Literature DB >> 17945208

Synthesis, cytotoxicity, and hemolytic activity of 6'-O-substituted dioscin derivatives.

Wei Li1, Zaozao Qiu, Yibing Wang, Yichun Zhang, Ming Li, Jia Yu, Lihong Zhang, Ziyan Zhu, Biao Yu.   

Abstract

Dioscin derivatives (1-12) with a variety of substitutions at the 6'-OH of the chacotriosyl residue and the 3',6'-anhydrosaponin derivatives (26, 30, and 32) were synthesized. All these derivatives showed much lower cytotoxicity than that of the parent dioscin, while their hemolytic activities were partially retained depending on the various 6'-O-substitutions.

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Year:  2007        PMID: 17945208     DOI: 10.1016/j.carres.2007.09.004

Source DB:  PubMed          Journal:  Carbohydr Res        ISSN: 0008-6215            Impact factor:   2.104


  3 in total

1.  Hemolytic mechanism of dioscin proposed by molecular dynamics simulations.

Authors:  Fu Lin; Renxiao Wang
Journal:  J Mol Model       Date:  2009-06-10       Impact factor: 1.810

Review 2.  Saponins from Chinese Medicines as Anticancer Agents.

Authors:  Xiao-Huang Xu; Ting Li; Chi Man Vivienne Fong; Xiuping Chen; Xiao-Jia Chen; Yi-Tao Wang; Ming-Qing Huang; Jin-Jian Lu
Journal:  Molecules       Date:  2016-10-05       Impact factor: 4.411

Review 3.  Synthesis, Modification and Biological Activity of Diosgenyl β-d-Glycosaminosides: An Overview.

Authors:  Daria Grzywacz; Beata Liberek; Henryk Myszka
Journal:  Molecules       Date:  2020-11-20       Impact factor: 4.411

  3 in total

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