16:00 - 18:00
Room: San Francisco
Poster session
Bioactive chemical constituents isolated from the root of Neolitsea acuminatissima
Ko Horng-Huey 1, 2, Chang Chih-Chi 1, Lin Chu-Hung 2, 3, Kuo Yueh-Hsiung 4, 5, Chen Ih-Sheng 3, Chang Hsun-Shuo 2, 3
1 Department of Fragrance and Cosmetic Science, Kaohsiung Medical University, Kaohsiung, Taiwan
2 Research Center for Natural Products and Drug Development, Kaohsiung Medical University, Kaohsiung, Taiwan
3 School of Pharmacy, Kaohsiung Medical University, Kaohsiung, Taiwan
4 Department of Chinese Pharmaceutical Science and Chinese Medicine Resources, China Medical University, Taichung, Taiwan
5 Department of Biotechnology, Asia University, Taichung, Taiwan

Neolitsea acuminatisima (Hayata) Kanehira & Sasaki is genus of Neolistea (Lauraceae), an endemic species in Taiwan. In fact, the chemical constituents of the root of this plant have seldom been investigated previously. It is worth to verify the phytochemistry and secondary metabolites of the root of N. acuminatissima. One new carboline alkaloid, demethoxydaibucarboline A (1) and three new eudesmanolide type sesquiterpenes, methylneolitacumone A (2), neolitacumone E (3), and dineolitacumone C (4), along with twelve known compounds neolitacumones A-C (5-7), b-sitosterol (8), quercetin (9), dihydroquercetin (10), epicatechin (11), oplopanone (12), zeorin (13), linderaggrine A (14), clovane-2β,9α-diol (15), and stigmast-5-ene-3b-yl formate (16) were isolated from the dichloromethane and ethyl acetate-soluble layers of the root of N. acuminatissima. All compounds were obtained by column chromatography and their structures were spectroscopically determined by 1D, 2D NMR and MS. In this present study, the bioactivity of the isolates was also reported.


Reference:
Mo-Poster Session 1-PO-96:
Session:
Poster Session 1
Presenter/s:
Horng-Huey Ko
Presentation type:
Poster presentation
Room:
San Francisco
Date:
Monday, 4th September, 2017
Time:
16:00 - 18:00
Session times:
16:00 - 18:00