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Iridoids and sfingolipids from Hedyotis diffusa
被引:25
|作者:
Wang, Changfu
[1
]
Xin, Ping
[2
]
Wang, Youzhi
[2
]
Zhou, Xuegang
[2
]
Wei, Donghua
[2
]
Deng, Chengjie
[2
]
Sun, Shiqin
[2
]
机构:
[1] Guangdong Pharmaceut Univ, Coll TCM, 280 Outside Loop East Rd Higher Educ Mega Ctr, Guangzhou 510006, Guangdong, Peoples R China
[2] Harbin Med Univ Daqing, Coll Pharm, Daqing 163319, Heilongjiang, Peoples R China
来源:
关键词:
Hedyotis diffusa;
Cytotoxicity;
Iridoid glycosides;
Cerebrosides;
Ceramides;
CHEMICAL-CONSTITUENTS;
CANCER CELLS;
GLYCOSIDES;
WILLD;
CEREBROSIDES;
APOPTOSIS;
CHROMATOGRAPHY;
CYTOTOXICITY;
INHIBITION;
FLAVONOIDS;
D O I:
10.1016/j.fitote.2017.11.004
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
Seven new compounds were isolated from the aerial part of Hedyotis diffusa, including three iridoid glycosides, hedyoiridoidside A - C (1-3), two cerebrosides, hedyocerenoside F (4) and G (5), and two new ceramides, hedyoceramide A (6) and B (7). And six known iridoid glycosides (8-13) were also obtained. Their structures were established by their physico-chemical constants and spectroscopic analysis. The cytotoxicity of all compounds against tumor cell lines of human cervical cancer HeLa, human leukemia HL-60, human lung cancer A459, human hepatoma HepG2, human gastric gland carcinoma BCG-823, human nasopharyngeal cancer CNE-2, human colon cancer HCT15, and human prostate cancer PC-3 were also evaluated in vitro. As a result, new compound 1 exhibited evident cytotoxicity to all tumor cell lines, and the IC50 values are from 9.5 mu M to 28.2 mu M, while new compound 2 exhibited evident cytotoxicity to Hela, HL-60, A459, HepG2, BGC-823, CNE-2, and HCT15, and the IC50 values are from 15.8 mu M to 26.2 mu M. Known compound 11 also exhibited evident cytotoxicity to HL-60, A459, HepG2, BGC-823, CNE-2, and HCT15, and the IC50 values are from 16.5 mu M to 40.4 mu M. New compounds 4-7 and known compounds 12 and 13 showed moderate cytotoxicity to some tumor cell lines.
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页码:152 / 159
页数:8
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