BDBM50076299 CHEMBL3416323

SMILES: [O-][N+](=O)c1ccc(Sc2cccc(Cl)c2)c2nonc12

InChI Key: InChIKey=RWTVQJMHWQOGAT-UHFFFAOYSA-N

Data: 3 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 3 hits for monomerid = 50076299   

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
Histone acetyltransferase GCN5 (Saccharomyces cerevisiae S288c)	BDBM50076299 (CHEMBL3416323) Show SMILES [O-][N+](=O)c1ccc(Sc2cccc(Cl)c2)c2nonc12 Show InChI InChI=1S/C12H6ClN3O3S/c13-7-2-1-3-8(6-7)20-10-5-4-9(16(17)18)11-12(10)15-19-14-11/h1-6H	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MMDB PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Mayo Clinic College of Medicine Curated by ChEMBL					Assay Description Inhibition of Vps75-stimulated recombinant Saccharomyces cerevisiae histone acetyltransferase Rtt109 using Asf1-dH3-H4 as substrate assessed as coenz...				J Med Chem 58: 2091-113 (2015) Article DOI: 10.1021/jm5019093 BindingDB Entry DOI: 10.7270/Q26M38J9
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase (Homo sapiens (Human))	BDBM50076299 (CHEMBL3416323) Show SMILES [O-][N+](=O)c1ccc(Sc2cccc(Cl)c2)c2nonc12 Show InChI InChI=1S/C12H6ClN3O3S/c13-7-2-1-3-8(6-7)20-10-5-4-9(16(17)18)11-12(10)15-19-14-11/h1-6H	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MMDB PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Auckland Curated by ChEMBL					Assay Description Inhibition of recombinant human IDO1 expressed in bacterial expression system using L-Tryptophan as substrate after 25 mins in absence of GSH and pre...				Eur J Med Chem 126: 983-996 (2017) Article DOI: 10.1016/j.ejmech.2016.12.029 BindingDB Entry DOI: 10.7270/Q2RX9F9K
					More data for this Ligand-Target Pair
Histone acetyltransferase GCN5 (Saccharomyces cerevisiae S288c)	BDBM50076299 (CHEMBL3416323) Show SMILES [O-][N+](=O)c1ccc(Sc2cccc(Cl)c2)c2nonc12 Show InChI InChI=1S/C12H6ClN3O3S/c13-7-2-1-3-8(6-7)20-10-5-4-9(16(17)18)11-12(10)15-19-14-11/h1-6H	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MMDB PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	6.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
Mayo Clinic College of Medicine Curated by ChEMBL					Assay Description Inhibition of Vps75-stimulated recombinant Saccharomyces cerevisiae histone acetyltransferase Rtt109 using Asf1-dH3-H4 as substrate assessed as coenz...				J Med Chem 58: 2091-113 (2015) Article DOI: 10.1021/jm5019093 BindingDB Entry DOI: 10.7270/Q26M38J9
					More data for this Ligand-Target Pair