Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Histone deacetylase 9' and Ligand = 'BDBM272144'   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Histone deacetylase 9 (Homo sapiens (Human))	BDBM272144 (E1-(abs)-5-(3-fluoro-2-methylphenyl)-N-hydroxy-3- ...) Show SMILES Cc1c(F)cccc1[C@@]1(Cc2snc(c2C1)-c1ccccc1)C(=O)NO |r| Show InChI InChI=1S/C20H17FN2O2S/c1-12-15(8-5-9-16(12)21)20(19(24)22-25)10-14-17(11-20)26-23-18(14)13-6-3-2-4-7-13/h2-9,25H,10-11H2,1H3,(H,22,24)/t20-/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	79	n/a	n/a	n/a	n/a	n/a	n/a
CHDI Foundation, Inc. US Patent					Assay Description The potency of the compounds is quantified by measuring the Histone Deacetylase 9 (HDAC9) enzymatic activity using the fluorogenic substrate, Boc-Lys...				US Patent US10457675 (2019) BindingDB Entry DOI: 10.7270/Q22J6F7J
					More data for this Ligand-Target Pair
Histone deacetylase 9 (Homo sapiens (Human))	BDBM272144 (E1-(abs)-5-(3-fluoro-2-methylphenyl)-N-hydroxy-3- ...) Show SMILES Cc1c(F)cccc1[C@@]1(Cc2snc(c2C1)-c1ccccc1)C(=O)NO |r| Show InChI InChI=1S/C20H17FN2O2S/c1-12-15(8-5-9-16(12)21)20(19(24)22-25)10-14-17(11-20)26-23-18(14)13-6-3-2-4-7-13/h2-9,25H,10-11H2,1H3,(H,22,24)/t20-/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	79	n/a	n/a	n/a	n/a	n/a	n/a
CHDI Foundation, Inc. US Patent					Assay Description The potency of the compounds is quantified by measuring the Histone Deacetylase 9 (HDAC9) enzymatic activity using the fluorogenic substrate, Boc-Lys...				US Patent US10065948 (2018) BindingDB Entry DOI: 10.7270/Q2154K23
					More data for this Ligand-Target Pair