Ecological, Physiological and Biochemical Adaptation in Helminth: Trends in Evolution of Anthelminthic Chemical Agents

IF 0.4 Q4 PHARMACOLOGY & PHARMACY Advances in Pharmacology and Pharmacy Pub Date : 2021-10-01 DOI:10.13189/app.2021.090404
M. Gorbachev
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Abstract

This paper discusses the landmark anthelminthic substances – traditional medicine components, different categories of pluripotential synthetic and naturally occurring compounds. Much attention is paid to the sections devoted to recent discoveries (Emodepside, Monepantel, Derquantel, Tribendimidine) and to some promising works. This review focused on some aspects of molecular mechanisms of action of anthelminthic substances and of helminth adaptation to anthelminthic substances, and on alternative worming treatment options. A new substance development, be it designing a new compound or identification of properties of any existing compounds, is a time-consuming and expensive process. Application of the diversification (different types of compounds) and the focused (related compounds) screenings, software-based evaluation of anthelminthic activity in silico, chemical and genetic trials on model small animals (nematodes Artemia salina, Caenorhabditis elegans, etc.) are intended to accelerate introduction of new substances. Further knowledge in molecular action mechanisms of anthelminthic agents and in resistance development would improve planning of helminthoses control protocols. Based on the systemic analysis of particular features of the chemical structure of anthelminthic substances, the hypothesis on the viability of the targeted search for such compounds among the derivatives of conditionally progenitor cyclic hydrocarbons – benzene, indene, naphthalene, 1Н-cyclopenth [a]-naphthalene, anthracene and phenanthrene – by alternating absolutely unsaturated and saturated structures, including heterocyclic analogues containing nitrogen, oxygen and sulfur and different substitutes and functional groups, was voiced.
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寄生虫的生态、生理和生化适应:寄生虫化学制剂的进化趋势
本文讨论了具有里程碑意义的驱虫物质——传统药物成分、不同类别的多能合成化合物和天然化合物。大部分注意力都放在了最近发现的部分(Emodepside, Monepantel, Derquantel, Tribendimidine)和一些有前途的作品。本文就驱虫物质的分子作用机制、寄生虫对驱虫物质的适应以及驱虫的替代治疗方案等方面进行了综述。一种新物质的开发,无论是设计一种新化合物还是鉴定任何现有化合物的性质,都是一个耗时且昂贵的过程。应用多样化(不同类型的化合物)和重点(相关化合物)筛选,基于软件的硅驱虫活性评价,模型小动物(盐蒿线虫,秀丽隐杆线虫等)的化学和遗传试验,旨在加速新物质的引入。进一步了解驱虫剂的分子作用机制和耐药性的发展将改善驱虫控制方案的规划。在系统分析蚁类物质化学结构特征的基础上,提出了通过绝对不饱和结构和饱和结构(包括含氮杂环类似物)交替在条件祖先环烃(苯、茚、萘、1Н-cyclopenth [a]-萘、蒽和菲)的衍生物中定向寻找这类化合物的可行性假设。氧和硫以及不同的取代基和官能团,都被表示出来了。
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Advances in Pharmacology and Pharmacy
Advances in Pharmacology and Pharmacy PHARMACOLOGY & PHARMACY-
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