New and cytotoxic components from Antrodia Camphorata
Journal
Molecules
Journal Volume
19
Journal Issue
12
Pages
21378 - 21385
Date Issued
2014
Author(s)
Chen, Chien-Chih
Chen, Jih-Jung
Liao, Hui-Fen
Chang, Hsun-Shuo
Sung, Ping-Jyun
Tseng, Mei-Hwei
Wang, Sheng-Yang
Ko, Horng-Huey
Kuo, Yueh-Hsiung
Abstract
The solid-state cultured products of Antrodia camphorata as health foods has been blooming for the past few decades in Taiwan. In continuing our studies on the chemical constituents of the solid-state cultured products of this fungus, 6-methoxy-4-methyl-2,3-(methylenedioxy)phenol (1) and 4,4′-(ethane-1,2-diyl)bis(2,3,6-trimethoxyphenol)(2) together with 2,3,6-trimethoxy-4-methylphenol (3), 1(10→6)abeo-ergosta-5,7,9,22-tetraen-3α-ol (4), citreoanthrasteroid B (5) and dankasterones A (6) and B (7) were purified by a series of column chromatography. Their structures were elucidated by spectral data analysis. For bioactivity assay, compounds 4-7 showed significant cytotoxicity toward murine colorectal CT26 and human leukemia K562 cancer cell lines with IC50 values ranging from 6.7 to 15.3 μM and from 12.5 to 23.1 μM, respectively. ? 2014 by the authors; licensee MDPI, Basel, Switzerland.
Subjects
Abeo-ergostane; Antrodia camphorata; Cytotoxicity; Dihydrostilbene; Phenylmethanoid
SDGs
Other Subjects
antineoplastic agent; staurosporine; animal; Antrodia; chemistry; drug screening; human; IC50; isolation and purification; K562 cell line; mouse; Animals; Antineoplastic Agents; Antrodia; Drug Screening Assays, Antitumor; Humans; Inhibitory Concentration 50; K562 Cells; Mice; Staurosporine
Type
journal article