化学
小分子
药理学
药物输送
医学
纳米技术
生物化学
材料科学
作者
Sotirios Katsamakas,Theodora Chatzisideri,Savvas Thysiadis,Vasiliki Sarli
标识
DOI:10.4155/fmc-2017-0008
摘要
Conjugates of cytotoxic agents with RGD peptides (Arg-Gly-Asp) addressed to ανβ3, α5β1 and ανβ6 integrin receptors overexpressed by cancer cells, have recently gained attention as potential selective anticancer chemotherapeutics. In this review, the design and the development of RGD conjugates coupled to different small molecules including known cytotoxic drugs and natural products will be discussed.
科研通智能强力驱动
Strongly Powered by AbleSci AI