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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Taylor and Francis Ltd.
2024
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2-s2.0-85191227422 Abang Heilman D.N.A.; Zamakshshari N.H.; Yi Mian V.J.; Chee Hui A.Y.; Lizazman M.A.; Ahmad F.B. Soulaxanthone, a new xanthone derivative from Calophyllum soulattri 2024 Natural Product Research 10.1080/14786419.2024.2345752 https://www.scopus.com/inward/record.uri?eid=2-s2.0-85191227422&doi=10.1080%2f14786419.2024.2345752&partnerID=40&md5=1ffff8828c2a20cc5e19e0c9607bcadf 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 µg/mL. Hexane (non-polar) extract from both plants exhibited moderate activity against Enterobacter cloacae (MIC = 250 µg/mL). Calopolyanolide E (3) and friedelin (5) showed bactericidal activity against Enterobacter cloacae (MBC = 50 µg/mL), thus the compounds have the potential to serve as a new lead for developing effective antibacterial medication. © 2024 Informa UK Limited, trading as Taylor & Francis Group. Taylor and Francis Ltd. 14786419 English Article |
author |
Abang Heilman D.N.A.; Zamakshshari N.H.; Yi Mian V.J.; Chee Hui A.Y.; Lizazman M.A.; Ahmad F.B. |
spellingShingle |
Abang Heilman D.N.A.; Zamakshshari N.H.; Yi Mian V.J.; Chee Hui A.Y.; Lizazman M.A.; Ahmad F.B. Soulaxanthone, a new xanthone derivative from Calophyllum soulattri |
author_facet |
Abang Heilman D.N.A.; Zamakshshari N.H.; Yi Mian V.J.; Chee Hui A.Y.; Lizazman M.A.; Ahmad F.B. |
author_sort |
Abang Heilman D.N.A.; Zamakshshari N.H.; Yi Mian V.J.; Chee Hui A.Y.; Lizazman M.A.; Ahmad F.B. |
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 |
publishDate |
2024 |
container_title |
Natural Product Research |
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container_issue |
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doi_str_mv |
10.1080/14786419.2024.2345752 |
url |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85191227422&doi=10.1080%2f14786419.2024.2345752&partnerID=40&md5=1ffff8828c2a20cc5e19e0c9607bcadf |
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 µg/mL. Hexane (non-polar) extract from both plants exhibited moderate activity against Enterobacter cloacae (MIC = 250 µg/mL). Calopolyanolide E (3) and friedelin (5) showed bactericidal activity against Enterobacter cloacae (MBC = 50 µg/mL), thus the compounds have the potential to serve as a new lead for developing effective antibacterial medication. © 2024 Informa UK Limited, trading as Taylor & Francis Group. |
publisher |
Taylor and Francis Ltd. |
issn |
14786419 |
language |
English |
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Article |
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scopus |
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Scopus |
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1818940557352763392 |