H synthase 2 in chinese hamster ovary (CHO) cells |
Bioorg Med Chem Lett 7: 57-62 (1997)
Article DOI: 10.1016/S0960-894X(96)00582-3
BindingDB Entry DOI: 10.7270/Q29W0FG1 |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50289316
(6-(4-Fluoro-phenyl)-5-(4-methanesulfonyl-phenyl)-t...)Show SMILES CS(=O)(=O)c1ccc(cc1)-c1sc2ncnn2c1-c1ccc(F)cc1 Show InChI InChI=1S/C17H12FN3O2S2/c1-25(22,23)14-8-4-12(5-9-14)16-15(11-2-6-13(18)7-3-11)21-17(24-16)19-10-20-21/h2-10H,1H3 | PDB
MMDB
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| n/a | n/a | 36 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Tested in vitro for the ability to inhibit Prostaglandin G/H synthase 2 in chinese hamster ovary (CHO) cells |
Bioorg Med Chem Lett 7: 57-62 (1997)
Article DOI: 10.1016/S0960-894X(96)00582-3
BindingDB Entry DOI: 10.7270/Q29W0FG1 |
More data for this
Ligand-Target Pair | |
Polyunsaturated fatty acid 5-lipoxygenase
(Homo sapiens (Human)) | BDBM50280968
(4-(3-Methoxy-phenyl)-3H-naphtho[2,3-c]furan-1-one ...)Show InChI InChI=1S/C19H14O3/c1-21-14-7-4-6-13(9-14)18-15-8-3-2-5-12(15)10-16-17(18)11-22-19(16)20/h2-10H,11H2,1H3 | PDB
MMDB
Reactome pathway
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| n/a | n/a | 42 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Compound was evaluated in vitro for inhibition of LTB4 biosynthesis by human leukocytes |
Bioorg Med Chem Lett 3: 2063-2066 (1993)
Article DOI: 10.1016/S0960-894X(01)81016-7
BindingDB Entry DOI: 10.7270/Q2T43T1Z |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50289326
(6-(3,4-Difluoro-phenyl)-5-(4-methanesulfonyl-pheny...)Show SMILES CS(=O)(=O)c1ccc(cc1)-c1sc2ncnn2c1-c1ccc(F)c(F)c1 Show InChI InChI=1S/C17H11F2N3O2S2/c1-26(23,24)12-5-2-10(3-6-12)16-15(22-17(25-16)20-9-21-22)11-4-7-13(18)14(19)8-11/h2-9H,1H3 | PDB
MMDB
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KEGG
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| n/a | n/a | 48 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
In vivo ability to inhibit Prostaglandin G/H synthase 2 in human whole blood assay |
Bioorg Med Chem Lett 7: 57-62 (1997)
Article DOI: 10.1016/S0960-894X(96)00582-3
BindingDB Entry DOI: 10.7270/Q29W0FG1 |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 1
(Homo sapiens (Human)) | BDBM50029600
(5-Bromo-2-(4-fluoro-phenyl)-3-(4-methanesulfonyl-p...)Show SMILES CS(=O)(=O)c1ccc(cc1)-c1cc(Br)sc1-c1ccc(F)cc1 Show InChI InChI=1S/C17H12BrFO2S2/c1-23(20,21)14-8-4-11(5-9-14)15-10-16(18)22-17(15)12-2-6-13(19)7-3-12/h2-10H,1H3 | PDB
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| n/a | n/a | 59 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Tested in vitro for the ability to inhibit Prostaglandin G/H synthase 1 in chinese hamster ovary (CHO) cells |
Bioorg Med Chem Lett 7: 57-62 (1997)
Article DOI: 10.1016/S0960-894X(96)00582-3
BindingDB Entry DOI: 10.7270/Q29W0FG1 |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 1
(Homo sapiens (Human)) | BDBM50029600
(5-Bromo-2-(4-fluoro-phenyl)-3-(4-methanesulfonyl-p...)Show SMILES CS(=O)(=O)c1ccc(cc1)-c1cc(Br)sc1-c1ccc(F)cc1 Show InChI InChI=1S/C17H12BrFO2S2/c1-23(20,21)14-8-4-11(5-9-14)15-10-16(18)22-17(15)12-2-6-13(19)7-3-12/h2-10H,1H3 | PDB
