Institute of Pharmaceutical Biology and Biotechnology, Heinrich-Heine-Universität, 40225 Düsseldorf, Germany; Department of Pharmacognosy, Faculty of Pharmacy, Ain Shams University, 11566 Cairo, Egypt.
Department of Pharmacognosy, Faculty of Pharmacy, Ain Shams University, 11566 Cairo, Egypt.
Fitoterapia. 2024 Dec;179:106254. doi: 10.1016/j.fitote.2024.106254. Epub 2024 Oct 11.
Chemical prospection for the mycelial extract of the fungus Acremonium sp. Strain MNA-F-1, derived from the inner tissue of anise roots (Pimpnella anisum L., family Apiaceae), led to the isolation and characterization of one previously undescribed natural product, acremochlorin S (1), together with five related derivatives (2-6) and an alkaloidal metabolite, ilicicolin H (7). Structure elucidation of the isolated compounds was determined through comprehensive 1D/2D NMR spectroscopic analyses and HR-ESI-MS measurements. The absolute configuration of acremochlorin S (1) was concluded based on the comparison of its experimental and calculated electronic circular dichroism (ECD) spectra implementing Time-dependent density functional theory (TDDFT). All isolated compounds were assessed for their antibacterial activity against Staphylococcus aureus, Escherichia coli and Mycobacterium tuberculosis, where several compounds revealed potent activities against tested Gram-positive strains.
从八角(Pimpnella anisum L.,伞形科)的内部组织中分离出来的真菌 Acrenonium sp. 菌株 MNA-F-1 的菌丝体提取物进行化学勘探,导致分离和鉴定了一种以前未描述的天然产物 acremochlorin S(1),以及五个相关的衍生物(2-6)和一种生物碱代谢物ilicicolin H(7)。通过综合的 1D/2D NMR 光谱分析和 HR-ESI-MS 测量确定了分离化合物的结构。根据实验和计算电子圆二色谱(ECD)光谱的比较,基于时间相关密度泛函理论(TDDFT),得出了 acremochlorin S(1)的绝对构型。所有分离的化合物都评估了它们对金黄色葡萄球菌、大肠杆菌和结核分枝杆菌的抗菌活性,其中几种化合物对测试的革兰氏阳性菌株显示出很强的活性。