Isopimarane diterpenes and flavan derivatives from the twigs of Caesalpinia furfuracea
The first phytochemical investigation of Caesalpinia furfuracea twigs led to the isolation and identification of four new compounds including two isopimarane diterpenes, caesalfurfuric acids A (1) and B (2), and two flavans, (2R)-caesalflavans A (5) and B (6), together with four known compounds, 4-e...
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th-cmuir.6653943832-72692014-08-30T03:51:46Z Isopimarane diterpenes and flavan derivatives from the twigs of Caesalpinia furfuracea Siridechakorn I. Cheenpracha S. Ritthiwigrom T. Phakhodee W. Deachathai S. Machan T. Ruankeaw N. Laphookhieo S. The first phytochemical investigation of Caesalpinia furfuracea twigs led to the isolation and identification of four new compounds including two isopimarane diterpenes, caesalfurfuric acids A (1) and B (2), and two flavans, (2R)-caesalflavans A (5) and B (6), together with four known compounds, 4-epi-isopimaric acid (3), methyl (E)-3-(3,4-dihydroxyphenyl)acrylate (4), (E)-resveratrol (7) and oxyresveratrol (8). Their structures were elucidated by intensive spectroscopic analysis. Compound 1 was found to exhibit antibacterial activity against MRSA SK1 with an MIC value of 16 μg/mL. © 2013 Phytochemical Society of Europe. Published by Elsevier B.V. All rights reserved. 2014-08-30T03:51:46Z 2014-08-30T03:51:46Z 2014 Article 18743900 10.1016/j.phytol.2013.12.003 PLHEB http://www.scopus.com/inward/record.url?eid=2-s2.0-84891603038&partnerID=40&md5=aa5576cb6b5b8bfa63723199c5cc1b53 http://cmuir.cmu.ac.th/handle/6653943832/7269 English |
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The first phytochemical investigation of Caesalpinia furfuracea twigs led to the isolation and identification of four new compounds including two isopimarane diterpenes, caesalfurfuric acids A (1) and B (2), and two flavans, (2R)-caesalflavans A (5) and B (6), together with four known compounds, 4-epi-isopimaric acid (3), methyl (E)-3-(3,4-dihydroxyphenyl)acrylate (4), (E)-resveratrol (7) and oxyresveratrol (8). Their structures were elucidated by intensive spectroscopic analysis. Compound 1 was found to exhibit antibacterial activity against MRSA SK1 with an MIC value of 16 μg/mL. © 2013 Phytochemical Society of Europe. Published by Elsevier B.V. All rights reserved. |
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Article |
author |
Siridechakorn I. Cheenpracha S. Ritthiwigrom T. Phakhodee W. Deachathai S. Machan T. Ruankeaw N. Laphookhieo S. |
spellingShingle |
Siridechakorn I. Cheenpracha S. Ritthiwigrom T. Phakhodee W. Deachathai S. Machan T. Ruankeaw N. Laphookhieo S. Isopimarane diterpenes and flavan derivatives from the twigs of Caesalpinia furfuracea |
author_facet |
Siridechakorn I. Cheenpracha S. Ritthiwigrom T. Phakhodee W. Deachathai S. Machan T. Ruankeaw N. Laphookhieo S. |
author_sort |
Siridechakorn I. |
title |
Isopimarane diterpenes and flavan derivatives from the twigs of Caesalpinia furfuracea |
title_short |
Isopimarane diterpenes and flavan derivatives from the twigs of Caesalpinia furfuracea |
title_full |
Isopimarane diterpenes and flavan derivatives from the twigs of Caesalpinia furfuracea |
title_fullStr |
Isopimarane diterpenes and flavan derivatives from the twigs of Caesalpinia furfuracea |
title_full_unstemmed |
Isopimarane diterpenes and flavan derivatives from the twigs of Caesalpinia furfuracea |
title_sort |
isopimarane diterpenes and flavan derivatives from the twigs of caesalpinia furfuracea |
publishDate |
2014 |
url |
http://www.scopus.com/inward/record.url?eid=2-s2.0-84891603038&partnerID=40&md5=aa5576cb6b5b8bfa63723199c5cc1b53 http://cmuir.cmu.ac.th/handle/6653943832/7269 |
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1681420768820330496 |