Department of Chemistry, University of Delhi, Delhi-110007, India.
Curr Med Chem. 2011;18(25):3889-928. doi: 10.2174/092986711803414340.
Trioxane based compounds such as artemisinin and its synthetic and semi-synthetic analogues constitute promising class of antimalarial agents. The pharmaceutical development of artemisinin was started in 1971 after the isolation from Chinese medicinal plant Artemisia annua and this compound has drawn much attention from medical chemist and pharmacologist worldwide. Researchers from across the globe have independently and collaboratively conducted various studies on the artemisinin system in an attempt to identify lead molecules for malaria chemotherapy. This systematic study led to the discovery of artemether, arteether, dihydroartemisinin, and sodium artesunate which are being used as antimalarial drug for the treatment of Plasmodium falciparum related infections. These studies also revealed that the trioxane bridge is essential for the antimalarial activity of this class of compounds. Another class of structurally simple peroxides that emerged from these studies was the 1,2,4,5-tetraoxanes. Some of the tetraoxane based compounds have shown promising antimalarial potential, and much of work has been done on this type of compound in recent years. Apart from their antimalarial activity, these classes of compounds have also shown promising anticancer and antibacterial activity. To this end, an attempt has been made to describe the medicinal potential of trioxane and tetraoxane-based compounds. Literature from 1999 has been critically reviewed and an attempt has been made to discuss structure activity relationship study among the series of trioxane and tetraoxane based compounds.
基于三氧杂环己烷的化合物,如青蒿素及其合成和半合成类似物,构成了有前途的抗疟药物类别。青蒿素的药物开发始于 1971 年,当时从中药青蒿中分离出来,这种化合物引起了全球医学家和药理学家的关注。世界各地的研究人员独立地和合作地对青蒿素系统进行了各种研究,试图确定用于疟疾化疗的先导分子。这项系统研究发现了青蒿琥酯、蒿甲醚、双氢青蒿素和青蒿琥酯钠,它们被用作治疗恶性疟原虫感染的抗疟药物。这些研究还表明,三氧杂环己烷桥对于这类化合物的抗疟活性是必不可少的。从这些研究中出现的另一类结构简单的过氧化物是 1,2,4,5-四氧杂环己烷。一些基于四氧杂环己烷的化合物表现出有希望的抗疟潜力,近年来对这类化合物进行了大量的研究。除了它们的抗疟活性外,这些类别的化合物还显示出有希望的抗癌和抗菌活性。为此,我们试图描述基于三氧杂环己烷和四氧杂环己烷的化合物的药用潜力。对 1999 年以来的文献进行了批判性回顾,并试图讨论三氧杂环己烷和四氧杂环己烷类化合物的构效关系研究。