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| n/a | n/a | 59 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
In vitro inhibition of the production of PGE-2 in arachidonic acid stimulated chinese hamster ovary (CHO) cellstransfected with human cyclooxygenase-... |
Bioorg Med Chem Lett 7: 47-52 (1997)
Article DOI: 10.1016/S0960-894X(96)00580-X
BindingDB Entry DOI: 10.7270/Q2FN166R |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50029600
(5-Bromo-2-(4-fluoro-phenyl)-3-(4-methanesulfonyl-p...)Show SMILES CS(=O)(=O)c1ccc(cc1)-c1cc(Br)sc1-c1ccc(F)cc1 Show InChI InChI=1S/C17H12BrFO2S2/c1-23(20,21)14-8-4-11(5-9-14)15-10-16(18)22-17(15)12-2-6-13(19)7-3-12/h2-10H,1H3 | PDB
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| n/a | n/a | 60 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
In vivo ability to inhibit Prostaglandin G/H synthase 2 in human whole blood assay |
Bioorg Med Chem Lett 7: 57-62 (1997)
Article DOI: 10.1016/S0960-894X(96)00582-3
BindingDB Entry DOI: 10.7270/Q29W0FG1 |
More data for this
Ligand-Target Pair | |
Polyunsaturated fatty acid 5-lipoxygenase
(Homo sapiens (Human)) | BDBM50280961
(9-Benzo[1,3]dioxol-5-yl-8H-furo[3',4':6,7]naphtho[...)Show InChI InChI=1S/C20H12O6/c21-20-13-3-11-5-17-18(26-9-25-17)6-12(11)19(14(13)7-22-20)10-1-2-15-16(4-10)24-8-23-15/h1-6H,7-9H2 | PDB
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| n/a | n/a | 70 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Compound was evaluated in vitro for inhibition of LTB4 biosynthesis by human leukocytes |
Bioorg Med Chem Lett 3: 2063-2066 (1993)
Article DOI: 10.1016/S0960-894X(01)81016-7
BindingDB Entry DOI: 10.7270/Q2T43T1Z |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 1
(Homo sapiens (Human)) | BDBM50289300
(6-(4-Methylsulfanyl-phenyl)-5-phenyl-imidazo[2,1-b...)Show InChI InChI=1S/C18H14N2S2/c1-21-15-9-7-13(8-10-15)16-17(14-5-3-2-4-6-14)20-11-12-22-18(20)19-16/h2-12H,1H3 | PDB
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| n/a | n/a | 78 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
In vitro inhibition of the production of PGE-2 in arachidonic acid stimulated chinese hamster ovary (CHO) cellstransfected with human cyclooxygenase-... |
Bioorg Med Chem Lett 7: 47-52 (1997)
Article DOI: 10.1016/S0960-894X(96)00580-X
BindingDB Entry DOI: 10.7270/Q2FN166R |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50289330
(6-(3,5-Difluoro-phenyl)-5-(4-methanesulfonyl-pheny...)Show SMILES CS(=O)(=O)c1ccc(cc1)-c1sc2ncnn2c1-c1cc(F)cc(F)c1 Show InChI InChI=1S/C17H11F2N3O2S2/c1-26(23,24)14-4-2-10(3-5-14)16-15(22-17(25-16)20-9-21-22)11-6-12(18)8-13(19)7-11/h2-9H,1H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
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GoogleScholar
AffyNet
| CHEMBL
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PC sid
UniChem
Similars
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| n/a | n/a | 80 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Tested in vitro for the ability to inhibit Prostaglandin G/H synthase 2 in chinese hamster ovary (CHO) cells |
Bioorg Med Chem Lett 7: 57-62 (1997)
Article DOI: 10.1016/S0960-894X(96)00582-3
BindingDB Entry DOI: 10.7270/Q29W0FG1 |
More data for this
Ligand-Target Pair | |
Polyunsaturated fatty acid 5-lipoxygenase
