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.6653943832-451912018-01-24T06:06:37Z Isopimarane diterpenes and flavan derivatives from the twigs of Caesalpinia furfuracea Ittipon Siridechakorn Sarot Cheenpracha Thunwadee Ritthiwigrom Wong Phakhodee Suwanna Deachathai Theeraphan Machan Nirun Ruankeaw Surat Laphookhieo 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. 2018-01-24T06:06:37Z 2018-01-24T06:06:37Z 2014-02-01 Journal 18767486 18743900 2-s2.0-84891603038 10.1016/j.phytol.2013.12.003 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84891603038&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/45191 |
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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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Journal |
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Ittipon Siridechakorn Sarot Cheenpracha Thunwadee Ritthiwigrom Wong Phakhodee Suwanna Deachathai Theeraphan Machan Nirun Ruankeaw Surat Laphookhieo |
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Ittipon Siridechakorn Sarot Cheenpracha Thunwadee Ritthiwigrom Wong Phakhodee Suwanna Deachathai Theeraphan Machan Nirun Ruankeaw Surat Laphookhieo Isopimarane diterpenes and flavan derivatives from the twigs of Caesalpinia furfuracea |
author_facet |
Ittipon Siridechakorn Sarot Cheenpracha Thunwadee Ritthiwigrom Wong Phakhodee Suwanna Deachathai Theeraphan Machan Nirun Ruankeaw Surat Laphookhieo |
author_sort |
Ittipon Siridechakorn |
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 |
2018 |
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https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84891603038&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/45191 |
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