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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.
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页码:3004 / 3012
页数:9
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