Design and synthesis of novel chalcones as potent selective monoamine oxidase-B inhibitors

A Hammuda, R Shalaby, S Rovida… - European journal of …, 2016 - Elsevier
A novel series of substituted chalcones were designed and synthesized to be evaluated as
selective human MAO-B inhibitors. A combination of either methylsulfonyl or trifluoromethyl …

Design and synthesis of novel chalcones as potent selective monoamine oxidase-B inhibitors

A Hammuda, R Shalaby, S Rovida, DE Edmondson… - 2016 - qspace.qu.edu.qa
A novel series of substituted chalcones were designed and synthesized to be evaluated as
selective human MAO-B inhibitors. A combination of either methylsulfonyl or trifluoromethyl …

Design and synthesis of novel chalcones as potent selective monoamine oxidase-B inhibitors.

A Hammuda, R Shalaby, S Rovida… - EUROPEAN JOURNAL …, 2016 - iris.unipv.it
A novel series of substituted chalcones were designed and synthesized to be evaluated as
selective human MAO-B inhibitors. A combination of either methylsulfonyl or trifluoromethyl …

Design and synthesis of novel chalcones as potent selective monoamine oxidase-B inhibitors.

A Hammuda, R Shalaby, S Rovida… - European Journal of …, 2016 - europepmc.org
A novel series of substituted chalcones were designed and synthesized to be evaluated as
selective human MAO-B inhibitors. A combination of either methylsulfonyl or trifluoromethyl …

Design and synthesis of novel chalcones as potent selective monoamine oxidase-B inhibitors

A Hammuda, R Shalaby, S Rovida… - European Journal of …, 2016 - infona.pl
A novel series of substituted chalcones were designed and synthesized to be evaluated as
selective human MAO-B inhibitors. A combination of either methylsulfonyl or trifluoromethyl …

Design and synthesis of novel chalcones as potent selective monoamine oxidase-B inhibitors

A Hammuda, R Shalaby, S Rovida… - European journal …, 2016 - pubmed.ncbi.nlm.nih.gov
A novel series of substituted chalcones were designed and synthesized to be evaluated as
selective human MAO-B inhibitors. A combination of either methylsulfonyl or trifluoromethyl …

Design and synthesis of novel chalcones as potent selective monoamine oxidase-B inhibitors

A Hammuda, R Shalaby, S Rovida, DE Edmondson… - 2016 - qspace.qu.edu.qa
A novel series of substituted chalcones were designed and synthesized to be evaluated as
selective human MAO-B inhibitors. A combination of either methylsulfonyl or trifluoromethyl …