BDBM50413392 CHEMBL524043

SMILES: CCCc1cc(OC)c(OC)cc1Cc1cnc(N)nc1N

InChI Key: InChIKey=RSAYXWLOHLCKLF-UHFFFAOYSA-N

Data: 2 IC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50413392   

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
P2X purinoceptor 2 (Homo sapiens (Human))	BDBM50413392 (CHEMBL524043) Show SMILES CCCc1cc(OC)c(OC)cc1Cc1cnc(N)nc1N Show InChI InChI=1S/C16H22N4O2/c1-4-5-10-7-13(21-2)14(22-3)8-11(10)6-12-9-19-16(18)20-15(12)17/h7-9H,4-6H2,1-3H3,(H4,17,18,19,20)	UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	<1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Roche Palo Alto LLC Curated by ChEMBL					Assay Description Inhibition of P2X2 receptor				Bioorg Med Chem Lett 19: 1628-31 (2009) Article DOI: 10.1016/j.bmcl.2009.02.003 BindingDB Entry DOI: 10.7270/Q29023NX
					More data for this Ligand-Target Pair
P2X purinoceptor 3 (RAT)	BDBM50413392 (CHEMBL524043) Show SMILES CCCc1cc(OC)c(OC)cc1Cc1cnc(N)nc1N Show InChI InChI=1S/C16H22N4O2/c1-4-5-10-7-13(21-2)14(22-3)8-11(10)6-12-9-19-16(18)20-15(12)17/h7-9H,4-6H2,1-3H3,(H4,17,18,19,20)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	<1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Roche Palo Alto LLC Curated by ChEMBL					Assay Description Antagonist activity at rat recombinant P2X3 receptor expressed in CHO cells by FLIPR assay				Bioorg Med Chem Lett 19: 1628-31 (2009) Article DOI: 10.1016/j.bmcl.2009.02.003 BindingDB Entry DOI: 10.7270/Q29023NX
					More data for this Ligand-Target Pair