Encountering unpredicted off-target effects of pharmacological inhibitors

被引:16
|
作者
Miyazawa, Keiji [1 ]
机构
[1] Univ Yamanashi, Dept Biochem, Interdisciplinary Grad Sch Med & Engn, Chuo Ku, Yamanashi 4093898, Japan
来源
JOURNAL OF BIOCHEMISTRY | 2011年 / 150卷 / 01期
关键词
Inhibitor; Kinase; JNK; off-target; PI3K; PROTEIN-KINASE INHIBITORS; TYROSINE KINASE; SP600125;
D O I
10.1093/jb/mvr053
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
With the emergence of chemical biology, the use of pharmacological inhibitors in biological research has been expanding. SP600125 is a low-molecular weight compound that has been widely used to inhibit c-Jun-N-terminal kinase (JNK). A recent publication by Tanemura et al. (J. Biochem. 145:345-354, 2009) indicated that SP600125 also inhibits phosphatidylinositol 3-kinase (PI3K) in an isoform-selective fashion: it efficiently inhibited the delta isoform of p110 catalytic subunit (p110 delta), which is primarily expressed in leucocytes, but neither of the ubiquitously expressed isoforms, p110 alpha and p110 gamma. Here, I discuss what we learn from such unpredicted off-target effects of pharmacological inhibitors.
引用
收藏
页码:1 / 3
页数:3
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