A new ß- carboline-type alkaloid from the flowers of Calotropis gigantea ( L.) WTAiton

被引:1
|
作者
Dang, Phu H. H. [1 ,2 ,3 ]
Tran, Tu H. H. [1 ,2 ,3 ]
Le, Tho H. H. [1 ,2 ,3 ]
Do, Truong N. V. [1 ,2 ,3 ]
Nguyen, Hai X. X. [1 ,2 ,3 ]
Nguyen, Mai T. T. [1 ,2 ,3 ]
Nguyen, Nhan T. T. [1 ,2 ,3 ]
机构
[1] Univ Sci, Fac Chem, Ho Chi Minh City, Vietnam
[2] Vietnam Natl Univ, Ho Chi Minh City, Vietnam
[3] Univ Sci, Res Lab Drug Discovery & Dev, Ho Chi Minh City, Vietnam
关键词
Calotropis gigantea (L.); WTAiton; Apocynaceae; beta-carboline-type alkaloid; DPPH assay; biosynthetic pathway; ANTIOXIDANT ACTIVITY; OXIDATIVE STRESS; NATURAL-PRODUCTS; PHARMACOLOGY;
D O I
10.1080/14786419.2023.2208259
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
In our antioxidant screening of some Vietnamese plant extracts, the CHCl3-soluble fraction from Calotropis gigantea (L.) W.T.Aiton flowers showed moderate DPPH free radical scavenging activity with an IC50 value of 55.8 mu g/mL. Thus, a further phytochemical study was carried out to obtain five alkaloids, including a new ss-carboline-type alkaloid, caloside H (1). These known compounds were identified as 5-hydroxy-( 2-methoxymethyl)pyridine (2), nicotinic acid (3), p-(acetylamino)phenol (4), and thymine (5). These structures were determined based on the NMR spectroscopic analysis. In antioxidant assay, caloside H at concentration of 100 mu M showed DPPH radical scavenging capacity with a percentage of inhibition of 40.2%. In addition, a plausible biosynthetic pathway for the formation of caloside H was proposed based on the Schiff base formation and Mannich-like reaction.
引用
收藏
页码:3004 / 3012
页数:9
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