Reaction Details |
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Target | Prostaglandin E synthase |
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Ligand | BDBM50270615 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1510157 (CHEMBL3606528) |
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IC50 | 1300±n/a nM |
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Citation | Noha, SM; Fischer, K; Koeberle, A; Garscha, U; Werz, O; Schuster, D Discovery of novel, non-acidic mPGES-1 inhibitors by virtual screening with a multistep protocol. Bioorg Med Chem23:4839-45 (2015) [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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BDBM50270615 |
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n/a |
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Name | BDBM50270615 |
Synonyms: | CHEMBL521286 | N-(4-chloro-3-(5-methylbenzo[d]oxazol-2-yl)phenyl)-2-(trifluoromethyl)benzamide |
Type | Small organic molecule |
Emp. Form. | C22H14ClF3N2O2 |
Mol. Mass. | 430.807 |
SMILES | Cc1ccc2oc(nc2c1)-c1cc(NC(=O)c2ccccc2C(F)(F)F)ccc1Cl |
Structure |
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