金缕莲的植物成分研究-淀粉酶和-葡萄糖苷酶的降糖作用及分子对接研究。

IF 1.9 3区 化学 Q3 CHEMISTRY, APPLIED Natural Product Research Pub Date : 2024-12-01 Epub Date: 2023-11-27 DOI:10.1080/14786419.2023.2283759
Nurul Najihah Husna Tanazi, Ahmad Nazif Aziz, Mohamad Nurul Azmi, Mohamad Hafizi Abu Bakar, Muhamad Fairus Noor Hassim, Nurul Huda Abdul Wahab, Nurulfazlina Edayah Rasol, Nurunajah Ab Ghani, M Maulidiani, Khalijah Awang
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引用次数: 0

摘要

对金家花树皮进行了植物化学研究,得到了10个化合物,包括6个多酮类化合物,即金家花苷a1、金家花苷b2、金家花苷e3、金家花苷f4、金家花苷k5和金家花苷l6,以及3种内生酸;王元酸a7、参贝林b8和烯二花酸m9,以及一个倍半萜;daibuoxide 10。除大布肟外,其余化合物均为外消旋混合物。通过详细的光谱分析和比较文献数据分析阐明了它们的结构。这是关于倍半萜存在的第一份报告;大黄花属。体外酶法生物评价表明,4对α-淀粉酶和α-葡萄糖苷酶的抑制活性最好,IC50值分别为181.54±6.27µg/mL和237.87±0.07µg/mL。此外,分子对接分析证实了4所证实的α-淀粉酶和α-葡萄糖苷酶抑制活性。
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Phytoconstituents of Endiandra kingiana; antidiabetic effects and molecular docking studies on alpha-amylase and alpha-glucosidase.

Phytochemical investigation on the bark of E. kingiana plant afforded ten compounds, including six polyketides namely kingianin A 1, kingianin B 2, kingianin E 3, kingianin F 4, kingianin K 5 and kingianin L 6, three endiandric acids; kingianic acid A 7, tsangibeilin B 8 and endiandric acid M 9, and one sesquiterpene; daibuoxide 10. All compounds were separated as racemic mixture by recycling high-performance liquid chromatography (RHPLC), except for daibuoxide. Their structures were elucidated by detailed spectroscopic and comparative literature data analysis. This is the first report on the presence of the sesquiterpene; daibuoxide in Endiandra genus. In vitro enzymatic bio-evaluation of the isolated compounds against α-amylase and α-glucosidase showed that 4 demonstrated the best α-amylase and α-glucosidase inhibitory activity with IC50 values of 181.54 ± 6.27 µg/mL and 237.87 ± 0.07 µg/mL, respectively. In addition, molecular docking analysis confirmed the α-amylase and α-glucosidase inhibitory activities demonstrated by 4.

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来源期刊
Natural Product Research
Natural Product Research 化学-医药化学
CiteScore
5.10
自引率
9.10%
发文量
605
审稿时长
2.1 months
期刊介绍: The aim of Natural Product Research is to publish important contributions in the field of natural product chemistry. The journal covers all aspects of research in the chemistry and biochemistry of naturally occurring compounds. The communications include coverage of work on natural substances of land and sea and of plants, microbes and animals. Discussions of structure elucidation, synthesis and experimental biosynthesis of natural products as well as developments of methods in these areas are welcomed in the journal. Finally, research papers in fields on the chemistry-biology boundary, eg. fermentation chemistry, plant tissue culture investigations etc., are accepted into the journal. Natural Product Research issues will be subtitled either ""Part A - Synthesis and Structure"" or ""Part B - Bioactive Natural Products"". for details on this , see the forthcoming articles section. All manuscript submissions are subject to initial appraisal by the Editor, and, if found suitable for further consideration, to peer review by independent, anonymous expert referees. All peer review is single blind and submission is online via ScholarOne Manuscripts.
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