Maydisens, Sesterterpenoids with Anti-MDR Activity from <i>Bipolaris maydis</i>

Fourteen previously undescribed sesterterpenoids (<b>1</b>-<b>14</b>) were isolated from <i>Bipolaris maydis</i>. Their structures with absolute configurations were elucidated by NMR, HRESIMS, DP4+ calculations, ECD calculations, single-crystal X-ray diffraction analyses, and the modified Mosher's method. Compounds <b>1</b>-<b>5</b> possess an uncommon 5/11 bicyclic ring system identified from <i>B. maydis</i> for the first time. Compounds <b>6</b>-<b>14</b> have a 5/8/5 tricyclic ring system, and these compounds both possess carbonyl groups in ring A. Compound <b>10</b> showed significant reversal of paclitaxel resistance in cancer cells.

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Publication Details

Journal
Journal of Natural Products
Published
2024-10-02
DOI
https://doi.org/10.1021/acs.jnatprod.4c00658
Citations
3
Primary Topic
Allelopathy and phytotoxic interactions
Type
article
Field-Weighted Citation Impact
1.80

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article

Maydisens, Sesterterpenoids with Anti-MDR Activity from Bipolaris maydis

Lianghu Gu, Yong Shen, Yonghui Zhang, Qin Li et al.
3 citations
Journal of Natural Products
Allelopathy and phytotoxic interactions
1.80
article

Maydisens, Sesterterpenoids with Anti-MDR Activity from Bipolaris maydis

Lianghu Gu, Yong Shen, Yonghui Zhang, Qin Li, Chunmei Chen, Nanjin Ding, Hucheng Zhu, Mengru Yu, Weiguang Sun
article en
3 citations

Abstract

Fourteen previously undescribed sesterterpenoids (<b>1</b>-<b>14</b>) were isolated from <i>Bipolaris maydis</i>. Their structures with absolute configurations were elucidated by NMR, HRESIMS, DP4+ calculations, ECD calculations, single-crystal X-ray diffraction analyses, and the modified Mosher's method. Compounds <b>1</b>-<b>5</b> possess an uncommon 5/11 bicyclic ring system identified from <i>B. maydis</i> for the first time. Compounds <b>6</b>-<b>14</b> have a 5/8/5 tricyclic ring system, and these compounds both possess carbonyl groups in ring A. Compound <b>10</b> showed significant reversal of paclitaxel resistance in cancer cells.

Journal of Natural ProductsVol. 87(10)
Huazhong University of Science and Technology (CN)
National Natural Science Foundation of China, Science and Technology Department of Hubei Province, National Key Research and Development Program of China
Zero hunger
Openalex Percentile: Top 13%
Allelopathy and phytotoxic interactions
1.80
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