BDBM50413398 CHEMBL500550

SMILES: COc1cc(C(C)C)c(Oc2cnc(N)nc2N)cc1C(O)=O

InChI Key: InChIKey=UMZMQINYOLOMAX-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 = 50413398   

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 3 (RAT)	BDBM50413398 (CHEMBL500550) Show SMILES COc1cc(C(C)C)c(Oc2cnc(N)nc2N)cc1C(O)=O Show InChI InChI=1S/C15H18N4O4/c1-7(2)8-4-10(22-3)9(14(20)21)5-11(8)23-12-6-18-15(17)19-13(12)16/h4-7H,1-3H3,(H,20,21)(H4,16,17,18,19)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	158	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
P2X purinoceptor 2 (Homo sapiens (Human))	BDBM50413398 (CHEMBL500550) Show SMILES COc1cc(C(C)C)c(Oc2cnc(N)nc2N)cc1C(O)=O Show InChI InChI=1S/C15H18N4O4/c1-7(2)8-4-10(22-3)9(14(20)21)5-11(8)23-12-6-18-15(17)19-13(12)16/h4-7H,1-3H3,(H,20,21)(H4,16,17,18,19)	UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	316	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