Literature DB >> 20851441

Cytotoxic tirucallane C26 triterpenoids from the stem barks of Aphanamixis grandifolia.

Yao Zhang1, Junsong Wang, Dandan Wei, Xiaobing Wang, Jun Luo, Jianguang Luo, Lingyi Kong.   

Abstract

Five tirucallane type C(26) triterpenoids, accompanied by two known compounds, 3α-hydroxy-24,25,26,27-tetranortirucall-7-ene-23(21)-lactone and 3-oxo-24,25,26,27-tetranortirucall-7-ene-23(21)-lactone, were isolated from the stem barks of Aphanamixis grandifolia. Their structures were established mainly by means of a combination of 1D and 2D NMR spectroscopic and mass spectrometry techniques as 3α-hydroxyl-21α-methoxy-24,25,26,27-tetranortirucall-7-ene-23(21)-lactone, 3α-hydroxy-21β-methoxy-24,25,26,27-tetranortirucall-7-ene-23(21)-lactone, 3-oxo-21α-methoxy-24,25,26,27-tetranortirucall-7-ene-23(21)-lactone, 3-oxo-21β-methoxy-24,25,26,27-tetranortirucall-7-ene-23(21)-lactone, and 3-oxo-21α-ethoxy-24,25,26,27-tetranortirucall-7-ene-23(21)-lactone. All isolates were in vitro evaluated for their cytotoxic activities against five tumor cell lines (MCF-7, HeLa, HepG2, SGC-7901 and BGC-823).
Copyright © 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 20851441     DOI: 10.1016/j.phytochem.2010.08.017

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


  4 in total

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3.  Cytotoxic and radical scavenging nor-dammarane triterpenoids from Viburnum mongolicum.

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Journal:  Molecules       Date:  2013-01-24       Impact factor: 4.411

4.  Cytotoxic Activity of Inositol Angelates and Tirucallane-Type Alkaloids from Amoora Dasyclada.

Authors:  Sheng-Xiang Yang; Cheng-Gang Song; Yi Kuang; Bing Liu; Yan-Xin Zhang; Ming-Zhe Zhang; Chun-Ying Zhang; Gang Ding; Jian-Chun Qin
Journal:  Molecules       Date:  2020-03-09       Impact factor: 4.411

  4 in total

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