Аннотация
High biological activity of natural furocoumarins is often linked to a series of adverse side effects, e.g., genotoxicity. This makes it desirable to develop semi-synthetic derivatives with reduced negative activity while retaining or even enhancing the positive properties. Previously, we have studied the genotoxic activity of a library of twenty-one 1,2,3-triazolyl-modified furocoumarins and 2,3-dihydrofurocoumarins and identified modifications that minimize the negative properties. In the current article, we report on an investigation into the cytotoxic activity of the same library. We have aimed to rank the substances in order of the severity of their cytotoxicity and therefore to predict, with the use of statistical processing, the most promising substituents for the furocoumarin scaffold.
Язык оригинала | английский |
---|---|
Страницы (с-по) | 1321-1330 |
Число страниц | 10 |
Журнал | Protoplasma |
Том | 259 |
Номер выпуска | 5 |
Ранняя дата в режиме онлайн | 26 янв. 2022 |
DOI | |
Состояние | Опубликовано - сент. 2022 |
Предметные области OECD FOS+WOS
- 1.06 БИОЛОГИЧЕСКИЕ НАУКИ
- 1.06.DE НАУКИ О РАСТЕНИЯХ
- 1.06.DR КЛЕТОЧНАЯ БИОЛОГИЯ