Discovery and Semisynthesis of Arthritacins A–J—Terpestacin-Derived Sesterterpenoids from the Plant Endophytic Fungus Arthrinium sp. HS66

Arthrinium species are promising producers of terpenoids with diverse architectures and noteworthy pharmacological properties. In this work, ten undescribed terpestacin-type sesterterpenoids, arthritacins A–J (1–10), together with five known analogues (11–15), were obtained from the endophytic fungus Arthrinium sp. HS66 isolated from the stems of Isodon xerophilus. Their structures were established through comprehensive spectroscopic analysis, semisynthesis, and NMR calculations, further supported by DP4+ probability analysis. The semisynthetic studies further helped confirm the biosynthetically ambiguous configurations at C-11 and C-23 in terpestacin derivatives. All compounds were evaluated for cytotoxic activity against human neuroblastoma cells. Among them, compounds 1, 2, 4, 6, 7, 9, 12 and 13 showed moderate antiproliferative effects, with IC50 values ranging from 21.13 to 36.54 µM.

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Publication Details

Journal
Journal of Fungi
Published
2026-09-16
DOI
https://doi.org/10.3390/jof12090693
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
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article

Discovery and Semisynthesis of Arthritacins A–J—Terpestacin-Derived Sesterterpenoids from the Plant Endophytic Fungus Arthrinium sp. HS66

Xiao‐Zheng Su, Xing‐Ren Li, Pema‐Tenzin Puno, Han-Dong Sun et al.
Journal of Fungi
Microbial Natural Products and Biosynthesis
article

Discovery and Semisynthesis of Arthritacins A–J—Terpestacin-Derived Sesterterpenoids from the Plant Endophytic Fungus Arthrinium sp. HS66

Xiao‐Zheng Su, Xing‐Ren Li, Pema‐Tenzin Puno, Han-Dong Sun, Kun Hu
article en

Abstract

Arthrinium species are promising producers of terpenoids with diverse architectures and noteworthy pharmacological properties. In this work, ten undescribed terpestacin-type sesterterpenoids, arthritacins A–J (1–10), together with five known analogues (11–15), were obtained from the endophytic fungus Arthrinium sp. HS66 isolated from the stems of Isodon xerophilus. Their structures were established through comprehensive spectroscopic analysis, semisynthesis, and NMR calculations, further supported by DP4+ probability analysis. The semisynthetic studies further helped confirm the biosynthetically ambiguous configurations at C-11 and C-23 in terpestacin derivatives. All compounds were evaluated for cytotoxic activity against human neuroblastoma cells. Among them, compounds 1, 2, 4, 6, 7, 9, 12 and 13 showed moderate antiproliferative effects, with IC50 values ranging from 21.13 to 36.54 µM.

Journal of FungiVol. 12(9)
Kunming Institute of Botany (CN), Chinese Academy of Sciences (CN)
Life in Land
Openalex Percentile: Top 13%
Microbial Natural Products and Biosynthesis
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