Related Experiment Video
Updated: Sep 18, 2025

Functionalized Spirocyclic Heterocycle Synthesis and Cytotoxicity Assay
Published on: February 9, 2021
Synthesis, characterization, and biological activity evaluation of 4,6-dihydropyrano[3,2-c]isochromene-3-carbonitrile
Salehe Sabouri1, Fatemeh Haghani2, Mehdi Abaszadeh3
1. ssabouri@kmu.ac.ir.
Abstract:
Herein, a series of new 2-amino-4,6-dihydropyrano[3,2-c]isochromene-3-carbonitrile derivatives (4a-o) have been synthesized by one-pot three component reaction of 4-hydroxyisocoumarin, various aromatic aldehydes, and malononitrile in the presence of triethylamine in EtOH at reflux conditions. All the newly synthesized compounds were characterized using standard spectroscopic techniques (FT-IR, 1H and 13C NMR) and elemental analysis. The cytotoxicity of the synthesized compounds was determined by MTT assay on one normal (3T3) and two cancer cell lines (A549 and MCF-7). It was revealed that some of these compounds (4b, 4f, and 4j) are toxic especially for MCF-7 cell line and can be considered as lead compounds for further investigation. Howevere, the other compounds had low cytotoxicity and can be suitable candidates for other pharmacological effects such as antibacterial, antifungal, antiviral, etc.
More Related Videos
07:30A Direct, Regioselective and Atom-Economical Synthesis of 3-Aroyl-N-hydroxy-5-nitroindoles by Cycloaddition of 4-Nitronitrosobenzene with Alkynones
Published on: January 21, 2020
07:12Cercosporin-Photocatalyzed [4+1]- and [4+2]-Annulations of Azoalkenes Under Mild Conditions
Published on: July 17, 2020
Related Concept Videos
Inhibition of Cdk Activity
Mutagenicity and Carcinogenicity
Aromatic Hydrocarbon Cations: Structural Overview
Removing one hydrogen from the intervening CH2 group...