(Homo sapiens (Human)) | BDBM50280963
(4-Phenyl-7-(quinolin-2-ylmethoxy)-3H-naphtho[2,3-c...)Show SMILES O=C1OCc2c1cc1cc(OCc3ccc4ccccc4n3)ccc1c2-c1ccccc1 Show InChI InChI=1S/C28H19NO3/c30-28-24-15-20-14-22(31-16-21-11-10-18-6-4-5-9-26(18)29-21)12-13-23(20)27(25(24)17-32-28)19-7-2-1-3-8-19/h1-15H,16-17H2 | PDB
MMDB
Reactome pathway
KEGG
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| CHEMBL
PC cid
PC sid
UniChem
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| n/a | n/a | 88 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Compound was evaluated in vitro for inhibition of LTB4 biosynthesis by human leukocytes |
Bioorg Med Chem Lett 3: 2063-2066 (1993)
Article DOI: 10.1016/S0960-894X(01)81016-7
BindingDB Entry DOI: 10.7270/Q2T43T1Z |
More data for this
Ligand-Target Pair | |
Polyunsaturated fatty acid 5-lipoxygenase
(Homo sapiens (Human)) | BDBM50280959
(7-Benzyloxy-4-phenyl-3H-naphtho[2,3-c]furan-1-one ...)Show InChI InChI=1S/C25H18O3/c26-25-22-14-19-13-20(27-15-17-7-3-1-4-8-17)11-12-21(19)24(23(22)16-28-25)18-9-5-2-6-10-18/h1-14H,15-16H2 | PDB
MMDB
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UniChem
Similars
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| n/a | n/a | 100 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Compound was evaluated in vitro for inhibition of LTB4 biosynthesis by human leukocytes |
Bioorg Med Chem Lett 3: 2063-2066 (1993)
Article DOI: 10.1016/S0960-894X(01)81016-7
BindingDB Entry DOI: 10.7270/Q2T43T1Z |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50289314
(6-(4-Methanesulfonyl-phenyl)-2-methyl-5-phenyl-imi...)Show SMILES Cc1cn2c(c(nc2s1)-c1ccc(cc1)S(C)(=O)=O)-c1ccccc1 Show InChI InChI=1S/C19H16N2O2S2/c1-13-12-21-18(15-6-4-3-5-7-15)17(20-19(21)24-13)14-8-10-16(11-9-14)25(2,22)23/h3-12H,1-2H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
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PC sid
UniChem
Similars
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| n/a | n/a | 140 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
In vitro inhibition of the production of PGE-2 in arachidonic acid stimulated chinese hamster ovary (CHO) cellstransfected with human cyclooxygenase-... |
Bioorg Med Chem Lett 7: 47-52 (1997)
Article DOI: 10.1016/S0960-894X(96)00580-X
BindingDB Entry DOI: 10.7270/Q2FN166R |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50289315
(6-(3-Fluoro-phenyl)-5-(4-methanesulfonyl-phenyl)-2...)Show SMILES Cc1nc2sc(c(-c3cccc(F)c3)n2n1)-c1ccc(cc1)S(C)(=O)=O Show InChI InChI=1S/C18H14FN3O2S2/c1-11-20-18-22(21-11)16(13-4-3-5-14(19)10-13)17(25-18)12-6-8-15(9-7-12)26(2,23)24/h3-10H,1-2H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
| n/a | n/a | 150 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
In vivo ability to inhibit Prostaglandin G/H synthase 2 in human whole blood assay |
Bioorg Med Chem Lett 7: 57-62 (1997)
Article DOI: 10.1016/S0960-894X(96)00582-3
BindingDB Entry DOI: 10.7270/Q29W0FG1 |
More data for this
Ligand-Target Pair | |
Polyunsaturated fatty acid 5-lipoxygenase
(Homo sapiens (Human)) | BDBM50280979
(9-Phenyl-8H-furo[3',4':6,7]naphtho[2,3-d][1,3]diox...)Show InChI InChI=1S/C19H12O4/c20-19-14-6-12-7-16-17(23-10-22-16)8-13(12)18(15(14)9-21-19)11-4-2-1-3-5-11/h1-8H,9-10H2 | PDB
