Reaction Details |
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Target | Lactoylglutathione lyase |
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Ligand | BDBM50016893 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1355172 (CHEMBL3280975) |
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Ki | 34700000±n/a nM |
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Citation | Hall, SS; Doweyko, LM; Doweyko, AM; Zilenovski, JS Synthesis and evaluation of alpha-hydroxythiol esters as antitumor agents and glyoxalase I inhibitors. J Med Chem20:1239-42 (1977) [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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BDBM50016893 |
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n/a |
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Name | BDBM50016893 |
Synonyms: | CHEMBL3277445 |
Type | Small organic molecule |
Emp. Form. | C14H18O4S |
Mol. Mass. | 282.355 |
SMILES | CCCCOC(=O)CSC(=O)C(O)c1ccccc1 |
Structure |
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