Reaction Details |
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Target | Lactoylglutathione lyase |
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Ligand | BDBM50355548 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_776454 (CHEMBL1913551) |
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IC50 | 54600±n/a nM |
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Citation | Takasawa, R; Tao, A; Saeki, K; Shionozaki, N; Tanaka, R; Uchiro, H; Takahashi, S; Yoshimori, A; Tanuma, S Discovery of a new type inhibitor of human glyoxalase I by myricetin-based 4-point pharmacophore. Bioorg Med Chem Lett21:4337-42 (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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BDBM50355548 |
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n/a |
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Name | BDBM50355548 |
Synonyms: | CHEMBL1910549 |
Type | Small organic molecule |
Emp. Form. | C17H17NO4S |
Mol. Mass. | 331.386 |
SMILES | COc1ccc(cc1)C(=O)Nc1sc2CCCCc2c1C(O)=O |
Structure |
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