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
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.
引用
收藏
页码:152 / 159
页数:8
相关论文
共 50 条
  • [1] IRIDOIDS FROM HEDYOTIS-DIFFUSA
    WU, HM
    TAO, XL
    CHEN, Q
    LAO, XF
    JOURNAL OF NATURAL PRODUCTS, 1991, 54 (01): : 254 - 256
  • [2] Biologically Active Iridoids from Hedyotis diffusa
    Ding, Bo
    Ma, Wei-Wei
    Dai, Yi
    Gao, Hao
    Yu, Yang
    Tao, Ye
    Zhong, Yi
    Yao, Xin-Sheng
    HELVETICA CHIMICA ACTA, 2010, 93 (12) : 2488 - 2494
  • [3] Iridoids from Hedyotis hedyotidea
    Peng, JN
    Feng, XZ
    Liang, XT
    PHYTOCHEMISTRY, 1998, 47 (08) : 1657 - 1659
  • [4] Four anthraquinones from Hedyotis diffusa
    Huang, Wei-Hua
    Yu, Shun-Hui
    Li, You-Bin
    Jiang, Jian-Qin
    JOURNAL OF ASIAN NATURAL PRODUCTS RESEARCH, 2008, 10 (09) : 887 - 889
  • [5] AN ANTHRAQUINONE FROM HEDYOTIS-DIFFUSA
    HO, TI
    CHEN, GP
    LIN, YC
    LIN, YM
    CHEN, FC
    PHYTOCHEMISTRY, 1986, 25 (08) : 1988 - 1989
  • [6] Neuroprotective constituents from Hedyotis diffusa
    Kim, Y
    Park, EJ
    Kim, J
    Kim, YB
    Kim, SR
    Kim, YC
    JOURNAL OF NATURAL PRODUCTS, 2001, 64 (01): : 75 - 78
  • [7] Two new iridoids from Hedyotis chrysotricha
    Peng, JN
    Feng, XZ
    Liang, XT
    JOURNAL OF NATURAL PRODUCTS, 1999, 62 (04): : 611 - 612
  • [8] The Antitumor Constituents from Hedyotis Diffusa Willd
    Wang, Changfu
    Zhou, Xuegang
    Wang, Youzhi
    Wei, Donghua
    Deng, Chengjie
    Xu, Xiaoyun
    Xin, Ping
    Sun, Shiqin
    MOLECULES, 2017, 22 (12):
  • [9] Two new anthraquinones from Hedyotis diffusa
    Huang, Wei-Hua
    Yu, Shun-Hui
    Li, You-Bin
    Jiang, Jian-Qin
    JOURNAL OF ASIAN NATURAL PRODUCTS RESEARCH, 2008, 10 (05) : 467 - 471
  • [10] NEW IRIDOIDS FROM OLDENLANDIA DIFFUSA ROXB
    HUANG, JT
    ARCHIV DER PHARMAZIE, 1981, 314 (10) : 831 - 836