Reaction Details |
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Target | Prostaglandin E synthase |
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Ligand | BDBM50360826 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_796762 (CHEMBL1938077) |
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IC50 | 4116±n/a nM |
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Citation | Shiro, T; Takahashi, H; Kakiguchi, K; Inoue, Y; Masuda, K; Nagata, H; Tobe, M Synthesis and SAR study of imidazoquinolines as a novel structural class of microsomal prostaglandin E2 synthase-1 inhibitors. Bioorg Med Chem Lett22:285-8 (2011) [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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BDBM50360826 |
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n/a |
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Name | BDBM50360826 |
Synonyms: | CHEMBL1934804 |
Type | Small organic molecule |
Emp. Form. | C16H10BrN3O |
Mol. Mass. | 340.174 |
SMILES | Oc1ccccc1-c1nc2c(cnc3cc(Br)ccc23)[nH]1 |
Structure |
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