140480-22-4

Upstream product

• 70-34-8 2,4-Dinitrofluorobenzene 
• 101485-34-1 N^α-(benzyloxycarbonyl)-erythro-β-hydroxy-L-histidine 

Downstream Products

• 140480-27-9 ethyl (S)-4-<α-<<6-<amino>ethyl>-N-<(o-nitrophenyl)thio>amino>methyl>-4-methoxy-2-pyridyl>carbonyl>-erythro-β-tert-butoxy-L-histidyl>amino>pentanoate 
• 123993-14-6 (S)-4-<α-<<6-<amino>ethyl>-N-<(o-nitrophenyl)thio>amino>methyl>-4-methoxy-2-pyridyl>carbonyl>-erythro-β-tert-butoxy-L-histidyl>amino>pentanoic acid 
• 140480-25-7 ethyl (S)-4-<α-(benzyloxycarbonyl)-erythro-β-tert-butoxy-L-histidyl>amino>pentanoate 
• 140480-24-6 ethyl (S)-4-<α-(benzyloxycarbonyl)-erythro-β-hydroxy-L-histidyl>amino>pentanoate 

Relevant academic research and scientific papers

Man-designed bleomycins: Significance of the binding sites as enzyme models and of the stereochemistry of the linker moiety

Comparison of the DNA cleavage activity of man-designed bleomycins demonstrates that belomycins are small enzymes comprised of a catalytic site and a binding site. The linker moiety is shown to be significant for DNA binding, and inversion of its stereoch