BDBM50005912 2-Benzyl-1,8-dihydroxy-anthraquinone::CHEMBL41525

SMILES: Oc1cccc2C(=O)c3ccc(Cc4ccccc4)c(O)c3C(=O)c12

InChI Key: InChIKey=ZSGODHJXXNFJIM-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 = 50005912   

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
Cathepsin G (Homo sapiens (Human))	BDBM50005912 (2-Benzyl-1,8-dihydroxy-anthraquinone | CHEMBL41525) Show SMILES Oc1cccc2C(=O)c3ccc(Cc4ccccc4)c(O)c3C(=O)c12 Show InChI InChI=1S/C21H14O4/c22-16-8-4-7-14-17(16)21(25)18-15(20(14)24)10-9-13(19(18)23)11-12-5-2-1-3-6-12/h1-10,22-23H,11H2	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	5.60E+4	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry and Biochemistry Curated by ChEMBL					Assay Description Inhibition of Cathepsin G (CatG)				J Med Chem 35: 1597-605 (1992) BindingDB Entry DOI: 10.7270/Q2QN67D7
					More data for this Ligand-Target Pair
Leukocyte elastase (Homo sapiens (Human))	BDBM50005912 (2-Benzyl-1,8-dihydroxy-anthraquinone | CHEMBL41525) Show SMILES Oc1cccc2C(=O)c3ccc(Cc4ccccc4)c(O)c3C(=O)c12 Show InChI InChI=1S/C21H14O4/c22-16-8-4-7-14-17(16)21(25)18-15(20(14)24)10-9-13(19(18)23)11-12-5-2-1-3-6-12/h1-10,22-23H,11H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry and Biochemistry Curated by ChEMBL					Assay Description In vitro inhibition of human leukocyte elastase.				J Med Chem 35: 1597-605 (1992) BindingDB Entry DOI: 10.7270/Q2QN67D7
					More data for this Ligand-Target Pair