A new chromanone acid from the stem bark of Calophyllum teysmannii

A new chromanone acid, namely caloteysmannic acid (1), along with three known compounds, calolongic acid (2), isocalolongic acid (3) and stigmasterol (4) were isolated from the stem bark of Calophyllum teysmannii. All these compounds were evaluated for their cytotoxic and antioxidant activities in t...

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Published in:Natural Product Research
Main Author: Lim C.K.; Subramaniam H.; Say Y.H.; Jong V.Y.M.; Khaledi H.; Chee C.F.
Format: Article
Language:English
Published: Taylor and Francis Ltd. 2015
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-84941599822&doi=10.1080%2f14786419.2015.1015020&partnerID=40&md5=61acff65e6bb83fd0166d9ef72677fd3
id 2-s2.0-84941599822
spelling 2-s2.0-84941599822
Lim C.K.; Subramaniam H.; Say Y.H.; Jong V.Y.M.; Khaledi H.; Chee C.F.
A new chromanone acid from the stem bark of Calophyllum teysmannii
2015
Natural Product Research
29
21
10.1080/14786419.2015.1015020
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84941599822&doi=10.1080%2f14786419.2015.1015020&partnerID=40&md5=61acff65e6bb83fd0166d9ef72677fd3
A new chromanone acid, namely caloteysmannic acid (1), along with three known compounds, calolongic acid (2), isocalolongic acid (3) and stigmasterol (4) were isolated from the stem bark of Calophyllum teysmannii. All these compounds were evaluated for their cytotoxic and antioxidant activities in the MTT and DPPH assays, respectively. The structure of compound 1 was determined by means of spectroscopic methods including 1D and 2D NMR experiments as well as HR-EIMS spectrometry. The stereochemical assignment of compound 1 was done based on the NMR results and X-ray crystallographic analysis. The preliminary assay results revealed that all the test compounds displayed potent inhibitory activity against HeLa cancer cell line, in particular with compound 1 which exhibited the highest cytotoxic activity comparable to the positive control used, cisplatin. However, no significant antioxidant activity was observed for all the test compounds in the DPPH radical scavenging capacity assay. © 2015 Taylor & Francis.
Taylor and Francis Ltd.
14786419
English
Article

author Lim C.K.; Subramaniam H.; Say Y.H.; Jong V.Y.M.; Khaledi H.; Chee C.F.
spellingShingle Lim C.K.; Subramaniam H.; Say Y.H.; Jong V.Y.M.; Khaledi H.; Chee C.F.
A new chromanone acid from the stem bark of Calophyllum teysmannii
author_facet Lim C.K.; Subramaniam H.; Say Y.H.; Jong V.Y.M.; Khaledi H.; Chee C.F.
author_sort Lim C.K.; Subramaniam H.; Say Y.H.; Jong V.Y.M.; Khaledi H.; Chee C.F.
title A new chromanone acid from the stem bark of Calophyllum teysmannii
title_short A new chromanone acid from the stem bark of Calophyllum teysmannii
title_full A new chromanone acid from the stem bark of Calophyllum teysmannii
title_fullStr A new chromanone acid from the stem bark of Calophyllum teysmannii
title_full_unstemmed A new chromanone acid from the stem bark of Calophyllum teysmannii
title_sort A new chromanone acid from the stem bark of Calophyllum teysmannii
publishDate 2015
container_title Natural Product Research
container_volume 29
container_issue 21
doi_str_mv 10.1080/14786419.2015.1015020
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-84941599822&doi=10.1080%2f14786419.2015.1015020&partnerID=40&md5=61acff65e6bb83fd0166d9ef72677fd3
description A new chromanone acid, namely caloteysmannic acid (1), along with three known compounds, calolongic acid (2), isocalolongic acid (3) and stigmasterol (4) were isolated from the stem bark of Calophyllum teysmannii. All these compounds were evaluated for their cytotoxic and antioxidant activities in the MTT and DPPH assays, respectively. The structure of compound 1 was determined by means of spectroscopic methods including 1D and 2D NMR experiments as well as HR-EIMS spectrometry. The stereochemical assignment of compound 1 was done based on the NMR results and X-ray crystallographic analysis. The preliminary assay results revealed that all the test compounds displayed potent inhibitory activity against HeLa cancer cell line, in particular with compound 1 which exhibited the highest cytotoxic activity comparable to the positive control used, cisplatin. However, no significant antioxidant activity was observed for all the test compounds in the DPPH radical scavenging capacity assay. © 2015 Taylor & Francis.
publisher Taylor and Francis Ltd.
issn 14786419
language English
format Article
accesstype
record_format scopus
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