Rosanoid diterpenoids: structural diversity, classification and biological activities.

IF 5.1 Q2 CHEMISTRY, MEDICINAL
ADMET and DMPK Pub Date : 2026-03-06 eCollection Date: 2026-01-01 DOI:10.5599/admet.3165
Sabrin R M Ibrahim, Hani Z Asfour, Gamal A Mohamed, Nabil A Alhakamy, Hossam M Abdallah, Hagar M Mohamed
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引用次数: 0

Abstract

Background and purpose: Rosanoid diterpenoids, including ent-rosane and rosane diterpenoids, are structurally unique and bioactive subclass diterpenes characterized by a tricyclic carbon skeleton. This work aims to provide a comprehensive review of the literature on these diterpenoids from 1975. to September 2025., including their occurrence, structural diversity, and biological activities.

Approach: An extensive literature search was conducted through scientific databases (ScienceDirect, PubMed, Scopus, Web of Science, and Google Scholar) and publishers' webpages (Elsevier, Wiley, ACS, RSC, Taylor & Francis, Springer, Bentham, Thieme, and MDPI), covering reports from 1975 to September 2025.

Key results: Rosanoid diterpenoids have been isolated from various natural sources, including fungi, liverworts, and higher plant families such as Euphorbiaceae, Lamiaceae, Alismataceae, Asteraceae, Velloziaceae, and Celastraceae. They are predominantly found in Euphorbia species, revealing their chemotaxonomic relevance to the Euphorbiaceae family. These compounds exhibit extensive structural diversity, encompassing a broad spectrum of biological activities, including anti-inflammatory, antimicrobial, antiviral, cytotoxic, enzyme-inhibitory, neuroactive, and anti-adipogenic effects.

Conclusion: The reported findings highlight the chemical variability and pharmacological potential of rosanoid diterpenoids, making them promising building blocks for future drug discovery and natural product development. However, further studies are warranted to explore their pharmacokinetics, mechanisms of action, safety profiles, and biosynthetic pathways.

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蔷薇二萜:结构多样性、分类及生物活性。
背景与目的:迷迭香二萜包括对-迷迭香和迷迭香二萜,是一种结构独特且具有生物活性的亚类二萜,其特征为三环碳骨架。本文旨在对1975年以来有关这些二萜的文献进行全面综述。到2025年9月。,包括它们的发生、结构多样性和生物活动。方法:通过科学数据库(ScienceDirect、PubMed、Scopus、Web of Science和谷歌Scholar)和出版商的网页(Elsevier、Wiley、ACS、RSC、Taylor & Francis、施普林格、Bentham、Thieme和MDPI)进行了广泛的文献检索,涵盖了1975年至2025年9月的报告。从真菌、苔类植物和高等植物科(如大戟科、Lamiaceae、泽泻科、Asteraceae、Velloziaceae和Celastraceae)中分离到了玫瑰类二萜。它们主要存在于大戟属植物中,揭示了它们在化学分类上与大戟科植物的相关性。这些化合物表现出广泛的结构多样性,包括广泛的生物活性,包括抗炎、抗菌、抗病毒、细胞毒性、酶抑制、神经活性和抗脂肪生成作用。结论:报告的发现突出了玫瑰二萜的化学变异性和药理潜力,使其成为未来药物发现和天然产物开发的有希望的基石。然而,需要进一步研究它们的药代动力学、作用机制、安全性和生物合成途径。
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来源期刊
ADMET and DMPK
ADMET and DMPK Multiple-
CiteScore
4.40
自引率
0.00%
发文量
22
审稿时长
4 weeks
期刊介绍: ADMET and DMPK is an open access journal devoted to the rapid dissemination of new and original scientific results in all areas of absorption, distribution, metabolism, excretion, toxicology and pharmacokinetics of drugs. ADMET and DMPK publishes the following types of contributions: - Original research papers - Feature articles - Review articles - Short communications and Notes - Letters to Editors - Book reviews The scope of the Journal involves, but is not limited to, the following areas: - physico-chemical properties of drugs and methods of their determination - drug permeabilities - drug absorption - drug-drug, drug-protein, drug-membrane and drug-DNA interactions - chemical stability and degradations of drugs - instrumental methods in ADMET - drug metablic processes - routes of administration and excretion of drug - pharmacokinetic/pharmacodynamic study - quantitative structure activity/property relationship - ADME/PK modelling - Toxicology screening - Transporter identification and study
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