Solid-phase synthesis of the antifungal tetrapeptide from the culture of penicilli-um canescens / 药学实践杂志
Journal of Pharmaceutical Practice
;
(6): 342-343,378, 2014.
Article
Dans Chinois
| WPRIM
| ID: wpr-790355
ABSTRACT
Objective To synthesize the antifungal tetrapetide by solid-phase synthesis method .Methods The solid-phase peptide synthesis was chosen for getting the desired target tetrapeptide and its structure was confirmed by MS and 1 H NMR.Results The synthesis of the D-Phe-Val-D-Val-Tyr-OH was realized with yield of 47%.Conclusion The synthetic method was feasible and practical.The desired target tetrapeptide could be used for screening of antifungal activity .
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
langue:
Chinois
Texte intégral:
Journal of Pharmaceutical Practice
Année:
2014
Type:
Article
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