BDBM50421166 CHEMBL2086766

SMILES: B[P@](=O)(OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cc(OC)c(=O)[nH]c1=O)OP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cc(OC)c(=O)[nH]c1=O

InChI Key: InChIKey=GJNNGZJKVSNGHN-IAFXRAFASA-N

Data: 1 EC50

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 1 hit for monomerid = 50421166   

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
P2Y purinoceptor 6 (Homo sapiens (Human))	BDBM50421166 (CHEMBL2086766) Show SMILES B[P@](=O)(OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cc(OC)c(=O)[nH]c1=O)OP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cc(OC)c(=O)[nH]c1=O |r| Show InChI InChI=1S/C20H30BN4O21P3/c1-39-7-3-24(19(32)22-15(7)30)17-13(28)11(26)9(43-17)5-41-47(21,34)45-49(37,38)46-48(35,36)42-6-10-12(27)14(29)18(44-10)25-4-8(40-2)16(31)23-20(25)33/h3-4,9-14,17-18,26-29H,5-6,21H2,1-2H3,(H,35,36)(H,37,38)(H,22,30,32)(H,23,31,33)/t9-,10-,11-,12-,13-,14-,17-,18-,47+/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	2.20E+3	n/a	n/a	n/a	n/a
Bar-Ilan University Curated by ChEMBL					Assay Description Agonist activity at human GFP-tagged P2Y6 receptor expressed in human 1321N1 cells assessed as intracellular calcium mobilization by fura2/AM-based f...				Bioorg Med Chem 20: 5483-95 (2012) Article DOI: 10.1016/j.bmc.2012.07.042 BindingDB Entry DOI: 10.7270/Q21837S1
					More data for this Ligand-Target Pair