Design, Synthesis and Anticancer Evaluation of Carbazole Fused Aminopyrimidine Derivatives

Author:

Spandana Zanjam1,Sreenivasulu Reddymasu2,Basaveswara Rao Mandava V.1

Affiliation:

1. Department of Chemistry, Krishna University, Machilipatnam-521 001, Andhra Pradesh, India

2. Department of Chemistry, University College of Engineering (Autonomous), Jawaharlal Nehru Technological University, Kakinada-533003, Andhra Pradesh, India

Abstract

Carbazole is an important type of tricyclic nitrogen containing compound and isolated first from coal tar in 1872 by Graebe and Glazer. Carbazole alkaloids have received considerable attention since their discovery in the 1960’s and their derivatives are well known for their pharmacological activities. Many recent studies have reported that carbazole derivatives exhibit a variety of biological activities. Toxicity of test compound in cells was determined by MTT assay based on mitochondrial reduction of yellow MTT tetrazolium dye to a highly blue colored formazan product. Among the ten synthesized compounds, 12c, 12d, 12e, 12f, 12g and 12i were showed good activity. In which 12c, 12d and 12e showed moderate activity on MCF-7 cancer cell line. Compounds 12f, 12g and 12i showed more potent activity than control. Compounds 12f, 12g and 12i showed more potent activity than control adriamycin. In future, we will plan further mechanistic studies on most potent active compounds 12f, 12g and 12i.

Publisher

Bentham Science Publishers Ltd.

Subject

Organic Chemistry,Biochemistry

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