Department of Pharmaceutical Chemistry, Faculty of Pharmacy and Health Sciences, Universiti Kuala Lumpur Royal College of Medicine Perak, Ipoh, Perak, Malaysia.
School of Pharmacy, Monash University Malaysia, Bandar Sunway, Selangor, Malaysia.
Drug Des Devel Ther. 2021 Jun 21;15:2721-2746. doi: 10.2147/DDDT.S299753. eCollection 2021.
Swertiamarin, a seco-iridoid glycoside, is mainly found in Blume () and exhibits therapeutic activities for various diseases. The present study aimed to provide a review of swertiamarin in terms of its phytochemistry, physicochemical properties, biosynthesis, pharmacology and therapeutic potential. Relevant literature was collected from several scientific databases, including PubMed, ScienceDirect, Scopus and Google Scholar, between 1990 and the present. This review included the distribution of swertiamarin in medicinal plants and its isolation, characterization, physicochemical properties and possible biosynthetic pathways. A comprehensive summary of the pharmacological activities, therapeutic potential and metabolic pathways of swertiamarin was also included after careful screening and tabulation. Based on the reported evidence, swertiamarin meets all five of Lipinski's rules for drug-like properties. Thereafter, the physicochemical properties of swertiamarin were detailed and analyzed. A simple and rapid method for isolating swertiamarin from has been described. The present review proposed that swertiamarin may be biosynthesized by the mevalonate or nonmevalonate pathways, followed by the seco-iridoid pathway. It has also been found that swertiamarin is a potent compound with diverse pharmacological activities, including hepatoprotective, analgesic, anti-inflammatory, antiarthritis, antidiabetic, antioxidant, neuroprotective and gastroprotective activities. The anticancer activity of swertiamarin against different cancer cell lines has been recently reported. The underlying mechanisms of all these pharmacological effects are diverse and seem to involve the regulation of different molecular targets, including growth factors, inflammatory cytokines, protein kinases, apoptosis-related proteins, receptors and enzymes. Swertiamarin also modulates the activity of several transcription factors, and their signaling pathways in various pathological conditions are also discussed. Moreover, we have highlighted the toxicity profile, pharmacokinetics and possible structural modifications of swertiamarin. The pharmacological activities and therapeutic potential of swertiamarin have been extensively investigated. However, more advanced studies are required including clinical trials and studies on the bioavailability, permeability and administration of safe doses to offer swertiamarin as a novel candidate for future drug development.
獐芽菜苦苷,一种裂环环烯醚萜类糖苷,主要存在于獐牙菜属()中,具有治疗多种疾病的活性。本研究旨在综述獐牙菜苦苷的植物化学、理化性质、生物合成、药理学和治疗潜力。从 1990 年至今,从多个科学数据库(包括 PubMed、ScienceDirect、Scopus 和 Google Scholar)中收集了相关文献。本综述包括獐牙菜苦苷在药用植物中的分布及其分离、鉴定、理化性质和可能的生物合成途径。在仔细筛选和制表后,还包括了獐牙菜苦苷的药理学活性、治疗潜力和代谢途径的综合总结。根据报道的证据,獐牙菜苦苷符合类药性的五个利宾斯基规则。此后,详细分析了獐牙菜苦苷的理化性质。描述并详细介绍了从獐牙菜中分离獐牙菜苦苷的简单快速方法。本综述提出,獐牙菜苦苷可能通过甲羟戊酸或非甲羟戊酸途径合成,然后通过裂环环烯醚萜途径合成。还发现獐牙菜苦苷是一种具有多种药理活性的有效化合物,包括保肝、镇痛、抗炎、抗关节炎、抗糖尿病、抗氧化、神经保护和胃保护活性。最近报道了獐牙菜苦苷对不同癌细胞系的抗癌活性。所有这些药理作用的潜在机制多种多样,似乎涉及不同分子靶点的调节,包括生长因子、炎症细胞因子、蛋白激酶、凋亡相关蛋白、受体和酶。獐牙菜苦苷还调节几种转录因子的活性,还讨论了它们在各种病理条件下的信号通路。此外,我们强调了獐牙菜苦苷的毒性概况、药代动力学和可能的结构修饰。獐牙菜苦苷的药理学活性和治疗潜力已得到广泛研究。然而,需要进行更先进的研究,包括临床试验和关于生物利用度、通透性和安全剂量给药的研究,以提供獐牙菜苦苷作为未来药物开发的新候选药物。