生物正交化学
前药
化学
组合化学
化学空间
同种类的
劈理(地质)
纳米技术
药物发现
键裂
生物化学
催化作用
点击化学
热力学
物理
工程类
断裂(地质)
岩土工程
材料科学
作者
Qingqiang Min,Xingyue Ji
标识
DOI:10.1021/acs.jmedchem.3c01459
摘要
Time- and space-resolved drug delivery is highly demanded for cancer treatment, which, however, can barely be achieved with a traditional prodrug strategy. In recent years, the prodrug strategy based on a bioorthogonal bond cleavage chemistry has emerged with the advantages of high temporospatial resolution over drug activation and homogeneous activation irrespective of individual heterogeneity. In the past five years, tremendous progress has been witnessed in this field with one such bioorthogonal prodrug entering Phase II clinical trials. This Perspective aims to highlight these new advances (2019–2023) and critically discuss their pros and cons. In addition, the remaining challenges and potential strategic directions for future progress will also be included.
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