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Synthesis of Chalcones Derivatives and Their Biological Activities: A Review.
Elkanzi, Nadia A A; Hrichi, Hajer; Alolayan, Ruba A; Derafa, Wassila; Zahou, Fatin M; Bakr, Rania B.
Afiliação
  • Elkanzi NAA; Chemistry Department, College of Science, Jouf University, Sakaka 2014, Saudi Arabia.
  • Hrichi H; Chemistry Department, College of Science, Jouf University, Sakaka 2014, Saudi Arabia.
  • Alolayan RA; Chemistry Department, College of Science, Jouf University, Sakaka 2014, Saudi Arabia.
  • Derafa W; Chemistry Department, College of Science, Jouf University, Sakaka 2014, Saudi Arabia.
  • Zahou FM; Biology Department, College of Science, Jouf University, Sakaka 2014, Saudi Arabia.
  • Bakr RB; Department of Pharmaceutical Organic Chemistry, Faculty of Pharmacy, Beni-Suef University, Beni-Suef 62514, Egypt.
ACS Omega ; 7(32): 27769-27786, 2022 Aug 16.
Article em En | MEDLINE | ID: mdl-35990442
ABSTRACT
Chalcone derivatives are considered valuable species because they possess a ketoethylenic moiety, CO-CH=CH-. Due to the presence of a reactive α,ß-unsaturated carbonyl group, chalcones and their derivatives possess a wide spectrum of antiproliferative, antifungal, antibacterial, antiviral, antileishmanial, and antimalarial pharmacological properties. Recent developments in heterocyclic chemistry have led to the synthesis of chalcone derivatives, which had been biologically investigated toward certain disease targets. The major aspect of this review is to present the most recent synthesis of chalcones bearing N, O, and/or S heterocycles, revealing their biological potential during the past decade (2010-2021). Based on a review of the literature, many chalcone-heterocycle hybrids appear to exhibit promise as future drug candidates owing to their similar or superior activities compared to those of the standards. Thus, this review may prove to be beneficial for the development and design of new potent therapeutic drugs based on previously developed strategies.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article