Reaction Details |
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Target | Prostaglandin E synthase |
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Ligand | BDBM50028864 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1439894 (CHEMBL3388594) |
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IC50 | 26±n/a nM |
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Citation | Banerjee, A; Pawar, MY; Patil, S; Yadav, PS; Kadam, PA; Kattige, VG; Deshpande, DS; Pednekar, PV; Pisat, MK; Gharat, LA Development of 2-aryl substituted quinazolin-4(3H)-one, pyrido[4,3-d]pyrimidin-4(3H)-one and pyrido[2,3-d]pyrimidin-4(3H)-one derivatives as microsomal prostaglandin E(2) synthase-1 inhibitors. Bioorg Med Chem Lett24:4838-44 (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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BDBM50028864 |
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n/a |
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Name | BDBM50028864 |
Synonyms: | CHEMBL3342705 |
Type | Small organic molecule |
Emp. Form. | C20H17ClF3N3O2 |
Mol. Mass. | 423.816 |
SMILES | CC(C)C(=O)NCc1ccc(Cl)c(c1)-c1nc2cc(ccc2c(=O)[nH]1)C(F)(F)F |
Structure |
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