Soulaxanthone, a new xanthone derivative from Calophyllum soulattri
In search for new metabolites from the stem bark of Calophyllum soulattri and Calophyllum gracilentum, led to the isolation of a new xanthone, soulaxanthone (1), along with four other known metabolites, euxanthone (2), calopolyanolide E (3), calanolide E (4) and friedelin (5). The structures of thes...
Published in: | NATURAL PRODUCT RESEARCH |
---|---|
Main Authors: | , , , , , , |
Format: | Article; Early Access |
Language: | English |
Published: |
TAYLOR & FRANCIS LTD
2024
|
Subjects: | |
Online Access: | https://www-webofscience-com.uitm.idm.oclc.org/wos/woscc/full-record/WOS:001209228300001 |
author |
Heilman Dayang Nurul Anisa Abang; Zamakshshari Nor Hisam; Mian Vivien Jong Yi; Hui Audrey Yong Chee; Lizazman Mas Atikah; Ahmad Fasihuddin Badruddin |
---|---|
spellingShingle |
Heilman Dayang Nurul Anisa Abang; Zamakshshari Nor Hisam; Mian Vivien Jong Yi; Hui Audrey Yong Chee; Lizazman Mas Atikah; Ahmad Fasihuddin Badruddin Soulaxanthone, a new xanthone derivative from Calophyllum soulattri Chemistry; Pharmacology & Pharmacy |
author_facet |
Heilman Dayang Nurul Anisa Abang; Zamakshshari Nor Hisam; Mian Vivien Jong Yi; Hui Audrey Yong Chee; Lizazman Mas Atikah; Ahmad Fasihuddin Badruddin |
author_sort |
Heilman |
spelling |
Heilman, Dayang Nurul Anisa Abang; Zamakshshari, Nor Hisam; Mian, Vivien Jong Yi; Hui, Audrey Yong Chee; Lizazman, Mas Atikah; Ahmad, Fasihuddin Badruddin Soulaxanthone, a new xanthone derivative from Calophyllum soulattri NATURAL PRODUCT RESEARCH English Article; Early Access In search for new metabolites from the stem bark of Calophyllum soulattri and Calophyllum gracilentum, led to the isolation of a new xanthone, soulaxanthone (1), along with four other known metabolites, euxanthone (2), calopolyanolide E (3), calanolide E (4) and friedelin (5). The structures of these compounds were identified and elucidated using spectroscopic techniques such as 1H NMR,13C NMR, COSY, DEPT, HSQC, HMBC, MS and FTIR. The antibacterial activities of compounds 1-5, as well as the extracts, were tested against five bacterial strains. Soulaxanthone (1) exhibited moderate activity against Pseudomonas aeruginosa with an MIC value of 25 mu g/mL. Hexane (non-polar) extract from both plants exhibited moderate activity against Enterobacter cloacae (MIC = 250 mu g/mL). Calopolyanolide E (3) and friedelin (5) showed bactericidal activity against Enterobacter cloacae (MBC = 50 mu g/mL), thus the compounds have the potential to serve as a new lead for developing effective antibacterial medication. [GRAPHICS] . TAYLOR & FRANCIS LTD 1478-6419 1478-6427 2024 10.1080/14786419.2024.2345752 Chemistry; Pharmacology & Pharmacy WOS:001209228300001 https://www-webofscience-com.uitm.idm.oclc.org/wos/woscc/full-record/WOS:001209228300001 |
title |
Soulaxanthone, a new xanthone derivative from Calophyllum soulattri |
title_short |
Soulaxanthone, a new xanthone derivative from Calophyllum soulattri |
title_full |
Soulaxanthone, a new xanthone derivative from Calophyllum soulattri |
title_fullStr |
Soulaxanthone, a new xanthone derivative from Calophyllum soulattri |
title_full_unstemmed |
Soulaxanthone, a new xanthone derivative from Calophyllum soulattri |
title_sort |
Soulaxanthone, a new xanthone derivative from Calophyllum soulattri |
container_title |
NATURAL PRODUCT RESEARCH |
language |
English |
format |
Article; Early Access |
description |
In search for new metabolites from the stem bark of Calophyllum soulattri and Calophyllum gracilentum, led to the isolation of a new xanthone, soulaxanthone (1), along with four other known metabolites, euxanthone (2), calopolyanolide E (3), calanolide E (4) and friedelin (5). The structures of these compounds were identified and elucidated using spectroscopic techniques such as 1H NMR,13C NMR, COSY, DEPT, HSQC, HMBC, MS and FTIR. The antibacterial activities of compounds 1-5, as well as the extracts, were tested against five bacterial strains. Soulaxanthone (1) exhibited moderate activity against Pseudomonas aeruginosa with an MIC value of 25 mu g/mL. Hexane (non-polar) extract from both plants exhibited moderate activity against Enterobacter cloacae (MIC = 250 mu g/mL). Calopolyanolide E (3) and friedelin (5) showed bactericidal activity against Enterobacter cloacae (MBC = 50 mu g/mL), thus the compounds have the potential to serve as a new lead for developing effective antibacterial medication. [GRAPHICS] . |
publisher |
TAYLOR & FRANCIS LTD |
issn |
1478-6419 1478-6427 |
publishDate |
2024 |
container_volume |
|
container_issue |
|
doi_str_mv |
10.1080/14786419.2024.2345752 |
topic |
Chemistry; Pharmacology & Pharmacy |
topic_facet |
Chemistry; Pharmacology & Pharmacy |
accesstype |
|
id |
WOS:001209228300001 |
url |
https://www-webofscience-com.uitm.idm.oclc.org/wos/woscc/full-record/WOS:001209228300001 |
record_format |
wos |
collection |
Web of Science (WoS) |
_version_ |
1809679004855173120 |