Reaction Details |
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Target | Lactoylglutathione lyase |
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Ligand | BDBM50336267 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_716548 (CHEMBL1670272) |
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Ki | 65000±n/a nM |
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Citation | Yuan, M; Luo, M; Song, Y; Xu, Q; Wang, X; Cao, Y; Bu, X; Ren, Y; Hu, X Identification of curcumin derivatives as human glyoxalase I inhibitors: A combination of biological evaluation, molecular docking, 3D-QSAR and molecular dynamics simulation studies. Bioorg Med Chem19:1189-96 (2011) [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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BDBM50336267 |
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n/a |
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Name | BDBM50336267 |
Synonyms: | CHEMBL1669737 | ethyl 2-(3-nitrobenzylidene)-3-oxobutanoate |
Type | Small organic molecule |
Emp. Form. | C13H13NO5 |
Mol. Mass. | 263.246 |
SMILES | CCOC(=O)C(=Cc1cccc(c1)[N+]([O-])=O)C(C)=O |w:6.6| |
Structure |
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