null

SMILES: Oc1cc(OCc2ccc(Cl)nc2)cc2oc(cc(=O)c12)-c1ccc(OCc2ccc(Cl)nc2)cc1

InChI Key: InChIKey=BATUOPVUCCEVJZ-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50321610   

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
Telomerase reverse transcriptase (Homo sapiens (Human))	BDBM50321610 (7-((6-chloropyridin-3-yl)methoxy)-2-(4-((6-chlorop...) Show SMILES Oc1cc(OCc2ccc(Cl)nc2)cc2oc(cc(=O)c12)-c1ccc(OCc2ccc(Cl)nc2)cc1 Show InChI InChI=1S/C27H18Cl2N2O5/c28-25-7-1-16(12-30-25)14-34-19-5-3-18(4-6-19)23-11-22(33)27-21(32)9-20(10-24(27)36-23)35-15-17-2-8-26(29)31-13-17/h1-13,32H,14-15H2	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	800	n/a	n/a	n/a	n/a	n/a	n/a
Nanjing University Curated by ChEMBL					Assay Description Inhibition of human telomerase in human SGC7901 cells by TRAP assay				Bioorg Med Chem Lett 20: 4163-7 (2010) Article DOI: 10.1016/j.bmcl.2010.05.080 BindingDB Entry DOI: 10.7270/Q28G8MPC
					More data for this Ligand-Target Pair
DNA polymerase I, thermostable (Thermus aquaticus)	BDBM50321610 (7-((6-chloropyridin-3-yl)methoxy)-2-(4-((6-chlorop...) Show SMILES Oc1cc(OCc2ccc(Cl)nc2)cc2oc(cc(=O)c12)-c1ccc(OCc2ccc(Cl)nc2)cc1 Show InChI InChI=1S/C27H18Cl2N2O5/c28-25-7-1-16(12-30-25)14-34-19-5-3-18(4-6-19)23-11-22(33)27-21(32)9-20(10-24(27)36-23)35-15-17-2-8-26(29)31-13-17/h1-13,32H,14-15H2	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Nanjing University Curated by ChEMBL					Assay Description Inhibition of Thermus aquaticus taq polymerase				Bioorg Med Chem Lett 20: 4163-7 (2010) Article DOI: 10.1016/j.bmcl.2010.05.080 BindingDB Entry DOI: 10.7270/Q28G8MPC
					More data for this Ligand-Target Pair