Reaction Details |
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Target | Glyoxalase I |
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Ligand | BDBM50092826 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_424952 (CHEMBL911358) |
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Ki | 1200±n/a nM |
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Citation | More, SS; Vince, R A metabolically stable tight-binding transition-state inhibitor of glyoxalase-I. Bioorg Med Chem Lett16:6039-42 (2006) [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 |
Synonyms: | GLO1 | LGUL_YEAST | Lactoylglutathione lyase |
Type: | PROTEIN |
Mol. Mass.: | 37210.98 |
Organism: | Saccharomyces cerevisiae |
Description: | ChEMBL_571116 |
Residue: | 326 |
Sequence: | MSTDSTRYPIQIEKASNDPTLLLNHTCLRVKDPARTVKFYTEHFGMKLLSRKDFEEAKFS
LYFLSFPKDDIPKNKNGEPDVFSAHGVLELTHNWGTEKNPDYKINNGNEEPHRGFGHICF
SVSDINKTCEELESQGVKFKKRLSEGRQKDIAFALGPDGYWIELITYSREGQEYPKGSVG
NKFNHTMIRIKNPTRSLEFYQNVLGMKLLRTSEHESAKFTLYFLGYGVPKTDSVFSCESV
LELTHNWGTENDPNFHYHNGNSEPQGYGHICISCDDAGALCKEIEVKYGDKIQWSPKFNQ
GRMKNIAFLKDPDGYSIEVVPHGLIA
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BDBM50092826 |
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n/a |
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Name | BDBM50092826 |
Synonyms: | (2S)-2-amino-5-{[(1R)-1-[({[(4-bromophenyl)(hydroxy)amino]carbonyl}thio)methyl]-2-(carboxyamino)-2-oxoethyl]amino}-5-oxopentanoic acid | (S)-2-amino-5-((R)-3-((4-bromophenyl)hydroxycarbamoylthio)-1-(carboxymethylamino)-1-oxopropan-2-ylamino)-5-oxopentanoic acid | CHEMBL128872 | S-(N-4bromophenyl-N-hydroxycarbamoyl)glutathione |
Type | Small organic molecule |
Emp. Form. | C17H21BrN4O8S |
Mol. Mass. | 521.34 |
SMILES | N[C@@H](CCC(=O)N[C@@H](CSC(=O)N(O)c1ccc(Br)cc1)C(=O)NCC(O)=O)C(O)=O |
Structure |
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