Reaction Details |
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Target | Lactoylglutathione lyase |
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Ligand | BDBM50517464 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1901787 (CHEMBL4404009) |
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Ki | 230±n/a nM |
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Citation | Jin, T; Zhao, L; Wang, HP; Huang, ML; Yue, Y; Lu, C; Zheng, ZB Recent advances in the discovery and development of glyoxalase I inhibitors. Bioorg Med Chem28:0 (2020) [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: | 4.4.1.5 | Aldoketomutase | Glo1 | Glx I | Glyoxalase I | Ketone-aldehyde mutase | LGUL_MOUSE | Lactoylglutathione lyase | Methylglyoxalase | S-D-lactoylglutathione methylglyoxal lyase |
Type: | PROTEIN |
Mol. Mass.: | 20805.83 |
Organism: | Mus musculus |
Description: | ChEMBL_10270 |
Residue: | 184 |
Sequence: | MAEPQPASSGLTDETAFSCCSDPDPSTKDFLLQQTMLRIKDPKKSLDFYTRVLGLTLLQK
LDFPAMKFSLYFLAYEDKNDIPKDKSEKTAWTFSRKATLELTHNWGTEDDETQSYHNGNS
DPRGFGHIGIAVPDVYSACKRFEELGVKFVKKPDDGKMKGLAFIQDPDGYWIEILNPNKI
ATII
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BDBM50517464 |
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n/a |
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Name | BDBM50517464 |
Synonyms: | CHEMBL1234300 |
Type | Small organic molecule |
Emp. Form. | C16H16O6 |
Mol. Mass. | 304.2946 |
SMILES | COC(=O)c1c(C)cc(Oc2cc(C)cc(O)c2O)cc1O |
Structure |
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