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A Simple and Efficient Procedure Toward 2-Thioxoquinazolin-4(1H)-One Derivatives Publisher



Ahmadi Shourkaei F1 ; Rashidi Ranjbar P1 ; Mahdavi M2 ; Tuzun B3 ; Taslimi P4
Authors
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Authors Affiliations
  1. 1. School of Chemistry, College of Science, University of Tehran, Tehran, Iran
  2. 2. Endocrinology and Metabolism Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Plant and Animal Production Department, Technical Sciences Vocational School of Sivas, Sivas Cumhuriyet University, Sivas, Turkey
  4. 4. Department of Biotechnology, Faculty of Science, Bartin University, Bartin, Turkey

Source: Iranian Journal of Chemistry and Chemical Engineering Published:2024


Abstract

A facile synthetic route for constructing 2-thioxoquinazolin-4(1H)-one derivative through cyclization reactions using readily available starting materials 2-aminobenzoic acids, alkyl/aryl amines, and carbon disulfide is described. These reactions occur under mild conditions, producing the desired products with good to high yields. Molecular docking was conducted to assess the activities of the 2-thioxoquinazolin-4(1H)-one derivative against breast cancer protein (PDB ID: 1JNX), liver cancer protein (PDB ID: 2H80), and colon cancer protein (PDB ID: 4UYA). Furthermore, an ADME/T analysis was performed to evaluate the impact of these compounds on human metabolism. © 2024, Iranian Institute of Research and Development in Chemical Industries. All rights reserved.