Reaction Details |
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Target | Lactoylglutathione lyase |
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Ligand | BDBM50069026 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_71304 (CHEMBL686107) |
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IC50 | 140500±n/a nM |
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Citation | Ly, HD; Clugston, SL; Sampson, PB; Honek, JF Syntheses and kinetic evaluation of hydroxamate-based peptide inhibitors of glyoxalase I. Bioorg Med Chem Lett8:705-10 (1999) [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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BDBM50069026 |
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n/a |
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Name | BDBM50069026 |
Synonyms: | 2-Amino-4-[1-(ethoxycarbonylmethyl-carbamoyl)-3-(hydroxy-methyl-carbamoyl)-propylcarbamoyl]-butyric acid anion | CHEMBL164262 |
Type | Small organic molecule |
Emp. Form. | C15H26N4O8 |
Mol. Mass. | 390.3889 |
SMILES | CCOC(=O)CNC(=O)C(CCC(=O)N(C)O)NC(=O)CCC([NH3+])C([O-])=O |
Structure |
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