Laboratory of Growth Regulators, The Czech Academy of Sciences, Institute of Experimental Botany & Palacký University, Šlechtitelů 27, CZ-78371, Olomouc, Czech Republic.
Prog Chem Org Nat Prod. 2021;115:115-176. doi: 10.1007/978-3-030-64853-4_3.
Secondary metabolites (SM) from organisms have served medicinal chemists over the past two centuries as an almost inexhaustible pool of new drugs, drug-like skeletons, and chemical probes that have been used in the "hunt" for new biologically active molecules with a "beneficial effect on human mind and body." Several secondary metabolites, or their derivatives, have been found to be the answer in the quest to search for new approaches to treat or even eradicate many types of diseases that oppress humanity. A special place among SM is occupied by lignans and neolignans. These phenolic compounds are generated biosynthetically via radical coupling of two phenylpropanoid monomers, and are known for their multitarget activity and low toxicity. The disadvantage of the relatively low specificity of phenylpropanoid-based SM turns into an advantage when structural modifications of these skeletons are made. Indeed, phenylpropanoid-based SM previously have proven to offer great potential as a starting point in drug development. Compounds such as Warfarin (a coumarin-based anticoagulant) as well as etoposide and teniposide (podophyllotoxin-based anticancer drugs) are just a few examples. At the beginning of the third decade of the twenty-first century, the call for the treatment of more than a dozen rare or previously "neglected" diseases remains for various reasons unanswered. Leishmaniasis, a neglected disease that desperately needs new ways of treatment, is just one of these. This disease is caused by more than 20 leishmanial parasites that are pathogenic to humans and are spread by as many as 800 sandfly species across subtropical areas of the world. With continuing climate changes, the presence of Leishmania parasites and therefore leishmaniasis, the disease caused by these parasites, is spreading from previous locations to new areas. Thus, leishmaniasis is affecting each year a larger proportion of the world's population. The choice of appropriate leishmaniasis treatment depends on the severity of the disease and its form of manifestation. The success of current drug therapy is often limited, due in most cases to requiring long hospitalization periods (weeks to months) and the toxicity (side effects) of administered drugs, in addition to the increasing resistance of the parasites to treatment. It is thus important to develop new drugs and treatments that are less toxic, can overcome drug resistance, and require shorter periods of treatment. These aspects are especially important for the populations of developing countries. It was reported that several phenylpropanoid-based secondary metabolites manifest interesting antileishmanial activities and are used by various indigenous people to treat leishmaniasis. In this chapter, the authors shed some light on the various biological activities of phenylpropanoid natural products, with the main focus being on their possible applications in the context of antileishmanial treatment.
次生代谢物(SM)来自生物体,在过去的两个世纪里,一直为药用化学家提供了一个几乎用之不竭的新药库、类似药物的骨架和化学探针,用于寻找具有“对人类身心有益的有益作用”的新生物活性分子。已经发现几种次生代谢物或其衍生物是寻找治疗甚至根除多种压迫人类疾病的新方法的答案。在次生代谢物中,木脂素和新木脂素占有特殊地位。这些酚类化合物通过两个苯丙素单体的自由基偶联生物合成产生,以多靶点活性和低毒性而闻名。基于苯丙素的次生代谢物的相对低特异性的缺点在对这些骨架进行结构修饰时变成了优点。事实上,基于苯丙素的次生代谢物之前已被证明具有作为药物开发起点的巨大潜力。华法林(香豆素类抗凝剂)、依托泊苷和替尼泊苷(鬼臼毒素类抗癌药物)等化合物就是几个例子。在 21 世纪的第三个十年开始时,由于各种原因,仍有十几种罕见或以前“被忽视”的疾病需要治疗,但仍未得到满足。利什曼病是一种急需新治疗方法的被忽视的疾病,就是其中之一。这种疾病是由 20 多种对人类致病的利什曼原虫寄生虫引起的,通过世界亚热带地区的 800 多种沙蝇物种传播。随着气候变化的继续,利什曼原虫寄生虫的存在以及由这些寄生虫引起的利什曼病正在从以前的地方传播到新的地方。因此,利什曼病每年影响到世界上更大比例的人口。适当的利什曼病治疗方法的选择取决于疾病的严重程度及其表现形式。由于大多数情况下需要长时间住院(数周到数月)以及所给予药物的毒性(副作用),再加上寄生虫对治疗的耐药性增加,当前药物治疗的成功率往往受到限制。因此,开发毒性较低、能克服耐药性、治疗时间较短的新药和治疗方法非常重要。这些方面对于发展中国家的人口尤为重要。据报道,几种基于苯丙素的次生代谢物表现出有趣的抗利什曼原虫活性,并被各种土著人民用于治疗利什曼病。在本章中,作者探讨了苯丙素天然产物的各种生物活性,主要关注它们在抗利什曼病治疗方面的可能应用。