• 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