891090-80-5

Upstream product

• 56047-52-0 4-(((tert-butoxycarbonyl)amino)methyl)-3-nitrobenzoic acid 
• 124-30-1 1-aminooctadecane 
• 130029-56-0 3-nitro-4-{[(trifluoroacetyl)amino]methyl}benzoic acid 
• 2372-51-2 4-(aminomethyl)-3-nitrobenzoic acid 
• 24424-99-5 di-tert-butyl dicarbonate 
• 56-91-7 p-aminomethylbenzoic acid 
• 130029-61-7 4-[[(2,2,2-trifluoroacetyl)amino]methyl]benzoic acid 

Downstream Products

• 891090-28-1 3-t-butoxycarbonylamino-N-(2-nitro-4-octadecylcarbamoylbenzyl)succinamic acid t-butyl ester 
• 891090-36-1 4-t-butoxycarbonylamino-4-(2-nitro-4-octadecylcarbamoylbenzylcarbamoyl)butyric acid t-butyl ester 
• 891090-44-1 [5-t-butoxycarbonylamino-1-(2-nitro-4-octadecylcarbamoylbenzylcarbamoyl)pentyl]carbamic acid t-butyl ester 
• 891090-20-3 N-stearyl-4-(aminomethyl)-3-nitrobenzamide 

Relevant academic research and scientific papers

Formulation of photocleavable liposomes and the mechanism of their content release

In pursuit of designing photocleavable liposomes as drug delivery vehicles, we synthesized several amphiphilic lipids by connecting stearyl amine (as the non-polar tail) and charged amino acids (as polar heads) via the o-nitrobenzyl derivatives. The lipid

Design of photocleavable lipids and their application in liposomal "uncorking"

The design of o-nitrobenzyl containing photocleavable lipid-amino acid conjugates, and their application in liposomal uncorking are described. The Royal Society of Chemistry 2005.