BDBM50035558 5-(2-Fluoro-phenyl)-2,3-dihydro-imidazo[2,1-a]isoquinoline::CHEMBL310238
SMILES: Fc1ccccc1C1=Cc2ccccc2C2=NCCN12
InChI Key: InChIKey=CRASKXTVWBAFRS-UHFFFAOYSA-N
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Polycomb protein EED (EED) (Homo sapiens (Human)) | BDBM50035558 (5-(2-Fluoro-phenyl)-2,3-dihydro-imidazo[2,1-a]isoq...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid PDB UniChem Patents Similars | PDB Article PubMed | n/a | n/a | 6.04E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Novartis Institutes for BioMedical Research Curated by ChEMBL | Assay Description Inhibition of EED in human G401 cells assessed as reduction in global H3K27me3 level after 48 hrs by ELISA | J Med Chem 60: 2215-2226 (2017) Article DOI: 10.1021/acs.jmedchem.6b01576 BindingDB Entry DOI: 10.7270/Q20G3NDT | |||||||||||
More data for this Ligand-Target Pair | 3D Structure (crystal) | ||||||||||||
Platelet activating factor receptor (Homo sapiens (Human)) | BDBM50035558 (5-(2-Fluoro-phenyl)-2,3-dihydro-imidazo[2,1-a]isoq...) | PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid PDB UniChem Patents Similars | PubMed | n/a | n/a | 5.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sandoz Research Institute Curated by ChEMBL | Assay Description Inhibition of [3H]-PAF binding to human platelet activating factor receptor | J Med Chem 38: 234-40 (1995) BindingDB Entry DOI: 10.7270/Q27M06Z1 | |||||||||||
More data for this Ligand-Target Pair |