143868-68-2

Upstream product

• 98714-71-7 methyl 2-[((2S)-2-[[(benzyloxy)carbonyl]amino]-3-phenylpropanoyl)amino]-2-methylpropanoate 
• 2637-44-7 N-benzyloxycarbonyl-L-tryptophylaminoethanol 
• 7432-21-5 N-carbobenzyloxy-L-tryptophane 
• 143868-61-5 Z-Trp-Aib-Trp-Glyol 
• 133641-28-8 Z-Trp-O-COO-isoBu 
• 143868-52-4 Z-Trp-Aib-OH 
• 143868-55-7 methyl 2-[(2S)-2-[[(benzyloxy)carbonyl]amino]-3-(1H-indol-3-yl)propanoyl]amino-2-methylpropanoate 
• 1685-28-5 (S)-2-amino-N-(2-hydroxyethyl)-3-(1H-indole-3-yl)propionamide 
• 41518-17-6 Z-Phe-O-COO-isoBu 
• 1161-13-3 N-Cbz-L-Phe 
• 109772-33-0 N-benzyloxycarbonyl-L-phenylalanyl-2-methylalanine 
• 143868-60-4 H-Trp-Aib-Trp-Glyol 

Downstream Products

• 143868-65-9 H-Trp-Aib-Phe-Aib-Trp-Aib-Trp-Glyol 
• 143868-66-0 Z-Trp-Aib-Phe-Aib-Trp-Aib-Trp-Glyol 
• 143868-67-1 H-Phe-Aib-Trp-Aib-Trp-Glyol 

Relevant academic research and scientific papers

Changes in Conformation and Antimicrobial Properties Caused by Replacement of D-Amino Acids with α-Aminoisobutyric Acid in the Gramicidin Backbone: Synthesis and Circular Dichroic Studies

In an attempt to mimic the stable helical structures of proteins with possible pore-forming ability in membranes, the linear gramicidin backbone has been changed by inserting achiral α-aminoisobutyric acids (Aib) in place of all of the alternatively seque