Cytotoxic activity of some benzo[4,5]imidazo[1,2-a]pyrimidine derivatives against the human cancer cell lines HepG2 and MCF-7

Document Type : Original Article

Authors

1 National Research Centre

2 Organometalic and Organometalliod Chemistry Department, National Research Centre

3 Organometallic chemistry Department, National research centre

4 Ain Shams university

5 Organometallic and Organometalloid Chemistry Department, National Research Centre, Cairo, Egypt.

6 Microbial Biotechnology Department, National Research Centre, Dokki, Cairo, Egypt

7 Biochemistry and Molecular Biology Department, Theodor Bilharz Research Institute,Cairo, Egypt.

Abstract

Different benzo[4,5]imidazo[1,2-a]pyrimidine derivatives were synthesized in high purity and yields with short reaction times by the reaction of 2-aminobenzimidazole, aldehydes and active carbonyl compounds in the presence of Silica sulfuric acid/ethylene glycol (SSA/EG) as a catalyst. Cytotoxicity of the synthesized benzo[4,5]imidazo[1,2-a]pyrimidine derivatives 1-6 was carried out against the two human cancer cell lines, hepatocellular carcinoma (HepG2) and breast carcinoma (MCF-7) as well as Vero cells (normal cells).

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