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SMILES: ONC(=O)CCCCCCN(c1nc2ccccc2o1)c1ccc(F)cn1

InChI Key: InChIKey=XZLSRIUXMLZDIG-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 310723   

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 deacetylase 6 (Homo sapiens (Human))	BDBM310723 (7-(Benzo[d]oxazol-2-yl(5-fluoropyridin-2-yl)amino)...) Show SMILES ONC(=O)CCCCCCN(c1nc2ccccc2o1)c1ccc(F)cn1 Show InChI InChI=1S/C19H21FN4O3/c20-14-10-11-17(21-13-14)24(12-6-2-1-3-9-18(25)23-26)19-22-15-7-4-5-8-16(15)27-19/h4-5,7-8,10-11,13,26H,1-3,6,9,12H2,(H,23,25)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	<500	n/a	n/a	n/a	n/a	n/a	n/a
Karus Therapeutics Limited US Patent					Assay Description The assay is described in WO2008/062201.				US Patent US10150763 (2018) BindingDB Entry DOI: 10.7270/Q2C82CC1
					More data for this Ligand-Target Pair
Histone deacetylase 1 (Homo sapiens (Human))	BDBM310723 (7-(Benzo[d]oxazol-2-yl(5-fluoropyridin-2-yl)amino)...) Show SMILES ONC(=O)CCCCCCN(c1nc2ccccc2o1)c1ccc(F)cn1 Show InChI InChI=1S/C19H21FN4O3/c20-14-10-11-17(21-13-14)24(12-6-2-1-3-9-18(25)23-26)19-22-15-7-4-5-8-16(15)27-19/h4-5,7-8,10-11,13,26H,1-3,6,9,12H2,(H,23,25)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Karus Therapeutics Limited US Patent					Assay Description The assay is described in WO2008/062201.				US Patent US10150763 (2018) BindingDB Entry DOI: 10.7270/Q2C82CC1
					More data for this Ligand-Target Pair