Organic Chemistry Unit, Department of Chemistry in Pharmaceutical Sciences, Faculty of Pharmacy, University Complutense of Madrid, Plza. Ramón y Cajal s/n, 28040 Madrid, Spain.
Department of Organic Chemistry, Faculty of Sciences, University Autónoma of Madrid, Cantoblanco, 28049 Madrid, Spain.
Int J Mol Sci. 2024 Sep 5;25(17):9615. doi: 10.3390/ijms25179615.
, commonly known as Aguaje or Moriche palm, is traditionally recognised in South America for its medicinal properties, particularly for its anti-inflammatory and antioxidant effects. However, the bioactive compounds responsible for these effects have not been thoroughly investigated. This study aims to isolate and characterise pentacyclic triterpenoid compounds from and to evaluate their therapeutic potential. Using various chromatographic and spectroscopic techniques including Nuclear Magnetic Resonance (NMR) and Mass Spectrometry (MS), three pentacyclic triterpenoid compounds were successfully isolated. Among them, compound (3,11-dioxours-12-en-28-oic acid) exhibited notable bioactivity, significantly inhibiting the activation of Nuclear Factor kappa-light-chain-enhancer of activated B cells (NF-κB) (IC = 7.39-8.11 μM) and of Nitric Oxide (NO) (IC = 4.75-6.59 μM), both of which are key processes in inflammation. Additionally, compound demonstrated potent antioxidant properties by activating the antioxidant enzyme Superoxide Dismutase (SOD) (EC = 1.87 μM) and the transcription factor Nuclear factor erythroid 2-related factor 2 (Nrf2) (EC = 243-547.59 nM), thus showing its potential in combating oxidative stress. This study is the first to isolate and characterise the three compounds from , suggesting that compound could be a promising candidate for the development of safer and more effective therapies for inflammatory and oxidative stress-related diseases.
玛卡巴卡, commonly known as Aguaje or Moriche palm, is traditionally recognised in South America for its medicinal properties, particularly for its anti-inflammatory and antioxidant effects. However, the bioactive compounds responsible for these effects have not been thoroughly investigated. This study aims to isolate and characterise pentacyclic triterpenoid compounds from and to evaluate their therapeutic potential. Using various chromatographic and spectroscopic techniques including Nuclear Magnetic Resonance (NMR) and Mass Spectrometry (MS), three pentacyclic triterpenoid compounds were successfully isolated. Among them, compound (3,11-dioxours-12-en-28-oic acid) exhibited notable bioactivity, significantly inhibiting the activation of Nuclear Factor kappa-light-chain-enhancer of activated B cells (NF-κB) (IC = 7.39-8.11 μM) and of Nitric Oxide (NO) (IC = 4.75-6.59 μM), both of which are key processes in inflammation. Additionally, compound demonstrated potent antioxidant properties by activating the antioxidant enzyme Superoxide Dismutase (SOD) (EC = 1.87 μM) and the transcription factor Nuclear factor erythroid 2-related factor 2 (Nrf2) (EC = 243-547.59 nM), thus showing its potential in combating oxidative stress. This study is the first to isolate and characterise the three compounds from, suggesting that compound could be a promising candidate for the development of safer and more effective therapies for inflammatory and oxidative stress-related diseases.
巴巴雅嘎,通常被称为 Aguaje 或 Moriche 棕榈树,在南美洲因其药用特性而被传统认可,特别是其抗炎和抗氧化作用。然而,负责这些作用的生物活性化合物尚未得到彻底研究。本研究旨在从 中分离和表征五环三萜类化合物,并评估其治疗潜力。使用各种色谱和光谱技术,包括核磁共振(NMR)和质谱(MS),成功分离出三种五环三萜类化合物。其中,化合物 (3,11-二氧乌苏-12-烯-28-酸)表现出显著的生物活性,显著抑制核因子 kappa-轻链增强子活化 B 细胞(NF-κB)(IC = 7.39-8.11 μM)和一氧化氮(NO)(IC = 4.75-6.59 μM)的激活,这两者都是炎症的关键过程。此外,化合物 通过激活抗氧化酶超氧化物歧化酶(SOD)(EC = 1.87 μM)和转录因子红细胞 2 相关因子 2(Nrf2)(EC = 243-547.59 nM)来显示出强大的抗氧化特性,从而显示出其在对抗氧化应激方面的潜力。本研究首次从 中分离和表征了这三种化合物,表明化合物 可能是开发更安全、更有效的炎症和氧化应激相关疾病治疗方法的有前途的候选药物。