Shafiq Nusrat, Noreen Sadia, Rafiq Naila, Ali Basharat, Parveen Shagufta, Mahmood Ayesha, Sajid Arfa, Akhtar Naseem, Bilal Muhammad
Department of Chemistry, Government College Women University, Madina Town, Pakistan.
Department of Biochemistry, Government College Women University, Faisalabad, Pakistan.
J Food Biochem. 2020 Aug;44(8):e13320. doi: 10.1111/jfbc.13320. Epub 2020 Jun 16.
Herein, the methanolic extract of Rumex hastatus was prepared and subjected to silica gel column chromatographic separation for purification. The chromatographic analysis yielded four bioactive compounds namely, 1,8-dihydroxy-3-methyl-anthraquinone (C1, chrysophanol), 3-methoxy-7-methyl-1,5-dihydroxy-anthraquinone (C2), 6-methyl-1,3,7-trihydroxy-anthraquinone (C3), and 4-hydroxycinnamic acid (C4). The structures of all the isolated bio-entities were elucidated by spectroscopic analysis (1D, 2D-NMR, and MS). The biological potentialities of bioactive compounds were evaluated by determining their antioxidant and anti-urease activities. The results revealed that compound 1 showed the highest nitrite radical scavenging activity (IC = 0.39 mM) followed by C2 and C4 (IC = 0.45) mM and C3 (IC = 0.47 mM). Similarly, the determined IC values for anti-urease activity were C2 (IC = 0.39 mM), C1 (IC = 0.40), C4 (IC = 0.41), and C3 (IC = 44). Molecular docking study revealed maximum interactions among the hydroxyl group of all compounds. In conclusion, Rumex hastatus extract could be a promising alternative to chemical additives in pharmaceutical industries due to its noteworthy biological activities. PRACTICAL APPLICATIONS: As we have shown in this study that Rumex hastatus is a prolific source of biologically active compounds with potent antioxidant and anti-urease activities, therefore, R. hastatus extract could be used as a promising alternative to chemical additives in pharmaceutical industries due to its unique compounds and noteworthy biological activities.
在此,制备了皱叶酸模的甲醇提取物,并通过硅胶柱色谱分离进行纯化。色谱分析得到了四种生物活性化合物,即1,8 - 二羟基 - 3 - 甲基蒽醌(C1,大黄酚)、3 - 甲氧基 - 7 - 甲基 - 1,5 - 二羟基蒽醌(C2)、6 - 甲基 - 1,3,7 - 三羟基蒽醌(C3)和4 - 羟基肉桂酸(C4)。所有分离出的生物实体的结构通过光谱分析(一维、二维核磁共振和质谱)得以阐明。通过测定其抗氧化和抗脲酶活性来评估生物活性化合物的生物学潜力。结果表明,化合物1表现出最高的亚硝酸根自由基清除活性(IC = 0.39 mM),其次是C2和C4(IC = 0.45 mM)以及C3(IC = 0.47 mM)。同样,抗脲酶活性的测定IC值分别为C2(IC = 0.39 mM)、C1(IC = 0.40)、C4(IC = 0.41)和C3(IC = 44)。分子对接研究揭示了所有化合物羟基之间的最大相互作用。总之,由于皱叶酸模提取物具有显著的生物学活性,它可能成为制药行业化学添加剂的一种有前途的替代品。实际应用:正如我们在本研究中所示,皱叶酸模是具有强大抗氧化和抗脲酶活性的生物活性化合物的丰富来源,因此,由于其独特的化合物和显著的生物学活性,皱叶酸模提取物可作为制药行业化学添加剂的一种有前途的替代品。