BDBM50268882 5-chloropyridin-3-yl 4-ethoxy-2-styryloxazole-5-carboxylate::CHEMBL496214

SMILES: CCOc1nc(\C=C\c2ccccc2)oc1C(=O)Oc1cncc(Cl)c1

InChI Key: InChIKey=QCUVCXVXWWGNTC-CMDGGOBGSA-N

Data: 1 IC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50268882   

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
Genome polyprotein (Human rhinovirus 16)	BDBM50268882 (5-chloropyridin-3-yl 4-ethoxy-2-styryloxazole-5-ca...) Show SMILES CCOc1nc(\C=C\c2ccccc2)oc1C(=O)Oc1cncc(Cl)c1 Show InChI InChI=1S/C19H15ClN2O4/c1-2-24-18-17(19(23)25-15-10-14(20)11-21-12-15)26-16(22-18)9-8-13-6-4-3-5-7-13/h3-12H,2H2,1H3/b9-8+	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	690	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Science and Technology Curated by ChEMBL					Assay Description Inhibition of HRV-16 protease 3C expressed in Escherichia coli BL21(DE3) by FRET assay				Bioorg Med Chem Lett 19: 3632-6 (2009) Article DOI: 10.1016/j.bmcl.2009.04.114 BindingDB Entry DOI: 10.7270/Q2542NHW
					More data for this Ligand-Target Pair