Reaction Details |
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Target | Lactoylglutathione lyase |
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Ligand | BDBM50039110 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_71288 (CHEMBL684992) |
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Ki | 1700±n/a nM |
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Citation | Murthy, NS; Bakeris, T; Kavarana, MJ; Hamilton, DS; Lan, Y; Creighton, DJ S-(N-aryl-N-hydroxycarbamoyl)glutathione derivatives are tight-binding inhibitors of glyoxalase I and slow substrates for glyoxalase II. J Med Chem37:2161-6 (1994) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Lactoylglutathione lyase |
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Name: | Lactoylglutathione lyase |
Synonyms: | Aldoketomutase | GLO1 | Glx I | Glyoxalase 1 (GLO1) | Glyoxalase I | Ketone-aldehyde mutase | LGUL_HUMAN | Methylglyoxalase | S-D-lactoylglutathione methylglyoxal lyase |
Type: | Enzyme |
Mol. Mass.: | 20772.95 |
Organism: | Homo sapiens (Human) |
Description: | Q04760 |
Residue: | 184 |
Sequence: | MAEPQPPSGGLTDEAALSCCSDADPSTKDFLLQQTMLRVKDPKKSLDFYTRVLGMTLIQK
CDFPIMKFSLYFLAYEDKNDIPKEKDEKIAWALSRKATLELTHNWGTEDDETQSYHNGNS
DPRGFGHIGIAVPDVYSACKRFEELGVKFVKKPDDGKMKGLAFIQDPDGYWIEILNPNKM
ATLM
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BDBM50039110 |
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n/a |
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Name | BDBM50039110 |
Synonyms: | S-(N-Methyl-N-hydroxycarbomyl)ethylglutathione |
Type | Small organic molecule |
Emp. Form. | C7H11N2O6S |
Mol. Mass. | 251.238 |
SMILES | CN(O)C(=O)SCC(C([NH3+])C([O-])=O)C([O-])=O |
Structure |
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