Molecules (Basel, Switzerland) · 2025
Assessment of the Biological Properties of N-Nonsubstituted Succinimides and Their Metallocarbonyl Complexes in Normal and Cancer Cells.
СтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Juszczak Michał, Tokarz Paulina, Kosińska Aneta, Rudolf Bogna, Woźniak Katarzyna
Аннотация
Succinimide derivatives display a broad spectrum of biological activities and are being explored for various medical applications, including the treatment of epilepsy, diabetes, and cancer, as well as cardiovascular and liver diseases. Ongoing research continues to yield new derivatives with promising therapeutic potential. This study evaluates the biological properties of 3-methoxysuccinimide (1), 3-butynyloxysuccinimide (2), and their metallocarbonyl complexes (η5-cyclopentadienyl)Fe(CO)2(η1-N-(3-methoxysuccinimidato)) (3) and (η5-cyclopentadienyl)Fe(CO)2(η1-N-(3-butynyloxysuccinimidato)) (4) in normal peripheral blood mononuclear cells (PBM) and HL-60 leukemic cells. We examined cytotoxicity, genotoxicity, oxidative, and antioxidative potential of these compounds. Succinimides and their complexes exhibited low cytotoxicity in both cell lines in the concentration range 3-50 μM. At 100 μM, only 3-methoxysuccinimide (1) reduced PBM cell viability, while all compounds significantly decreased HL-60 cell viability at this concentration. We also showed that all compounds caused a minor concentration-independent increase in DNA damage level. Interestingly, complex 3 was significantly less genotoxic for HL-60 cells compared to N-nonsubstituted analog (1). Succinimides 1 and 2 and their metallocarbonyl complexes 3 and 4 demonstrated strong antioxidant properties, especially in HL-60 cancer cells. They also restored SOD activity reduced by oxidative stress in cancer cells.