Natural products and chemotaxonomic studies from the twigs of Neobalanocarpus heimii (King) P.S. Ashton (Dipterocarpaceae, Malvales)
Neobalanocarpus heimii is one of the toughest timbers in the world and resistant to termites and fungi. Phytochemical investigation from the twigs of N. heimii led to the isolation of eight resveratrol oligomers namely trans-resveratrol (1), (−)-ε-viniferin (2), balanocarpol (3), ampelopsin A (4), (...
| Published in: | Biochemical Systematics and Ecology |
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| Format: | Article |
| Language: | English |
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Elsevier Ltd
2024
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| Online Access: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85205467236&doi=10.1016%2fj.bse.2024.104906&partnerID=40&md5=16aef2d2fa28e30bd74168b813d064e6 |
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2-s2.0-85205467236 Zakaria N.S.; Ab'lah N.; Kamarozaman A.S.; Azmin N.F.N.; Azman F.A.I.; Mohamad Yusof M.I.; Saidin S.; Ahmat N. Natural products and chemotaxonomic studies from the twigs of Neobalanocarpus heimii (King) P.S. Ashton (Dipterocarpaceae, Malvales) 2024 Biochemical Systematics and Ecology 117 10.1016/j.bse.2024.104906 https://www.scopus.com/inward/record.uri?eid=2-s2.0-85205467236&doi=10.1016%2fj.bse.2024.104906&partnerID=40&md5=16aef2d2fa28e30bd74168b813d064e6 Neobalanocarpus heimii is one of the toughest timbers in the world and resistant to termites and fungi. Phytochemical investigation from the twigs of N. heimii led to the isolation of eight resveratrol oligomers namely trans-resveratrol (1), (−)-ε-viniferin (2), balanocarpol (3), ampelopsin A (4), (+)-α-viniferin (5), vaticanol A (6), vaticanol B (7) and hopeaphenol (8). The structures of the isolated compounds were successfully elucidated using various spectroscopic techniques as well as comparison with the literature data. The chemotaxonomic significance of the isolated compounds was summarized, along with a compound-genus network analysis. © 2024 Elsevier Ltd Elsevier Ltd 03051978 English Article |
| author |
Zakaria N.S.; Ab'lah N.; Kamarozaman A.S.; Azmin N.F.N.; Azman F.A.I.; Mohamad Yusof M.I.; Saidin S.; Ahmat N. |
| spellingShingle |
Zakaria N.S.; Ab'lah N.; Kamarozaman A.S.; Azmin N.F.N.; Azman F.A.I.; Mohamad Yusof M.I.; Saidin S.; Ahmat N. Natural products and chemotaxonomic studies from the twigs of Neobalanocarpus heimii (King) P.S. Ashton (Dipterocarpaceae, Malvales) |
| author_facet |
Zakaria N.S.; Ab'lah N.; Kamarozaman A.S.; Azmin N.F.N.; Azman F.A.I.; Mohamad Yusof M.I.; Saidin S.; Ahmat N. |
| author_sort |
Zakaria N.S.; Ab'lah N.; Kamarozaman A.S.; Azmin N.F.N.; Azman F.A.I.; Mohamad Yusof M.I.; Saidin S.; Ahmat N. |
| title |
Natural products and chemotaxonomic studies from the twigs of Neobalanocarpus heimii (King) P.S. Ashton (Dipterocarpaceae, Malvales) |
| title_short |
Natural products and chemotaxonomic studies from the twigs of Neobalanocarpus heimii (King) P.S. Ashton (Dipterocarpaceae, Malvales) |
| title_full |
Natural products and chemotaxonomic studies from the twigs of Neobalanocarpus heimii (King) P.S. Ashton (Dipterocarpaceae, Malvales) |
| title_fullStr |
Natural products and chemotaxonomic studies from the twigs of Neobalanocarpus heimii (King) P.S. Ashton (Dipterocarpaceae, Malvales) |
| title_full_unstemmed |
Natural products and chemotaxonomic studies from the twigs of Neobalanocarpus heimii (King) P.S. Ashton (Dipterocarpaceae, Malvales) |
| title_sort |
Natural products and chemotaxonomic studies from the twigs of Neobalanocarpus heimii (King) P.S. Ashton (Dipterocarpaceae, Malvales) |
| publishDate |
2024 |
| container_title |
Biochemical Systematics and Ecology |
| container_volume |
117 |
| container_issue |
|
| doi_str_mv |
10.1016/j.bse.2024.104906 |
| url |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85205467236&doi=10.1016%2fj.bse.2024.104906&partnerID=40&md5=16aef2d2fa28e30bd74168b813d064e6 |
| description |
Neobalanocarpus heimii is one of the toughest timbers in the world and resistant to termites and fungi. Phytochemical investigation from the twigs of N. heimii led to the isolation of eight resveratrol oligomers namely trans-resveratrol (1), (−)-ε-viniferin (2), balanocarpol (3), ampelopsin A (4), (+)-α-viniferin (5), vaticanol A (6), vaticanol B (7) and hopeaphenol (8). The structures of the isolated compounds were successfully elucidated using various spectroscopic techniques as well as comparison with the literature data. The chemotaxonomic significance of the isolated compounds was summarized, along with a compound-genus network analysis. © 2024 Elsevier Ltd |
| publisher |
Elsevier Ltd |
| issn |
03051978 |
| language |
English |
| format |
Article |
| accesstype |
|
| record_format |
scopus |
| collection |
Scopus |
| _version_ |
1814778496707198976 |