Title of article
2-Amino-4-(nitroalkyl)-4H-chromene-3-carbonitriles as New Cytotoxic Agents
Author/Authors
Zonouzi, Afsaneh School of Chemistry - University College of Science - University of Tehran , Mirzazadeh, Roghieh School of Chemistry - University College of Science - University of Tehran , Safavi, Maliheh Faculty of Pharmacy and Pharmaceutical Sciences Research Center - Tehran University of Medical Sciences , Kabudanian Ardestani, Sussan Institute of Biochemistry and Biophysics - Department of Biochemistry - University of Tehran , Emami, Saeed Department of Medicinal Chemistry and Pharmaceutical Sciences Research Center - Faculty of Pharmacy - Mazandaran University of Medical Sciences, Sari , Foroumadi, Alireza Faculty of Pharmacy and Pharmaceutical Sciences Research Center - Tehran University of Medical Sciences - Drug Design and Development Research Center - Tehran University of Medical Sciences
Pages
7
From page
679
To page
685
Abstract
A series of 2-amino-4-(nitroalkyl)-4H-chromene-3-carbonitriles were synthesized by
an efficient multicomponent reaction in aqueous media using DBU as a catalyst at room temperature. Mild condition, environment friendly procedure and excellent yields are the main advantages of this procedure. The cytotoxic activity of target compounds were evaluated against three cancer cell lines MDA-MB-231, MCF-7 and T47D in comparison with etoposide as reference drug. Generally, all compounds showed good cell growth inhibitory activity with IC50 values less than 30 μg/mL. Their activities were comparable or more potent than standard drug etoposide. The 6-bromo- derivatives 7e and 7f showed promising cytotoxic activity with IC50 values in the range of 3.46–18.76 μg/mL, being more potent than etoposide against all tested cell lines.
Keywords
4H-chromenes , Benzopyran , DBU , One-pot synthesis , Cytotoxic activity
Journal title
Astroparticle Physics
Serial Year
2013
Record number
2415060
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