BindingDB logo
myBDB logout

Articleid 50029437

Compile data set for download or QSAR
Found 76 hits of Enzyme Inhibition Constant Data   
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
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403384
PNG
(CHEMBL17445)
Show SMILES NCc1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C21H17FN4/c22-18-7-5-15(6-8-18)19-20(16-9-11-24-12-10-16)26-21(25-19)17-3-1-14(13-23)2-4-17/h1-12H,13,23H2,(H,25,26)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
n/an/a 50n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM13531
PNG
(4-(4-Fluorophenyl)-2-(4-hydroxyphenyl)-5-(4-pyridy...)
Show SMILES Oc1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C20H14FN3O/c21-16-5-1-13(2-6-16)18-19(14-9-11-22-12-10-14)24-20(23-18)15-3-7-17(25)8-4-15/h1-12,25H,(H,23,24)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
Purchase

PC cid
PC sid
UniChem

Similars

Article
n/an/a 50n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50104352
PNG
(4-[4-(4-Fluoro-phenyl)-5-pyridin-4-yl-1H-imidazol-...)
Show SMILES Nc1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C20H15FN4/c21-16-5-1-13(2-6-16)18-19(14-9-11-23-12-10-14)25-20(24-18)15-3-7-17(22)8-4-15/h1-12H,22H2,(H,24,25)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
Purchase

CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
n/an/a 50n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50230001
PNG
(4-(4-(4-fluorophenyl)-2-(4-nitrophenyl)-1H-imidazo...)
Show SMILES [O-][N+](=O)c1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C20H13FN4O2/c21-16-5-1-13(2-6-16)18-19(14-9-11-22-12-10-14)24-20(23-18)15-3-7-17(8-4-15)25(26)27/h1-12H,(H,23,24)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
Purchase

CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
n/an/a 50n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403407
PNG
(CHEMBL17210)
Show SMILES NS(=O)(=O)c1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C20H15FN4O2S/c21-16-5-1-13(2-6-16)18-19(14-9-11-23-12-10-14)25-20(24-18)15-3-7-17(8-4-15)28(22,26)27/h1-12H,(H,24,25)(H2,22,26,27)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
n/an/a 50n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403386
PNG
(CHEMBL417087)
Show SMILES CN(C)Cc1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C23H21FN4/c1-28(2)15-16-3-5-19(6-4-16)23-26-21(17-7-9-20(24)10-8-17)22(27-23)18-11-13-25-14-12-18/h3-14H,15H2,1-2H3,(H,26,27)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
n/an/a 80n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM13336
PNG
(4-[4-(4-fluorophenyl)-2-(4-methanesulfinylphenyl)-...)
Show SMILES CS(=O)c1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C21H16FN3OS/c1-27(26)18-8-4-16(5-9-18)21-24-19(14-2-6-17(22)7-3-14)20(25-21)15-10-12-23-13-11-15/h2-13H,1H3,(H,24,25)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
Purchase

CHEMBL
MMDB
PC cid
PC sid
UniChem

Patents


Similars

Article
n/an/a 80n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403376
PNG
(CHEMBL17389)
Show SMILES CS(=O)c1ccc(cc1)-c1nc(c([nH]1)-c1cccc(Cl)c1)-c1ccncc1
Show InChI InChI=1S/C21H16ClN3OS/c1-27(26)18-7-5-15(6-8-18)21-24-19(14-9-11-23-12-10-14)20(25-21)16-3-2-4-17(22)13-16/h2-13H,1H3,(H,24,25)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
n/an/a 80n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50104373
PNG
(4-[4-(4-Fluoro-phenyl)-5-pyridin-4-yl-1H-imidazol-...)
Show SMILES Fc1ccc(cc1)-c1[nH]c(nc1-c1ccncc1)-c1ccc(cc1)C#N
Show InChI InChI=1S/C21H13FN4/c22-18-7-5-15(6-8-18)19-20(16-9-11-24-12-10-16)26-21(25-19)17-3-1-14(13-23)2-4-17/h1-12H,(H,25,26)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Patents


Similars

Article
n/an/a 100n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403397
PNG
(CHEMBL17334)
Show SMILES Fc1ccc(cc1)-c1[nH]c(nc1-c1ccncc1)-c1ccc(CNC=O)cc1
Show InChI InChI=1S/C22H17FN4O/c23-19-7-5-16(6-8-19)20-21(17-9-11-24-12-10-17)27-22(26-20)18-3-1-15(2-4-18)13-25-14-28/h1-12,14H,13H2,(H,25,28)(H,26,27)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
n/an/a 120n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50284507
PNG
(4-[4-(4-Fluoro-phenyl)-5-pyridin-4-yl-1H-imidazol-...)
Show SMILES ONC(=O)c1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C21H15FN4O2/c22-17-7-5-13(6-8-17)18-19(14-9-11-23-12-10-14)25-20(24-18)15-1-3-16(4-2-15)21(27)26-28/h1-12,28H,(H,24,25)(H,26,27)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Patents


