BDBM50426964 CHEMBL2325083

SMILES: Cc1cc2oc(nc2cc1Cl)N1CCC(CC1)C(=O)N[C@@H]1CC[C@H](CO)CC1

InChI Key: InChIKey=MUGVMTZRVAZLMI-FZNQNYSPSA-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 = 50426964   

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))	BDBM50426964 (CHEMBL2325083) Show SMILES Cc1cc2oc(nc2cc1Cl)N1CCC(CC1)C(=O)N[C@@H]1CC[C@H](CO)CC1 |r,wU:20.22,23.26,(25.8,-26.07,;27.13,-25.3,;28.47,-26.07,;29.8,-25.3,;31.27,-25.78,;32.19,-24.53,;31.27,-23.27,;29.8,-23.75,;28.46,-22.99,;27.13,-23.76,;25.8,-22.99,;33.72,-24.53,;34.48,-25.87,;36.01,-25.87,;36.79,-24.54,;36.02,-23.21,;34.48,-23.2,;38.33,-24.55,;39.1,-23.22,;39.09,-25.88,;40.63,-25.89,;41.4,-27.24,;42.93,-27.25,;43.71,-25.92,;45.25,-25.93,;46.01,-27.27,;42.95,-24.58,;41.41,-24.57,)| Show InChI InChI=1S/C21H28ClN3O3/c1-13-10-19-18(11-17(13)22)24-21(28-19)25-8-6-15(7-9-25)20(27)23-16-4-2-14(12-26)3-5-16/h10-11,14-16,26H,2-9,12H2,1H3,(H,23,27)/t14-,16+	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	39	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Inc. Curated by ChEMBL					Assay Description Inhibition of human mPGES1 by ELISA				Bioorg Med Chem Lett 23: 1120-6 (2013) Article DOI: 10.1016/j.bmcl.2012.11.107 BindingDB Entry DOI: 10.7270/Q26W9CDS
					More data for this Ligand-Target Pair
Prostaglandin E synthase (Homo sapiens (Human))	BDBM50426964 (CHEMBL2325083) Show SMILES Cc1cc2oc(nc2cc1Cl)N1CCC(CC1)C(=O)N[C@@H]1CC[C@H](CO)CC1 |r,wU:20.22,23.26,(25.8,-26.07,;27.13,-25.3,;28.47,-26.07,;29.8,-25.3,;31.27,-25.78,;32.19,-24.53,;31.27,-23.27,;29.8,-23.75,;28.46,-22.99,;27.13,-23.76,;25.8,-22.99,;33.72,-24.53,;34.48,-25.87,;36.01,-25.87,;36.79,-24.54,;36.02,-23.21,;34.48,-23.2,;38.33,-24.55,;39.1,-23.22,;39.09,-25.88,;40.63,-25.89,;41.4,-27.24,;42.93,-27.25,;43.71,-25.92,;45.25,-25.93,;46.01,-27.27,;42.95,-24.58,;41.41,-24.57,)| Show InChI InChI=1S/C21H28ClN3O3/c1-13-10-19-18(11-17(13)22)24-21(28-19)25-8-6-15(7-9-25)20(27)23-16-4-2-14(12-26)3-5-16/h10-11,14-16,26H,2-9,12H2,1H3,(H,23,27)/t14-,16+	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	600	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Inc. Curated by ChEMBL					Assay Description Inhibition of mPGES1 mediated PGE2 production in LPS-stimulated human whole blood by ELISA				Bioorg Med Chem Lett 23: 1120-6 (2013) Article DOI: 10.1016/j.bmcl.2012.11.107 BindingDB Entry DOI: 10.7270/Q26W9CDS
					More data for this Ligand-Target Pair