A New Benzophenone C-Glucoside and Other Constituents of Pseuduvaria fragrans and Their α-Glucosidase Inhibitory Activity

被引:17
|
作者
Panidthananon, Wongvarit [1 ]
Chaowasku, Tanawat [2 ,3 ]
Sritularak, Boonchoo [1 ]
Likhitwitayawuid, Kittisak [1 ]
机构
[1] Chulalongkorn Univ, Fac Pharmaceut Sci, Dept Pharmacognosy & Pharmaceut Bot, Bangkok 10330, Thailand
[2] Chiang Mai Univ, Fac Sci, Dept Biol, 239 Huay Kaew Rd, Chiang Mai 50200, Thailand
[3] Chiang Mai Univ, Ctr Excellence Bioresources Agr Ind & Med, Chiang Mai 50200, Thailand
来源
MOLECULES | 2018年 / 23卷 / 07期
关键词
benzophenone; glycoside; aporphine; azafluorenone; tyramine amide; alpha-glucosidase; uncompetitive inhibition; ALKALOIDS; AMIDES; INDOCHINENSIS; LEAVES; RUGOSA; STEMS; ACID;
D O I
10.3390/molecules23071600
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
Phytochemical investigations of the leaves and stems of Pseuduvaria fragrans led to the isolation of a new benzophenone C-glucoside named pseuduvarioside (1), together with six known compounds including (-)-guaiol (2), (+)-isocorydine (3), cyathocaline (4), isoursoline (5), N-trans-coumaroyltyramine (6), and N-trans-feruloyltyramine (7). Their structures were characterized by NMR spectroscopy and mass spectrometry. All of the isolates were evaluated for inhibitory activity against the enzyme alpha-glucosidase. N-trans-coumaroyltyramine and N-trans-feruloyltyramine showed higher activity than the drug acarbose. Kinetic studies revealed that both tyramine-derived amides were uncompetitive inhibitors of the enzyme.
引用
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页数:8
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