Similars

Article
n/an/a 120n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403404
PNG
(CHEMBL17346)
Show SMILES NC(=NO)c1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C21H16FN5O/c22-17-7-5-13(6-8-17)18-19(14-9-11-24-12-10-14)26-21(25-18)16-3-1-15(2-4-16)20(23)27-28/h1-12,28H,(H2,23,27)(H,25,26)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
n/an/a 190n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50284506
PNG
(4-[5-(4-Fluoro-phenyl)-2-(4-methanesulfonyl-phenyl...)
Show SMILES CS(=O)(=O)c1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C21H16FN3O2S/c1-28(26,27)18-8-4-16(5-9-18)21-24-19(14-2-6-17(22)7-3-14)20(25-21)15-10-12-23-13-11-15/h2-13H,1H3,(H,24,25)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
Purchase

CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
n/an/a 200n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403392
PNG
(CHEMBL17293)
Show SMILES NC(=O)N(O)Cc1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C22H18FN5O2/c23-18-7-5-15(6-8-18)19-20(16-9-11-25-12-10-16)27-21(26-19)17-3-1-14(2-4-17)13-28(30)22(24)29/h1-12,30H,13H2,(H2,24,29)(H,26,27)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
n/an/a 200n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403402
PNG
(CHEMBL17493)
Show SMILES CS(=O)(=O)Nc1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C21H17FN4O2S/c1-29(27,28)26-18-8-4-16(5-9-18)21-24-19(14-2-6-17(22)7-3-14)20(25-21)15-10-12-23-13-11-15/h2-13,26H,1H3,(H,24,25)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
n/an/a 270n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50284483
PNG
((3-{4-[4-(4-Fluoro-phenyl)-5-pyridin-4-yl-1H-imida...)
Show SMILES CN(C)CCCOc1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C25H25FN4O/c1-30(2)16-3-17-31-22-10-6-20(7-11-22)25-28-23(18-4-8-21(26)9-5-18)24(29-25)19-12-14-27-15-13-19/h4-15H,3,16-17H2,1-2H3,(H,28,29)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Patents


Similars

Article
n/an/a 290n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50104356
PNG
(4-[5-(4-Fluoro-phenyl)-2-phenyl-3H-imidazol-4-yl]-...)
Show SMILES Fc1ccc(cc1)-c1[nH]c(nc1-c1ccncc1)-c1ccccc1
Show InChI InChI=1S/C20H14FN3/c21-17-8-6-14(7-9-17)18-19(15-10-12-22-13-11-15)24-20(23-18)16-4-2-1-3-5-16/h1-13H,(H,23,24)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Patents


Similars

Article
n/an/a 300n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50284513
PNG
(CHEMBL17325 | {4-[4-(4-Fluoro-phenyl)-5-pyridin-4-...)
Show SMILES CN(C)c1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C22H19FN4/c1-27(2)19-9-5-17(6-10-19)22-25-20(15-3-7-18(23)8-4-15)21(26-22)16-11-13-24-14-12-16/h3-14H,1-2H3,(H,25,26)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Patents


Similars

Article
n/an/a 350n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50284516
PNG
(2,4,5-Triarylimidazole analogue | CHEMBL16925)
Show SMILES CC(N(O)C(N)=O)c1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C23H20FN5O2/c1-14(29(31)23(25)30)15-2-4-18(5-3-15)22-27-20(16-6-8-19(24)9-7-16)21(28-22)17-10-12-26-13-11-17/h2-14,31H,1H3,(H2,25,30)(H,27,28)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
n/an/a 350n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50104355
PNG
(4-[4-(4-Fluoro-phenyl)-5-pyridin-4-yl-1H-imidazol-...)
Show SMILES COC(=O)c1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C22H16FN3O2/c1-28-22(27)17-4-2-16(3-5-17)21-25-19(14-6-8-18(23)9-7-14)20(26-21)15-10-12-24-13-11-15/h2-13H,1H3,(H,25,26)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Patents


Similars

Article
n/an/a 370n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50104351
PNG
(4-[5-(4-Fluoro-phenyl)-2-(4-methoxy-phenyl)-3H-imi...)
Show SMILES COc1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C21H16FN3O/c1-26-18-8-4-16(5-9-18)21-24-19(14-2-6-17(22)7-3-14)20(25-21)15-10-12-23-13-11-15/h2-13H,1H3,(H,24,25)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Patents


