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TargetLactoylglutathione lyase
LigandBDBM54705
Substrate/Competitorn/a
Meas. Tech.ChEMBL_716548 (CHEMBL1670272)
Ki 383000±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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BDBM54705
n/a
NameBDBM54705
Synonyms:CHEMBL1297 | Fenoprofen | UNM-0000306101 | calcium;2-(3-phenoxyphenyl)propanoic acid;hydrate | calcium;2-(3-phenoxyphenyl)propionic acid;hydrate | cid_16219353
TypeSmall organic molecule
Emp. Form.C15H14O3
Mol. Mass.242.2699
SMILESCC(C(O)=O)c1cccc(Oc2ccccc2)c1
Structure
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