National Center for Natural Products Research, The University of Mississippi, Oxford, MS, USA.
Department of Biomolecular Sciences, Research Institute for Pharmaceutical Sciences, School of Pharmacy, The University of Mississippi, Oxford, MS, USA.
Nat Prod Res. 2022 Jun;36(12):2984-2992. doi: 10.1080/14786419.2021.1937157. Epub 2021 Jun 14.
Bioactivity guided isolation of an ethanol extract of the root of (Family Fabaceae) afforded a new prenylated isoflavone, named schottiin (5,7,5'-trihydroxy-4'--methyl-6'-(3,3-dimethylallyl)-isoflavone) (), together with four other isoflavones, including fremontone (), 5,7,4',5'-tetrahydroxy-2'-(3,3-dimethylallyl)-isoflavone (), glycyrrhisoflavone () and fremontin (), of which and identified as isomeric mixture. Structures of - were determined by full spectroscopic analyses. A comprehensive 2 D NMR spectral data has allowed revising the structure of fremontone as from previously reported Compound showed weak antibacterial activity against methicillin-resistant (MRSA). A combination study using a checkerboard assay between fremontone () and methicillin exhibited a synergistic activity with 8-fold decrease in MIC of methicillin, as well as an additive effect with vancomycin against MRSA ATCC 1708. Compounds and also showed moderate antiplasmodial activity against chloroquine-sensitive (D6) and -resistant (W2) strains of with no cytotoxicity to mammalian Vero cells.
从(豆科)根的乙醇提取物中经生物活性导向分离得到一个新的烯丙基化异黄酮,命名为()(5,7,5'-三羟基-4'--甲基-6'-(3,3-二甲基烯丙基)-异黄酮),连同其他四个异黄酮,包括()、5,7,4',5'-四羟基-2'-(3,3-二甲基烯丙基)-异黄酮()、甘草异黄酮()和(),其中和被鉴定为异构混合物。通过全光谱分析确定了 - 的结构。全面的 2D NMR 光谱数据允许修正先前报道的 fremontone 的结构为()。化合物表现出微弱的抗耐甲氧西林金黄色葡萄球菌(MRSA)的抗菌活性。使用棋盘试验对 fremontone()和甲氧西林进行联合研究表明,甲氧西林的 MIC 降低了 8 倍,与万古霉素对 MRSA ATCC 1708 具有相加作用。化合物和对氯喹敏感(D6)和-耐药(W2)株的疟原虫也表现出中度抗疟活性,对哺乳动物 Vero 细胞没有细胞毒性。