Similars

Article
n/an/a 400n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50284487
PNG
((1Z)-N'-cyano-2-{4-[4-(4-fluorophenyl)-5-pyridin-4...)
Show SMILES NC(Cc1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1)=NC#N
Show InChI InChI=1S/C23H17FN6/c24-19-7-5-16(6-8-19)21-22(17-9-11-27-12-10-17)30-23(29-21)18-3-1-15(2-4-18)13-20(26)28-14-25/h1-12H,13H2,(H2,26,28)(H,29,30)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
n/an/a 420n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50284492
PNG
(4-[5-(4-Fluoro-phenyl)-2-(4-methanesulfinyl-phenyl...)
Show SMILES Cc1cnccc1-c1nc([nH]c1-c1ccc(F)cc1)-c1ccc(cc1)S(C)=O
Show InChI InChI=1S/C22H18FN3OS/c1-14-13-24-12-11-19(14)21-20(15-3-7-17(23)8-4-15)25-22(26-21)16-5-9-18(10-6-16)28(2)27/h3-13H,1-2H3,(H,25,26)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
n/an/a 430n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403381
PNG
(CHEMBL17480)
Show SMILES Fc1ccc(cc1)-c1[nH]c(nc1-c1ccncc1)-c1ccc(cc1)N=[N+]=[N-]
Show InChI InChI=1S/C20H13FN6/c21-16-5-1-13(2-6-16)18-19(14-9-11-23-12-10-14)25-20(24-18)15-3-7-17(8-4-15)26-27-22/h1-12H,(H,24,25)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
n/an/a 440n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50110200
PNG
(4-[4-(4-Fluoro-phenyl)-5-pyridin-4-yl-1H-imidazol-...)
Show SMILES OC(=O)c1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C21H14FN3O2/c22-17-7-5-13(6-8-17)18-19(14-9-11-23-12-10-14)25-20(24-18)15-1-3-16(4-2-15)21(26)27/h1-12H,(H,24,25)(H,26,27)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Patents


Similars

Article
n/an/a 500n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403377
PNG
(CHEMBL17224)
Show SMILES CS(=O)(=O)NCc1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C22H19FN4O2S/c1-30(28,29)25-14-15-2-4-18(5-3-15)22-26-20(16-6-8-19(23)9-7-16)21(27-22)17-10-12-24-13-11-17/h2-13,25H,14H2,1H3,(H,26,27)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
n/an/a 500n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403398
PNG
(CHEMBL17688)
Show SMILES Fc1ccc(cc1)-c1[nH]c(nc1-c1ccncc1)-c1ccc(CN2CCOCC2)cc1
Show InChI InChI=1S/C25H23FN4O/c26-22-7-5-19(6-8-22)23-24(20-9-11-27-12-10-20)29-25(28-23)21-3-1-18(2-4-21)17-30-13-15-31-16-14-30/h1-12H,13-17H2,(H,28,29)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
n/an/a 550n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50075778
PNG
(4-[5-(4-Fluoro-phenyl)-2-(4-methylsulfanyl-phenyl)...)
Show SMILES CSc1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C21H16FN3S/c1-26-18-8-4-16(5-9-18)21-24-19(14-2-6-17(22)7-3-14)20(25-21)15-10-12-23-13-11-15/h2-13H,1H3,(H,24,25)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
Purchase

CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
n/an/a 580n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403399
PNG
(CHEMBL17238)
Show SMILES COc1cccc(c1)-c1[nH]c(nc1-c1ccncc1)-c1ccc(cc1)S(C)=O
Show InChI InChI=1S/C22H19N3O2S/c1-27-18-5-3-4-17(14-18)21-20(15-10-12-23-13-11-15)24-22(25-21)16-6-8-19(9-7-16)28(2)26/h3-14H,1-2H3,(H,24,25)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
n/an/a 590n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50284489
PNG
(4-[4-(4-Fluoro-phenyl)-5-pyridin-4-yl-1H-imidazol-...)
Show SMILES Cc1cc(cc(C)c1O)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C22H18FN3O/c1-13-11-17(12-14(2)21(13)27)22-25-19(15-3-5-18(23)6-4-15)20(26-22)16-7-9-24-10-8-16/h3-12,27H,1-2H3,(H,25,26)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Patents


