null

SMILES: Cn1ccc(n1)N(CCCCCCC(=O)NO)c1ccc(F)cn1

InChI Key: InChIKey=DTSWVZIEMROXHQ-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 310721   

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))	BDBM310721 (7-((5-Fluoropyridin-2-yl)(1-methyl-1H-pyrazol-3-yl...) Show SMILES Cn1ccc(n1)N(CCCCCCC(=O)NO)c1ccc(F)cn1 Show InChI InChI=1S/C16H22FN5O2/c1-21-11-9-15(19-21)22(14-8-7-13(17)12-18-14)10-5-3-2-4-6-16(23)20-24/h7-9,11-12,24H,2-6,10H2,1H3,(H,20,23)	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))	BDBM310721 (7-((5-Fluoropyridin-2-yl)(1-methyl-1H-pyrazol-3-yl...) Show SMILES Cn1ccc(n1)N(CCCCCCC(=O)NO)c1ccc(F)cn1 Show InChI InChI=1S/C16H22FN5O2/c1-21-11-9-15(19-21)22(14-8-7-13(17)12-18-14)10-5-3-2-4-6-16(23)20-24/h7-9,11-12,24H,2-6,10H2,1H3,(H,20,23)	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