Glutathionyl transferase catalyzed addition of glutathione to COMC: A new hypothesis for antitumor activity

被引:31
作者
Hamilton, DS
Ding, Z
Ganem, B [1 ]
Creighton, DJ
机构
[1] Univ Maryland, Dept Chem & Biochem, Baltimore, MD 21228 USA
[2] Cornell Univ, Baker Lab, Dept Chem & Chem Biol, Ithaca, NY 14853 USA
关键词
D O I
10.1021/ol025650h
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
[GRAPHICS] Data are presented indicating that the potent antitumor activity of 2-crotonyloxymethyl-(4R,5R,6R)-4,5,6-trihydroxy-2-cyclohexenone (COTC) and 2-crotonyloxymethyl-2-cyclohexenone (COMC) is not likely the result of glyoxalase I inhibition, as has long been assumed. An alternative hypothesis is presented, based on the finding that COMC is a substrate for human glutathionyl transferase, which produces a transient, highly electrophilic glutathionylated 2-exomethylenecyclohexanone that can covalently modify proteins and nucleic acids.
引用
收藏
页码:1209 / 1212
页数:4
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