125405-90-5

Upstream product

• 81782-59-4 Gly-Ala-Gly-OBzl 
• 15401-08-8 N-tert-butoxycarbonyl-L-prolyl-L-proline 
• 33294-56-3 symmetric anhydride of Boc-Pro-OH 
• 691843-74-0 ((S)-2-{2-[((S)-Pyrrolidine-2-carbonyl)-amino]-acetylamino}-propionylamino)-acetic acid benzyl ester 
• 15761-39-4 1-(tert-butoxycarbonyl)-L-proline 
• 125405-89-2 (S)-2-({[(S)-1-(Benzyloxycarbonylmethyl-carbamoyl)-ethylcarbamoyl]-methyl}-carbamoyl)-pyrrolidine-1-carboxylic acid tert-butyl ester 

Downstream Products

• 119798-88-8 Pro-Pro-Gly-Ala-Gly-OBzl 
• 125405-91-6 {(S)-2-[2-({(S)-1-[(S)-1-(2-Benzyloxycarbonylamino-acetyl)-pyrrolidine-2-carbonyl]-pyrrolidine-2-carbonyl}-amino)-acetylamino]-propionylamino}-acetic acid benzyl ester 

Relevant academic research and scientific papers

Peptide synthesis in alcoholic solvents using 1-(β-naphthalenesulfonyloxy)-benztriazole as a coupling reagent

The use of 1-(β-naphthalenesulfonyloxy)-benztriazole (NSBT) as a peptide coupling reagent in protic solvents is described.This reagent is useful for coupling peptide fragments with poor solubility in aprotic solvents.

SYNTHESIS, CONFORMATIONAL FEATURES AND BIOLOGICAL ACTIVITY OF 3> ANTIARRHYTHMIC PEPTIDE

Synthesis of Gly-Pro-Pro-Gly-Ala-Gly3>AAP in solution has been carried out.Solvent dependent conformational distribution of 3>AAP has been studied using CD and NMr spectroscopy.The CED spectra in water, methanol and trifluoro