Reaction Details |
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Target | Lactoylglutathione lyase |
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Ligand | BDBM50233538 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1901788 (CHEMBL4404010) |
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Ki | 290±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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BDBM50233538 |
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n/a |
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Name | BDBM50233538 |
Synonyms: | 18beta-glycyrrhetic acid | 3beta-hydroxy-11-oxoolean-12-en-30-oic acid | CHEMBL230006 | US11660306, Example 18beta Glycyrrhetinic acid | glycyrrhetinic acid |
Type | Small organic molecule |
Emp. Form. | C30H46O4 |
Mol. Mass. | 470.6838 |
SMILES | CC1(C)[C@@H](O)CC[C@@]2(C)[C@H]1CC[C@]1(C)[C@@H]2C(=O)C=C2[C@@H]3C[C@](C)(CC[C@]3(C)CC[C@@]12C)C(O)=O |r,t:19| |
Structure |
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