Azo-Schiff base derivatives of transition metal complexes as antimicrobial agents

M Pervaiz, S Sadiq, A Sadiq, U Younas, A Ashraf… - Coordination Chemistry …, 2021 - Elsevier
M Pervaiz, S Sadiq, A Sadiq, U Younas, A Ashraf, Z Saeed, M Zuber, A Adnan
Coordination Chemistry Reviews, 2021Elsevier
AMR (Antimicrobial-resistant) pathogens like MRSA (Methicillin-Resistant Staphylococcus
aureus) have become prodigious peril to human health in the past couple of years with the
failure of various antifungals and antibiotics in treating mild to chronic mycoses and
septicemia. In the grave concern for the rising contagions, Azo-Schiff Bases with dual
functionality and far-ranging pharmacological potential has been considered an excellent
target for antimicrobial investigations. A diversity of homocyclic and heterocyclic organic …
Abstract
AMR (Antimicrobial-resistant) pathogens like MRSA (Methicillin-Resistant Staphylococcus aureus) have become prodigious peril to human health in the past couple of years with the failure of various antifungals and antibiotics in treating mild to chronic mycoses and septicemia. In the grave concern for the rising contagions, Azo-Schiff Bases with dual functionality and far-ranging pharmacological potential has been considered an excellent target for antimicrobial investigations. A diversity of homocyclic and heterocyclic organic precursors has been utilized for submitting novelty in the Azo-Schiff Base Ligands (ASBLs). In addition, the d-block transition metal chelates of ASBLs with infinitely diverse features have also been synthesized and characterized exploiting the classical and advanced analytical techniques. These resourceful coordination compounds owing to their characteristic polydentate ligands with multiple coordination sites, the geometry of complexes, and redox nature of metal centres are bestowed with the structural tunability to reinvigorate their potential applications. A detailed literature survey divulged that no compendious review has yet been published on ASBL-metal derivatives. Therefore, the present study encompasses the research undertaken during the last two decennia for the development and in vitro antimicrobial screening of these prospective drug agents.
Elsevier
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