BDBM50184327 CHEMBL205303::phosphoric acid mono-[(2R,3R,4R,5S,6S)-5-hydroxy-2-hydroxymethyl-4-phosphonooxy-6-(3-phosphonooxy-propyl)-tetrahydro-pyran-3-yl] ester

SMILES: OC[C@H]1O[C@@H](CCCOP(O)(O)=O)[C@H](O)[C@@H](OP(O)(O)=O)[C@@H]1OP(O)(O)=O

InChI Key: InChIKey=IWTHYJFNJFRJKQ-KVEIKIFDSA-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 = 50184327   

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
Inositol 1,4,5-trisphosphate receptor type 1 (Rattus norvegicus)	BDBM50184327 (CHEMBL205303 | phosphoric acid mono-[(2R,3R,4R,5S,...) Show SMILES OC[C@H]1O[C@@H](CCCOP(O)(O)=O)[C@H](O)[C@@H](OP(O)(O)=O)[C@@H]1OP(O)(O)=O Show InChI InChI=1S/C9H21O15P3/c10-4-6-8(23-26(15,16)17)9(24-27(18,19)20)7(11)5(22-6)2-1-3-21-25(12,13)14/h5-11H,1-4H2,(H2,12,13,14)(H2,15,16,17)(H2,18,19,20)/t5-,6+,7-,8+,9+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	4.43E+3	n/a	n/a	n/a	n/a
Hokkaido University Curated by ChEMBL					Assay Description Agonistic potency at rat IP3 type 1 receptor expressed in chicken DT40 cells				J Med Chem 49: 1900-9 (2006) Article DOI: 10.1021/jm051039n BindingDB Entry DOI: 10.7270/Q2MK6CG5
					More data for this Ligand-Target Pair