| Literature DB >> 22098349 |
Nancy B Iannucci1, Giselle V Ripoll, Juan Garona, Osvaldo Cascone, Graciela N Ciccia, Daniel E Gomez, Daniel F Alonso.
Abstract
BACKGROUND: Desmopressin (dDAVP), a synthetic nonapeptide derivative of arginine vasopressin, is a safe antidiuretic and hemostatic compound that acts as a selective agonist for the vasopressin V2 membrane receptor (V2R). It is known that dDAVP can inhibit progression of residual metastatic cells in preclinical models. Among other mechanisms, the compound induces an agonist effect on V2R present in tumor cells. RESULTS/DISCUSSION: Looking for novel analogs with improved anti-tumor activity, positions 4 and 5, at the conformational peptide loop, were substituted. The analog [V(4)Q(5)]dDAVP ([4-valine 5-glutamine] desmopressin) exhibited a significantly higher antiproliferative effect than dDAVP in cultures of MCF-7, a V2R-expressing human breast carcinoma cell line. The chiral isomer of this analog and tetrapeptide fragments corresponding to the loop region were also assessed.Entities:
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Year: 2011 PMID: 22098349 DOI: 10.4155/fmc.11.152
Source DB: PubMed Journal: Future Med Chem ISSN: 1756-8919 Impact factor: 3.808