111324-56-2

Upstream product

• 624-83-9 methyl isocyanate 
• 111324-55-1 1-<<2-(dimethylamino)ethyl>amino>-7-<(tert-butyldiphenylsilyl)oxy>-4-(hydroxymethyl)-9H-thioxanthen-9-one 
• 111324-54-0 1-<<2-(dimethylamino)ethyl>amino>-7-<(tert-butyldiphenylsilyl)oxy>-9-oxo-9H-thioxanthene-4-carboxaldehyde 
• 111324-53-9 1-<<2-(dimethylamino)ethyl>amino>-9-oxo-7-(toluenesulfonyloxy)-9H-thioxanthene-4-carboxaldehyde 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 101339-44-0 1-<<2-(dimethylamino)ethyl>amino>-4-(hydroxymethyl)-7-(toluenesulfonyloxy)-9H-thioxanthen-9-one 
• 86456-32-8 1-<<2-(dimethylamino)ethyl>amino>-7-(toluenesulfonyloxy)-9H-thioxanthen-9-one 
• 86456-11-3 1-<<2-(dimethylamino)ethyl>amino>-7-hydroxy-9-oxo-9H-thioxanthene-4-carboxaldehyde 
• 86456-31-7 1-<<2-(dimethylamino)ethyl>amino>-7-hydroxy-9H-thioxanthen-9-one 

Relevant academic research and scientific papers

Preparation and antischistosomal and antitumor activity of hycanthone and some of its congeners. Evidence for the mode of action of hycanthone

The synthesis of a series of esters of hycanthone (HC) and 7-hydroxyhycanthone, their antitumor activity, and their antischistosomal effects on HC-sensitive and HC-resistant schistosomes are reported. Binding studies using tritium-labeled HC and hycanthon