Bioactive Naphthoquinone and Phenazine Analogs from the Endophytic Streptomyces sp. PH9030 as α-Glucosidase Inhibitors

被引:0
|
作者
Ma, Qingxian [1 ]
Zhong, Yani [1 ]
Huang, Pingzhi [1 ]
Li, Aijie [1 ]
Jiang, Ting [2 ]
Jiang, Lin [3 ]
Yang, Hao [1 ]
Wang, Zhong [1 ]
Wu, Guangling [1 ]
Huang, Xueshuang [1 ]
Pu, Hong [1 ]
Liu, Jianxin [1 ]
机构
[1] Hunan Univ Med, Sch Pharmaceut Sci, Hunan Prov Key Lab Synthet Biol Tradit Chinese Med, China Pakistan Int Sci & Technol Innovat Cooperat, Huaihua 418000, Peoples R China
[2] Jiangxi Drug Inspect Ctr, Nanchang 330029, Peoples R China
[3] Hunan Univ Chinese Med, Hunan Engn Technol Res Ctr Bioact Subst Discovery, Sch Pharm, Changsha 410208, Peoples R China
来源
MOLECULES | 2024年 / 29卷 / 15期
基金
中国国家自然科学基金;
关键词
Kadsura coccinea; Streptomyces; naphthoquinone; phenazine; alpha-glucosidase inhibitor; PHENAZINE-1-CARBOXYLIC ACID; BIOSYNTHESIS; METABOLITES; MICROORGANISMS; FERMENTATION; ANTIBIOTICS; BACTERIUM; PRODUCTS;
D O I
10.3390/molecules29153450
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A talented endophytic Streptomyces sp. PH9030 is derived from the medicinal plant Kadsura coccinea (Lem.) A.C. Smith. The undescribed naphthoquinone naphthgeranine G (5) and seven previously identified compounds, 6-12, were obtained from Streptomyces sp. PH9030. The structure of 5 was identified by comprehensive examination of its HRESIMS, 1D NMR, 2D NMR and ECD data. The inhibitory activities of all the compounds toward alpha-glucosidase and their antibacterial properties were investigated. The alpha-glucosidase inhibitory activities of 5, 6, 7 and 9 were reported for the first time, with IC50 values ranging from 66.4 +/- 6.7 to 185.9 +/- 0.2 mu M, as compared with acarbose (IC50 = 671.5 +/- 0.2 mu M). The molecular docking and molecular dynamics analysis of 5 with alpha-glucosidase further indicated that it may have a good binding ability with alpha-glucosidase. Both 9 and 12 exhibited moderate antibacterial activity against methicillin-resistant Staphylococcus aureus, with minimum inhibitory concentration (MIC) values of 16 mu g/mL. These results indicate that 5, together with the naphthoquinone scaffold, has the potential to be further developed as a possible inhibitor of alpha-glucosidase.
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页数:14
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