4.6 Article

Novel Lycorine Derivatives as Anticancer Agents: Synthesis and In Vitro Biological Evaluation

期刊

MOLECULES
卷 19, 期 2, 页码 2469-2480

出版社

MDPI AG
DOI: 10.3390/molecules19022469

关键词

lycorine derivatives; anticancer; synthesis

资金

  1. National Natural Science Foundation of China [21202087]
  2. National Basic Research Program of China (973 program) [2013CB911104]
  3. Fundamental Research Funds for the Central Universities [65124002]
  4. Higher Education Ministry of Education of China [20120031120049]
  5. Tianjin Science and Technology Program [13JCYBJC24300, 13JCQNJC13100]
  6. Scientific Research Starting Foundation of Returned Overseas Chinese Scholars, Ministry of Education of China
  7. Ministry of Education of China [B06005]

向作者/读者索取更多资源

Lycorine, which is the most abundant alkaloid isolated from the Amaryllidaceae family of plants, reportedly exhibits promising anticancer activities. Herein, a series of novel lycorine derivatives were synthesized and evaluated for their in vitro inhibitory activities against seven different cancer cell lines, including A549, HCT116, SK-OV-3, NCI-H460, K562, MCF-7 and HL-60. The results indicated that compounds bearing diverse amine substituents at the C-2 position demonstrated good anticancer activities. The selectivity towards different cancer cell lines of the synthesized derivatives is discussed.

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