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基于橡胶籽油构建作为α-葡萄糖苷酶抑制剂的橡胶籽油脂肪酸衍生物。

Construction of fatty acid derivatives from rubber seed oil as α-glucosidase inhibitors based on rubber seed oil.

作者信息

Liu Jiahao, Zhang Renwei, Nie Kaili, Liu Changsheng, Deng Li, Wang Fang

机构信息

Beijing Bioprocess Key Laboratory and State Key Laboratory of Chemical Resource Engineering, College of Life Science and Technology, Beijing University of Chemical Technology (BUCT), Beijing, 100029, People's Republic of China.

Sinovac Biotech Ltd, Beijing, China.

出版信息

Bioresour Bioprocess. 2022 Mar 21;9(1):23. doi: 10.1186/s40643-022-00492-9.

Abstract

Natural free fatty acids show inhibitory effects on α-glucosidase and can hence have potential applications in diabetes treatment. This study indicated that the inhibitory effect of fatty acids showed a significant negative correlation with affinity energy (- 0.87) and melting point (- 0.88). Guided by this relationship, two promotion strategies of hydration and esterification were put forward to increase the inhibitory effect of fatty acids on α-glucosidase. The hydration can import an extra hydroxy group into the C=C bond of fatty acids, that will enhance the interaction with α-glucosidase, while the esterification will lower the melting point of fatty acids, and promote the inhibitory effect. Hydroxy fatty acids and fatty acid isopropyl esters possessed higher inhibitory effects than the natural fatty acids. Then, rubber seed oil was modified into novel fatty acid derivatives with higher inhibitory effect on α-glucosidase. The inhibitory IC50 of hydroxy products and isopropanol esters was 0.42 ± 0.01 μM and 0.57 ± 0.01 μM, respectively. The result reveals a feasible route to construct fatty acid derivatives from natural oil with α-glucosidase inhibitory effect.

摘要

天然游离脂肪酸对α-葡萄糖苷酶具有抑制作用,因此在糖尿病治疗中具有潜在应用价值。本研究表明,脂肪酸的抑制作用与亲和能(-0.87)和熔点(-0.88)呈显著负相关。基于这种关系,提出了水合和酯化两种促进策略,以增强脂肪酸对α-葡萄糖苷酶的抑制作用。水合作用可在脂肪酸的C=C键中引入一个额外的羟基,这将增强与α-葡萄糖苷酶的相互作用,而酯化作用会降低脂肪酸的熔点,并促进抑制作用。羟基脂肪酸和脂肪酸异丙酯比天然脂肪酸具有更高的抑制作用。然后,将橡胶籽油改性为对α-葡萄糖苷酶具有更高抑制作用的新型脂肪酸衍生物。羟基产物和异丙醇酯的抑制IC50分别为0.42±0.01μM和0.57±0.01μM。该结果揭示了一条从天然油构建具有α-葡萄糖苷酶抑制作用的脂肪酸衍生物的可行途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acdd/10992144/a5093fdb6d0f/40643_2022_492_Fig1_HTML.jpg

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