Journal of Enzyme Inhibition and Medicinal Chemistry (Jan 2021)

Carbonic anhydrase activation profile of indole-based derivatives

  • Elisabetta Barresi,
  • Rahul Ravichandran,
  • Lorenzo Germelli,
  • Andrea Angeli,
  • Emma Baglini,
  • Silvia Salerno,
  • Anna Maria Marini,
  • Barbara Costa,
  • Eleonora Da Pozzo,
  • Claudia Martini,
  • Federico Da Settimo,
  • Claudiu Supuran,
  • Sandro Cosconati,
  • Sabrina Taliani

DOI
https://doi.org/10.1080/14756366.2021.1959573
Journal volume & issue
Vol. 36, no. 1
pp. 1783 – 1797

Abstract

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Carbonic Anhydrase Activators (CAAs) could represent a novel approach for the treatment of Alzheimer’s disease, ageing, and other conditions that require remedial achievement of spatial learning and memory therapy. Within a research project aimed at developing novel CAAs selective for certain isoforms, three series of indole-based derivatives were investigated. Enzyme activation assay on human CA I, II, VA, and VII isoforms revealed several effective micromolar activators, with promising selectivity profiles towards the brain-associated cytosolic isoform hCA VII. Molecular modelling studies suggested a theoretical model of the complex between hCA VII and the new activators and provide a possible explanation for their modulating as well as selectivity properties. Preliminary biological evaluations demonstrated that one of the most potent CAA 7 is not cytotoxic and is able to increase the release of the brain-derived neurotrophic factor (BDNF) from human microglial cells, highlighting its possible application in the treatment of CNS-related disorders.

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