Indopexines A and B: Two Prenylated Isoindoline Alkaloids from the Fungus <i>Aspergillus</i> sp. TJ507

Indopexines A (<b>1</b>) and B (<b>2</b>), two prenylated isoindoline alkaloids, were isolated from <i>Aspergillus</i> sp. TJ507. Their structures were determined by extensive spectroscopic analysis, CASE algorithms, quantum <sup>1</sup>H and <sup>13</sup>C NMR DP4+, and electronic circular dichroism calculations. Structurally, <b>1</b> was the first examples of isoindoline alkaloids bearing a 6/5/5/6 ring based on the 2-oxa-10-azatetracyclo-[7.7.0.0<sup>1,12</sup>.0<sup>3,8</sup>]cetane core, while <b>2</b> featured an 5,20-bioxa-1-azapencyclo-[10.7.1.0<sup>1,12</sup>.0<sup>6,11</sup>.0<sup>13,18</sup>]lcosane moiety. Furthermore, <b>1</b> displayed an inhibitory effect toward triple-negative breast cancer cells through the Rap1/PI3K/AKT signaling pathway.

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Journal
Organic Letters
Published
2025-10-03
DOI
https://doi.org/10.1021/acs.orglett.5c03829
Citations
1
Primary Topic
Cancer Treatment and Pharmacology
Type
article
Field-Weighted Citation Impact
1.05
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article

Indopexines A and B: Two Prenylated Isoindoline Alkaloids from the Fungus Aspergillus sp. TJ507

Jinlong Zhang, Xueqi Lan, Kuansong Wang, Changxing Qi et al.
1 citations
Organic Letters
Cancer Treatment and Pharmacology
1.05
article

Indopexines A and B: Two Prenylated Isoindoline Alkaloids from the Fungus Aspergillus sp. TJ507

Jinlong Zhang, Xueqi Lan, Kuansong Wang, Changxing Qi, Xinye Huang, Yeting Zhang, Ming Chen, Qiang Li, Zhengyi Shi
article en
1 citations

Abstract

Indopexines A (<b>1</b>) and B (<b>2</b>), two prenylated isoindoline alkaloids, were isolated from <i>Aspergillus</i> sp. TJ507. Their structures were determined by extensive spectroscopic analysis, CASE algorithms, quantum <sup>1</sup>H and <sup>13</sup>C NMR DP4+, and electronic circular dichroism calculations. Structurally, <b>1</b> was the first examples of isoindoline alkaloids bearing a 6/5/5/6 ring based on the 2-oxa-10-azatetracyclo-[7.7.0.0<sup>1,12</sup>.0<sup>3,8</sup>]cetane core, while <b>2</b> featured an 5,20-bioxa-1-azapencyclo-[10.7.1.0<sup>1,12</sup>.0<sup>6,11</sup>.0<sup>13,18</sup>]lcosane moiety. Furthermore, <b>1</b> displayed an inhibitory effect toward triple-negative breast cancer cells through the Rap1/PI3K/AKT signaling pathway.

Organic LettersVol. 27(41)
Ministry of Education of the People's Republic of China (CN), Central South University (CN), Zhengzhou University (CN), Culture Resource (EG), Office of Basic Energy Sciences (US), Xiangya Hospital Central South University (CN), Huazhong University of Science and Technology (CN)
Openalex Percentile: Top 17%
Cancer Treatment and Pharmacology
1.05
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Indopexines A and B: Two Prenylated Isoindoline Alkaloids from the Fungus <i>Aspergillus</i> sp. TJ507 — Jinlong Zhang, Xueqi Lan, et al. · Organic Letters (2025) | TGRS Research Map | TGRS