2. Academic Validation
  3. The cytotoxic and tyrosine kinase inhibitory properties of C21 steroids and iridoids from the tubers of Alocasia cucullata

The cytotoxic and tyrosine kinase inhibitory properties of C21 steroids and iridoids from the tubers of Alocasia cucullata

  • J Nat Med. 2016 Jul;70(3):602-9. doi: 10.1007/s11418-016-0982-4.
Wei Peng 1 2,  Shuang Liang 3,  JiaLiang Hu 3,  ZhiYu Chen 1 2,  Xiangwei Zheng 4
Affiliations

Affiliations

  • 1 Department of Medical Oncology, Fudan University Shanghai Cancer Center, Fudan University, Shanghai, People's Republic of China.
  • 2 Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, People's Republic of China.
  • 3 Engineering Research Center of Modern Preparation Technology of TCM, Ministry of Education, Shanghai University of Traditional Chinese Medicine, Room 1107, No. 1200 Cai Lun Road, Pudong District, Shanghai, People's Republic of China.
  • 4 Engineering Research Center of Modern Preparation Technology of TCM, Ministry of Education, Shanghai University of Traditional Chinese Medicine, Room 1107, No. 1200 Cai Lun Road, Pudong District, Shanghai, People's Republic of China. zhengxwsh@hotmail.com.
PMID: 27120176 DOI: 10.1007/s11418-016-0982-4
Abstract

Ten Steroids and Iridoids were isolated from the tubers of Alocasia cucullata (Lour.) G. Don. Among them, alocasgenin A (1) and alocasgenoside B-C (2-3) were new compounds and the aglycone of compound 1, obtained from the acid hydrolysis of 1, was named alocasgenol (1a). Also, for the first time, tenacigenin B (4), 17β-tenacigenin-B (5), 3-O-6-deoxy-3-O-methyl-β-D-allopyranosyl-(1→4)-β-D-oleandropyranosyl-tenacigenin C (6), marsdenoside A-B (7-8) and tenacigenoside A-B (9-10) were isolated from the genus Alocasia. The chemical structures were elucidated by the extensive analysis of spectral data and compared with the literature. By evaluation of the cytotoxic and tyrosine kinase inhibition, compounds 1-10, 1a and compound 2 showed significant growth inhibition against two tumour cell lines, MGC-803 and HT-29, while compounds 1, 1a, 3, 6 and 8 presented moderate inhibition. Furthermore, compound 2 had the inhibitory property against the Enzyme activity biochemically.

Keywords

Alocasia cucullata; Cytotoxicity; Steroid; Terpene; Tyrosine kinase.

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