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Synthesis and Biological Evaluation of Chalcone-Triazole Hybrid Derivatives As 15-Lox Inhibitors Publisher



Asadipour A2 ; Noushini S3 ; Moghimi S3 ; Mahdavi M4 ; Nadri H5 ; Moradi A5 ; Shabani S3 ; Firoozpour L3 ; Foroumadi A1, 2
Authors
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Authors Affiliations
  1. 1. Department of Medicinal Chemistry, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Department of Medicinal Chemistry, Faculty of Pharmacy and Neuroscience Research Center, Institute of Neuropharmacology, Kerman University of Medical Sciences, Kerman, Iran
  3. 3. Drug Design and Development Research Center, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Endocrinology and Metabolism Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran
  5. 5. Department of Medicinal Chemistry, Faculty of Pharmacy, Shahid Sadoughi University of Medical Sciences, Yazd, Iran

Source: Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences Published:2018


Abstract

An efficient aldol condensation/click reaction sequence is employed for the synthesis of chalcone-triazole-based derivatives in moderate to good yields. The ability of target compounds to inhibit 15-lipoxygenase enzyme was investigated and moderate to low inhibitory activities were observed for the synthesized compounds. © 2018 Walter de Gruyter GmbH, Berlin/Boston.