BDBM50416555 CHEMBL1215230

SMILES: OCc1cccc(c1)-c1ccc(s1)C(=O)NC(c1ccccc1)c1ccccc1

InChI Key: InChIKey=MFVURJXQWWTYIK-UHFFFAOYSA-N

Data: 1 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 1 hit for monomerid = 50416555   

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
Prostaglandin D Synthase (Homo sapiens (Human))	BDBM50416555 (CHEMBL1215230) Show SMILES OCc1cccc(c1)-c1ccc(s1)C(=O)NC(c1ccccc1)c1ccccc1 Show InChI InChI=1S/C25H21NO2S/c27-17-18-8-7-13-21(16-18)22-14-15-23(29-22)25(28)26-24(19-9-3-1-4-10-19)20-11-5-2-6-12-20/h1-16,24,27H,17H2,(H,26,28)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.38E+4	n/a	n/a	n/a	n/a	n/a	n/a
The University of Queensland Curated by ChEMBL					Assay Description Inhibition of human H-PGDS expressed in Escherichia coli BL21 DE2 by enzyme immuno assay at 50 uM				J Med Chem 53: 5536-48 (2010) Article DOI: 10.1021/jm100194a BindingDB Entry DOI: 10.7270/Q21J99Z4
					More data for this Ligand-Target Pair