BDBM50288096 5-Chloro-2-ethoxy-benzo[d][1,3]oxazin-4-one::CHEMBL79597

SMILES: CCOc1nc2cccc(Cl)c2c(=O)o1

InChI Key: InChIKey=IKBJPGAZNDONQO-UHFFFAOYSA-N

Data: 2 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 2 hits for monomerid = 50288096   

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
Rhomboid protease GluP (Bacillus subtilis (strain 168))	BDBM50288096 (5-Chloro-2-ethoxy-benzo[d][1,3]oxazin-4-one | CHEM...) Show SMILES CCOc1nc2cccc(Cl)c2c(=O)o1 Show InChI InChI=1S/C10H8ClNO3/c1-2-14-10-12-7-5-3-4-6(11)8(7)9(13)15-10/h3-5H,2H2,1H3	PDB UniProtKB/SwissProt UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
KU Leuven Curated by ChEMBL					Assay Description Competitive inhibition of Bacillus subtilis rhomboid YqgP preincubated for 30 mins followed by FP-Rh addition measured after 1 hr by gel-based ABPP m...				Bioorg Med Chem Lett 28: 1423-1427 (2018) Article DOI: 10.1016/j.bmcl.2017.12.056 BindingDB Entry DOI: 10.7270/Q2WH2SM6
					More data for this Ligand-Target Pair
Human herpesvirus 1 protease (Human herpesvirus 1 (strain 17) (HHV-1) (Human her...)	BDBM50288096 (5-Chloro-2-ethoxy-benzo[d][1,3]oxazin-4-one | CHEM...) Show SMILES CCOc1nc2cccc(Cl)c2c(=O)o1 Show InChI InChI=1S/C10H8ClNO3/c1-2-14-10-12-7-5-3-4-6(11)8(7)9(13)15-10/h3-5H,2H2,1H3	MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	7.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against herpes simplex type 1 protease (HSV-1 pr).				Bioorg Med Chem Lett 6: 2463-2466 (1996) Article DOI: 10.1016/0960-894X(96)00455-6 BindingDB Entry DOI: 10.7270/Q2F47P4R
					More data for this Ligand-Target Pair