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Origin of Antimicrobial Drug Design | OMICS International| Abstract

World Journal of Pharmacology and Toxicology
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Origin of Antimicrobial Drug Design

Amman Kurdish1* and Alex David2
1Department of Pharmacology, University of Minnesota, U.S.A
2Department of Pharmacology, University of Minnesota, U.S.A
*Corresponding Author : Amman Kurdish, Department of Pharmacology, University of Minnesota, U.S.A, Email: kurdishamman@um.ac.org

Received Date: Nov 01, 2023 / Accepted Date: Nov 30, 2023 / Published Date: Nov 30, 2023

Abstract

The presentation of anti-infection agents into clinical practice altered the treatment and the executives of irresistible illnesses. Before the resentation of anti-toxins, these sicknesses were the main source of morbidity and mortality in human populaces. This survey presents a short history of disclosure of the fundamental antimicrobial classes (arsphenamines, b-lactams, sulphonamides, polypeptides, aminoglycosides, tetracyclines, amphenicols, lipopeptides, macrolides, oxazolidinones, glycopeptides, streptogramins, ansamycins, quinolones, and lincosamides) that have changed the scene of contemporary medication. Given inside a verifiable course of events setting, the survey examines how the presentation of specific antimicrobial classes impacted the horribleness and death rates because of bacterial irresistible illnesses in human populations. Issues of protection from anti-infection agents of various classes are likewise widely talked about.

Citation: Kurdish A (2023) Origin of Antimicrobial Drug Design. World J PharmacolToxicol 6: 219.

Copyright: © 2023 Kurdish A. This is an open-access article distributed under theterms of the Creative Commons Attribution License, which permits unrestricteduse, distribution, and reproduction in any medium, provided the original author andsource are credited.

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