BDBM50337645 1-benzyl-1-(3-((4-chlorophenyl)ethynyl)benzyl)-3-isopropylurea::CHEMBL1683202

SMILES: CC(C)NC(=O)N(Cc1ccccc1)Cc1cccc(c1)C#Cc1ccc(Cl)cc1

InChI Key: InChIKey=VHDDVMOBBOZRTR-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 = 50337645   

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 E synthase (Homo sapiens (Human))	BDBM50337645 (1-benzyl-1-(3-((4-chlorophenyl)ethynyl)benzyl)-3-i...) Show SMILES CC(C)NC(=O)N(Cc1ccccc1)Cc1cccc(c1)C#Cc1ccc(Cl)cc1 Show InChI InChI=1S/C26H25ClN2O/c1-20(2)28-26(30)29(18-23-7-4-3-5-8-23)19-24-10-6-9-22(17-24)12-11-21-13-15-25(27)16-14-21/h3-10,13-17,20H,18-19H2,1-2H3,(H,28,30)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	22	n/a	n/a	n/a	n/a	n/a	n/a
Merck Frosst Center for Therapeutic Research Curated by ChEMBL					Assay Description Inhibition of mPGES1				Bioorg Med Chem Lett 21: 1488-92 (2011) Article DOI: 10.1016/j.bmcl.2011.01.006 BindingDB Entry DOI: 10.7270/Q2XS5VNP
					More data for this Ligand-Target Pair
Prostaglandin E synthase (Homo sapiens (Human))	BDBM50337645 (1-benzyl-1-(3-((4-chlorophenyl)ethynyl)benzyl)-3-i...) Show SMILES CC(C)NC(=O)N(Cc1ccccc1)Cc1cccc(c1)C#Cc1ccc(Cl)cc1 Show InChI InChI=1S/C26H25ClN2O/c1-20(2)28-26(30)29(18-23-7-4-3-5-8-23)19-24-10-6-9-22(17-24)12-11-21-13-15-25(27)16-14-21/h3-10,13-17,20H,18-19H2,1-2H3,(H,28,30)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Merck Frosst Center for Therapeutic Research Curated by ChEMBL					Assay Description Inhibition of mPGES1 in IL-1beta treated human A549 cell microsome assessed as inhibition of PGE2 production after 1 min in presence of 50% FBS				Bioorg Med Chem Lett 21: 1488-92 (2011) Article DOI: 10.1016/j.bmcl.2011.01.006 BindingDB Entry DOI: 10.7270/Q2XS5VNP
					More data for this Ligand-Target Pair