A new symmetrical tetramer oligostilbenoid containing tetrahydrofuran ring from the stem bark of Dryobalanops lanceolata

A new symmetrical tetramer oligostilbenoid containing tetrahydrofuran ring from the stem bark of Dryobalanops lanceolata

A new tetramer oligostilbenoid possessing tetrahydrofuran ring, malaysianol C (1), was isolated from the acetone extract of the stem bark of Dryobalanops lanceolata, together with four known oligostilbenoids nepalensinol E (2), ε-viniferin (3), laevifonol (4), and ampelopsin F (5). The structures of...

Full description

Bibliographic Details
Published in:Journal of Asian Natural Products Research
Main Author: Ahmat N.; Wibowo A.; Mohamad S.A.S.; Low A.L.M.; Sufian A.S.; Yusof M.I.M.; Latip J.
Format: Article
Language:English
Published: Taylor and Francis Ltd. 2014
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-84911952425&doi=10.1080%2f10286020.2014.938059&partnerID=40&md5=de138333635e5a17415554bfcd40fc67
id 2-s2.0-84911952425
spelling 2-s2.0-84911952425
Ahmat N.; Wibowo A.; Mohamad S.A.S.; Low A.L.M.; Sufian A.S.; Yusof M.I.M.; Latip J.
A new symmetrical tetramer oligostilbenoid containing tetrahydrofuran ring from the stem bark of Dryobalanops lanceolata
2014
Journal of Asian Natural Products Research
16
11
10.1080/10286020.2014.938059
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84911952425&doi=10.1080%2f10286020.2014.938059&partnerID=40&md5=de138333635e5a17415554bfcd40fc67
A new tetramer oligostilbenoid possessing tetrahydrofuran ring, malaysianol C (1), was isolated from the acetone extract of the stem bark of Dryobalanops lanceolata, together with four known oligostilbenoids nepalensinol E (2), ε-viniferin (3), laevifonol (4), and ampelopsin F (5). The structures of isolated compounds were elucidated on the basis of spectral evidence. The antibacterial activity of the isolated compounds was evaluated using resazurin microtitre-plate assay, whereas the cytotoxic activity was tested using MTT assay. The plausible biogenetic routes of the isolated compounds are also discussed. © 2014 Taylor & Francis.
Taylor and Francis Ltd.
10286020
English
Article
author Ahmat N.; Wibowo A.; Mohamad S.A.S.; Low A.L.M.; Sufian A.S.; Yusof M.I.M.; Latip J.
spellingShingle Ahmat N.; Wibowo A.; Mohamad S.A.S.; Low A.L.M.; Sufian A.S.; Yusof M.I.M.; Latip J.
A new symmetrical tetramer oligostilbenoid containing tetrahydrofuran ring from the stem bark of Dryobalanops lanceolata
author_facet Ahmat N.; Wibowo A.; Mohamad S.A.S.; Low A.L.M.; Sufian A.S.; Yusof M.I.M.; Latip J.
author_sort Ahmat N.; Wibowo A.; Mohamad S.A.S.; Low A.L.M.; Sufian A.S.; Yusof M.I.M.; Latip J.
title A new symmetrical tetramer oligostilbenoid containing tetrahydrofuran ring from the stem bark of Dryobalanops lanceolata
title_short A new symmetrical tetramer oligostilbenoid containing tetrahydrofuran ring from the stem bark of Dryobalanops lanceolata
title_full A new symmetrical tetramer oligostilbenoid containing tetrahydrofuran ring from the stem bark of Dryobalanops lanceolata
title_fullStr A new symmetrical tetramer oligostilbenoid containing tetrahydrofuran ring from the stem bark of Dryobalanops lanceolata
title_full_unstemmed A new symmetrical tetramer oligostilbenoid containing tetrahydrofuran ring from the stem bark of Dryobalanops lanceolata
title_sort A new symmetrical tetramer oligostilbenoid containing tetrahydrofuran ring from the stem bark of Dryobalanops lanceolata
publishDate 2014
container_title Journal of Asian Natural Products Research
container_volume 16
container_issue 11
doi_str_mv 10.1080/10286020.2014.938059
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-84911952425&doi=10.1080%2f10286020.2014.938059&partnerID=40&md5=de138333635e5a17415554bfcd40fc67
description A new tetramer oligostilbenoid possessing tetrahydrofuran ring, malaysianol C (1), was isolated from the acetone extract of the stem bark of Dryobalanops lanceolata, together with four known oligostilbenoids nepalensinol E (2), ε-viniferin (3), laevifonol (4), and ampelopsin F (5). The structures of isolated compounds were elucidated on the basis of spectral evidence. The antibacterial activity of the isolated compounds was evaluated using resazurin microtitre-plate assay, whereas the cytotoxic activity was tested using MTT assay. The plausible biogenetic routes of the isolated compounds are also discussed. © 2014 Taylor & Francis.
publisher Taylor and Francis Ltd.
issn 10286020
language English
format Article
accesstype
record_format scopus
collection Scopus
_version_ 1809677911826890752

Similar Items