null

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

InChI Key: InChIKey=UCJMDMYGVGENKA-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50395945   

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))	BDBM50395945 (CHEMBL2164565) Show SMILES CCN(CCO)C(=O)c1cc2cccnn2c1-c1cccc(c1)C(F)(F)F Show InChI InChI=1S/C19H18F3N3O2/c1-2-24(9-10-26)18(27)16-12-15-7-4-8-23-25(15)17(16)13-5-3-6-14(11-13)19(20,21)22/h3-8,11-12,26H,2,9-10H2,1H3	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	100	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))	BDBM50395945 (CHEMBL2164565) Show SMILES CCN(CCO)C(=O)c1cc2cccnn2c1-c1cccc(c1)C(F)(F)F Show InChI InChI=1S/C19H18F3N3O2/c1-2-24(9-10-26)18(27)16-12-15-7-4-8-23-25(15)17(16)13-5-3-6-14(11-13)19(20,21)22/h3-8,11-12,26H,2,9-10H2,1H3	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	2.34E+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