Alstolarsines A–E, Indoline Alkaloids with Two Different Carbon Skeletons from <i>Alstonia scholaris</i>

Five complex indoline alkaloids, alstolarsines A-E (<b>1</b>-<b>5</b>) possessing two unprecedented carbon skeletons of 6/5/5/7/6/6(5) fused polycyclic systems, were isolated from <i>Alstonia scholaris</i>. Their structures were characterized using various methods including spectroscopic data, ECD spectra, and single-crystal X-ray diffraction. The inhibitory activities of alstolarsines A-D (<b>1</b>-<b>4</b>) on DRAK2 phosphorylation and ATP-citrate lyase were evaluated, but all of them were inactive.

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Publication Details

Journal
Journal of Natural Products
Published
2025-03-14
DOI
https://doi.org/10.1021/acs.jnatprod.5c00027
Citations
3
Primary Topic
Alkaloids: synthesis and pharmacology
Type
article
Field-Weighted Citation Impact
4.67

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article

Alstolarsines A–E, Indoline Alkaloids with Two Different Carbon Skeletons from Alstonia scholaris

Yao‐Yue Fan, Xu-Xin Zhu, Jian‐Min Yue, Cheng‐Yu Zheng et al.
3 citations
Journal of Natural Products
Alkaloids: synthesis and pharmacology
4.67
article

Alstolarsines A–E, Indoline Alkaloids with Two Different Carbon Skeletons from Alstonia scholaris

Yao‐Yue Fan, Xu-Xin Zhu, Jian‐Min Yue, Cheng‐Yu Zheng, Hongying Yang, Kun Gao
article en
3 citations

Abstract

Five complex indoline alkaloids, alstolarsines A-E (<b>1</b>-<b>5</b>) possessing two unprecedented carbon skeletons of 6/5/5/7/6/6(5) fused polycyclic systems, were isolated from <i>Alstonia scholaris</i>. Their structures were characterized using various methods including spectroscopic data, ECD spectra, and single-crystal X-ray diffraction. The inhibitory activities of alstolarsines A-D (<b>1</b>-<b>4</b>) on DRAK2 phosphorylation and ATP-citrate lyase were evaluated, but all of them were inactive.

Journal of Natural ProductsVol. 88(3)
Chinese Academy of Sciences (CN), Shanghai Institute of Materia Medica (CN), Lanzhou University (CN)
National Natural Science Foundation of China, Shanghai Rising-Star Program
Openalex Percentile: Top 7%
Alkaloids: synthesis and pharmacology
4.67
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