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N-Cycloamino substituent effects on the packing architecture of ortho-sulfanilamide molecular crystals and their in silico carbonic anhydrase II and IX inhibitory activities

In the search for new ‘sulfa drugs’ with therapeutic properties, o-nitrosulfonamides and N-cycloamino-o-sulfanilamides were synthesized and characterized using techniques including (1)H NMR, (13)C NMR and FT–IR spectroscopy, and single-crystal X-ray diffraction (SC-XRD). The calculated density...

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Detalles Bibliográficos
Autores principales:	Kolade, Sherif O., Izunobi, Josephat U., Gordon, Allen T., Hosten, Eric C., Olasupo, Idris A., Ogunlaja, Adeniyi S., Asekun, Olayinka T., Familoni, Oluwole B.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	International Union of Crystallography 2022
Materias:	Research Papers
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720883/ https://www.ncbi.nlm.nih.gov/pubmed/36468556 http://dx.doi.org/10.1107/S2053229622010130

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