Three New Diterpenoids From <i>Phyllanthus emblica</i> Roots: Structure and Anti‐HIV Activity

Three undescribed aromatic diterpenoids (1-3), were isolated from the roots of Phyllanthus emblica and structurally characterized. Compounds 1 and 2 are cleistanthane-type diterpenoids, and the latter possesses a rare 4,5-seco-20(10→5)-abeo-ent-cleistanthane scaffold with an acetenyl at C-14. Compound 3 was elucidated as a new podocarpane trinorditerpenoid. The structural elucidation, including absolute configuration determination, was achieved through comprehensive spectroscopic analysis (nuclear magnetic resonance, mass spectrometry, ultraviolet, and infrared) combined with time-dependent density functional theory-based electronic circular dichroism calculations. Compound 2 showed potential activity against HIV-1<sub>Bal</sub> PsV infection with an IC<sub>50</sub> value of 3.30 µM.

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Publication Details

Journal
Chemistry & Biodiversity
Published
2025-04-07
DOI
https://doi.org/10.1002/cbdv.202500783
Citations
1
Primary Topic
Phytochemistry and Bioactivity Studies
Type
article
Field-Weighted Citation Impact
1.56

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article

Three New Diterpenoids From Phyllanthus emblica Roots: Structure and Anti‐HIV Activity

Zhou Bin, Jian‐Min Yue, Qian Wang
1 citations
Chemistry & Biodiversity
Phytochemistry and Bioactivity Studies
1.56
article

Three New Diterpenoids From Phyllanthus emblica Roots: Structure and Anti‐HIV Activity

Zhou Bin, Jian‐Min Yue, Qian Wang
article en
1 citations

Abstract

Three undescribed aromatic diterpenoids (1-3), were isolated from the roots of Phyllanthus emblica and structurally characterized. Compounds 1 and 2 are cleistanthane-type diterpenoids, and the latter possesses a rare 4,5-seco-20(10→5)-abeo-ent-cleistanthane scaffold with an acetenyl at C-14. Compound 3 was elucidated as a new podocarpane trinorditerpenoid. The structural elucidation, including absolute configuration determination, was achieved through comprehensive spectroscopic analysis (nuclear magnetic resonance, mass spectrometry, ultraviolet, and infrared) combined with time-dependent density functional theory-based electronic circular dichroism calculations. Compound 2 showed potential activity against HIV-1<sub>Bal</sub> PsV infection with an IC<sub>50</sub> value of 3.30 µM.

Chemistry & BiodiversityVol. 22(8)
Shanghai Medical College of Fudan University (CN), Nanchang University (CN), Chinese Academy of Sciences (CN), Fudan University (CN), Shanghai Institute of Materia Medica (CN), State Key Laboratory of Drug Research
National Natural Science Foundation of China, Hainan University, National Key Research and Development Program of China
Good health and well-being
Openalex Percentile: Top 21%
Phytochemistry and Bioactivity Studies
1.56
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Three New Diterpenoids From <i>Phyllanthus emblica</i> Roots: Structure and Anti‐HIV Activity — Zhou Bin, Jian‐Min Yue, et al. · Chemistry & Biodiversity (2025) | TGRS Research Map | TGRS