BDBM41890 2-(1-benzimidazolyl)-1-(3,4-dihydroxyphenyl)ethanone;hydrochloride::2-(benzimidazol-1-yl)-1-(3,4-dihydroxyphenyl)ethanone;hydrochloride::2-(benzimidazol-1-yl)-1-[3,4-bis(oxidanyl)phenyl]ethanone;hydrochloride::CHEMBL608723::MLS-0315853.0001::cid_25067493

SMILES: Oc1ccc(cc1O)C(=O)Cn1cnc2ccccc12

InChI Key: InChIKey=ILEKMJJREWCPRD-UHFFFAOYSA-N

Data: 7 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 7 hits for monomerid = 41890   

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
Alkaline phosphatase placental-like (Homo sapiens (Human))	BDBM41890 (2-(1-benzimidazolyl)-1-(3,4-dihydroxyphenyl)ethano...) Show SMILES Oc1ccc(cc1O)C(=O)Cn1cnc2ccccc12 Show InChI InChI=1S/C15H12N2O3/c18-13-6-5-10(7-14(13)19)15(20)8-17-9-16-11-3-1-2-4-12(11)17/h1-7,9,18-19H,8H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PCBioAssay	n/a	n/a	1.48E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sanford-Burnham Center for Chemical Genomics Curated by PubChem BioAssay					Assay Description Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, C...				PubChem Bioassay (2009) BindingDB Entry DOI: 10.7270/Q2JQ0ZDS
					More data for this Ligand-Target Pair
Alkaline phosphatase, tissue-nonspecific isozyme (Homo sapiens (Human))	BDBM41890 (2-(1-benzimidazolyl)-1-(3,4-dihydroxyphenyl)ethano...) Show SMILES Oc1ccc(cc1O)C(=O)Cn1cnc2ccccc12 Show InChI InChI=1S/C15H12N2O3/c18-13-6-5-10(7-14(13)19)15(20)8-17-9-16-11-3-1-2-4-12(11)17/h1-7,9,18-19H,8H2	KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PCBioAssay	n/a	n/a	1.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
Burnham Center for Chemical Genomics Curated by PubChem BioAssay					Assay Description Sanford-Burnham Center for Chemical Genomics (SBCCG) Sanford-Burnham Medical Research Institute (SBMRI, San Diego, CA) NIH Molecular Libraries Screen...				PubChem Bioassay (2010) BindingDB Entry DOI: 10.7270/Q2CR5RRG
					More data for this Ligand-Target Pair
Alkaline phosphatase placental-like (Homo sapiens (Human))	BDBM41890 (2-(1-benzimidazolyl)-1-(3,4-dihydroxyphenyl)ethano...) Show SMILES Oc1ccc(cc1O)C(=O)Cn1cnc2ccccc12 Show InChI InChI=1S/C15H12N2O3/c18-13-6-5-10(7-14(13)19)15(20)8-17-9-16-11-3-1-2-4-12(11)17/h1-7,9,18-19H,8H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PCBioAssay	n/a	n/a	1.53E+3	n/a	n/a	n/a	n/a	n/a	n/a
Burnham Center for Chemical Genomics Curated by PubChem BioAssay					Assay Description Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, C...				PubChem Bioassay (2009) BindingDB Entry DOI: 10.7270/Q29S1PG8
					More data for this Ligand-Target Pair
Alkaline phosphatase placental-like (Homo sapiens (Human))	BDBM41890 (2-(1-benzimidazolyl)-1-(3,4-dihydroxyphenyl)ethano...) Show SMILES Oc1ccc(cc1O)C(=O)Cn1cnc2ccccc12 Show InChI InChI=1S/C15H12N2O3/c18-13-6-5-10(7-14(13)19)15(20)8-17-9-16-11-3-1-2-4-12(11)17/h1-7,9,18-19H,8H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
Human BioMolecular Research Institute Curated by ChEMBL					Assay Description Inhibition of GCAP by analogous luminescence assay				Bioorg Med Chem 18: 573-9 (2010) Article DOI: 10.1016/j.bmc.2009.12.012 BindingDB Entry DOI: 10.7270/Q24T6JHR
					More data for this Ligand-Target Pair
Alkaline phosphatase, tissue-nonspecific isozyme (Homo sapiens (Human))	BDBM41890 (2-(1-benzimidazolyl)-1-(3,4-dihydroxyphenyl)ethano...) Show SMILES Oc1ccc(cc1O)C(=O)Cn1cnc2ccccc12 Show InChI InChI=1S/C15H12N2O3/c18-13-6-5-10(7-14(13)19)15(20)8-17-9-16-11-3-1-2-4-12(11)17/h1-7,9,18-19H,8H2	KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.80E+4	n/a	n/a	n/a	n/a	n/a	n/a
Human BioMolecular Research Institute Curated by ChEMBL					Assay Description Inhibition of TNAP by analogous luminescence assay				Bioorg Med Chem 18: 573-9 (2010) Article DOI: 10.1016/j.bmc.2009.12.012 BindingDB Entry DOI: 10.7270/Q24T6JHR
					More data for this Ligand-Target Pair
Intestinal alkaline phosphatase (Homo sapiens (Human))	BDBM41890 (2-(1-benzimidazolyl)-1-(3,4-dihydroxyphenyl)ethano...) Show SMILES Oc1ccc(cc1O)C(=O)Cn1cnc2ccccc12 Show InChI InChI=1S/C15H12N2O3/c18-13-6-5-10(7-14(13)19)15(20)8-17-9-16-11-3-1-2-4-12(11)17/h1-7,9,18-19H,8H2	PDB MMDB KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.48E+4	n/a	n/a	n/a	n/a	n/a	n/a
Human BioMolecular Research Institute Curated by ChEMBL					Assay Description Inhibition of IAP by analogous luminescence assay				Bioorg Med Chem 18: 573-9 (2010) Article DOI: 10.1016/j.bmc.2009.12.012 BindingDB Entry DOI: 10.7270/Q24T6JHR
					More data for this Ligand-Target Pair
Phospholipase A-2-activating protein (Homo sapiens (Human))	BDBM41890 (2-(1-benzimidazolyl)-1-(3,4-dihydroxyphenyl)ethano...) Show SMILES Oc1ccc(cc1O)C(=O)Cn1cnc2ccccc12 Show InChI InChI=1S/C15H12N2O3/c18-13-6-5-10(7-14(13)19)15(20)8-17-9-16-11-3-1-2-4-12(11)17/h1-7,9,18-19H,8H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	800	n/a	n/a	n/a	n/a	n/a	n/a
Human BioMolecular Research Institute Curated by ChEMBL					Assay Description Inhibition of PLAP by analogous luminescence assay				Bioorg Med Chem 18: 573-9 (2010) Article DOI: 10.1016/j.bmc.2009.12.012 BindingDB Entry DOI: 10.7270/Q24T6JHR
					More data for this Ligand-Target Pair