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Secondary Metabolites from a Marine-Derived Endophytic Fungus Penicillium chrysogenum QEN-24S

机译:海洋来源的内生真菌Chensogenum QEN-24S的次生代谢产物

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摘要

Penicillium chrysogenum QEN-24S, an endophytic fungus isolated from an unidentified marine red algal species of the genus Laurencia, displayed inhibitory activity against the growth of pathogen Alternaria brassicae in dual culture test. Chemical investigation of this fungal strain resulted in the isolation of four new (1–3 and 5) and one known (4) secondary metabolites. Their structures were identified as two polyketide derivatives penicitides A and B (1 and 2), two glycerol derivatives 2-(2,4-dihydroxy-6-methylbenzoyl)-glycerol (3) and 1-(2,4-dihydroxy-6-methylbenzoyl)- glycerol (4), and one monoterpene derivative penicimonoterpene (5). Penicitides A and B (1 and 2) feature a unique 10-hydroxy- or 7,10-dihydroxy-5,7-dimethylundecyl moiety substituting at C-5 of the α-tetrahydropyrone ring, which is not reported previously among natural products. Compound 5 displayed potent activity against the pathogen A. brassicae, while compound 1 exhibited moderate cytotoxic activity against the human hepatocellular liver carcinoma cell line.
机译:产自青霉菌的青霉菌QEN-24S是从劳伦西亚属的一个未鉴定的海洋红藻物种中分离出来的一种内生真菌,在双重培养试验中显示出对病原体交链孢霉生长的抑制活性。对这种真菌菌株进行化学研究后,分离出了四个新的(1-3和5)和一个已知的(4)次级代谢产物。它们的结构被鉴定为两个聚酮化合物衍生物Penicitides A和B(1和2),两个甘油衍生物2-(2,4-dihydroxy-6-methylbenzoyl)-glycerol(3)和1-(2,4-dihydroxy-6 -甲基苯甲酰基)-甘油(4)和一种单萜衍生物青单萜(5)。除草剂A和B(1和2)具有一个独特的10-羟基或7,10-二羟基-5,7-二甲基十一烷基部分取代在α-四氢吡喃环的C-5处,这在天然产物中以前没有报道。化合物5显示出对病原芽孢杆菌的有效活性,而化合物1显示出对人肝细胞肝癌细胞系的中等细胞毒性活性。

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