Similars

Article
n/an/a 600n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403394
PNG
(CHEMBL17252)
Show SMILES Fc1ccc(cc1)-c1[nH]c(nc1-c1ccnc2ccccc12)-c1ccc(cc1)C#N
Show InChI InChI=1S/C25H15FN4/c26-19-11-9-17(10-12-19)23-24(21-13-14-28-22-4-2-1-3-20(21)22)30-25(29-23)18-7-5-16(15-27)6-8-18/h1-14H,(H,29,30)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
n/an/a 600n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403382
PNG
(CHEMBL17273)
Show SMILES CS(=O)(=O)c1cccc(c1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C21H16FN3O2S/c1-28(26,27)18-4-2-3-16(13-18)21-24-19(14-5-7-17(22)8-6-14)20(25-21)15-9-11-23-12-10-15/h2-13H,1H3,(H,24,25)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
n/an/a 620n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403400
PNG
(CHEMBL17204)
Show SMILES Ic1cccc(c1)-c1[nH]c(nc1-c1ccncc1)-c1ccc(cc1)N=[N+]=[N-]
Show InChI InChI=1S/C20H13IN6/c21-16-3-1-2-15(12-16)19-18(13-8-10-23-11-9-13)24-20(25-19)14-4-6-17(7-5-14)26-27-22/h1-12H,(H,24,25)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
n/an/a 640n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403408
PNG
(CHEMBL275365)
Show SMILES Cn1c(nc(c1-c1ccncc1)-c1ccc(F)cc1)-c1ccc(cc1)S(C)=O
Show InChI InChI=1S/C22H18FN3OS/c1-26-21(16-11-13-24-14-12-16)20(15-3-7-18(23)8-4-15)25-22(26)17-5-9-19(10-6-17)28(2)27/h3-14H,1-2H3
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
n/an/a 650n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403375
PNG
(CHEMBL276114)
Show SMILES CS(=O)c1ccc(cc1)-c1nc(c([nH]1)-c1cccc2ccccc12)-c1ccncc1
Show InChI InChI=1S/C25H19N3OS/c1-30(29)20-11-9-19(10-12-20)25-27-23(18-13-15-26-16-14-18)24(28-25)22-8-4-6-17-5-2-3-7-21(17)22/h2-16H,1H3,(H,27,28)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
n/an/a 650n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403391
PNG
(CHEMBL17220)
Show SMILES CSc1ccc(cc1)-c1nc(c([nH]1)-c1cccc(N)c1)-c1ccncc1
Show InChI InChI=1S/C21H18N4S/c1-26-18-7-5-15(6-8-18)21-24-19(14-9-11-23-12-10-14)20(25-21)16-3-2-4-17(22)13-16/h2-13H,22H2,1H3,(H,24,25)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403409
PNG
(CHEMBL276529)
Show SMILES CS(=O)c1cccc(c1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C21H16FN3OS/c1-27(26)18-4-2-3-16(13-18)21-24-19(14-5-7-17(22)8-6-14)20(25-21)15-9-11-23-12-10-15/h2-13H,1H3,(H,24,25)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
n/an/a 700n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403379
PNG
(CHEMBL277587)
Show SMILES CS(=O)c1ccccc1-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C21H16FN3OS/c1-27(26)18-5-3-2-4-17(18)21-24-19(14-6-8-16(22)9-7-14)20(25-21)15-10-12-23-13-11-15/h2-13H,1H3,(H,24,25)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
n/an/a 710n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50284495
PNG
(4-[5-(4-Fluoro-phenyl)-2-(4-methanesulfinyl-phenyl...)
Show SMILES CS(=O)c1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccnc2ccccc12
Show InChI InChI=1S/C25H18FN3OS/c1-31(30)19-12-8-17(9-13-19)25-28-23(16-6-10-18(26)11-7-16)24(29-25)21-14-15-27-22-5-3-2-4-20(21)22/h2-15H,1H3,(H,28,29)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Patents


Similars

Article
n/an/a 710n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403395
PNG
(CHEMBL17792)
Show SMILES CS(=O)(=O)c1ccccc1-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C21H16FN3O2S/c1-28(26,27)18-5-3-2-4-17(18)21-24-19(14-6-8-16(22)9-7-14)20(25-21)15-10-12-23-13-11-15/h2-13H,1H3,(H,24,25)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
n/an/a 740n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403403
PNG
(CHEMBL16926)
Show SMILES CN1CCC(CC1)S(=O)(=O)c1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C26H25FN4O2S/c1-31-16-12-23(13-17-31)34(32,33)22-8-4-20(5-9-22)26-29-24(18-2-6-21(27)7-3-18)25(30-26)19-10-14-28-15-11-19/h2-11,14-15,23H,12-13,16-17H2,1H3,(H,29,30)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
n/an/a 740n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50217610
PNG
(4-(2-(4-(methylsulfinyl)phenyl)-4-(naphthalen-2-yl...)
Show SMILES CS(=O)c1ccc(cc1)-c1nc(c([nH]1)-c1ccc2ccccc2c1)-c1ccncc1
Show InChI InChI=1S/C25H19N3OS/c1-30(29)22-10-8-19(9-11-22)25-27-23(18-12-14-26-15-13-18)24(28-25)21-7-6-17-4-2-3-5-20(17)16-21/h2-16H,1H3,(H,27,28)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Patents


Similars

Article
n/an/a 770n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
Arachidonate 5-lipoxygenase


