null

SMILES: CCN(CCO)C(=O)c1cc2cccnn2c1-c1cccc(C)c1

InChI Key: InChIKey=UZTROBSZBAPWOG-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50395944   

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
Transient receptor potential cation channel subfamily V member 1 (Homo sapiens (Human))	BDBM50395944 (CHEMBL2164571) Show SMILES CCN(CCO)C(=O)c1cc2cccnn2c1-c1cccc(C)c1 Show InChI InChI=1S/C19H21N3O2/c1-3-21(10-11-23)19(24)17-13-16-8-5-9-20-22(16)18(17)15-7-4-6-14(2)12-15/h4-9,12-13,23H,3,10-11H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	251	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Antagonist activity at human TRPV1 expressed in CHO cells by IonWorks assay				Bioorg Med Chem Lett 22: 6888-95 (2012) Article DOI: 10.1016/j.bmcl.2012.09.059 BindingDB Entry DOI: 10.7270/Q26W9C63
					More data for this Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2 (Homo sapiens (Human))	BDBM50395944 (CHEMBL2164571) Show SMILES CCN(CCO)C(=O)c1cc2cccnn2c1-c1cccc(C)c1 Show InChI InChI=1S/C19H21N3O2/c1-3-21(10-11-23)19(24)17-13-16-8-5-9-20-22(16)18(17)15-7-4-6-14(2)12-15/h4-9,12-13,23H,3,10-11H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>3.16E+4	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of human ERG expressed in CHO cells by IonWorks assay				Bioorg Med Chem Lett 22: 6888-95 (2012) Article DOI: 10.1016/j.bmcl.2012.09.059 BindingDB Entry DOI: 10.7270/Q26W9C63
					More data for this Ligand-Target Pair