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Novel lycorine derivatives as anticancer agents: synthesis and in vitro biological evaluation.
Wang, Peng; Yuan, Hui-Hui; Zhang, Xue; Li, Yun-Ping; Shang, Lu-Qing; Yin, Zheng.
Affiliation
  • Wang P; College of Pharmacy & State Key Laboratory of Elemento-Organic Chemistry, Nankai University, Tianjin 300071, China.
  • Yuan HH; College of Life Sciences, Nankai University, Tianjin 300071, China.
  • Zhang X; College of Pharmacy & State Key Laboratory of Elemento-Organic Chemistry, Nankai University, Tianjin 300071, China.
  • Li YP; College of Life Sciences, Nankai University, Tianjin 300071, China.
  • Shang LQ; College of Pharmacy & State Key Laboratory of Elemento-Organic Chemistry, Nankai University, Tianjin 300071, China. shanglq@nankai.edu.cn.
  • Yin Z; College of Pharmacy & State Key Laboratory of Elemento-Organic Chemistry, Nankai University, Tianjin 300071, China. zheng_yin@nankai.edu.cn.
Molecules ; 19(2): 2469-80, 2014 Feb 21.
Article in En | MEDLINE | ID: mdl-24566315
ABSTRACT
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.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Phenanthridines / Amaryllidaceae Alkaloids / Antineoplastic Agents Language: En Journal: Molecules Year: 2014 Type: Article Affiliation country: China

Full text: 1 Database: MEDLINE Main subject: Phenanthridines / Amaryllidaceae Alkaloids / Antineoplastic Agents Language: En Journal: Molecules Year: 2014 Type: Article Affiliation country: China