null

SMILES: Clc1cc(Cl)cc(COC(=O)NC2CC3(C2)CN(C3)S(=O)(=O)c2ccc3[nH]c(=O)oc3c2)c1

InChI Key: InChIKey=VAWHLBLARXWUKL-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 258515   

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
Ataxin-2 (Homo sapiens (Human))	BDBM258515 (US10633384, Example 3.5 | US9493486, 3.5) Show SMILES Clc1cc(Cl)cc(COC(=O)NC2CC3(C2)CN(C3)S(=O)(=O)c2ccc3[nH]c(=O)oc3c2)c1 Show InChI InChI=1S/C21H19Cl2N3O6S/c22-13-3-12(4-14(23)5-13)9-31-19(27)24-15-7-21(8-15)10-26(11-21)33(29,30)16-1-2-17-18(6-16)32-20(28)25-17/h1-6,15H,7-11H2,(H,24,27)(H,25,28)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	20	n/a	n/a	n/a	n/a	n/a	n/a
Hoffmann-La Roche Inc. US Patent					Assay Description ATX inhibition was measured by a fluorescence quenching assay using a specifically labeled substrate analogue (MR121 substrate). To obtain this MR121...				US Patent US10633384 (2020)
					More data for this Ligand-Target Pair
Ectonucleotide pyrophosphatase/phosphodiesterase family member 2 (Homo sapiens (Human))	BDBM258515 (US10633384, Example 3.5 | US9493486, 3.5) Show SMILES Clc1cc(Cl)cc(COC(=O)NC2CC3(C2)CN(C3)S(=O)(=O)c2ccc3[nH]c(=O)oc3c2)c1 Show InChI InChI=1S/C21H19Cl2N3O6S/c22-13-3-12(4-14(23)5-13)9-31-19(27)24-15-7-21(8-15)10-26(11-21)33(29,30)16-1-2-17-18(6-16)32-20(28)25-17/h1-6,15H,7-11H2,(H,24,27)(H,25,28)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	20	n/a	n/a	n/a	n/a	8.0	30
Hoffmann-La Roches Inc. US Patent					Assay Description ATX inhibition was measured by a fluorescence quenching assay using a specifically labeled substrate analogue (MR121 substrate). To obtain this MR121...				US Patent US9493486 (2016) BindingDB Entry DOI: 10.7270/Q2VT1R1K
					More data for this Ligand-Target Pair