Comprehensive insights into carbonic anhydrase inhibition: A triad of In vitro, In silico, and In vivo perspectives.

Journal: Enzyme and microbial technology
Published Date:

Abstract

Carbonic anhydrases (CAs) are zinc-dependent metalloenzymes essential for sustaining physiological balance by facilitating the reversible conversion of carbon dioxide to its hydrated form. Their biological significance, coupled with their involvement in a wide array of pathological conditions, makes them attractive targets for therapeutic intervention. This review presents a comprehensive analysis of carbonic anhydrase inhibition through an integrated triad of in vitro, In silico, and In vivo perspectives. In vitro studies provide critical insights into the mechanisms of enzyme inhibition, enabling the identification and optimization of potent inhibitors while elucidating their structure-activity relationships. In silico methodologies, including docking, molecular dynamics (MD) simulation, virtual screening, ADMET, and QSAR analyses, have emerged as invaluable tools in rational drug design, streamlining the discovery and development of isoform-specific inhibitors. Complementing these efforts, In vivo investigations validate the pharmacokinetics, pharmacodynamics, and therapeutic efficacy of CA inhibitors (CAIs) in disease models, bridging the gap between laboratory findings and clinical applications. The therapeutic relevance of CAIs extends across multiple domains, including glaucoma, epilepsy, cancer, metabolic disorders, and infectious diseases. Emerging applications, such as their potential use in combating antimicrobial resistance and modulating immune responses, further underscore their versatility. However, challenges such as achieving isoform selectivity, minimizing off-target effects, and translating preclinical findings into clinical success persist. Advances in fragment-based drug design, artificial intelligence-driven discovery, and innovative experimental techniques are poised to address these limitations, paving the way for the next generation of CAIs.

Authors

  • Ahmed A Allam
    Department of Biology, College of Science, Imam Mohammad Ibn Saud Islamic University (IMSIU), Riyadh 11623, Saudi Arabia.
  • Hassan A Rudayni
    Biology Department, College of Science, Imam Mohammad Ibn Saud Islamic University, Riyadh 11623, Saudi Arabia.
  • Noha A Ahmed
    Physiology Division, Zoology Department, Faculty of Science, Beni-Suef University, P.O. Box 62521, Beni-Suef, Egypt.
  • Faris F Aba Alkhayl
    Department of Medical Laboratories, College of Applied Medical Sciences, Qassim University, Buraydah, 51452, Saudi Arabia.
  • Al Mokhtar Lamsabhi
    Departamento de Química and Institute for advanced research in chemical Science (IAdChem), Facultad de Ciencias, Módulo 13, Universidad Autónoma de Madrid, Madrid 28049, Spain.
  • Emadeldin M Kamel
    Chemistry Department, Faculty of Science, Beni-Suef University, Beni-Suef 62514, Egypt. Electronic address: emad.abdelhameed@science.bsu.edu.eg.