Abstract
AbstractHeterocyclic compounds with different heterocycle moieties, namely benzoxazinone, benzimidazole, quinazolinone, and benzofuranone heterocyclic rings, were synthesized, characterized, and evaluated for their anticancer activity against human hepatocellular carcinoma cell line (HepG2) using sulforhodamine B (SRB) and dimethylthiazol‐diphenyltetrazolium bromide (MTT) assays. Also, their cytotoxic activities were tested against human epithelioid carcinoma (Hela) cell line in comparison with normal cell, amniotic epithelial (WISH) cell line, as an in vitro toxicity estimation model. The results showed clearly that 2‐(2‐benzyl‐4‐oxoquinazolin‐3(4H)‐yl)acetohydrazide 4 is the most potent antioxidant and anticancer agents. Although, 3‐amino‐2‐benzylquinazolin‐4(3H)‐one 5 is less potent anticancer agent against Hela but it is more safe against normal cell (WISH).
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