Abstract
Sixteen convolvulaceous glycolipids selected from the tricolorin (1 - 7) and orizabin (8 - 16) series, proved to be strong in vitro inhibitors of the enzyme that catalyzes the synthesis of 1,3-β-D-glucan, a major polymer of fungal cell-walls. Results provide an insight into function
of the specific structures of these complex macrocyclic lactones as inhibitors of
the 1,3-β-D-glucan synthase and open the possibility of using these compounds as starting points
for the development of antifungal agents that act by inhibiting fungal cell-wall synthesis.
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Prof. Dra Susana A. Zacchino
Farmacognosia, Facultad Ciencias Bioquímicas y Farmacéuticas
Universidad Nacional de Rosario
Suipacha 531(2000)-Rosario
Argentina
Fax: +54-341-4375315
eMail: szaabgil@citynet.net.ar