Antitumor activity of novel amino substituted pentacyclic benzimidazole derivatives tested in 2D and 3D cell culture system (CROSBI ID 637360)
Prilog sa skupa u zborniku | sažetak izlaganja sa skupa | međunarodna recenzija
Podaci o odgovornosti
Perin, Nataša ; Bobanović, Kristina ; Brajša, Karmen ; Jelić, Dubravko ; Zlatar, Ivo ; Hranjec, Marijana
engleski
Antitumor activity of novel amino substituted pentacyclic benzimidazole derivatives tested in 2D and 3D cell culture system
Over the past few years substituted benzimidazoles, as a one of the most important groups of nitrogen heterocycles, are important and fundamental building skeletons of various essential synthetic and natural pharmacological compounds. Due to the structural similarity with naturally occurring compounds such as purine, benzimidazole derivatives can easily interact with biomolecules of the living systems. Recently, we have reported on the synthesis and biological activity of several groups of tetracyclic benzimidazo[1, 2-a]quinolines [1, 2]. Detailed biological studies confirmed the promissing anticancer potential of this class of compounds. As a part of our continuing research in the field of medicinal chemistry, novel amino substituted pentacyclic benzimidazole derivatives were synthesized by uncatalyzed microwave assisted amination from halogeno substituted precursors. Antitumor activity in vitro of novel pentacyclic and earlier prepared tetracyclic benzimidazole derivatives was tested on tree breast cell lines (MDA-MB-231, SK-BR-3 and T-47D) in 2D and 3D cell culture system [3].
benzimidazoles; antitumor activity; amino substituents; 2D and 3D system
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Podaci o prilogu
16-16.
2016.
objavljeno
Podaci o matičnoj publikaciji
17th Tetrahedron Symposium Challenges in Biological, Bioorganic, Organic & Medicinal Chemistry, Sitges, Španjolska 2016.
Elsevier
Podaci o skupu
17th Tetrahedron Symposium - Challenges in Biological, Bioorganic, Organic & Medicinal Chemistry
poster
28.06.2016-01.07.2016
Sitges, Španjolska