1271925-54-2

Upstream product

• 1192235-33-8 3-(2-phenyl-benzo[b]thiophen-3-yl)-prop-2-ynyl 4-O-acetyl-2,3,6-trideoxy-α-L-erythro-hexopyranoside 
• 1271934-16-7 3-(2-phenyl-benzo[b]thiophen-3-yl)-propyl 4-amino-2,3,4,6-tetradeoxy-α-L-threo-hexopyranoside 
• 1271934-20-3 3-(2-phenyl-benzo[b]thiophen-3-yl)-propyl 4-O-acetyl-2,3,6-trideoxy-α-L-erythro-hexopyranoside 
• 1271934-24-7 3-(2-phenyl-benzo[b]thiophen-3-yl)-propyl 2,3,6-trideoxy-α-L-erythro-hexopyranoside 
• 1271925-52-0 3-(2-phenyl-benzo[b]thiophen-3-yl)-prop-2-ynyl 4-O-benzoyl-2,3,6-trideoxy-α-L-threo-hexopyranoside 
• 1271925-53-1 3-(2-phenyl-benzo[b]thiophen-3-yl)-prop-2-ynyl 2,3,6-trideoxy-α-L-threo-hexopyranoside 

Downstream Products

• 1271925-55-3 3-(2-phenyl-benzo[b]thiophen-3-yl)-prop-2-ynyl 4-amino-2,3,4,6-tetradeoxy-α-L-erythro-hexopyranoside 

Relevant academic research and scientific papers

Structure-activity relationships in glycosylated 2-phenyl-indoles, 2-phenyl-benzo[b]thiophenes and 2-phenyl-benzo[b]furans as DNA binding and potential antitumor agents

In earlier investigations we have described the synthesis and biological evaluation of a panel of novel glycosylated heteroaromatics (1-12). It was found that these compounds can bind to DNA in vitro and are cytotoxic against several cancer cell lines at