Literature DB >> 30818173

Natural barrigenol-like triterpenoids: A comprehensive review of their contributions to medicinal chemistry.

Xinxin Zhang1, Song Zhang1, Yiren Yang1, Da Wang2, Huiyuan Gao3.   

Abstract

Barrigenol-like triterpenoids (BATs), which contain an unusual oleanane substituted by many hydroxyl groups as the skeleton, are subdivided into five subtypes: barrigenol A1, barrigenol A2, barrigenol R1, barringtogenol C, and 16-deoxybarringtogenol C. The variations in acyl derivatives, hydroxyl groups, and carbohydrate chains in their structures have enhanced the diversity of BATs. Moreover, the stable polyhydroxy-replaced pentacyclic skeleton provides an ideal platform for structural modifications. To date, more than 500 BAT derivatives have been isolated from plants. Synchronously, BATs possess anti-tumour, anti-Alzheimer's disease, anti-inflammatory, anti-microbial, anti-obesity and anti-allergic activities by regulating numerous cellular molecules. Some BAT derivatives, such as escin obtained from Aesculus hippocastanum L. and xanthoceraside isolated from Xanthoceras sorbifolia Bunge, have been used to treat encephaloedema or inflammatory diseases. This review aims to provide comprehensive information about the chemistry, sources, bioavailability, and anti-tumour effects of BATs, with a particular emphasis on the molecular mechanisms of action. The pharmacokinetics and clinical progress are also concerned. More than 300 structures identified over past 25 years are summarized here (249 compounds) and in the supplementary information (114 compounds). Accordingly, the pharmaceutical activity of barrigenol triterpenoids suggests that some compounds should be developed as promising anti-tumour or anti- Alzheimer's disease agents in future.
Copyright © 2019 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Anti-Alzheimer's disease; Anti-tumour; Barrigenol-like triterpenoid; Chemical structures; Pharmacological mechanism

Mesh:

Substances:

Year:  2019        PMID: 30818173     DOI: 10.1016/j.phytochem.2019.01.017

Source DB:  PubMed          Journal:  Phytochemistry        ISSN: 0031-9422            Impact factor:   4.072


  7 in total

1.  Metabolomic insights into the browning of the peel of bagging 'Rui Xue' apple fruit.

Authors:  Hui Wang; Shuang Wang; Miao-Miao Fan; Shu-Hui Zhang; Lu-Long Sun; Zheng-Yang Zhao
Journal:  BMC Plant Biol       Date:  2021-05-08       Impact factor: 4.215

2.  Amyloid β aggregation inhibitory activity of triterpene saponins from the cactus Stenocereus pruinosus.

Authors:  Koji Fujihara; Takuya Shimoyama; Ryo Kawazu; Hiroaki Sasaki; Kiyotaka Koyama; Kunio Takahashi; Kaoru Kinoshita
Journal:  J Nat Med       Date:  2020-11-24       Impact factor: 2.343

3.  Preliminary Biological Activity Screening of Plectranthus spp. Extracts for the Search of Anticancer Lead Molecules.

Authors:  Epole Ntungwe; Eva María Domínguez-Martín; Catarina Teodósio; Silvia Teixidó-Trujillo; Natalia Armas Capote; Lucilia Saraiva; Ana María Díaz-Lanza; Noélia Duarte; Patrícia Rijo
Journal:  Pharmaceuticals (Basel)       Date:  2021-04-23

4.  Cytotoxic Polyhydroxylated Oleanane Triterpenoids from Cissampelos pareira var. hirsuta.

Authors:  Yanjun Sun; Ruyi Pan; Haojie Chen; Chen Zhao; Ruijie Han; Meng Li; Guimin Xue; Hui Chen; Kun Du; Junmin Wang; Weisheng Feng
Journal:  Molecules       Date:  2022-02-10       Impact factor: 4.411

5.  16-Tigloyl linked barrigenol-like triterpenoid from Semen Aesculi and its anti-tumor activity in vivo and in vitro.

Authors:  Yiren Yang; Liping Long; Xinxin Zhang; Kairu Song; Da Wang; Xin Xiong; Huiyuan Gao; Luping Sha
Journal:  RSC Adv       Date:  2019-10-07       Impact factor: 4.036

6.  Oriented Deep Eutectic Solvents as Efficient Approach for Selective Extraction of Bioactive Saponins from Husks of Xanthoceras sorbifolia Bunge.

Authors:  Jinteng Cao; Guangwei Wu; Lei Wang; Fuliang Cao; Yan Jiang; Linguo Zhao
Journal:  Antioxidants (Basel)       Date:  2022-04-08

Review 7.  The Biosurfactant β-Aescin: A Review on the Physico-Chemical Properties and Its Interaction with Lipid Model Membranes and Langmuir Monolayers.

Authors:  Ramsia Geisler; Carina Dargel; Thomas Hellweg
Journal:  Molecules       Date:  2019-12-27       Impact factor: 4.411

  7 in total

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