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

• Үндсэн зохиолчид: Tanvi V. Wani (Зохиогч), Silvia Bua (Зохиогч), Pravin S. Khude (Зохиогч), Abdul H. Chowdhary (Зохиогч), Claudiu T. Supuran (Зохиогч), Mrunmayee P. Toraskar (Зохиогч)
• Формат: Ном
• Хэвлэсэн: Taylor & Francis Group, 2018-01-01T00:00:00Z.
• Нөхцлүүд: article
• Онлайн хандалт: Connect to this object online.

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,...