35157-96-1

Upstream product

• 86571-08-6 2,2'-selenedibenzoic acid 
• 17333-86-7 o-Carboxybenzenediazonium 
• 6512-83-0 2,2'-diselanediyl-di-benzoic acid 
• 118-92-3 anthranilic acid 

Downstream Products

• 1256612-34-6 bis[2-(N-n-propylcarbamoyl)phenyl] selenide 
• 155228-83-4 bis[2-(N-phenylcarbamoyl)phenyl] selenide 
• 1256612-29-9 bis[2-(N-methylcarbamoyl)phenyl] selenide 
• 1402034-89-2 2,2'-selenobis(N-(2-methoxyphenyl)benzamide) 
• 1402034-96-1 C₂₈H₂₂N₂O₄Se 
• 1402034-88-1 C₂₈H₂₀N₂O₆Se 
• 1402034-95-0 C₂₈H₁₈N₂O₆Se 
• 1402034-87-0 C₂₈H₂₄N₂O₂Se 
• 1402034-86-9 C₂₆H₁₈Br₂N₂O₂Se 
• 1402034-93-8 C₂₆H₁₆Br₂N₂O₂Se 
• 1402034-85-8 C₂₆H₁₈Cl₂N₂O₂Se 
• 1402034-92-7 C₂₆H₁₆Cl₂N₂O₂Se 
• 1402034-84-7 2,2'-selenobis(N-(3-methoxyphenyl)benzamide) 
• 1402034-91-6 C₂₈H₂₂N₂O₄Se 

Relevant academic research and scientific papers

Crucial role of selenium in the virucidal activity of benzisoselenazol- 3(2h)-ones and related diselenides

Various N-substituted benzisoselenazol-3(2H)-ones and their non-seleniumcontaining analogues have been synthesized and tested against selected viruses (HHV-1, EMCV and VSV) to determine the extent to which selenium plays a role in antiviral activity. The data presented here show that the presence of selenium is crucial for the antiviral properties of benzisoselenazol-3(2H)-ones since their isostructural analogues having different groups but lacking selenium either did not show any antiviral activity or their activity was substantially lower. The open-chain analogues of benzisoselenazol- 3(2H)-ones-diselenides also exhibited high antiviral activity while selenides and disulfides were completely inactive towards model viruses.