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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Taylor and Francis Ltd.
2015
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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 |
collection |
Scopus |
_version_ |
1809678161613422592 |