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TargetLactoylglutathione lyase
LigandBDBM50569134
Substrate/Competitorn/a
Meas. Tech.ChEMBL_2108109 (CHEMBL4816784)
IC50 2900±n/a nM
Citation Azuma, MInoue, MNishida, AAkahane, HKitajima, MNatani, SChimori, RYoshimori, AMano, YUchiro, HTanuma, SITakasawa, 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
More Info.:Get all data from this article,  Assay Method
 
Lactoylglutathione lyase
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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  Blast E-value cutoff:
BDBM50569134
n/a
NameBDBM50569134
Synonyms:CHEMBL4863408
TypeSmall organic molecule
Emp. Form.C20H22N4O4S
Mol. Mass.414.478
SMILESCc1nn(C2CCS(=O)(=O)C2)c(C)c1\C=C(/CC(O)=O)c1nc2ccccc2[nH]1
Structure
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