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Penicillium sp. KHMM 中的多种聚酮化合物和生物碱:结构阐明、生物和分子对接研究。

Diverse polyketides and alkaloids from Penicillium sp. KHMM: structural elucidation, biological and molecular docking studies.

机构信息

Organic and Bioorganic Chemistry, Department of Chemistry, Bielefeld University, Universitätsstraße 25, D-33501 Bielefeld, Germany.

Chemistry Department, Faculty of Science, Al-Azhar University, Nasr City-Cairo 11884, Egypt.

出版信息

Z Naturforsch C J Biosci. 2019 May 27;74(5-6):131-137. doi: 10.1515/znc-2018-0145.

DOI:10.1515/znc-2018-0145
PMID:30645191
Abstract

As a continuation of our earlier research concerning the investigation of microbial bioactive secondary metabolites from the terrestrial Penicillium sp.KH Link 1809 isolate KHMM, the fungus was re-cultivated on a large scale to explore its bioactive compounds intensively. Fifteen compounds, including seven alkaloids (1-7), one sesquiterpene (8), an acetylenic system (9), two sterols, and sphengolipid, were identified. Their structures were established on the bases of extensive one- and two-dimensional nuclear magnetic resonance and mass measurements, and by comparison with literature data. The antimicrobial activity of the fungal extract and the corresponding compounds were studied using a panel of pathogenic microorganisms, and their in vitro cytotoxicity against the human cervix carcinoma cell line (KB-3-1) was reported as well. The molecular docking of the isolated compounds showed promising affinities for the alkaloidal compounds 4-6 towards α, β tubulins.

摘要

作为我们之前研究的延续,我们对陆地青霉 KH Link 1809 菌株 KHMM 的微生物生物活性次生代谢产物进行了研究,该真菌被大规模再培养,以深入探索其生物活性化合物。鉴定了 15 种化合物,包括 7 种生物碱(1-7)、1 种倍半萜(8)、1 个炔属系统(9)、2 种甾醇和 sphengolipid。根据广泛的一维和二维核磁共振和质谱测量,并与文献数据进行比较,确定了它们的结构。使用一系列致病菌研究了真菌提取物和相应化合物的抗菌活性,并报告了它们对人宫颈癌细胞系(KB-3-1)的体外细胞毒性。分离化合物的分子对接表明,生物碱化合物 4-6 对α,β微管蛋白具有良好的亲和力。

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