1313055-17-2

Upstream product

• 98-61-3 p-Iodobenzenesulfonyl chloride 
• 20099-89-2 4-Cyanophenacyl bromide 
• 1313054-94-2 4-[2-(4-iodophenylsulfonyl)acetyl]benzonitrile 
• 1313055-05-8 4-[5-benzyl-3-(4-iodophenylsulfonyl)-5-methyl-4,5-dihydrofuran-2-yl]benzonitrile 

Relevant academic research and scientific papers

Synthesis and evaluation of monoamidoxime derivatives: Toward new antileishmanial compounds

A new series of monoamidoxime derivatives was synthesized using manganese(III) acetate by microwave irradiation. Several amidoximes (27-31, 33, 38) showed valuable in vitro activities toward Leishmania donovani promastigotes, exhibiting IC50 values between 5.21 and 7.89 μM. In parallel, the cytotoxicity of these compounds was evaluated on murine J774A.1 cells, revealing the corresponding selectivity index (SI). Among the 13 tested compounds, 4 monoamidoximes (27-30) exhibited an SI more than 20 times better than pentamidine. Moreover, monoamidoxime 28 (4-[5-Benzyl-3-(4- fluorophenylsulfonyl)-5-methyl-4,5-dihydrofuran-2-yl]-N′- hydroxybenzimidamide) is 40 times more selective than pentamidine, and 1.6 times more than amphotericin B, used as reference drug compounds.