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Synthesis, antimicrobial, and mitotic toxicity evaluation of new 6-substituted 2-(benzo[4,5]imidazo[1,2-c]quinazolin-5(6H)-yl)acetic acids

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JOURNAL OF HETEROCYCLIC CHEMISTRY
卷 58, 期 1, 页码 212-225

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WILEY
DOI: 10.1002/jhet.4161

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A series of novel compounds were synthesized and characterized, showing significant cytotoxicity for meristematic cells and slight susceptibility to some microbial strains.
A series of novel 6-substituted 2-(benzo[4,5]imidazo[1,2-c]quinazolin-5(6H)-yl)acetic acids were synthesized and characterized by(1)H,C-13,F-19 NMR,H-1-H-1-COSY,H-1-C-13-HSQC, NOESY, LC-MS, IR, and elemental analysis. The mitotic toxicity of the synthesized compounds was determined according to the Allium test procedure. The 2-(6-(pentafluorophenyl)benzo[4,5]imidazo[1,2-c]quinazolin-5(6H)-yl)acetic acid inhibited mitotic spindle formation, which resulted in significant cytotoxic effect for meristematic cells ofAllium cepal. roots. In a preliminary antimicrobial evaluation, onlyStreptococcus pyogenesandCandida albicanswere slightly susceptible to some of the synthesized compounds.

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