Synthesis of calix[4]azacrown substituted sulphonamides with antioxidant, acetylcholinesterase, butyrylcholinesterase, tyrosinase and carbonic anhydrase inhibitory action

A series of novel calix[4]azacrown substituted sulphonamide Schiff bases was synthesised by the reaction of calix[4]azacrown aldehydes with different substituted primary and secondary sulphonamides. The obtained novel compounds were investigated as inhibitors of six human (h) isoforms of carbonic an...

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Veröffentlicht in:J Enzyme Inhib Med Chem
Hauptverfasser: Oguz, Mehmet, Kalay, Erbay, Akocak, Suleyman, Nocentini, Alessio, Lolak, Nebih, Boga, Mehmet, Yilmaz, Mustafa, Supuran, Claudiu T.
Format: Artigo
Sprache:Inglês
Veröffentlicht: Taylor & Francis 2020
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Research Paper
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7269057/
https://ncbi.nlm.nih.gov/pubmed/32401067
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/14756366.2020.1765166
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