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TargetLactoylglutathione lyase
LigandBDBM62042
Substrate/Competitorn/a
Meas. Tech.ChEMBL_776454 (CHEMBL1913551)
IC50 93200±n/a nM
Citation Takasawa, RTao, ASaeki, KShionozaki, NTanaka, RUchiro, HTakahashi, SYoshimori, ATanuma, 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
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:
BDBM62042
n/a
NameBDBM62042
Synonyms:2-(p-anisoylamino)benzoic acid | 2-[(4-methoxybenzoyl)amino]benzoic acid | 2-[(4-methoxyphenyl)carbonylamino]benzoic acid | 2-[[(4-methoxyphenyl)-oxomethyl]amino]benzoic acid | KSC-20-006 | KUC106458N | cid_721421
TypeSmall organic molecule
Emp. Form.C15H13NO4
Mol. Mass.271.268
SMILESCOc1ccc(cc1)C(=O)Nc1ccccc1C(O)=O
Structure
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