New 2-Imino-2H-Chromene-3(N-aryl)carboxamides as Potential Cytotoxic Agents

Author(s):

Rupinder Kaur Gill, Jyoti Kumari and Jitender Bariwal   Pages 85 - 92 ( 8 )

Abstract:

Synthesis and structure activity relationships of four series of novel 2-imino-2H-chromene-3(N-aryl) carboxamides (V-VIII) have been described by bioisosteric replacement of usually present ketone at 2nd position of coumarin with imine. Various substitutents are introduced on aryl and chromene ring of iminocoumarin to investigate the effect of lipophilicity and electronic properties of substituents on cytotoxic activity against four human cancer cell lines. Novel 2-imino-2H-chromene-3(N-aryl)carboxamides (V-VIII) were synthesized by the reaction of substituted 2- cyanoacetamides with different salicyaldehydes in the presence of sodium acetate in glacial acetic acid. Compound VIa showed potent activity against MCF-7 (IC₅₀ = 8.5 μM), PC-3 (IC₅₀ = 35.0 μM), A-549 (IC₅₀ = 0.9 μM) and Caco-2 (IC₅₀ = 9.9 μM) cell lines. The anticancer results revealed that most of the synthesized compounds showed equipotent activity with the standard 5-fluorouracil and docetaxel on Caco-2 and MCF-7 cell lines, respectively.

Keywords:

Coumarin, cytotoxicity, bioisosteric, carboxamides, MCF-7.

Affiliation:

, , Department of Pharmaceutical Chemistry, ISF College of Pharmacy, Moga-142001, Punjab, India.

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