New Antifungal Pyranoisoflavone from <em>Ficus tikoua </em>Bur.

Considering the undesirable attributes of synthetic fungicides and the availability of Ficus<em> </em>species in China, the stem of<em> Ficus tikoua </em>Bur. was investigated. One<strong> </strong>new antifungal pyr...

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Main Authors: Shaopeng Wei, Zhiqin Ji, Wenjun Wu
Format: Article
Language:English
Published: MDPI AG 2012-06-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:http://www.mdpi.com/1422-0067/13/6/7375
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spelling doaj-5f4b34596dbd4320bbbca5a8fab31f342020-11-25T00:20:32ZengMDPI AGInternational Journal of Molecular Sciences1422-00672012-06-011367375738210.3390/ijms13067375New Antifungal Pyranoisoflavone from <em>Ficus tikoua </em>Bur.Shaopeng WeiZhiqin JiWenjun WuConsidering the undesirable attributes of synthetic fungicides and the availability of Ficus<em> </em>species in China, the stem of<em> Ficus tikoua </em>Bur. was investigated. One<strong> </strong>new antifungal pyranoisoflavone, 5,3',4'-trihydroxy-2",2"-dimethylpyrano (5",6":7,8) isoflavone (<strong>1</strong>), together with two known isoflavones, wighteone (<strong>2</strong>) and lupiwighteone (<strong>3</strong>) (with previously reported antifungal activities), were isolated from ethyl acetate extract by bioassay-guided fractionation. Their structures were determined by spectroscopic analysis, such as NMR (<sup>1</sup>H-<sup>1</sup>H COSY, HMQC, HMBC and NOESY), IR, UV and HRMS, as well as ESI-MS<sup>n</sup> analyses. The antifungal activities of <strong>1</strong>–<strong>3</strong> against <em>Phytophthora infestans</em> were evaluated by direct spore germination assay, and the IC<sub>50</sub> values were 262.442, 198.153 and 90.365 µg·mL<sup>−1</sup>, respectively.http://www.mdpi.com/1422-0067/13/6/7375<em>Ficus tikoua </em>Bur.pyranoisoflavoneantifungal activity
collection DOAJ
language English
format Article
sources DOAJ
author Shaopeng Wei
Zhiqin Ji
Wenjun Wu
spellingShingle Shaopeng Wei
Zhiqin Ji
Wenjun Wu
New Antifungal Pyranoisoflavone from <em>Ficus tikoua </em>Bur.
International Journal of Molecular Sciences
<em>Ficus tikoua </em>Bur.
pyranoisoflavone
antifungal activity
author_facet Shaopeng Wei
Zhiqin Ji
Wenjun Wu
author_sort Shaopeng Wei
title New Antifungal Pyranoisoflavone from <em>Ficus tikoua </em>Bur.
title_short New Antifungal Pyranoisoflavone from <em>Ficus tikoua </em>Bur.
title_full New Antifungal Pyranoisoflavone from <em>Ficus tikoua </em>Bur.
title_fullStr New Antifungal Pyranoisoflavone from <em>Ficus tikoua </em>Bur.
title_full_unstemmed New Antifungal Pyranoisoflavone from <em>Ficus tikoua </em>Bur.
title_sort new antifungal pyranoisoflavone from <em>ficus tikoua </em>bur.
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1422-0067
publishDate 2012-06-01
description Considering the undesirable attributes of synthetic fungicides and the availability of Ficus<em> </em>species in China, the stem of<em> Ficus tikoua </em>Bur. was investigated. One<strong> </strong>new antifungal pyranoisoflavone, 5,3',4'-trihydroxy-2",2"-dimethylpyrano (5",6":7,8) isoflavone (<strong>1</strong>), together with two known isoflavones, wighteone (<strong>2</strong>) and lupiwighteone (<strong>3</strong>) (with previously reported antifungal activities), were isolated from ethyl acetate extract by bioassay-guided fractionation. Their structures were determined by spectroscopic analysis, such as NMR (<sup>1</sup>H-<sup>1</sup>H COSY, HMQC, HMBC and NOESY), IR, UV and HRMS, as well as ESI-MS<sup>n</sup> analyses. The antifungal activities of <strong>1</strong>–<strong>3</strong> against <em>Phytophthora infestans</em> were evaluated by direct spore germination assay, and the IC<sub>50</sub> values were 262.442, 198.153 and 90.365 µg·mL<sup>−1</sup>, respectively.
topic <em>Ficus tikoua </em>Bur.
pyranoisoflavone
antifungal activity
url http://www.mdpi.com/1422-0067/13/6/7375
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AT zhiqinji newantifungalpyranoisoflavonefromltemgtficustikoualtemgtbur
AT wenjunwu newantifungalpyranoisoflavonefromltemgtficustikoualtemgtbur
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