Reaction Details |
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Target | Prostaglandin E synthase |
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Ligand | BDBM50443831 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1455679 (CHEMBL3366024) |
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IC50 | 700±n/a nM |
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Citation | Hanke, T; Lamers, C; Gomez, RC; Schneider, G; Werz, O; Schubert-Zsilavecz, M Identification of pirinixic acid derivatives bearing a 2-aminothiazole moiety combines dual PPARa/¿ activation and dual 5-LO/mPGES-1 inhibition. Bioorg Med Chem Lett24:3757-63 (2014) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Prostaglandin E synthase |
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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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BDBM50443831 |
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n/a |
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Name | BDBM50443831 |
Synonyms: | CHEMBL3091499 |
Type | Small organic molecule |
Emp. Form. | C22H25ClN4O2S2 |
Mol. Mass. | 477.043 |
SMILES | CCCCCCC(Sc1nc(Cl)cc(Nc2nc(cs2)-c2ccc(C)cc2)n1)C(O)=O |
Structure |
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