Phytochemicals from the Stem Bark of Calophyllum havilandii P. F. Stevens and their Biological Activities
The genus Calophyllum from the family Calophyllaceae has been extensively investigated in the past due to its rich source of bioactive phenolics such as coumarins, chromanones, and xanthones. In this study, phytochemical investigation on the stem bark of Calophyllum havilandii has afforded a new 4-p...
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John Wiley and Sons Inc
2024
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2-s2.0-85184738971 Zailan A.A.D.; Karunakaran T.; Santhanam R.; Suriaty Yaakop A.; Mohan S.; Abu Bakar M.H.; Jong Yi Mian V. Phytochemicals from the Stem Bark of Calophyllum havilandii P. F. Stevens and their Biological Activities 2024 Chemistry and Biodiversity 21 3 10.1002/cbdv.202301936 https://www.scopus.com/inward/record.uri?eid=2-s2.0-85184738971&doi=10.1002%2fcbdv.202301936&partnerID=40&md5=b6ab433fbc783c4ffb144d4838905bc4 The genus Calophyllum from the family Calophyllaceae has been extensively investigated in the past due to its rich source of bioactive phenolics such as coumarins, chromanones, and xanthones. In this study, phytochemical investigation on the stem bark of Calophyllum havilandii has afforded a new 4-propyldihydrocoumarin derivative, havilarin (1) together with calolongic acid (2), caloteysmannic acid (3), isocalolongic acid (4), euxanthone (5), and β-sitosterol (6). The chemical structure of compound 1 was elucidated and established based on detailed spectroscopic techniques, including MS, IR, UV, 1D and 2D NMR. The results of anti-bacillus study indicated that the chloroform extract showed promising activities with MIC value ranging between 0.5 to 1 μg/mL on selected bacillus strains. Besides, the plant extracts and compounds 1–4 were assessed for their cytotoxicity potential on HL-7702 cell line. All the tested plant extracts and respective chemical constituents displayed non-cytotoxic activity on HL-7702 cell line. © 2024 Wiley-VHCA AG, Zurich, Switzerland. John Wiley and Sons Inc 16121872 English Article |
author |
Zailan A.A.D.; Karunakaran T.; Santhanam R.; Suriaty Yaakop A.; Mohan S.; Abu Bakar M.H.; Jong Yi Mian V. |
spellingShingle |
Zailan A.A.D.; Karunakaran T.; Santhanam R.; Suriaty Yaakop A.; Mohan S.; Abu Bakar M.H.; Jong Yi Mian V. Phytochemicals from the Stem Bark of Calophyllum havilandii P. F. Stevens and their Biological Activities |
author_facet |
Zailan A.A.D.; Karunakaran T.; Santhanam R.; Suriaty Yaakop A.; Mohan S.; Abu Bakar M.H.; Jong Yi Mian V. |
author_sort |
Zailan A.A.D.; Karunakaran T.; Santhanam R.; Suriaty Yaakop A.; Mohan S.; Abu Bakar M.H.; Jong Yi Mian V. |
title |
Phytochemicals from the Stem Bark of Calophyllum havilandii P. F. Stevens and their Biological Activities |
title_short |
Phytochemicals from the Stem Bark of Calophyllum havilandii P. F. Stevens and their Biological Activities |
title_full |
Phytochemicals from the Stem Bark of Calophyllum havilandii P. F. Stevens and their Biological Activities |
title_fullStr |
Phytochemicals from the Stem Bark of Calophyllum havilandii P. F. Stevens and their Biological Activities |
title_full_unstemmed |
Phytochemicals from the Stem Bark of Calophyllum havilandii P. F. Stevens and their Biological Activities |
title_sort |
Phytochemicals from the Stem Bark of Calophyllum havilandii P. F. Stevens and their Biological Activities |
publishDate |
2024 |
container_title |
Chemistry and Biodiversity |
container_volume |
21 |
container_issue |
3 |
doi_str_mv |
10.1002/cbdv.202301936 |
url |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85184738971&doi=10.1002%2fcbdv.202301936&partnerID=40&md5=b6ab433fbc783c4ffb144d4838905bc4 |
description |
The genus Calophyllum from the family Calophyllaceae has been extensively investigated in the past due to its rich source of bioactive phenolics such as coumarins, chromanones, and xanthones. In this study, phytochemical investigation on the stem bark of Calophyllum havilandii has afforded a new 4-propyldihydrocoumarin derivative, havilarin (1) together with calolongic acid (2), caloteysmannic acid (3), isocalolongic acid (4), euxanthone (5), and β-sitosterol (6). The chemical structure of compound 1 was elucidated and established based on detailed spectroscopic techniques, including MS, IR, UV, 1D and 2D NMR. The results of anti-bacillus study indicated that the chloroform extract showed promising activities with MIC value ranging between 0.5 to 1 μg/mL on selected bacillus strains. Besides, the plant extracts and compounds 1–4 were assessed for their cytotoxicity potential on HL-7702 cell line. All the tested plant extracts and respective chemical constituents displayed non-cytotoxic activity on HL-7702 cell line. © 2024 Wiley-VHCA AG, Zurich, Switzerland. |
publisher |
John Wiley and Sons Inc |
issn |
16121872 |
language |
English |
format |
Article |
accesstype |
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record_format |
scopus |
collection |
Scopus |
_version_ |
1814778500000776192 |