Jeong Woo-Jin, Kang Dong-Min, Khalil Atif Ali Khan, Neupane Bashu Dev, Cho Seong-Joon, Yang Na-In, Kim Ki-Hyun, Ahn Mi-Jeong
College of Pharmacy and Research Institute of Pharmaceutical Sciences, Gyeongsang National University, Jinju 52828, Republic of Korea.
Department of Biotechnology, Yeungnam University, Gyeongsan 38541, Republic of Korea.
Plants (Basel). 2025 Aug 17;14(16):2558. doi: 10.3390/plants14162558.
Hance (Viburnaceae), the Korean elderberry, is widely used in herbal medicine and in the food industry. It is known to have various pharmacological effects, including antitumor, antioxidant, anti-inflammatory, and antimicrobial activities. During our search for anti- compounds from natural resources, the methanol extract of the branch significantly inhibited the growth of . Three phenolic and four lignan compounds were isolated from the methylene chloride fraction that had shown the most potent anti- activity among the hexane, methylene chloride, ethyl acetate, butanol, and water fractions. The chemical structures were identified to be three phenolics of sylvopinol (), dihydroconiferyl alcohol (), and (7,8)-guaiacylglycerol () and four lignans of boehmenan (), (7,8)-guaiacylglycerol -coniferyl ether () and lawsonicin () with a new lignan, (7,8)-sambucanol (), the structure of which was established by H- and C-NMR, and HRESI-MS, as well as quantum chemical electronic circular dichroism (ECD) calculations. Among the isolates, compounds and exhibited significant anti- activity against strains 51 and 26695. Compound displayed more potent antibacterial activity with MIC values of 3.13 and 6.25 μM, and MIC values of 28.5 and 56.8 μM against the two strains, respectively. Their inhibitory activities were higher than those of a positive control, quercetin. Furthermore, these two compounds showed moderate urease inhibitory activity. A molecular docking simulation revealed the high binding ability of and to the active site of urease. These results will provide further insights into the design of more potent natural products for eradicating .
接骨木属植物(忍冬科),即朝鲜接骨木,在草药和食品工业中广泛应用。已知其具有多种药理作用,包括抗肿瘤、抗氧化、抗炎和抗菌活性。在我们从自然资源中寻找抗化合物的过程中,该植物枝条的甲醇提取物显著抑制了[具体微生物名称未给出]的生长。从己烷、二氯甲烷、乙酸乙酯、丁醇和水馏分中表现出最强抗[具体微生物名称未给出]活性的二氯甲烷馏分中分离出了三种酚类和四种木脂素化合物。化学结构经鉴定为三种酚类化合物,即西洛品醇()、二氢松柏醇()和(7,8)-愈创木基甘油(),以及四种木脂素化合物,即波美南()、(7,8)-愈创木基甘油-松柏醚()和劳森尼辛(),还有一种新的木脂素(7,8)-接骨木醇(),其结构通过氢核磁共振(H-NMR)、碳核磁共振(C-NMR)、高分辨电喷雾电离质谱(HRESI-MS)以及量子化学电子圆二色光谱(ECD)计算得以确定。在分离出的化合物中,化合物[具体化合物编号未给出]和[具体化合物编号未给出]对菌株51和26695表现出显著的抗[具体微生物名称未给出]活性。化合物[具体化合物编号未给出]显示出更强的抗菌活性,对这两种菌株的最低抑菌浓度(MIC)值分别为3.13和6.25μM,以及28.5和56.8μM。它们的抑制活性高于阳性对照槲皮素。此外,这两种化合物还表现出适度的脲酶抑制活性。分子对接模拟显示化合物[具体化合物编号未给出]和[具体化合物编号未给出]与脲酶活性位点具有高结合能力。这些结果将为设计更有效的天然产物以根除[具体微生物名称未给出]提供进一步的见解。