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TargetProstaglandin E synthase
LigandBDBM50443827
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1277572 (CHEMBL3096448)
IC50 600±n/a nM
Citation Hanke, TDehm, FLiening, SPopella, SDMaczewsky, JPillong, MKunze, JWeinigel, CBarz, DKaiser, AWurglics, MLämmerhofer, MSchneider, GSautebin, LSchubert-Zsilavecz, MWerz, O Aminothiazole-featured pirinixic acid derivatives as dual 5-lipoxygenase and microsomal prostaglandin E2 synthase-1 inhibitors with improved potency and efficiency in vivo. J Med Chem56:9031-44 (2013) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Prostaglandin E synthase
Name:Prostaglandin E synthase
Synonyms:MGST1L1 | MPGES1 | PGES | PIG12 | PTGES | PTGES_HUMAN | Prostaglandin E synthase (PGES-1) | Prostaglandin E synthase 1 (mPGES-1) | Prostaglandin E synthase-1 (PGES-1) | Prostaglandin E synthase/G/H synthase 2 | Prostaglandin E2 synthase-1 ( mPGES-1)
Type:Protein
Mol. Mass.:17112.22
Organism:Homo sapiens (Human)
Description:n/a
Residue:152
Sequence:
MPAHSLVMSSPALPAFLLCSTLLVIKMYVVAIITGQVRLRKKAFANPEDALRHGGPQYCR
SDPDVERCLRAHRNDMETIYPFLFLGFVYSFLGPNPFVAWMHFLVFLVGRVAHTVAYLGK
LRAPIRSVTYTLAQLPCASMALQILWEAARHL
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BDBM50443827
n/a
NameBDBM50443827
Synonyms:CHEMBL3094413
TypeSmall organic molecule
Emp. Form.C25H25ClN4O2S2
Mol. Mass.513.075
SMILESCCCCCC[C@@H](Sc1nc(Cl)cc(Nc2nc(cs2)-c2ccc3ccccc3c2)n1)C(O)=O |r|
Structure
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