| Literature DB >> 28135059 |
Carlos Carbajales1, Jun-Ichi Sawada2, Giovanni Marzaro3, Eddy Sotelo1,4, Luz Escalante1, Antonio Sánchez-Díaz Marta1, Xerardo García-Mera4, Akira Asai2, Alberto Coelho1,4.
Abstract
The potent kinesin spindle protein inhibitor CPUYJ039 and a set of analogues were prepared by a target-oriented approach based on a Ugi reaction that uses 2-nitrophenyl isocyanides as key building blocks. The herein documented strategy provides straightforward and atom economical access to potent benzimidazole-based antimitotic agents by exploring the versatility and exploratory power of the Ugi reaction. The results of docking studies and biological activity evaluations of the benzimidazole compounds are also reported.Entities:
Keywords: CPUYJ039; Ugi reaction; antimitotic agent; kinesin spindle protein inhibitor
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Year: 2017 PMID: 28135059 DOI: 10.1021/acscombsci.6b00166
Source DB: PubMed Journal: ACS Comb Sci ISSN: 2156-8944 Impact factor: 3.784