Reaction Details |
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Target | Prostaglandin E synthase |
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Ligand | BDBM50060279 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_794980 (CHEMBL1936307) |
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IC50 | 800±n/a nM |
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Citation | Wiegard, A; Hanekamp, W; Griessbach, K; Fabian, J; Lehr, M Pyrrole alkanoic acid derivatives as nuisance inhibitors of microsomal prostaglandin E2 synthase-1. Eur J Med Chem48:153-63 (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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BDBM50060279 |
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n/a |
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Name | BDBM50060279 |
Synonyms: | 3-(4-Dodecanoyl-1,3,5-trimethyl-1H-pyrrol-2-yl)-propionic acid | CHEMBL442012 |
Type | Small organic molecule |
Emp. Form. | C22H37NO3 |
Mol. Mass. | 363.5341 |
SMILES | CCCCCCCCCCCC(=O)c1c(C)c(CCC(O)=O)n(C)c1C |
Structure |
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