Antifungal of modified neolignans from Mitrephora wangii Hu

© 2016, The Korean Society for Applied Biological Chemistry. Chromatographic separation of leaves and twigs from M. wangii had led to the isolation of conocarpan (1) and 3′-methoxyconocarpan (2). These structures were assigned on the basis of spectroscopic methods. Compound 1 was modified by organic...

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Main Authors:	Sanyacharernkul S., Nantapap S., Sangrueng K., Nuntasaen N., Pompimon W., Meepowpan P.
Format:	Journal
Published:	2017
Online Access:	https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84977566665&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/41858
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Institution:	Chiang Mai University

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spelling	th-cmuir.6653943832-418582017-09-28T04:23:47Z Antifungal of modified neolignans from Mitrephora wangii Hu Sanyacharernkul S. Nantapap S. Sangrueng K. Nuntasaen N. Pompimon W. Meepowpan P. © 2016, The Korean Society for Applied Biological Chemistry. Chromatographic separation of leaves and twigs from M. wangii had led to the isolation of conocarpan (1) and 3′-methoxyconocarpan (2). These structures were assigned on the basis of spectroscopic methods. Compound 1 was modified by organic reactions and the modified compound 5 exhibited potent antifungal, Pyricularia oryzae. The method used poisoned food technique with mycelial growth inhibition for 14 days, 57 % (100 ppm). Compound 5 was stronger than mancozeb which the fungi toxicity drug used as a positive control. 2017-09-28T04:23:47Z 2017-09-28T04:23:47Z 2016-06-01 Journal 24680834 2-s2.0-84977566665 10.1007/s13765-016-0178-3 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84977566665&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/41858
institution	Chiang Mai University
building	Chiang Mai University Library
country	Thailand
collection	CMU Intellectual Repository
description	© 2016, The Korean Society for Applied Biological Chemistry. Chromatographic separation of leaves and twigs from M. wangii had led to the isolation of conocarpan (1) and 3′-methoxyconocarpan (2). These structures were assigned on the basis of spectroscopic methods. Compound 1 was modified by organic reactions and the modified compound 5 exhibited potent antifungal, Pyricularia oryzae. The method used poisoned food technique with mycelial growth inhibition for 14 days, 57 % (100 ppm). Compound 5 was stronger than mancozeb which the fungi toxicity drug used as a positive control.
format	Journal
author	Sanyacharernkul S. Nantapap S. Sangrueng K. Nuntasaen N. Pompimon W. Meepowpan P.
spellingShingle	Sanyacharernkul S. Nantapap S. Sangrueng K. Nuntasaen N. Pompimon W. Meepowpan P. Antifungal of modified neolignans from Mitrephora wangii Hu
author_facet	Sanyacharernkul S. Nantapap S. Sangrueng K. Nuntasaen N. Pompimon W. Meepowpan P.
author_sort	Sanyacharernkul S.
title	Antifungal of modified neolignans from Mitrephora wangii Hu
title_short	Antifungal of modified neolignans from Mitrephora wangii Hu
title_full	Antifungal of modified neolignans from Mitrephora wangii Hu
title_fullStr	Antifungal of modified neolignans from Mitrephora wangii Hu
title_full_unstemmed	Antifungal of modified neolignans from Mitrephora wangii Hu
title_sort	antifungal of modified neolignans from mitrephora wangii hu
publishDate	2017
url	https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84977566665&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/41858
_version_	1681422080102367232

Antifungal of modified neolignans from Mitrephora wangii Hu

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