Dehydrogenated and Aromatized <i>ent</i>‐Cleistanthane Diterpenoids From the Roots of <i>Glochidion philippicum</i>

The first comprehensive phytochemical investigation of Glochidion philippicum roots resulted in the isolation and characterization of seven new ent-cleistanthane-type diterpenoids, glochiphenols A-G (1-7), along with two known analogs (8 and 9). Compounds 1-6 all feature a rare alkynyl group, with 1-3 representing highly aromatized 20-nor-ent-cleistanthane diterpenoids. Their structures were elucidated by comprehensive spectroscopic analysis, and absolute configurations were established via electronic circular dichroism (ECD) calculations. Notably, bioactivity assays revealed that compounds 1 and 7 display potent inhibitory effects against DGKζ with IC<sub>50</sub> values of 1.19 and 1.28 µM, respectively.

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Journal
Chemistry & Biodiversity
Published
2025-06-03
DOI
https://doi.org/10.1002/cbdv.202501481
Primary Topic
Phytochemistry and Biological Activities
Type
article
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article

Dehydrogenated and Aromatized ent‐Cleistanthane Diterpenoids From the Roots of Glochidion philippicum

Yao‐Yue Fan, Yang Yao, Yanan Duan, Zhou Bin et al.
1 links
Chemistry & Biodiversity
Phytochemistry and Biological Activities
article

Dehydrogenated and Aromatized ent‐Cleistanthane Diterpenoids From the Roots of Glochidion philippicum

Yao‐Yue Fan, Yang Yao, Yanan Duan, Zhou Bin, Jian‐Min Yue, Christina Z Li, Jingya Li
article en

Abstract

The first comprehensive phytochemical investigation of Glochidion philippicum roots resulted in the isolation and characterization of seven new ent-cleistanthane-type diterpenoids, glochiphenols A-G (1-7), along with two known analogs (8 and 9). Compounds 1-6 all feature a rare alkynyl group, with 1-3 representing highly aromatized 20-nor-ent-cleistanthane diterpenoids. Their structures were elucidated by comprehensive spectroscopic analysis, and absolute configurations were established via electronic circular dichroism (ECD) calculations. Notably, bioactivity assays revealed that compounds 1 and 7 display potent inhibitory effects against DGKζ with IC<sub>50</sub> values of 1.19 and 1.28 µM, respectively.

Chemistry & BiodiversityVol. 22(10)
Nanjing University of Chinese Medicine (CN), Chinese Academy of Sciences (CN), Shanghai Institute of Materia Medica (CN)
Openalex Percentile: Top 91%
Phytochemistry and Biological Activities
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