97423-72-8

Upstream product

• 13139-15-6 N-tert-butoxycarbonyl-L-leucine 
• 97423-71-7 D-Phe-Pro-OCH₂Ph 
• 41324-66-7 H-Pro-OBzl 
• 96935-61-4 H-D-Phe-L-Pro-OCH₂Ph hydrochloride 
• 64471-88-1 (S)-benzyl 1-((R)-2-(tert-butoxycarbonylamino)-3-phenylpropanoyl)pyrrolidine-2-carboxylate 
• 16652-71-4 benzyl (2S)-2-pyrrolidinecarboxylate hydrochloride 
• 18942-49-9 Boc-D-Phe-OH 

Downstream Products

• 121504-91-4 H-D-Leu-Val-Orn(Z)-Leu-Leu-D-Phe-Pro-OH 
• 121504-89-0 H-Leu-Val-Orn(Z)-Leu-Leu-D-Phe-Pro-OH 
• 121504-74-3 Boc-D-Leu-Val-Orn(Z)-Leu-Leu-D-Phe-Pro-OH 
• 121504-72-1 Boc-Leu-Val-Orn(Z)-Leu-Leu-D-Phe-Pro-OH 
• 121504-69-6 Boc-Leu-Val-Orn(Z)-Leu-Leu-D-Phe-Pro-OBzl 
• 121504-71-0 Boc-D-Leu-Val-Orn(Z)-Leu-Leu-D-Phe-Pro-OBzl 
• 121504-75-4 Boc-Leu-Val-Orn(Z)-Leu-Leu-D-Phe-Pro-OSu 
• 121504-77-6 Boc-D-Leu-Val-Orn(Z)-Leu-Leu-D-Phe-Pro-OSu 
• 97423-78-4 (S)-1-{(R)-2-[(S)-2-((S)-2-Amino-4-methyl-pentanoylamino)-4-methyl-pentanoylamino]-3-phenyl-propionyl}-pyrrolidine-2-carboxylic acid benzyl ester 
• 133693-06-8 HCl*H-Val-D-Lys(Z)-Leu-D-Phe-Pro-OH 
• 133693-04-6 Boc-Val-D-Lys(Z)-Leu-D-Phe-Pro-OH 
• 133693-05-7 Boc-Val-D-Lys(Z)-Leu-D-Phe-Pro-ONSu 
• 133693-03-5 Boc-Val-D-Lys(Z)-Leu-D-Phe-Pro-OBzl 
• 97475-37-1 Boc-D-Phe-Val-Orn(Z)-Leu-D-Phe-Pro-N₃ 

Relevant academic research and scientific papers

CONFIGURATIONAL REQUIREMENTS OF AROMATIC AMINO ACID RESIDUES FOR THE ACTIVITY OF PRP-HEXAPEPTIDE

The three analogues with D-amino acid substituents at position 1 and 5 of PRP-hexapeptide were synthesized and tested for its biological activity to check the influence of the spatial orientation of aromatic rings on the immune response.One of the analogs

Synthesis and properties of gramicidin S analogs containing Pro-D-Phe sequence in place of D-Phe-Pro sequence in the β-turn part of the antibiotic

Two analogs of gramicidin S, [L-Pro4, D-Phe5]-gramicidin S and [L-Pro(4,4'), D-Phe(5,5')]-gramicidin S, were synthesized in order to investigate the relationships among positions of Pro residues, antibiotic activity and CD spectra. [

Studies on peptide antibiotic 'gratisin'

According to a primary structure proposed for an antibiotic peptide, gratisin, four peptides containing respectively partial sequences, L-Phe-L-Pro-L-Tyr, D-Phe-L-Pro-L-Tyr, L-Phe-L-Pro-D-Tyr, and D-Phe-L-Pro-D-Tyr, were synthesized by a liquid phase meth