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

Internet

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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