Department of Pharmacognosy, Faculty of Pharmacy, Ain-Shams University, Abbassia, Cairo 11566, Egypt.
Institute of Pharmaceutical Biology and Biotechnology, Heinrich Heine University, Universitätsstrasse 1, 40225 Düsseldorf, Germany.
Molecules. 2023 Nov 18;28(22):7650. doi: 10.3390/molecules28227650.
In this study, we report the isolation of two new meroterpenoids, miniolutelide D () and miniolutelide E (13--miniolutelide C) (), along with two meroterpenoidal analogues ( and ) and two phenolic compounds ( and ) from the endophytic fungus derived from fruits. Their structures were elucidated using extensive MS, 1D, and 2D NMR spectroscopic analyses as well as by comparing with data in the literature. The absolute configurations of and were determined using TDDFT-ECD calculations. Antimicrobial activity was evaluated. Compound displayed significant activity against methicillin-resistant strain ATCC 700699 and moderate activity against strain ATCC 29213.
在这项研究中,我们报告了两种新的倍半萜类化合物的分离,即 miniolutelide D () 和 miniolutelide E (13--miniolutelide C) (),以及两种倍半萜类似物 () 和 () 和两种酚类化合物 () 和 (),它们均来自于果实内生真菌 。通过与文献数据进行比较,采用 MS、1D 和 2D NMR 光谱分析等方法确定了它们的结构。通过 TDDFT-ECD 计算确定了 和 的绝对构型。对其进行了抗菌活性评价。化合物 对耐甲氧西林金黄色葡萄球菌 ATCC 700699 菌株表现出显著的活性,对 菌株 ATCC 29213 表现出中等活性。