Literature DB >> 15922837

Synthesis and evaluation of double bond substituted combretastatins.

John A Hadfield1, Keira Gaukroger, Nicholas Hirst, Anna P Weston, Nicholas J Lawrence, Alan T McGown.   

Abstract

A series of combretastatins substituted with epoxides, amides and small alkyl groups has been synthesised and evaluated for cytotoxicity and their ability to inhibit the assembly of tubulin. The methyl and ethyl substituted phenols 36, 44 have shown potent antimitotic effects whilst exhibiting reduced cytotoxicity.

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Year:  2005        PMID: 15922837     DOI: 10.1016/j.ejmech.2004.12.008

Source DB:  PubMed          Journal:  Eur J Med Chem        ISSN: 0223-5234            Impact factor:   6.514


  3 in total

Review 1.  An overview of tubulin inhibitors that interact with the colchicine binding site.

Authors:  Yan Lu; Jianjun Chen; Min Xiao; Wei Li; Duane D Miller
Journal:  Pharm Res       Date:  2012-07-20       Impact factor: 4.200

2.  Design, Synthesis and Biochemical Evaluation of Novel Selective Estrogen Receptor Ligand Conjugates Incorporating an Endoxifen-Combretastatin Hybrid Scaffold.

Authors:  Niall O Keely; Miriam Carr; Bassem Yassin; Gloria Ana; David G Lloyd; Daniela Zisterer; Mary J Meegan
Journal:  Biomedicines       Date:  2016-07-20

3.  One-pot synthesis of epoxides from benzyl alcohols and aldehydes.

Authors:  Edwin Alfonzo; Jesse W L Mendoza; Aaron B Beeler
Journal:  Beilstein J Org Chem       Date:  2018-09-03       Impact factor: 2.883

  3 in total

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