Rare Sesterterpenoids from the Soil Derived Fungus,  Aspergillus variecolor Strain SDG, Therapeutic Potential of Stellatic Acid and Docking Studies.

IF 2.3 3区 化学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Chemistry & Biodiversity Pub Date : 2024-11-08 DOI:10.1002/cbdv.202401951
Mangala Gowri Ponnapalli, Pranay Kumar Koochana, S Ch V Appa Rao Annam, Kavya Sunkara, Uma Rajeswari Batchu, Umme Ummarah Fariha, Sunil Misra
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Abstract

Ethyl acetate extract of the cultures of the soil-derived filamentous fungus, Aspergillus variecolor SDG strain from Nallamala forest resulted in the isolation of extremely rare sesterterpenoids, stellatic acid (1) and andilesin C (2). We report a thorough chemical characterization of these compounds using various spectroscopic techniques and evaluation of their in vitro preclinical therapeutic potential. Stellatic acid exhibits potent antioxidant activity with an IC50 of 38 µg/mL and significant anticancer activity against HeLa, HepG2, MCF7, and A549 cancer cell lines with an IC50 of 7-12 µM. On the other hand, andilesin C displayed moderate cytotoxicity against DU145 and B16F10 cancer cell lines but lacked antioxidant activity. Furthermore, the potential hypoglycemic property of stellatic acid was evaluated by measuring its inhibitory effect against α-glucosidase. It exhibited tenfold potency against yeast  α-glucosidase (IC50 101.73 µg/mL) than mammalian α-glucosidase (IC50 1000.00 µg/mL). Docking studies were also performed to suggest the interaction mode of stellatic acid in the α-glucosidase enzyme active site. Notably, yeast α-glucosidase shows a higher affinity towards stellatic acid than mammalian α-glucosidase (3TOP). Thus, the in vitro preclinical study of stellatic acid suggests its potential efficacy in therapeutic drug development.

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从土壤衍生真菌变色曲霉菌株 SDG 中提取的稀有酯类物质、Stellatic Acid 的治疗潜力和对接研究。
从纳拉马拉森林的土壤丝状真菌 Aspergillus variecolor SDG 菌株的培养物中提取乙酸乙酯后,分离出了极为罕见的酯萜类化合物--星状酸(1)和ilesin C(2)。我们利用各种光谱技术对这些化合物进行了全面的化学鉴定,并对其体外临床前治疗潜力进行了评估。石蒜酸具有很强的抗氧化活性,其 IC50 值为 38 µg/mL,对 HeLa、HepG2、MCF7 和 A549 癌细胞株具有显著的抗癌活性,其 IC50 值为 7-12 µM。另一方面,andilesin C 对 DU145 和 B16F10 癌细胞株显示出中等程度的细胞毒性,但缺乏抗氧化活性。此外,还通过测量黄腐酸对α-葡萄糖苷酶的抑制作用,评估了其潜在的降血糖特性。它对酵母α-葡萄糖苷酶的抑制作用(IC50 101.73 µg/mL)是哺乳动物α-葡萄糖苷酶(IC50 1000.00 µg/mL)的十倍。此外,还进行了对接研究,以揭示星盘酸在α-葡萄糖苷酶活性位点的相互作用模式。值得注意的是,酵母α-葡萄糖苷酶与星形酸的亲和力高于哺乳动物α-葡萄糖苷酶(3TOP)。因此,黄腐酸的体外临床前研究表明,它在治疗药物开发方面具有潜在的功效。
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来源期刊
Chemistry & Biodiversity
Chemistry & Biodiversity 环境科学-化学综合
CiteScore
3.40
自引率
10.30%
发文量
475
审稿时长
2.6 months
期刊介绍: Chemistry & Biodiversity serves as a high-quality publishing forum covering a wide range of biorelevant topics for a truly international audience. This journal publishes both field-specific and interdisciplinary contributions on all aspects of biologically relevant chemistry research in the form of full-length original papers, short communications, invited reviews, and commentaries. It covers all research fields straddling the border between the chemical and biological sciences, with the ultimate goal of broadening our understanding of how nature works at a molecular level. Since 2017, Chemistry & Biodiversity is published in an online-only format.
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