Faculdade de Farmácia, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Instituto de Pesquisas de Produtos Naturais Walter Mors, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Curr Pharm Des. 2024;30(36):2835-2849. doi: 10.2174/0113816128314974240724045220.
Chronic venous disease (CVD) significantly impacts global health, presenting a complex challenge in medical management. Despite its prevalence and the burden it places on healthcare systems, CVD remains underdiagnosed and undertreated. This review aims to provide a comprehensive analysis of the bioactive compounds in the genus, exploring their therapeutic potential in CVD treatment and addressing the gap in current treatment modalities. A narrative review methodology was adopted, focusing on the pharmacological effects of -derived bioactive compounds, including flavonoids and terpenes. Additionally, the review introduced the DBsimilarity method for analyzing the chemical space and structural similarities among compounds. The review highlights the genus as a rich source of pharmacologically active compounds, notably flavonoids and terpenes, which exhibit significant anti-inflammatory, antioxidant, and veno-protective properties. Some of these compounds have been integrated into existing therapies, underscoring their potential for CVD management. The DBsimilarity analysis further identified many clusters of compounds with more than 85% structural similarity. -derived bioactive compounds offer promising therapeutic potential for managing CVD, showcasing significant anti-inflammatory, antioxidant, and veno-protective effects. The need for further comparative studies, as well as safety and efficacy investigations specific to CVD treatment, is evident. This review underlines the importance of advancing our understanding of these natural compounds and encouraging the development of novel treatments and formulations for effective CVD management. The DBsimilarity method's introduction provides a novel approach to exploring the chemical diversity within the genus, opening new pathways for pharmacological research.
慢性静脉疾病(CVD)对全球健康有重大影响,是医学管理中面临的一个复杂挑战。尽管 CVD 发病率高,给医疗系统带来了沉重负担,但它仍然存在漏诊和治疗不足的情况。本综述旨在全面分析 属植物中的生物活性化合物,探讨其在 CVD 治疗中的潜在治疗价值,并解决当前治疗方法中的空白。本综述采用叙述性综述方法,重点研究了 属植物来源的生物活性化合物的药理作用,包括类黄酮和萜类化合物。此外,还介绍了 DBsimilarity 方法,用于分析 属化合物的化学空间和结构相似性。本综述强调了 属植物作为具有药理活性的化合物的丰富来源,特别是类黄酮和萜类化合物,它们具有显著的抗炎、抗氧化和静脉保护作用。其中一些化合物已被整合到现有治疗方法中,突出了它们在 CVD 管理中的应用潜力。DBsimilarity 分析进一步确定了许多具有超过 85%结构相似性的化合物簇。 属植物来源的生物活性化合物在管理 CVD 方面具有有前途的治疗潜力,表现出显著的抗炎、抗氧化和静脉保护作用。显然,需要进一步开展比较研究,并对 CVD 治疗的安全性和疗效进行调查。本综述强调了深入了解这些天然化合物的重要性,并鼓励开发新的治疗方法和制剂,以有效管理 CVD。DBsimilarity 方法的引入为探索 属植物中的化学多样性提供了一种新方法,为药理学研究开辟了新途径。