a series of benzodioxole compounds were synthesized and evaluated for their cytotoxic activity against cervical (Hela), colorectal (Caco-2), and liver (Hep3B) cancer cell lines. Compounds 5a, 5b, 6a, 6b, 7a and 7b showed very weak or negligible anticancer activity with IC₅₀ 3.94-9.12 mM. On the contrary, carboxamide containing compounds 2a and 2b showed anticancer activity. Both 2a and 2b reduced Hep3B secretions of α-fetoprotein (α-FP) to 1625.8 ng/ml and 2340 ng/ml, respectively, compared to 2519.17 ng/ml in untreated cells. The results also showed that compound 2a has potent anticancer activity against Hep3B cancer cell line. Furthermore, in cell cycle analysis, compound 2a induced arrest in the G2-M phase in value of 8.07% that was very close to the activity of doxorubicin (7.4%). These results indicate that compound 2ahas a potent and promising antitumor activity. However, benzodiazepine derivatives (7a and 7b) showed moderate antioxidant activity with IC₅₀ values of 39.85 and 79.95 μM, respectively compared with the potent antioxidant agent Trolox (IC₅₀ = 7.72 μM).

العنوان

Heterocyclic Communications

الناشر

DeGruyter

بلد الناشر

بولندا

Indexing

Thomson Reuters

معامل التأثير

1,13

نوع المنشور

Both (Printed and Online)

المجلد

26

السنة

2020

الصفحات

157–167