Biological Bulletin · 1969 · 32 citations · 6 references
Life SciencesBiochemistryEntomologyHormone BiochemistryInsect PhysiologySteroid BiochemistryInsect EndocrinologyPlant-insect Chemical InteractionsDouble BondsInsecticide ChemistryJuvenile Hormone AnalogsJuvenile Hormone Esters
The juvenile hormone activity of both farnesenic acid esters and their dihydrodichloro derivatives increased from the methyl to the ethyl ester, then decreased again. In some hemipteran insects enormous increases in activity were obtained after addition of two hydrogen chloride molecules to the two double bonds of farnesenic acid esters. The same change in chemical structure considerably decreased the activity on Tenebrio pupae. On Pyrrhocoris apterus, the highest activity (at the 0.1 nanogram level) was obtained with the ethyl ester of trans-3,7,11-trimethyl-7,11-dichloro-2-dodecenic acid.
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The Structure of the Juvenile Hormone
Herbert Röller, Karl H. Dahm, C. C. Sweely et al. · Angewandte Chemie International Edition in English · 1967 · 307 citations
Juvenile Hormone: Identification of an Active Compound from Balsam Fir
William S. Bowers, Henry M. Fales, M. J. Thompson et al. · Science · 1966 · 198 citations