MMDB
Reactome pathway
KEGG
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| CHEMBL
PC cid
PC sid
UniChem
Similars
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| n/a | n/a | 160 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Compound was evaluated in vitro for inhibition of LTB4 biosynthesis by human leukocytes |
Bioorg Med Chem Lett 3: 2063-2066 (1993)
Article DOI: 10.1016/S0960-894X(01)81016-7
BindingDB Entry DOI: 10.7270/Q2T43T1Z |
More data for this
Ligand-Target Pair | |
Polyunsaturated fatty acid 5-lipoxygenase
(Homo sapiens (Human)) | BDBM50280962
(7-Methoxy-4-phenyl-3H-naphtho[2,3-c]furan-1-one | ...)Show InChI InChI=1S/C19H14O3/c1-21-14-7-8-15-13(9-14)10-16-17(11-22-19(16)20)18(15)12-5-3-2-4-6-12/h2-10H,11H2,1H3 | PDB
MMDB
Reactome pathway
KEGG
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| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
| n/a | n/a | 180 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Compound was evaluated in vitro for inhibition of LTB4 biosynthesis by human leukocytes |
Bioorg Med Chem Lett 3: 2063-2066 (1993)
Article DOI: 10.1016/S0960-894X(01)81016-7
BindingDB Entry DOI: 10.7270/Q2T43T1Z |
More data for this
Ligand-Target Pair | |
Polyunsaturated fatty acid 5-lipoxygenase
(Homo sapiens (Human)) | BDBM50280974
(5-Benzo[1,3]dioxol-5-yl-6,8-dihydro-furo[3',4':6,7...)Show InChI InChI=1S/C20H14O5/c1-2-16-17(23-9-22-16)4-11(1)20-14-6-19-18(24-10-25-19)5-12(14)3-13-7-21-8-15(13)20/h1-6H,7-10H2 | PDB
MMDB
Reactome pathway
KEGG
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B.MOAD
DrugBank
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
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| n/a | n/a | 230 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Compound was evaluated in vitro for inhibition of LTB4 biosynthesis by human leukocytes |
Bioorg Med Chem Lett 3: 2063-2066 (1993)
Article DOI: 10.1016/S0960-894X(01)81016-7
BindingDB Entry DOI: 10.7270/Q2T43T1Z |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50289322
(5-(4-Methanesulfonyl-phenyl)-6-phenyl-thiazolo[2,3...)Show SMILES CS(=O)(=O)c1ccc(cc1)-c1c(sc2nncn12)-c1ccccc1 Show InChI InChI=1S/C17H13N3O2S2/c1-24(21,22)14-9-7-12(8-10-14)15-16(13-5-3-2-4-6-13)23-17-19-18-11-20(15)17/h2-11H,1H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
| n/a | n/a | 230 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Tested in vitro for the ability to inhibit Prostaglandin G/H synthase 2 in chinese hamster ovary (CHO) cells |
Bioorg Med Chem Lett 7: 57-62 (1997)
Article DOI: 10.1016/S0960-894X(96)00582-3
BindingDB Entry DOI: 10.7270/Q29W0FG1 |
More data for this
Ligand-Target Pair | |
Polyunsaturated fatty acid 5-lipoxygenase
(Homo sapiens (Human)) | BDBM50280966
(4-Phenyl-3H-naphtho[2,3-c]furan-1-one | CHEMBL6189...)Show InChI InChI=1S/C18H12O2/c19-18-15-10-13-8-4-5-9-14(13)17(16(15)11-20-18)12-6-2-1-3-7-12/h1-10H,11H2 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
| n/a | n/a | 250 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Compound was evaluated in vitro for inhibition of LTB4 biosynthesis by human leukocytes |
Bioorg Med Chem Lett 3: 2063-2066 (1993)
Article DOI: 10.1016/S0960-894X(01)81016-7
BindingDB Entry DOI: 10.7270/Q2T43T1Z |
