Reaction Details |
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Target | Lactoylglutathione lyase |
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Ligand | BDBM50027952 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_754309 (CHEMBL1799085) |
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Ki | 335300±n/a nM |
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Citation | Liu, M; Yuan, M; Li, Z; Cheng, YK; Luo, HB; Hu, X Structural investigation into the inhibitory mechanisms of indomethacin and its analogues towards human glyoxalase I. Bioorg Med Chem Lett21:4243-7 (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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BDBM50027952 |
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n/a |
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Name | BDBM50027952 |
Synonyms: | 5-(4-chlorobenzoyl)-1,4-dimethyl-1H-pyrrole-2-acetic acid | CHEMBL19490 | Zomepirac | [5-(4-chlorobenzoyl)-1,4-dimethyl-1H-pyrrol-2-yl]acetic acid |
Type | Small organic molecule |
Emp. Form. | C15H14ClNO3 |
Mol. Mass. | 291.73 |
SMILES | Cc1cc(CC(O)=O)n(C)c1C(=O)c1ccc(Cl)cc1 |
Structure |
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