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TargetProstaglandin E synthase
LigandBDBM50140688
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1548641 (CHEMBL3757641)
IC50 2100±n/a nM
Citation Di Micco, SSpatafora, CCardullo, NRiccio, RFischer, KPergola, CKoeberle, AWerz, OChalal, MVervandier-Fasseur, DTringali, CBifulco, G 2,3-Dihydrobenzofuran privileged structures as new bioinspired lead compounds for the design of mPGES-1 inhibitors. Bioorg Med Chem24:820-6 (2016) [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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  Blast E-value cutoff:
BDBM50140688
n/a
NameBDBM50140688
Synonyms:CHEMBL3754377
TypeSmall organic molecule
Emp. Form.C26H30O8
Mol. Mass.470.5116
SMILESCCCCOC(=O)\C=C\c1cc2[C@H]([C@@H](Oc2c(O)c1)c1ccc(O)c(O)c1)C(=O)OCCCC |r|
Structure
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