BDBM50416550 CHEMBL1215372

SMILES: CC(C)C(NC(=O)c1ccc(cc1)-c1cccc(O)c1)C(N)=O

InChI Key: InChIKey=LIHXFKSRELDIPD-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 = 50416550   

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))	BDBM50416550 (CHEMBL1215372) Show SMILES CC(C)C(NC(=O)c1ccc(cc1)-c1cccc(O)c1)C(N)=O Show InChI InChI=1S/C18H20N2O3/c1-11(2)16(17(19)22)20-18(23)13-8-6-12(7-9-13)14-4-3-5-15(21)10-14/h3-11,16,21H,1-2H3,(H2,19,22)(H,20,23)	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	5.33E+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