Department of Chemistry & Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Private Bag X3, Rondebosch 7701, South Africa.
Expert Opin Ther Pat. 2012 Oct;22(10):1179-203. doi: 10.1517/13543776.2012.724063. Epub 2012 Sep 13.
The isolation of artemisinin from an ancient Chinese remedy in the early 1970s heralded the beginning of a new era in antimalarial drug therapy culminating in artemisinin-based combination therapies currently being the mainstay of malaria treatment worldwide. Ongoing research on this compound and its derivatives has revealed its potential use in treating other infectious and noninfectious diseases.
This review provides a summary of patents published globally from January 2006 to June 2012 covering promising artemisinin derivatives and artemisinin-based drug combinations developed for use in various therapeutic areas.
The diversity of semi-synthetic artemisinin derivatives has been limited to the same design strategy of modifying the artemisinin molecule at the same positions due to inherent synthetic challenges. To address this, future endeavors should include: the use of biotransformation strategies to modify other positions in the sesquiterpene ring while retaining the endoperoxide bridge; the design and synthesis of synthetic ozonides based on the pharmacophoric endoperoxide motif and drug repositioning approaches to artemisinin-based combination therapy. A better understanding of the mechanism of action of artemisinin derivatives and their biomolecular targets may provide an invaluable tool for the development of derivatives with a wider array of activity and greater clinical utility than currently appreciated.
20 世纪 70 年代初,从一种中国古方中分离出青蒿素,标志着抗疟药物治疗新时代的开始,最终青蒿素类复方疗法成为目前全球治疗疟疾的主要方法。对这种化合物及其衍生物的持续研究揭示了其在治疗其他传染病和非传染病方面的潜在用途。
本文综述了 2006 年 1 月至 2012 年 6 月期间全球公布的专利,涵盖了有前途的青蒿素衍生物和青蒿素类药物组合,这些药物组合针对各种治疗领域开发。
由于固有的合成挑战,半合成青蒿素衍生物的多样性仅限于对青蒿素分子在相同位置进行修饰的相同设计策略。为了解决这个问题,未来的努力应包括:使用生物转化策略来修饰倍半萜环中的其他位置,同时保留过氧化物桥;基于药效团的内过氧化物设计和合成合成臭氧化物,以及青蒿素类药物组合的重新定位方法。更好地了解青蒿素衍生物的作用机制及其生物分子靶标,可能为开发具有比目前更广泛的活性和更大临床应用价值的衍生物提供宝贵的工具。