Reaction Details |
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Target | Lactoylglutathione lyase |
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Ligand | BDBM50402209 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_885082 (CHEMBL2212266) |
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IC50 | >10000±n/a nM |
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Citation | Chiba, T; Ohwada, J; Sakamoto, H; Kobayashi, T; Fukami, TA; Irie, M; Miura, T; Ohara, K; Koyano, H Design and evaluation of azaindole-substituted N-hydroxypyridones as glyoxalase I inhibitors. Bioorg Med Chem Lett22:7486-9 (2012) [PubMed] Article |
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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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BDBM50402209 |
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n/a |
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Name | BDBM50402209 |
Synonyms: | CHEMBL2203973 |
Type | Small organic molecule |
Emp. Form. | C15H17NO2 |
Mol. Mass. | 243.301 |
SMILES | CCCCc1cc(-c2ccccc2)n(O)c(=O)c1 |
Structure |
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