By means of pheromone traps containing synthetic sex pheromones, areas of the most harmful click beetle species,Agriotes obscurus,A. lineatus, A. sputator, A. gurgistanus, A. ustulatus, A. tauricus Heyd, andA. lineatus, occurring in southern regions and differing biologically from the so-called northern species, have been specified and charted in the European and central Siberian areas of the former USSR.
It has been shown earlier that various geranyl and (E,E)-farnesyl esters are major components of natural sex pheromones of click beetles,Agriotes. In addition, some isomeric terpene esters have an inhibiting or synergistic influence upon the sex communication of some species ofAgriotes. In this paper the influence of synthetic terpene esters in pheromone compositions on the sex communication of differentAgriotes species occurring in different climatic zones has been studied. The relationship between the biological activity of sex attractants and their chemical structure has been established.
A series of novel acyclic thymine nucleoside analogues were prepared by the Mitsunobu reaction from appropriately protected chiral triols. The enantiomeric triols were obtained from substituted gamma-lactone acids, prepared by asymmetric oxidation of 3-substituted-1,2-cyclopentanediones. The cytotoxic activity of new analogues was evaluated on MCF-7 human breast cancer and HeLa cells, and antiviral activities on human immunodeficiency virus type 1 and hepatitis C virus models. The synthesized compounds revealed specific anti-retroviral activity and no cytotoxic side effects.
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