BDBM50289017 2-(2-Iodo-phenyl)-7-nitro-benzo[d][1,3]oxazin-4-one::CHEMBL159105

SMILES: [O-][N+](=O)c1ccc2c(c1)nc(oc2=O)-c1ccccc1I

InChI Key: InChIKey=RSARXMAIDILOCC-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 = 50289017   

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
Complement C1r (Homo sapiens (Human))	BDBM50289017 (2-(2-Iodo-phenyl)-7-nitro-benzo[d][1,3]oxazin-4-on...) Show SMILES [O-][N+](=O)c1ccc2c(c1)nc(oc2=O)-c1ccccc1I Show InChI InChI=1S/C14H7IN2O4/c15-11-4-2-1-3-9(11)13-16-12-7-8(17(19)20)5-6-10(12)14(18)21-13/h1-7H	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	n/a	n/a	>6.25E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against C1r serine protease				Bioorg Med Chem Lett 6: 679-682 (1996) Article DOI: 10.1016/0960-894X(96)00094-7 BindingDB Entry DOI: 10.7270/Q2P84BVF
					More data for this Ligand-Target Pair
Complement C1r subcomponent (Homo sapiens (Human))	BDBM50289017 (2-(2-Iodo-phenyl)-7-nitro-benzo[d][1,3]oxazin-4-on...) Show SMILES [O-][N+](=O)c1ccc2c(c1)nc(oc2=O)-c1ccccc1I Show InChI InChI=1S/C14H7IN2O4/c15-11-4-2-1-3-9(11)13-16-12-7-8(17(19)20)5-6-10(12)14(18)21-13/h1-7H	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	n/a	n/a	2.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against C1r serine protease				Bioorg Med Chem Lett 6: 679-682 (1996) Article DOI: 10.1016/0960-894X(96)00094-7 BindingDB Entry DOI: 10.7270/Q2P84BVF
					More data for this Ligand-Target Pair