175085-91-3

Upstream product

• 3556-56-7 4-nitrophenyl N-[(benzyloxy)carbonyl]-L-tyrosinate 
• 24424-99-5 di-tert-butyl dicarbonate 
• 130203-35-9 N-carbobenzoxy-L-tyrosine-spermine amide 
• 71-44-3 Spermine 

Downstream Products

• 175085-93-5 (5-{(S)-1-[3-(tert-Butoxycarbonyl-{4-[tert-butoxycarbonyl-(3-tert-butoxycarbonylamino-propyl)-amino]-butyl}-amino)-propylcarbamoyl]-2-[4-(tetrahydro-pyran-2-yloxy)-phenyl]-ethylcarbamoyl}-pentyl)-carbamic acid benzyl ester 
• 175085-92-4 {5-[(S)-1-[3-(tert-Butoxycarbonyl-{4-[tert-butoxycarbonyl-(3-tert-butoxycarbonylamino-propyl)-amino]-butyl}-amino)-propylcarbamoyl]-2-(4-hydroxy-phenyl)-ethylcarbamoyl]-pentyl}-carbamic acid benzyl ester 
• 175085-90-2 {4-[(3-{(S)-2-(6-Amino-hexanoylamino)-3-[4-(tetrahydro-pyran-2-yloxy)-phenyl]-propionylamino}-propyl)-tert-butoxycarbonyl-amino]-butyl}-(3-tert-butoxycarbonylamino-propyl)-carbamic acid tert-butyl ester 
• 144117-57-7 L-tyrosine-N',N'',N'''-tri-tert-butoxycarbonyl-spermine amide 

Relevant academic research and scientific papers

Synthesis of philanthotoxin analogs with bulky heads including porphyrins. Self-assembly monitored by circular dichroism

Philanthotoxin (PhTX) analogs with bulky bis-iminodibenzyl and porphyrin head groups have been prepared. Exciton coupled CD studies show that dependent on the hydrophobicity of the head group PhTX analogs may get amphiphilic properties forming micelles in