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Journal of Cellular and Molecular Pharmacology
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  • Commentary   
  • J Cell Mol Pharmacol 7: 193,

Enzyme Kinetics in Drug Discovery Accelerating Therapeutic Innovation

Daisuke Nakanishi*
Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Japan
*Corresponding Author : Daisuke Nakanishi, Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Japan, Email: daisuke.nakanishi@gmail.com

Received Date: Dec 01, 2023 / Published Date: Dec 29, 2023

Abstract

Enzyme kinetics is a fundamental discipline within biochemistry that has emerged as a key player in revolutionizing drug discovery. This article explores the pivotal role of enzyme kinetics in accelerating therapeutic innovation. The molecular dance between enzymes and substrates provides critical insights into reaction mechanisms, substrate specificity, and catalytic efficiency. Leveraging these insights, researchers can design drugs with unparalleled precision, leading to the development of targeted and effective therapeutic interventions. The article discusses how enzyme kinetics expedites the drug discovery process, from optimizing drug formulations to dissecting complex biological pathways. Furthermore, it highlights the synergy between experimental and computational approaches, paving the way for a new era of precision medicine. The journey from bench to bedside is illuminated, emphasizing the translation of kinetic discoveries into tangible therapeutic solutions. Finally, the article glimpses into the future, where emerging technologies promise to propel enzyme kinetics into new frontiers, fostering continued acceleration in therapeutic innovation

Citation: Nakanishi D (2023) Enzyme Kinetics in Drug Discovery AcceleratingTherapeutic Innovation. J Cell Mol Pharmacol 7: 193.

Copyright: © 2023 Nakanishi D. This is an open-access article distributed underthe terms 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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