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TargetLactoylglutathione lyase
LigandBDBM50336263
Substrate/Competitorn/a
Meas. Tech.ChEMBL_716548 (CHEMBL1670272)
Ki 91000±n/a nM
Citation Yuan, MLuo, MSong, YXu, QWang, XCao, YBu, XRen, YHu, X Identification of curcumin derivatives as human glyoxalase I inhibitors: A combination of biological evaluation, molecular docking, 3D-QSAR and molecular dynamics simulation studies. Bioorg Med Chem19:1189-96 (2011) [PubMed]  Article
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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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BDBM50336263
n/a
NameBDBM50336263
Synonyms:3-(3-nitrobenzylidene)pentane-2,4-dione | CHEMBL1669733
TypeSmall organic molecule
Emp. Form.C12H11NO4
Mol. Mass.233.22
SMILES[#6]-[#6](=O)-[#6](=[#6]\c1cccc(c1)-[#7+](-[#8-])=O)\[#6](-[#6])=O
Structure
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