(Rattus norvegicus)
BDBM50284481
PNG
(Benzyl-{4-[4-(4-fluoro-phenyl)-5-pyridin-4-yl-1H-i...)
Show SMILES CN(Cc1ccccc1)Cc1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C29H25FN4/c1-34(19-21-5-3-2-4-6-21)20-22-7-9-25(10-8-22)29-32-27(23-11-13-26(30)14-12-23)28(33-29)24-15-17-31-18-16-24/h2-18H,19-20H2,1H3,(H,32,33)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
n/an/a 800n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against 5-lipoxygenase enzyme from RBL-1 cells


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403396
PNG
(CHEMBL16838)
Show SMILES CSc1ccccc1-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C21H16FN3S/c1-26-18-5-3-2-4-17(18)21-24-19(14-6-8-16(22)9-7-14)20(25-21)15-10-12-23-13-11-15/h2-13H,1H3,(H,24,25)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
n/an/a 820n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403383
PNG
(CHEMBL280457)
Show SMILES Fc1ccc(cc1)-c1nc([nH]c1-c1ccncc1)-c1ccc(cc1)-c1nc(=O)o[nH]1
Show InChI InChI=1S/C22H14FN5O2/c23-17-7-5-13(6-8-17)18-19(14-9-11-24-12-10-14)26-20(25-18)15-1-3-16(4-2-15)21-27-22(29)30-28-21/h1-12H,(H,25,26)(H,27,28,29)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
n/an/a 860n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403393
PNG
(CHEMBL17641)
Show SMILES CSc1cccc(c1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C21H16FN3S/c1-26-18-4-2-3-16(13-18)21-24-19(14-5-7-17(22)8-6-14)20(25-21)15-9-11-23-12-10-15/h2-13H,1H3,(H,24,25)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
n/an/a 930n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50284475
PNG
(4-[4-(4-Fluoro-phenyl)-5-pyridin-4-yl-1H-imidazol-...)
Show SMILES CCOC(=O)c1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C23H18FN3O2/c1-2-29-23(28)18-5-3-17(4-6-18)22-26-20(15-7-9-19(24)10-8-15)21(27-22)16-11-13-25-14-12-16/h3-14H,2H2,1H3,(H,26,27)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Patents


Similars

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



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403380
PNG
(CHEMBL17135)
Show SMILES COc1ccccc1-c1[nH]c(nc1-c1ccncc1)-c1ccc(cc1)S(C)=O
Show InChI InChI=1S/C22H19N3O2S/c1-27-19-6-4-3-5-18(19)21-20(15-11-13-23-14-12-15)24-22(25-21)16-7-9-17(10-8-16)28(2)26/h3-14H,1-2H3,(H,24,25)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
n/an/a 1.14E+3n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403385
PNG
(CHEMBL17482)
Show SMILES Cc1nc(no1)-c1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C23H16FN5O/c1-14-26-23(29-30-14)18-4-2-17(3-5-18)22-27-20(15-6-8-19(24)9-7-15)21(28-22)16-10-12-25-13-11-16/h2-13H,1H3,(H,27,28)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
n/an/a 1.32E+3n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50284481
PNG
(Benzyl-{4-[4-(4-fluoro-phenyl)-5-pyridin-4-yl-1H-i...)
Show SMILES CN(Cc1ccccc1)Cc1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C29H25FN4/c1-34(19-21-5-3-2-4-6-21)20-22-7-9-25(10-8-22)29-32-27(23-11-13-26(30)14-12-23)28(33-29)24-15-17-31-18-16-24/h2-18H,19-20H2,1H3,(H,32,33)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Patents


Similars

Article
n/an/a 2.30E+3n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
Arachidonate 5-lipoxygenase


(Rattus norvegicus)
BDBM50284475
PNG
(4-[4-(4-Fluoro-phenyl)-5-pyridin-4-yl-1H-imidazol-...)
Show SMILES CCOC(=O)c1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C23H18FN3O2/c1-2-29-23(28)18-5-3-17(4-6-18)22-26-20(15-7-9-19(24)10-8-15)21(27-22)16-11-13-25-14-12-16/h3-14H,2H2,1H3,(H,26,27)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
n/an/a 2.40E+3n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against 5-lipoxygenase enzyme from RBL-1 cells


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
Arachidonate 5-lipoxygenase


(Rattus norvegicus)
BDBM50075778
PNG
(4-[5-(4-Fluoro-phenyl)-2-(4-methylsulfanyl-phenyl)...)
Show SMILES CSc1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C21H16FN3S/c1-26-18-8-4-16(5-9-18)21-24-19(14-2-6-17(22)7-3-14)20(25-21)15-10-12-23-13-11-15/h2-13H,1H3,(H,24,25)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
Purchase

CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
n/an/a 2.70E+3n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against 5-lipoxygenase enzyme from RBL-1 cells


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403390
PNG
(CHEMBL17410)
Show SMILES CSc1ccc(cc1)-c1nc(c([nH]1)-c1cccc(c1)[N+]([O-])=O)-c1ccncc1
Show InChI InChI=1S/C21H16N4O2S/c1-28-18-7-5-15(6-8-18)21-23-19(14-9-11-22-12-10-14)20(24-21)16-3-2-4-17(13-16)25(26)27/h2-13H,1H3,(H,23,24)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
n/an/a 2.77E+3n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50284482
PNG
(2-[4-(4-Fluoro-phenyl)-5-pyridin-4-yl-1H-imidazol-...)
Show SMILES Oc1ccccc1-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C20H14FN3O/c21-15-7-5-13(6-8-15)18-19(14-9-11-22-12-10-14)24-20(23-18)16-3-1-2-4-17(16)25/h1-12,25H,(H,23,24)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
n/an/a 3.00E+3n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
Arachidonate 5-lipoxygenase


(Rattus norvegicus)
BDBM50284489
PNG
(4-[4-(4-Fluoro-phenyl)-5-pyridin-4-yl-1H-imidazol-...)
Show SMILES Cc1cc(cc(C)c1O)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C22H18FN3O/c1-13-11-17(12-14(2)21(13)27)22-25-19(15-3-5-18(23)6-4-15)20(26-22)16-7-9-24-10-8-16/h3-12,27H,1-2H3,(H,25,26)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
n/an/a 3.10E+3n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against 5-lipoxygenase enzyme from RBL-1 cells


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
Arachidonate 5-lipoxygenase


(Rattus norvegicus)
BDBM50284487
PNG
((1Z)-N'-cyano-2-{4-[4-(4-fluorophenyl)-5-pyridin-4...)
Show SMILES NC(Cc1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1)=NC#N
Show InChI InChI=1S/C23H17FN6/c24-19-7-5-16(6-8-19)21-22(17-9-11-27-12-10-17)30-23(29-21)18-3-1-15(2-4-18)13-20(26)28-14-25/h1-12H,13H2,(H2,26,28)(H,29,30)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
n/an/a 3.80E+3n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against 5-lipoxygenase enzyme from RBL-1 cells


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
Arachidonate 5-lipoxygenase


(Rattus norvegicus)
BDBM50284482
PNG
(2-[4-(4-Fluoro-phenyl)-5-pyridin-4-yl-1H-imidazol-...)
Show SMILES Oc1ccccc1-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C20H14FN3O/c21-15-7-5-13(6-8-15)18-19(14-9-11-22-12-10-14)24-20(23-18)16-3-1-2-4-17(16)25/h1-12,25H,(H,23,24)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
n/an/a 4.10E+3n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against 5-lipoxygenase enzyme from RBL-1 cells


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403378
PNG
(CHEMBL278491)
Show SMILES CSc1ccc(cc1)-c1nc(c([nH]1)-c1cccc(NC(C)=O)c1)-c1ccncc1
Show InChI InChI=1S/C23H20N4OS/c1-15(28)25-19-5-3-4-18(14-19)22-21(16-10-12-24-13-11-16)26-23(27-22)17-6-8-20(29-2)9-7-17/h3-14H,1-2H3,(H,25,28)(H,26,27)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
n/an/a 4.32E+3n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
Arachidonate 5-lipoxygenase


(Rattus norvegicus)
BDBM50284507
PNG
(4-[4-(4-Fluoro-phenyl)-5-pyridin-4-yl-1H-imidazol-...)
Show SMILES ONC(=O)c1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C21H15FN4O2/c22-17-7-5-13(6-8-17)18-19(14-9-11-23-12-10-14)25-20(24-18)15-1-3-16(4-2-15)21(27)26-28/h1-12,28H,(H,24,25)(H,26,27)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
n/an/a 4.70E+3n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against 5-lipoxygenase enzyme from RBL-1 cells