More data for this
Ligand-Target Pair | |
Polyunsaturated fatty acid 5-lipoxygenase
(Homo sapiens (Human)) | BDBM50280971
(5-Benzo[1,3]dioxol-5-yl-8H-furo[3',4':6,7]naphtho[...)Show InChI InChI=1S/C20H12O6/c21-20-19-12(7-22-20)3-11-5-16-17(26-9-25-16)6-13(11)18(19)10-1-2-14-15(4-10)24-8-23-14/h1-6H,7-9H2 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
| n/a | n/a | 250 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Compound was evaluated in vitro for inhibition of LTB4 biosynthesis by human leukocytes |
Bioorg Med Chem Lett 3: 2063-2066 (1993)
Article DOI: 10.1016/S0960-894X(01)81016-7
BindingDB Entry DOI: 10.7270/Q2T43T1Z |
More data for this
Ligand-Target Pair | |
Polyunsaturated fatty acid 5-lipoxygenase
(Homo sapiens (Human)) | BDBM50280976
(5-Benzo[1,3]dioxol-5-yl-6,7-dimethyl-naphtho[2,3-d...)Show InChI InChI=1S/C20H16O4/c1-11-5-14-7-18-19(24-10-23-18)8-15(14)20(12(11)2)13-3-4-16-17(6-13)22-9-21-16/h3-8H,9-10H2,1-2H3 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
| n/a | n/a | 250 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Compound was evaluated in vitro for inhibition of LTB4 biosynthesis by human leukocytes |
Bioorg Med Chem Lett 3: 2063-2066 (1993)
Article DOI: 10.1016/S0960-894X(01)81016-7
BindingDB Entry DOI: 10.7270/Q2T43T1Z |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50289320
(5-(4-Methanesulfonyl-phenyl)-6-(3-methoxy-phenyl)-...)Show SMILES COc1cccc(c1)-c1c(sc2ncnn12)-c1ccc(cc1)S(C)(=O)=O Show InChI InChI=1S/C18H15N3O3S2/c1-24-14-5-3-4-13(10-14)16-17(25-18-19-11-20-21(16)18)12-6-8-15(9-7-12)26(2,22)23/h3-11H,1-2H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
| n/a | n/a | 260 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Tested in vitro for the ability to inhibit Prostaglandin G/H synthase 2 in chinese hamster ovary (CHO) cells |
Bioorg Med Chem Lett 7: 57-62 (1997)
Article DOI: 10.1016/S0960-894X(96)00582-3
BindingDB Entry DOI: 10.7270/Q29W0FG1 |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 1
(Homo sapiens (Human)) | BDBM50289304
(5-(4-Methylsulfanyl-phenyl)-6-phenyl-imidazo[2,1-b...)Show InChI InChI=1S/C18H14N2S2/c1-21-15-9-7-14(8-10-15)17-16(13-5-3-2-4-6-13)19-18-20(17)11-12-22-18/h2-12H,1H3 | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
| n/a | n/a | 320 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
In vitro inhibition of the production of PGE-2 in arachidonic acid stimulated chinese hamster ovary (CHO) cellstransfected with human cyclooxygenase-... |
Bioorg Med Chem Lett 7: 47-52 (1997)
Article DOI: 10.1016/S0960-894X(96)00580-X
BindingDB Entry DOI: 10.7270/Q2FN166R |
More data for this
Ligand-Target Pair | |
Polyunsaturated fatty acid 5-lipoxygenase
(Homo sapiens (Human)) | BDBM50280970
(4-Benzo[1,3]dioxol-5-yl-3H-naphtho[2,3-c]furan-1-o...)Show InChI InChI=1S/C19H12O4/c20-19-14-7-11-3-1-2-4-13(11)18(15(14)9-21-19)12-5-6-16-17(8-12)23-10-22-16/h1-8H,9-10H2 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
| n/a | n/a | 380 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Compound was evaluated in vitro for inhibition of LTB4 biosynthesis by human leukocytes |
Bioorg Med Chem Lett 3: 2063-2066 (1993)
Article DOI: 10.1016/S0960-894X(01)81016-7
