Benzothiazole carbamates and amides as antiproliferative species.

Videnović Milica; Mojsin Marija; Stevanović Milena; Opsenica Igor; Srdić-Rajić Tatjana; Šolaja Bogdan

doi:10.1016/j.ejmech.2018.08.067

Published August 25, 2018 | Version v.1.

Journal article Open

Benzothiazole carbamates and amides as antiproliferative species.

1. Faculty of Chemistry Innovative Centre, Studentski trg 12-16, 11158 Belgrade, Serbia
2. Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Vojvode Stepe 444a, 11010 Belgrade, Serbia
3. Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Vojvode Stepe 444a, 11010 Belgrade, Serbia; University of Belgrade – Faculty of Biology, Studentski trg 16, 11158 Belgrade, Serbia, Serbian Academy of Sciences and Arts, Knez Mihailova 35, 11158 Belgrade, Serbia
4. University of Belgrade – Faculty of Chemistry, Studentski trg 16, P.O. Box 51, 11158 Belgrade, Serbia
5. Institute for Oncology and Radiology of Serbia, Pasterova 14, 11000 Belgrade, Serbia
6. University of Belgrade – Faculty of Chemistry, Studentski trg 16, P.O. Box 51, 11158 Belgrade, Serbia; Serbian Academy of Sciences and Arts, Knez Mihailova 35, 11158 Belgrade, Serbia; Faculty of Chemistry Innovative Centre, Studentski trg 12-16, 11158 Belgrade, Serbia

A series of new benzothiazole-based carbamates and amides were synthesized and their antiproliferative activity was determined. Derivatives with profound activity were identified and further investigated for their possible mechanism of action. It was found that these compounds induce specific apoptosis, G2/M cell cycle arrest and decrease ROS level in MCF-7 human breast cancer cell line. Moreover, submicromolar antiproliferative activity of examined carbamates against NT2/D1 testicular embryonal carcinoma was shown. The most potent derivatives strongly inhibited NT2/D1 cell migration and invasiveness

Notes

This work is also supported by Serbian Academy of Sciences and Arts (BŠ, MS).

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