| Reaction Details |
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 | Report a problem with these data |
| Target | Glyoxalase I |
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| Ligand | BDBM50213420 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | ChEMBL_456126 (CHEMBL888135) |
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| Ki | 66880±n/a nM |
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| Citation |  More, SS; Vince, R Design, synthesis, and binding studies of bidentate Zn-chelating peptidic inhibitors of glyoxalase-I. Bioorg Med Chem Lett17:3793-7 (2007) [PubMed] Article |
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| More Info.: | Get all data from this article, Assay Method |
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| Glyoxalase I |
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| Name: | Glyoxalase I |
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| Synonyms: | GLO1 | LGUL_YEAST | Lactoylglutathione lyase |
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| Type: | PROTEIN |
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| Mol. Mass.: | 37210.98 |
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| Organism: | Saccharomyces cerevisiae |
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| Description: | ChEMBL_571116 |
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| Residue: | 326 |
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| Sequence: | MSTDSTRYPIQIEKASNDPTLLLNHTCLRVKDPARTVKFYTEHFGMKLLSRKDFEEAKFS
LYFLSFPKDDIPKNKNGEPDVFSAHGVLELTHNWGTEKNPDYKINNGNEEPHRGFGHICF
SVSDINKTCEELESQGVKFKKRLSEGRQKDIAFALGPDGYWIELITYSREGQEYPKGSVG
NKFNHTMIRIKNPTRSLEFYQNVLGMKLLRTSEHESAKFTLYFLGYGVPKTDSVFSCESV
LELTHNWGTENDPNFHYHNGNSEPQGYGHICISCDDAGALCKEIEVKYGDKIQWSPKFNQ
GRMKNIAFLKDPDGYSIEVVPHGLIA
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| BDBM50213420 |
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| n/a |
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| Name | BDBM50213420 |
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| Synonyms: | (S)-5-((S)-7-(4-bromobenzyloxy)-1-(carboxymethylamino)-1,5,7-trioxoheptan-2-ylamino)-2-amino-5-oxopentanoic acid | CHEMBL246554 |
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| Type | Small organic molecule |
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| Emp. Form. | C21H26BrN3O9 |
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| Mol. Mass. | 544.35 |
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| SMILES | N[C@@H](CCC(=O)N[C@@H](CCC(=O)CC(=O)OCc1ccc(Br)cc1)C(=O)NCC(O)=O)C(O)=O |
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| Structure | 
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