Activation of carbonic anhydrases from human brain by amino alcohol oxime ethers: towards human carbonic anhydrase VII selective activators.

J Enzyme Inhib Med Chem

Section of Pharmaceutical and Nutraceutical Sciences, Department of Neuroscience, Psychology, Drug Research and Child's Health (Neurofarba), University of Florence, Sesto Fiorentino, Italy.

Published: December 2021

AI Article Synopsis

  • The study explores the effects of a range of oxime ether-based amino alcohols on activating four human carbonic anhydrase (CA) isoforms (hCA I, II, IV, and VII) found in the brain.
  • Most of these amino alcohol derivatives showed a consistent activation of the CAs, with effectiveness measured in low micromolar to medium nanomolar ranges, particularly enhancing the activity of hCA II and VII.
  • The findings highlight hCA VII's significance in brain metabolism, suggesting that the newly identified selective activators could be valuable for therapeutic research and the development of more potent CA activators.

Article Abstract

The synthesis and carbonic anhydrase (CA; EC 4.2.1.1) activating effects of a series of oxime ether-based amino alcohols towards four human (h) CA isoforms expressed in human brain, hCA I, II, IV and VII, are described. Most investigated amino alcohol derivatives induced a consistent activation of the tested CAs, with Ks spanning from a low micromolar to a medium nanomolar range. Specifically, hCA II and VII, putative main CA targets when central nervous system (CNS) diseases are concerned, were most efficiently activated by these oxime ether derivatives. Furthermore, a multitude of selective hCA VII activators were identified. As hCA VII is one of the key isoforms involved in brain metabolism and other brain functions, the identified potent and selective hCA VII activators may be considered of interest for investigations of various therapeutic applications or as lead compounds in search of even more potent and selective CA activators.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7594847PMC
http://dx.doi.org/10.1080/14756366.2020.1838501DOI Listing

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