BDBM50425327 CHEMBL2315866

SMILES: Clc1ccc2oc(nc2c1)N1CCC(CC1)C(=O)NC1CCCC1c1ccccc1

InChI Key: InChIKey=VDADWYKVUHMQAE-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 = 50425327   

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))	BDBM50425327 (CHEMBL2315866) Show SMILES Clc1ccc2oc(nc2c1)N1CCC(CC1)C(=O)NC1CCCC1c1ccccc1 Show InChI InChI=1S/C24H26ClN3O2/c25-18-9-10-22-21(15-18)27-24(30-22)28-13-11-17(12-14-28)23(29)26-20-8-4-7-19(20)16-5-2-1-3-6-16/h1-3,5-6,9-10,15,17,19-20H,4,7-8,11-14H2,(H,26,29)	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	291	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Inc. Curated by ChEMBL					Assay Description Inhibition of human recombinant mPGES-1 using PGH2 as substrate incubated 20 mins prior to substrate addition measured after 30 secs by EIA				Bioorg Med Chem Lett 23: 907-11 (2013) Article DOI: 10.1016/j.bmcl.2012.10.040 BindingDB Entry DOI: 10.7270/Q2Z3210H
					More data for this Ligand-Target Pair