Title of article :
Structure–antifungal activity relationship of His-Phe-Arg-Trp-Gly-Lys-Pro-Val-NH2 and analogues Original Research Article
Author/Authors :
Marcelo F. Masman، نويسنده , , Csaba Somlai، نويسنده , , Francisco M. Garibotto، نويسنده , , Ana M. Rodr?guez، نويسنده , , Agustina de la Iglesia، نويسنده , , Susana A. Zacchino، نويسنده , , Botond Penke، نويسنده , , Ricardo D. Enriz، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2008
Pages :
12
From page :
4347
To page :
4358
Abstract :
The synthesis, in vitro evaluation and conformational study of His-Phe-Arg-Trp-Gly-Lys-Pro-Val-NH2 and analogues acting as antifungal agents are reported. Among them, His-Phe-Lys-Trp-Gly-Arg-Phe-Val-NH2 exhibited a moderate but significant antifungal activity against Cryptococcus neoformans, Candida albicans and Candida tropicalis. A theoretical study allows us to propose a biologically relevant conformation for these octapeptides acting as antifungal agents. In addition, these theoretical calculations allow us to determine the minimal structural requirements to produce the antifungal response and can provide a guide for the design of compounds with this biological activity.
Keywords :
?-MSH analogues , octapeptides , Antifungal peptides , conformation , Electronic properties
Journal title :
Bioorganic and Medicinal Chemistry
Serial Year :
2008
Journal title :
Bioorganic and Medicinal Chemistry
Record number :
1304265
Link To Document :
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