BDBM50090412 4-(2,5-Dioxo-3-phenyl-2,5-dihydro-pyrrol-1-ylamino)-2-trifluoromethyl-pyrimidine-5-carboxylic acid ethyl ester::CHEMBL290656::ethyl 4-(2,5-dioxo-3-phenyl-2H-pyrrol-1(5H)-ylamino)-2-(trifluoromethyl)pyrimidine-5-carboxylate
SMILES: CCOC(=O)c1cnc(nc1NN1C(=O)C=C(C1=O)c1ccccc1)C(F)(F)F
InChI Key: InChIKey=LCSVPHQXHLYQJW-UHFFFAOYSA-N
Data: 1 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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Proto-oncogene c-JUN/protein c-fos (Homo sapiens (Human)) | BDBM50090412 (4-(2,5-Dioxo-3-phenyl-2,5-dihydro-pyrrol-1-ylamino...) | PDB KEGG UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | 2.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Signal Pharmaceuticals, Inc. Curated by ChEMBL | Assay Description Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells | Bioorg Med Chem Lett 10: 1645-8 (2000) BindingDB Entry DOI: 10.7270/Q2F190XH | |||||||||||
More data for this Ligand-Target Pair |