Abdel-Kader Maged S, Almutib Fahad S, Aldosari Abdullah F, Soliman Gamal A, Elzorba Hisham Y, Alqarni Mohammed H, Ibrahim Reham S, Zaatout Hala H
Department of Pharmacognosy, College of Pharmacy, Prince Sattam Bin Abdulaziz University, Al Kharj 11942, Saudi Arabia.
Department of Pharmacognosy, College of Pharmacy, Alexandria University, Alexandria 21521, Egypt.
Metabolites. 2023 Jun 13;13(6):750. doi: 10.3390/metabo13060750.
The total alcohol extract obtained from the aerial parts of and fractions of the liquid-liquid fractionation process were tested against picornavirus-causing foot-and-mouth disease (FMD) based on the traditional use of the plant in Saudi Arabia. The most active petroleum ether soluble fraction was subjected to chromatographic purification, and nine compounds were isolated, identified using various chemical and spectroscopic methods, and tested for their anti-viral potential. The new ester identified as -Amyrin 3-(3'R-hydroxy)-hexadecanoate () was the most active compound with 51% inhibition of the viral growth and was given the name Rhazyin A. Compounds with ursane skeleton were more active than those with lupane skeleton except in the case of the acid derivatives where betulenic acid showed 26.1% inhibition against the viral growth, while ursolic acid showed only 16.6% inhibition. Moreover, molecular docking analysis using a glide extra-precision module was utilized for investigating the possible molecular interactions accounting for anti-viral activity against picornavirus of the nine isolated compounds. Molecular docking studies revealed a strong binding of the discovered hits within the active site of FMDV 3C. Compound showed the lowest docking score within the nine isolated compounds comparable to the two known anti-viral drugs; glycyrrhizic acid and ribavirin. The results of this research will provide lead candidates from natural origin with potential safety and efficacy compared to the synthetic ones with lower production costs for managing FMVD.
根据该植物在沙特阿拉伯的传统用途,对从其地上部分获得的总醇提取物以及液-液分馏过程的馏分进行了针对引起口蹄疫的小核糖核酸病毒(FMD)的测试。对活性最高的石油醚可溶馏分进行色谱纯化,分离出9种化合物,使用各种化学和光谱方法进行鉴定,并测试其抗病毒潜力。鉴定为β-香树脂醇3-(3'R-羟基)-十六烷酸酯()的新酯是活性最高的化合物,对病毒生长的抑制率为51%,并被命名为Rhazyin A。除了酸衍生物的情况外,具有乌苏烷骨架的化合物比具有羽扇豆烷骨架的化合物更具活性,其中桦木酸对病毒生长的抑制率为26.1%,而熊果酸仅显示16.6%的抑制率。此外,使用Glide超精确模块进行分子对接分析,以研究九种分离化合物对小核糖核酸病毒抗病毒活性的可能分子相互作用。分子对接研究表明,发现的命中物在口蹄疫病毒3C的活性位点内有很强的结合。化合物在九种分离化合物中显示出最低的对接分数,与两种已知的抗病毒药物甘草酸和利巴韦林相当。这项研究的结果将提供来自天然来源的潜在候选物,与合成候选物相比,具有潜在的安全性和有效性,且生产成本较低,可用于管理口蹄疫病毒病。