Synthesis and structure-activity relationship study of novel 3-heteroarylcoumarins based on pyridazine scaffold as selective MAO-B inhibitors

MC Costas-Lago, P Besada… - European Journal of …, 2017 - Elsevier
Compounds of hybrid structure pyridazine-coumarin were discovered as potent, selective
and reversible inhibitors of monoamine oxidase B (MAO-B). These compounds were …

Synthesis and structure-activity relationship study of novel 3-heteroarylcoumarins based on pyridazine scaffold as selective MAO-B inhibitors

MC Costas-Lago, P Besada… - European journal …, 2017 - pubmed.ncbi.nlm.nih.gov
Compounds of hybrid structure pyridazine-coumarin were discovered as potent, selective
and reversible inhibitors of monoamine oxidase B (MAO-B). These compounds were …

Synthesis and structure-activity relationship study of novel 3-heteroarylcoumarins based on pyridazine scaffold as selective MAO-B inhibitors.

MC Costas-Lago, P Besada… - European Journal of …, 2017 - europepmc.org
Compounds of hybrid structure pyridazine-coumarin were discovered as potent, selective
and reversible inhibitors of monoamine oxidase B (MAO-B). These compounds were …

Synthesis and structure-activity relationship study of novel 3-heteroarylcoumarins based on pyridazine scaffold as selective MAO-B inhibitors

MC Costas-Lago, P Besada, F Rodríguez-Enríquez… - 2017 - repositorio.uautonoma.cl
Compounds of hybrid structure pyridazine-coumarin were discovered as potent, selective
and reversible inhibitors of monoamine oxidase B (MAO-B). These compounds were …