97559-40-5

Upstream product

• 124482-89-9 H-Phe-Phe-Val-Gly-Leu-Met-OBn 
• 103321-59-1 N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-leucine, acid chloride 
• 103321-57-9 2S-flouren-9-ylmethoxycarbonylamino-3-phenylpropionyl chloride 
• 35661-40-6 N-Fmoc L-Phe 
• 103321-53-5 (S)-(9H-fluoren-9-yl)methyl 1-chloro-3-methyl-1-oxobutan-2-ylcarbamate 
• 738550-11-3 H-Leu-Met-OBn 
• 35661-60-0 Fmoc-Leu-OH 
• 68858-20-8 Fmoc-Val-OH 
• 89671-31-8 H-Phe-Val-Gly-Leu-Met-NH₂ 
• 89680-70-6 Boc-Phe-Val-Gly-Leu-Met-NH₂ 
• 91682-48-3 (S)-2-[2-((S)-2-Amino-3-methyl-butyrylamino)-acetylamino]-4-methyl-pentanoic acid ((S)-1-carbamoyl-3-methylsulfanyl-propyl)-amide 
• 16217-56-4 (S,S)-leucinylmethionine amide 
• 2575-66-8 Boc-Val-Gly-Leu-Met-NH₂ 
• 45233-75-8 2-[[(2S)-2-(tert-butoxycarbonylamino)-3-methyl-butanoyl]amino]acetic acid 

Relevant academic research and scientific papers

Rapid Continous Peptide Synthesis via FMOC Amino Acid Chloride Coupling and 4-(Aminomethyl)piperidine Deblocking

The recently described FMOC/4-AMP technique for rapid continous solution synthesis of peptides involving coupling by crystalline FMOC amino acid chlorides and deblocking via 4-(aminomethyl)piperidine (4-AMP) has been extended to the synthesis of a varied

NEUROKININ &α AND &β, SYNTHESIS AND PHARMACOLOGICAL PROPERTIES

Two novel neuropeptides, neurokinin α and β, isolated from porcine spinal cord were chemically synthesized by solution method.The amino acid sequences proposed were confirmed to be correct and pharmacological properties of neurokinin peptides were studied