BDBM50053410 4-(4-Fluorophenyl)-5-(pyridin-4-yl)-1H-imidazole::4-[5-(4-Fluoro-phenyl)-3H-imidazol-4-yl]-pyridine::CHEMBL63135
SMILES: Fc1ccc(cc1)-c1[nH]cnc1-c1ccncc1
InChI Key: InChIKey=MAOSUPNJVJGJEU-UHFFFAOYSA-N
Data: 6 IC50
Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kcal/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
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Prostaglandin G/H synthase (cyclooxygenase) (Ovis aries (Sheep)) | BDBM50053410 (4-(4-Fluorophenyl)-5-(pyridin-4-yl)-1H-imidazole |...) | PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
SmithKline Beecham Pharmaceuticals Curated by ChEMBL | Assay Description Inhibitory concentration against Prostaglandin H2 synthase 1 (PGHS-1) from ram seminal vesicle | J Med Chem 39: 3929-37 (1996) Article DOI: 10.1021/jm960415o BindingDB Entry DOI: 10.7270/Q29W0G4Z | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Mitogen-activated protein kinase 9 (Homo sapiens (Human)) | BDBM50053410 (4-(4-Fluorophenyl)-5-(pyridin-4-yl)-1H-imidazole |...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 195 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of c-Jun N-terminal kinase 2-alpha 1 | J Med Chem 42: 2180-90 (1999) Article DOI: 10.1021/jm9805236 BindingDB Entry DOI: 10.7270/Q2Q81C8D | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Arachidonate 5-lipoxygenase (Rattus norvegicus) | BDBM50053410 (4-(4-Fluorophenyl)-5-(pyridin-4-yl)-1H-imidazole |...) | PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
SmithKline Beecham Pharmaceuticals Curated by ChEMBL | Assay Description Inhibitory concentration against 5-lipoxygenase in rat RBL-1 cells | J Med Chem 39: 3929-37 (1996) Article DOI: 10.1021/jm960415o BindingDB Entry DOI: 10.7270/Q29W0G4Z | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
MAP kinase p38 (Mus musculus (mouse)) | BDBM50053410 (4-(4-Fluorophenyl)-5-(pyridin-4-yl)-1H-imidazole |...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | PubMed | n/a | n/a | 1.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Novartis Pharma AG Curated by ChEMBL | Assay Description In vivo inhibition of murine Mitogen-activated protein kinase p38 alpha activity, GST-ATF-2 as substrate in the presence of 120 microM ATP | Bioorg Med Chem Lett 12: 2109-12 (2002) BindingDB Entry DOI: 10.7270/Q2610ZNX | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Mitogen-activated protein kinase 14 (Homo sapiens (Human)) | BDBM50053410 (4-(4-Fluorophenyl)-5-(pyridin-4-yl)-1H-imidazole |...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 79 | n/a | n/a | n/a | n/a | n/a | n/a |
Islamic University of Gaza Curated by ChEMBL | Assay Description Inhibition of p38alpha MAP kinase (unknown origin) | J Med Chem 52: 2613-7 (2009) Article DOI: 10.1021/jm801467h BindingDB Entry DOI: 10.7270/Q21Z449S | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAF proto-oncogene serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50053410 (4-(4-Fluorophenyl)-5-(pyridin-4-yl)-1H-imidazole |...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 1.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibitory activity against recombinant human RAF proto-oncogene serine/threonine-protein kinase | J Med Chem 42: 2180-90 (1999) Article DOI: 10.1021/jm9805236 BindingDB Entry DOI: 10.7270/Q2Q81C8D | |||||||||||
More data for this Ligand-Target Pair |