| Literature DB >> 19269832 |
Jaime A Valderrama1, J Andrea Ibacache, Verónica Arancibia, Jaime Rodriguez, Cristina Theoduloz.
Abstract
A variety of 7-aminoisoquinoline-5,8-quinone derivatives were prepared from 2,5-dihydroxyacetophenone, methyl aminocrotonate, and the corresponding amines, through a highly efficient three-step sequence. The members of this series were tested on normal human fibroblasts and on a panel of three human cancer cell lines and their redox properties were determined by cyclic voltammetry in acetonitrile. Both the cytotoxicity and antitumor activity of 7-phenylaminoisoquinoline-5,8-quinone derivatives showed correlation with their half wave potentials and lipophilicities.Entities:
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Year: 2009 PMID: 19269832 DOI: 10.1016/j.bmc.2009.02.013
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641