Reaction Details |
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Target | Lactoylglutathione lyase |
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Ligand | BDBM50569134 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_2108109 (CHEMBL4816784) |
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IC50 | 2900±n/a nM |
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Citation | Azuma, M; Inoue, M; Nishida, A; Akahane, H; Kitajima, M; Natani, S; Chimori, R; Yoshimori, A; Mano, Y; Uchiro, H; Tanuma, SI; Takasawa, R Addition of hydrophobic side chains improve the apoptosis inducibility of the human glyoxalase I inhibitor, TLSC702. Bioorg Med Chem Lett40:0 (2021) [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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BDBM50569134 |
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n/a |
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Name | BDBM50569134 |
Synonyms: | CHEMBL4863408 |
Type | Small organic molecule |
Emp. Form. | C20H22N4O4S |
Mol. Mass. | 414.478 |
SMILES | Cc1nn(C2CCS(=O)(=O)C2)c(C)c1\C=C(/CC(O)=O)c1nc2ccccc2[nH]1 |
Structure |
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