Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Histone deacetylase 9' and Ligand = 'BDBM272091'   

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))	BDBM272091 ((S)-5-(3-Fluoro-2-methylphenyl)-N-hydroxy-2-(3- me...) Show SMILES Cc1cnccc1-n1cc2C[C@@](Cc2n1)(C(=O)NO)c1cccc(F)c1C |r| Show InChI InChI=1S/C20H19FN4O2/c1-12-10-22-7-6-18(12)25-11-14-8-20(19(26)24-27,9-17(14)23-25)15-4-3-5-16(21)13(15)2/h3-7,10-11,27H,8-9H2,1-2H3,(H,24,26)/t20-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	53	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))	BDBM272091 ((S)-5-(3-Fluoro-2-methylphenyl)-N-hydroxy-2-(3- me...) Show SMILES Cc1cnccc1-n1cc2C[C@@](Cc2n1)(C(=O)NO)c1cccc(F)c1C |r| Show InChI InChI=1S/C20H19FN4O2/c1-12-10-22-7-6-18(12)25-11-14-8-20(19(26)24-27,9-17(14)23-25)15-4-3-5-16(21)13(15)2/h3-7,10-11,27H,8-9H2,1-2H3,(H,24,26)/t20-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	53	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