BindingDB Entry DOI: 10.7270/Q2T43T1Z |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50289298
(6-(4-Fluoro-phenyl)-5-(4-methanesulfonyl-phenyl)-i...)Show SMILES CS(=O)(=O)c1ccc(cc1)-c1c(nc2sccn12)-c1ccc(F)cc1 Show InChI InChI=1S/C18H13FN2O2S2/c1-25(22,23)15-8-4-13(5-9-15)17-16(12-2-6-14(19)7-3-12)20-18-21(17)10-11-24-18/h2-11H,1H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
| n/a | n/a | 400 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
In vivo ability of the compound to inhibit cyclooxygenase-2 enzyme in human whole blood was determined |
Bioorg Med Chem Lett 7: 47-52 (1997)
Article DOI: 10.1016/S0960-894X(96)00580-X
BindingDB Entry DOI: 10.7270/Q2FN166R |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50289304
(5-(4-Methylsulfanyl-phenyl)-6-phenyl-imidazo[2,1-b...)Show InChI InChI=1S/C18H14N2S2/c1-21-15-9-7-14(8-10-15)17-16(13-5-3-2-4-6-13)19-18-20(17)11-12-22-18/h2-12H,1H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
| n/a | n/a | 420 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
In vitro inhibition of the production of PGE-2 in arachidonic acid stimulated chinese hamster ovary (CHO) cellstransfected with human cyclooxygenase-... |
Bioorg Med Chem Lett 7: 47-52 (1997)
Article DOI: 10.1016/S0960-894X(96)00580-X
BindingDB Entry DOI: 10.7270/Q2FN166R |
More data for this
Ligand-Target Pair | |
Polyunsaturated fatty acid 5-lipoxygenase
(Homo sapiens (Human)) | BDBM50280967
(5-Benzo[1,3]dioxol-5-yl-5,9-dihydro-furo[3',4':6,7...)Show InChI InChI=1S/C20H14O5/c1-2-16-17(23-9-22-16)4-11(1)20-14-6-19-18(24-10-25-19)5-12(14)3-13-7-21-8-15(13)20/h1-2,4-8,20H,3,9-10H2 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
| n/a | n/a | 420 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Compound was evaluated in vitro for inhibition of LTB4 biosynthesis by human leukocytes |
Bioorg Med Chem Lett 3: 2063-2066 (1993)
Article DOI: 10.1016/S0960-894X(01)81016-7
BindingDB Entry DOI: 10.7270/Q2T43T1Z |
More data for this
Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50289318
(6-(4-Methanesulfonyl-phenyl)-5-phenyl-thiazolo[2,3...)Show InChI InChI=1S/C17H13N3O2S2/c1-24(21,22)14-9-7-13(8-10-14)16-15(12-5-3-2-4-6-12)20-11-18-19-17(20)23-16/h2-11H,1H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
| n/a | n/a | 450 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Tested in vitro for the ability to inhibit Prostaglandin G/H synthase 2 in chinese hamster ovary (CHO) cells |
Bioorg Med Chem Lett 7: 57-62 (1997)
Article DOI: 10.1016/S0960-894X(96)00582-3
BindingDB Entry DOI: 10.7270/Q29W0FG1 |
More data for this
Ligand-Target Pair | |
Polyunsaturated fatty acid 5-lipoxygenase
(Homo sapiens (Human)) | BDBM50280977
(4-Phenyl-5H-6-oxa-1-thia-s-indacen-7-one | CHEMBL6...)Show InChI InChI=1S/C16H10O2S/c17-16-12-8-14-11(6-7-19-14)15(13(12)9-18-16)10-4-2-1-3-5-10/h1-8H,9H2 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
| n/a | n/a | 450 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Compound was evaluated in vitro for inhibition of LTB4 biosynthesis by human leukocytes |
Bioorg Med Chem Lett 3: 2063-2066 (1993)
Article DOI: 10.1016/S0960-894X(01)81016-7
BindingDB Entry DOI: 10.7270/Q2T43T1Z |
More data for this
Ligand-Target Pair | |
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