Euphabeones A–D, Rearranged Jatrophane Diterpenoids from Euphorbia hylonoma : Isolation, Structural Elucidation, and Anti-Senescence Evaluation

Abstract Euphabeones A–D (1–4), four rearranged jatrophane diterpenoids, were isolated from Euphorbia hylonoma. 1 and 2 possess a new 1(15→14),13(14→15)-diabeo-jatrophane skeleton featuring a 16-oxatricyclo[11.2.1.01,11]hexadecane core, while 3 and 4 are rare 1(15→14)-abeo-jatrophanes. Their structures were established by spectroscopic analysis, ECD calculation, and single-crystal X-ray diffraction. A plausible biosynthetic pathway for 1–4 was proposed and supported by biomimetic skeletal conversion. Compound 2 exhibited potent antisenescence activity, effectively ameliorating senescence phenotypes both in vitro and in vivo.

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Publication Details

Journal
Organic Letters
Published
2026-10-15
DOI
https://doi.org/10.1021/acs.orglett.6c04166
Primary Topic
Bioactive Natural Diterpenoids Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Euphabeones A–D, Rearranged Jatrophane Diterpenoids from Euphorbia hylonoma : Isolation, Structural Elucidation, and Anti-Senescence Evaluation

Fang-Yu Yuan, Yang Xian-yuan, Jia-Luo Huang, G.H. Tang et al.
Organic Letters
Bioactive Natural Diterpenoids Research
article

Euphabeones A–D, Rearranged Jatrophane Diterpenoids from Euphorbia hylonoma : Isolation, Structural Elucidation, and Anti-Senescence Evaluation

Fang-Yu Yuan, Yang Xian-yuan, Jia-Luo Huang, G.H. Tang, Sheng Yin, Weiye Wu, Ming-Ju Wen, Yun-yun Chen, Shu-Qi Wu, Peng-Cheng Huang
article en

Abstract

Abstract Euphabeones A–D (1–4), four rearranged jatrophane diterpenoids, were isolated from Euphorbia hylonoma. 1 and 2 possess a new 1(15→14),13(14→15)-diabeo-jatrophane skeleton featuring a 16-oxatricyclo[11.2.1.01,11]hexadecane core, while 3 and 4 are rare 1(15→14)-abeo-jatrophanes. Their structures were established by spectroscopic analysis, ECD calculation, and single-crystal X-ray diffraction. A plausible biosynthetic pathway for 1–4 was proposed and supported by biomimetic skeletal conversion. Compound 2 exhibited potent antisenescence activity, effectively ameliorating senescence phenotypes both in vitro and in vivo.

Organic Letters
Sun Yat-sen University (CN), Fuzhou University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 24%
Bioactive Natural Diterpenoids Research
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