Reaction Details |
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Target | Lactoylglutathione lyase |
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Ligand | BDBM50336254 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_716548 (CHEMBL1670272) |
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Ki | 18000±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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BDBM50336254 |
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n/a |
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Name | BDBM50336254 |
Synonyms: | 5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-7-(1H-pyrrol-2-yl)hepta-1,4,6-trien-3-one | CHEMBL1669726 |
Type | Small organic molecule |
Emp. Form. | C18H17NO4 |
Mol. Mass. | 311.3319 |
SMILES | COc1cc(C=CC(=O)CC(=O)C=Cc2ccc[nH]2)ccc1O |w:5.4,12.11| |
Structure |
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