New Flavonoids from the Leaves and Stems of Cinnamomum Reticulatum Hayate: Antioxidation and Antiproliferation Assay

Authors

  • Chi-Ming Liu Department of Nursing, Tzu Hui Institute of Technology, Pingtung County- 92641, Taiwan.
  • Hung-Chun Yeh Department of Nutrition and Health Sciences, School of Medical and Health Sciences, Fooyin University, Kaohsiung-83102, Taiwan.
  • Song-Chih Huang Department of Creative Product Design, College of Design, Ling Tung University, Taichung-40852, Taiwan.
  • Chung-Yi Chen Department of Nutrition and Health Sciences, School of Medical and Health Sciences, Fooyin University, Kaohsiung-83102, Taiwan.

DOI:

https://doi.org/10.9734/bpi/nacb/v2/18993D

Keywords:

Cinnamoum reticulatum Hayata, lauraceae, flavonoids, antioxidant

Abstract

The present study examined the anti-oxidation and anti-proliferation activity of the two new flavonoids compounds in cancer cells. Cinnamomum species have been used as important sources of traditional medicine, timber, edible fruits, spices, and perfumes in China for a long history. Cinnamoum reticulatum  Hayata (Lauraceae) is an indigenous tree species in Taiwan. We further isolated the two flavonoids compounds kaempferol-3-O-(2",4"-di-E-p-coumaroyl)-\(\alpha\)-L-rhamnopyranoside (1) and kaempferol-3-O-(3",4"-di-E-p-coumaroyl)-\(\alpha\)-L-rhamnopyranoside (2) from the leaves and stems of C. reticulatum Hayate. The phytochemical characteristics, antioxidant and cytotoxic activities of the two compounds were evaluated. Kaempferol-3-O-(2",4"-di-E-p-coumaroyl)-\(\alpha\)-L-rhamnopyranoside (1) and kaempferol-3-O-(3",4"-di-E-p-coumaroyl)-\(\alpha\)-L-rhamnopyranoside (2) have antiproliferation activity in lung cancer cell line (A549 and NCI-H460) and breast cancer cell line (MCF-7 and MDA-MB-231). However, (1) displays better antioxidant activity than (2). Our results showed that the two flavonoids from C. reticulatum might have good potential for further development as chemoprevention or antioxidant remedies. Flavonoids possess anti-oxidative effects as free radical scavengers and metal ion cheaters properties associated with the phenolic hydroxyl groups attached to ring structures. Intensity of the antioxidant activity of a flavonoid strongly depends on its chemical structure.

Published

2023-05-25

How to Cite

Chi-Ming Liu, Hung-Chun Yeh, Song-Chih Huang, & Chung-Yi Chen. (2023). New Flavonoids from the Leaves and Stems of Cinnamomum Reticulatum Hayate: Antioxidation and Antiproliferation Assay. Novel Aspects on Chemistry and Biochemistry Vol. 2, 108–116. https://doi.org/10.9734/bpi/nacb/v2/18993D