Reaction Details |
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Target | Prostaglandin E synthase |
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Ligand | BDBM50386162 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_824647 (CHEMBL2045705) |
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IC50 | >10000±n/a nM |
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Citation | Chini, MG; De Simone, R; Bruno, I; Riccio, R; Dehm, F; Weinigel, C; Barz, D; Werz, O; Bifulco, G Design and synthesis of a second series of triazole-based compounds as potent dual mPGES-1 and 5-lipoxygenase inhibitors. Eur J Med Chem54:311-23 (2012) [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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BDBM50386162 |
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n/a |
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Name | BDBM50386162 |
Synonyms: | CHEMBL2042363 |
Type | Small organic molecule |
Emp. Form. | C22H16N4O5 |
Mol. Mass. | 416.3862 |
SMILES | OC(=O)c1ccc(Cn2cc(nn2)-c2ccc(cc2)-c2ccc(O)cc2)c(c1)[N+]([O-])=O |
Structure |
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