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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Main Authors: Ittipon Siridechakorn, Sarot Cheenpracha, Thunwadee Ritthiwigrom, Wong Phakhodee, Suwanna Deachathai, Theeraphan Machan, Nirun Ruankeaw, Surat Laphookhieo
Format: Journal
Published: 2018
Online Access: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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Institution: Chiang Mai University
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spelling 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
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
description 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.
format Journal
author Ittipon Siridechakorn
Sarot Cheenpracha
Thunwadee Ritthiwigrom
Wong Phakhodee
Suwanna Deachathai
Theeraphan Machan
Nirun Ruankeaw
Surat Laphookhieo
spellingShingle 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
url 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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