Reaction Details |
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Target | Lactoylglutathione lyase |
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Ligand | BDBM50517465 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1869127 (CHEMBL4370193) |
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IC50 | 540±n/a nM |
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Citation | Perez, C; Barkley-Levenson, AM; Dick, BL; Glatt, PF; Martinez, Y; Siegel, D; Momper, JD; Palmer, AA; Cohen, SM Metal-Binding Pharmacophore Library Yields the Discovery of a Glyoxalase 1 Inhibitor. J Med Chem62:1609-1625 (2019) [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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BDBM50517465 |
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n/a |
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Name | BDBM50517465 |
Synonyms: | CHEMBL4457949 |
Type | Small organic molecule |
Emp. Form. | C20H13Cl2N3O2S |
Mol. Mass. | 430.307 |
SMILES | Clc1ccc(cc1Cl)-c1ccc(NS(=O)(=O)c2ccccn2)c2ncccc12 |
Structure |
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