3-Arylcoumarins as highly potent and selective monoamine oxidase B inhibitors: Which chemical features matter?

MARCO ANDRÉS MELLADO GARCÍA, Jaime Mella, César González, Dolores Viña, Eugenio Uriarte, Maria J. Matos

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

Monoamine oxidase B inhibitory activity is closely regulated by the interaction of the small molecules with the enzyme. It is therefore desirable to use theoretical approaches to design rational methods to develop new molecules to modulate specific interactions with the protein. Here, we report such methods, and we illustrate their successful implementation by studying six synthetized 3-arylcoumarins (71–76) based on them. Monoamine oxidase B inhibition is essential to maintain the balance of dopamine, and one of its major functions is to combat dopamine degradation, a phenomenon linked to Parkinson's disease. In this work, we study small-molecule inhibitors based on the 3-arylcoumarin scaffold and their monoamine oxidase B selective inhibition. We show that 3D-QSAR models, in particular CoMFA and CoMSIA, and molecular docking approaches, enhance the probability to find new interesting inhibitors, avoiding very costly and time-consuming synthesis and biological evaluations.

Original languageEnglish
Article number103964
JournalBioorganic Chemistry
Volume101
DOIs
StatePublished - Aug 2020
Externally publishedYes

Keywords

  • 3-Arylcoumarins
  • 3D-QSAR models
  • Drug design
  • Molecular docking
  • Monoamine oxidase B inhibitors

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