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403405
PNG
(CHEMBL274279)
Show SMILES CC(C)(C)c1cc(cc(c1O)C(C)(C)C)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C28H30FN3O/c1-27(2,3)21-15-19(16-22(25(21)33)28(4,5)6)26-31-23(17-7-9-20(29)10-8-17)24(32-26)18-11-13-30-14-12-18/h7-16,33H,1-6H3,(H,31,32)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403387
PNG
(CHEMBL277811)
Show SMILES CSc1ccc(cc1)-c1nc(c([nH]1)-c1cccc(NS(C)(=O)=O)c1)-c1ccncc1
Show InChI InChI=1S/C22H20N4O2S2/c1-29-19-8-6-16(7-9-19)22-24-20(15-10-12-23-13-11-15)21(25-22)17-4-3-5-18(14-17)26-30(2,27)28/h3-14,26H,1-2H3,(H,24,25)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50403401
PNG
(CHEMBL276548)
Show SMILES CS(=O)c1ccc(cc1)-c1nc(c([nH]1)-c1cccc(NS(C)(=O)=O)c1)-c1ccncc1
Show InChI InChI=1S/C22H20N4O3S2/c1-30(27)19-8-6-16(7-9-19)22-24-20(15-10-12-23-13-11-15)21(25-22)17-4-3-5-18(14-17)26-31(2,28)29/h3-14,26H,1-2H3,(H,24,25)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM67465
PNG
(2-(4-nitrophenyl)-4,5-diphenyl-1H-imidazole | SR-0...)
Show SMILES [O-][N+](=O)c1ccc(cc1)-c1nc(c([nH]1)-c1ccccc1)-c1ccccc1
Show InChI InChI=1S/C21H15N3O2/c25-24(26)18-13-11-17(12-14-18)21-22-19(15-7-3-1-4-8-15)20(23-21)16-9-5-2-6-10-16/h1-14H,(H,22,23)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
Purchase

PC cid
PC sid
UniChem

Similars

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



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50284510
PNG
(4-(4-ethyl-2-(4-methoxyphenyl)-1H-imidazol-5-yl)py...)
Show SMILES CCc1[nH]c(nc1-c1ccncc1)-c1ccc(OC)cc1
Show InChI InChI=1S/C17H17N3O/c1-3-15-16(12-8-10-18-11-9-12)20-17(19-15)13-4-6-14(21-2)7-5-13/h4-11H,3H2,1-2H3,(H,19,20)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
Purchase

CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

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



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
Arachidonate 5-lipoxygenase


(Rattus norvegicus)
BDBM50104355
PNG
(4-[4-(4-Fluoro-phenyl)-5-pyridin-4-yl-1H-imidazol-...)
Show SMILES COC(=O)c1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C22H16FN3O2/c1-28-22(27)17-4-2-16(3-5-17)21-25-19(14-6-8-18(23)9-7-14)20(26-21)15-10-12-24-13-11-15/h2-13H,1H3,(H,25,26)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

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



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against 5-lipoxygenase enzyme from RBL-1 cells


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
Arachidonate 5-lipoxygenase


(Rattus norvegicus)
BDBM50284513
PNG
(CHEMBL17325 | {4-[4-(4-Fluoro-phenyl)-5-pyridin-4-...)
Show SMILES CN(C)c1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C22H19FN4/c1-27(2)19-9-5-17(6-10-19)22-25-20(15-3-7-18(23)8-4-15)21(26-22)16-11-13-24-14-12-16/h3-14H,1-2H3,(H,25,26)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
n/an/a 5.60E+3n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against 5-lipoxygenase enzyme from RBL-1 cells


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
Arachidonate 5-lipoxygenase


(Rattus norvegicus)
BDBM50284516
PNG
(2,4,5-Triarylimidazole analogue | CHEMBL16925)
Show SMILES CC(N(O)C(N)=O)c1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C23H20FN5O2/c1-14(29(31)23(25)30)15-2-4-18(5-3-15)22-27-20(16-6-8-19(24)9-7-16)21(28-22)17-10-12-26-13-11-17/h2-14,31H,1H3,(H2,25,30)(H,27,28)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
n/an/a 6.20E+3n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against 5-lipoxygenase enzyme from RBL-1 cells


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
5-lipoxygenase/FLAP


(Homo sapiens (human))
BDBM50284499
PNG
(4-[2-[4-(5,5-Dimethyl-2,5-dihydro-[1,2,4]oxadiazol...)
Show SMILES CC1(C)NC(=NO1)c1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C24H20FN5O/c1-24(2)29-23(30-31-24)18-5-3-17(4-6-18)22-27-20(15-7-9-19(25)10-8-15)21(28-22)16-11-13-26-14-12-16/h3-14H,1-2H3,(H,27,28)(H,29,30)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
n/an/a 6.80E+3n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against interleukin-1(IL-1) synthesis, using intact human monocytes


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
Arachidonate 5-lipoxygenase


(Rattus norvegicus)
BDBM50284499
PNG
(4-[2-[4-(5,5-Dimethyl-2,5-dihydro-[1,2,4]oxadiazol...)
Show SMILES CC1(C)NC(=NO1)c1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C24H20FN5O/c1-24(2)29-23(30-31-24)18-5-3-17(4-6-18)22-27-20(15-7-9-19(25)10-8-15)21(28-22)16-11-13-26-14-12-16/h3-14H,1-2H3,(H,27,28)(H,29,30)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
n/an/a 7.20E+3n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against 5-lipoxygenase enzyme from RBL-1 cells


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
Arachidonate 5-lipoxygenase


