舒尼替尼
前药
药理学
酪氨酸激酶抑制剂
治疗指标
医学
耐受性
药代动力学
体内
药品
酪氨酸激酶
肿瘤科
内科学
不利影响
受体
生物
癌症
生物技术
作者
Qiang Huang,Changhua Zhou,Xiao Chen,Bi Rong Dong,Siqi Chen,Ning Zhang,Yawei Liu,An‐Rong Li,Meicun Yao,Ji Miao,Qing Li,Zhong Wang
出处
期刊:PLOS ONE
[Public Library of Science]
日期:2015-10-29
卷期号:10 (10): e0141395-e0141395
被引量:7
标识
DOI:10.1371/journal.pone.0141395
摘要
Patients have responded well to the multi-targeted tyrosine kinase inhibitor (TKI) Sunitinib in the clinic. But the severe toxic side effects associated with Sunitinib limit its therapeutic index. To improve the therapeutic index of Sunitinib, a prodrug strategy was employed to modify Sunitinib. The inactive prodrug AST-003 can be converted to Sunitinib in vitro and in vivo. Compared with Sunitinib, AST-003 has unique biochemical, cellular and pharmacokinetic properties with improved tolerability in mice and yield higher efficacy in tumor xenograft models. This prodrug strategy may constitute a novel paradigm to improve the therapeutic index of Sunitinib and other TKI or anti-angiogenesis drugs in general.
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