Evaluation of sulphonamide derivatives acting as inhibitors of human carbonic anhydrase isoforms I, II and Mycobacterium tuberculosisβ-class enzyme Rv3273

A series of novel sulphonamide derivatives was obtained from sulphanilamide which was N4-alkylated with ethyl bromoacetate followed by reaction with hydrazine hydrate. The hydrazide obtained was further reacted with various aromatic aldehydes. The novel sulphonamides were characterised by infrared,...

Descripción completa

Detalles Bibliográficos
Autores principales: Wani, Tanvi V., Bua, Silvia, Khude, Pravin S., Chowdhary, Abdul H., Supuran, Claudiu T., Toraskar, Mrunmayee P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6010129/
https://www.ncbi.nlm.nih.gov/pubmed/29772937
http://dx.doi.org/10.1080/14756366.2018.1471475

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6010129/
https://www.ncbi.nlm.nih.gov/pubmed/29772937
http://dx.doi.org/10.1080/14756366.2018.1471475

Ejemplares similares