(Rattus norvegicus)
BDBM50284495
PNG
(4-[5-(4-Fluoro-phenyl)-2-(4-methanesulfinyl-phenyl...)
Show SMILES CS(=O)c1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccnc2ccccc12
Show InChI InChI=1S/C25H18FN3OS/c1-31(30)19-12-8-17(9-13-19)25-28-23(16-6-10-18(26)11-7-16)24(29-25)21-14-15-27-22-5-3-2-4-20(21)22/h2-15H,1H3,(H,28,29)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
n/an/a 7.20E+3n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against 5-lipoxygenase enzyme from RBL-1 cells


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
Arachidonate 5-lipoxygenase


(Rattus norvegicus)
BDBM50104351
PNG
(4-[5-(4-Fluoro-phenyl)-2-(4-methoxy-phenyl)-3H-imi...)
Show SMILES COc1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C21H16FN3O/c1-26-18-8-4-16(5-9-18)21-24-19(14-2-6-17(22)7-3-14)20(25-21)15-10-12-23-13-11-15/h2-13H,1H3,(H,24,25)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
n/an/a 7.60E+3n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against 5-lipoxygenase enzyme from RBL-1 cells


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
Arachidonate 5-lipoxygenase


(Rattus norvegicus)
BDBM50230001
PNG
(4-(4-(4-fluorophenyl)-2-(4-nitrophenyl)-1H-imidazo...)
Show SMILES [O-][N+](=O)c1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C20H13FN4O2/c21-16-5-1-13(2-6-16)18-19(14-9-11-22-12-10-14)24-20(23-18)15-3-7-17(8-4-15)25(26)27/h1-12H,(H,23,24)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
Purchase

CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
n/an/a 8.00E+3n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against 5-lipoxygenase enzyme from RBL-1 cells


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
Arachidonate 5-lipoxygenase


(Rattus norvegicus)
BDBM50284492
PNG
(4-[5-(4-Fluoro-phenyl)-2-(4-methanesulfinyl-phenyl...)
Show SMILES Cc1cnccc1-c1nc([nH]c1-c1ccc(F)cc1)-c1ccc(cc1)S(C)=O
Show InChI InChI=1S/C22H18FN3OS/c1-14-13-24-12-11-19(14)21-20(15-3-7-17(23)8-4-15)25-22(26-21)16-5-9-18(10-6-16)28(2)27/h3-13H,1-2H3,(H,25,26)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
n/an/a 2.30E+4n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against 5-lipoxygenase enzyme from RBL-1 cells


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
Arachidonate 5-lipoxygenase


(Rattus norvegicus)
BDBM50284506
PNG
(4-[5-(4-Fluoro-phenyl)-2-(4-methanesulfonyl-phenyl...)
Show SMILES CS(=O)(=O)c1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C21H16FN3O2S/c1-28(26,27)18-8-4-16(5-9-18)21-24-19(14-2-6-17(22)7-3-14)20(25-21)15-10-12-23-13-11-15/h2-13H,1H3,(H,24,25)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
Purchase

CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
n/an/a 2.40E+4n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against 5-lipoxygenase enzyme from RBL-1 cells


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
Arachidonate 5-lipoxygenase


(Rattus norvegicus)
BDBM50284483
PNG
((3-{4-[4-(4-Fluoro-phenyl)-5-pyridin-4-yl-1H-imida...)
Show SMILES CN(C)CCCOc1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C25H25FN4O/c1-30(2)16-3-17-31-22-10-6-20(7-11-22)25-28-23(18-4-8-21(26)9-5-18)24(29-25)19-12-14-27-15-13-19/h4-15H,3,16-17H2,1-2H3,(H,28,29)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
n/an/a 4.90E+4n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against 5-lipoxygenase enzyme from RBL-1 cells


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
Arachidonate 5-lipoxygenase


(Rattus norvegicus)
BDBM13336
PNG
(4-[4-(4-fluorophenyl)-2-(4-methanesulfinylphenyl)-...)
Show SMILES CS(=O)c1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
Show InChI InChI=1S/C21H16FN3OS/c1-27(26)18-8-4-16(5-9-18)21-24-19(14-2-6-17(22)7-3-14)20(25-21)15-10-12-23-13-11-15/h2-13H,1H3,(H,24,25)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
Purchase

CHEMBL
MMDB
PC cid
PC sid
UniChem

Patents


Similars

Article
n/an/a 5.80E+4n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against 5-lipoxygenase enzyme from RBL-1 cells


Bioorg Med Chem Lett 5: 1171-1176 (1995)


Article DOI: 10.1016/0960-894X(95)00189-Z
BindingDB Entry DOI: 10.7270/Q28S4PV1
More data for this
Ligand-Target Pair
* indicates data uncertainty>20%