Design and synthesis of new pyranoxanthenones bearing a nitro group or an aminosubstituted side chain on the pyran ring. Evaluation of their growth inhibitory activity in breast cancer cells
- 4 December 2006
- journal article
- Published by Elsevier BV in European Journal of Medicinal Chemistry
- Vol. 42 (3), 307-319
- https://doi.org/10.1016/j.ejmech.2006.10.018
Abstract
No abstract availableKeywords
Funding Information
- Ministry of National Education and Religious Affairs
This publication has 17 references indexed in Scilit:
- Design, synthesis and antiproliferative activity of some new azapyranoxanthenone aminoderivativesEuropean Journal of Medicinal Chemistry, 2006
- The role of pixantrone in the treatment of non-Hodgkin’s lymphomaExpert Opinion on Investigational Drugs, 2005
- Antitumor acridines with diaminoalkylo pharmacophoric groupPublished by Walter de Gruyter GmbH ,2001
- Synthesis and Conformational Analysis of Some New Pyrano[2,3-c]xanthen-7-one and Pyrano[3,2-b]xanthen-6-one Derivatives with Cytotoxic ActivityHETEROCYCLES, 2000
- DNA recognition by two mitoxantrone analogues: Influence of the hydroxyl groupsFEBS Letters, 1996
- Synthesis and Cytotoxic Activity of Acronycine Derivatives Modified at the Pyran Ring.CHEMICAL & PHARMACEUTICAL BULLETIN, 1996
- 6,9-Bis[(aminoalkyl)amino]benzo[g]isoquinoline-5,10-diones. A Novel Class of Chromophore-Modified Antitumor Anthracene-9,10-diones: Synthesis and Antitumor EvaluationsJournal of Medicinal Chemistry, 1994
- Evaluation of the cytotoxic mechanisms mediated by the broad-spectrum antitumor alkaloid acronycine and selected semisynthetic derivativesChemico-Biological Interactions, 1992
- Synthesis, molecular modeling, DNA binding, and antitumor properties of some substituted amidoanthraquinonesJournal of Medicinal Chemistry, 1988
- Synthesis and biological activity of acronycine analogsJournal of Medicinal Chemistry, 1972