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Three new chromanes and one new flavone C-glycoside from Mallotus apelta
被引:4
|作者:
Nguyen Hoang Anh
[1
,2
]
Duong Thi Hai Yen
[3
]
Nguyen The Cuong
[4
]
Bui Huu Tai
[1
,3
]
Pham Hai Yen
[1
]
Pham The Chinh
[2
]
Pham Van Cuong
[3
]
Nguyen Hoai Nam
[3
]
Phan Van Kiem
[1
,3
]
Su-Hyeon Cho
[5
]
Park, SeonJu
[5
]
Nguyen Xuan Nhiem
[1
,3
]
机构:
[1] Vietnam Acad Sci & Technol VAST, Grad Univ Sci & Technol, Hanoi 10072, Vietnam
[2] Thai Nguyen Univ Sci, Fac Chem, Thai Nguyen 24118, Vietnam
[3] VAST, Inst Marine Biochem, 18 Hoang Quoc Viet, Hanoi 10072, Vietnam
[4] VAST, Inst Ecol & Biol Resources, Hanoi 10072, Vietnam
[5] Korea Basic Sci Inst, Chuncheon Ctr, 1 Kangwondaehak Gil, Chuncheon Si 24341, Gangwon Do, South Korea
关键词:
Mallotus apelta;
Euphorbiaceae;
chromane;
flavone C-glycoside;
malloapelta;
malloflavoside;
D O I:
10.1080/10286020.2022.2051494
中图分类号:
Q94 [植物学];
学科分类号:
071001 ;
摘要:
Three new chromanes, malloapeltas J-L (1-3), and one new flavone C-glycoside, malloflavoside (4), together with four known compounds, apigenin 6-C-beta-D-xylopyranosyl-8-C-alpha-L-arabinopyranoside (5), apigenin 6-C-beta-D-glucopyranosyl-8-C-alpha-L-arabinopyranoside (6), apigenin 7-O-beta-D-apiofuranosyl-(1 -> 2)-beta-D-glucopyranoside (7), and acantrifoside E (8) were isolated from the methanol extract of the leaves of Mallotus apelta. Their chemical structures were determined using spectroscopic methods, including 1D, 2D NMR, and HR-ESI-MS methods. All the isolated compounds were evaluated their cytotoxic activity against human prostate cancer (PC-3) and human breast cancer (MCF-7) cells, but none of them showed cytotoxicities on both human cancer cell lines.
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页码:18 / 26
页数:9
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