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...

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Published in:NATURAL PRODUCT RESEARCH
Main Authors: Heilman, Dayang Nurul Anisa Abang; Zamakshshari, Nor Hisam; Mian, Vivien Jong Yi; Hui, Audrey Yong Chee; Lizazman, Mas Atikah; Ahmad, Fasihuddin Badruddin
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
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