Hanultarin, a cytotoxic lignan as an inhibitor of actin cytoskeleton polymerization from the seeds of Trichosanthes kirilowii
- Authors
- Moon, Surk-Sik; Rahman, Aziz Abdur; Kim, Joo-Young; Kee, Sun-Ho
- Issue Date
- 1-8월-2008
- Publisher
- PERGAMON-ELSEVIER SCIENCE LTD
- Keywords
- Trichosanthes kirilowii; actin cytoskeleton; actin polymerization; hanultarin; secoisolariciresinol
- Citation
- BIOORGANIC & MEDICINAL CHEMISTRY, v.16, no.15, pp.7264 - 7269
- Indexed
- SCIE
SCOPUS
- Journal Title
- BIOORGANIC & MEDICINAL CHEMISTRY
- Volume
- 16
- Number
- 15
- Start Page
- 7264
- End Page
- 7269
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/122878
- DOI
- 10.1016/j.bmc.2008.06.032
- ISSN
- 0968-0896
- Abstract
- Bioactivity-directed fractionation of extracts from the seeds of Trichosanthes kirilowii led to the isolation of (-)-1-O-feruloylsecoisolariciresinol (2), named hanultarin, In addition, four known lignans were also isolated, including (-)-secoisolariciresinol (1), 1,4-O-diferuloylsecoisolariciresinol (3), (-)-pinoresinol (4), and 4-ketopinoresinol (5). Their structures were elucidated on the basis of spectroscopic data. Compounds 2 and 3 exhibited strong cytotoxic effects against human lung carcinoma A549 cells, melanoma SK-Mel-2 cells, and mouse skin melanoma B16F1 cells with IC50 ranges of 3 -13 mu g/mL. Compound 2 showed an inhibitory effect on the polymerization of the actin cytoskeleton in normal epidermal keratinocyte (HaCaT cells), suggesting unique biological properties of compound 2 compared to those of the other isolates. (C) 2008 Elsevier Ltd. All rights reserved.
- Files in This Item
- There are no files associated with this item.
- Appears in
Collections - Graduate School > Department of Biomedical Sciences > 1. Journal Articles
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.