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  • Ceratitus capitata  (2)
  • Springer  (2)
  • American Association for the Advancement of Science (AAAS)
  • Nature Publishing Group (NPG)
  • Oxford University Press
Document type
Publisher
  • Springer  (2)
  • American Association for the Advancement of Science (AAAS)
  • Nature Publishing Group (NPG)
  • Oxford University Press
Years
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical ecology 19 (1993), S. 1323-1335 
    ISSN: 1573-1561
    Keywords: Trimedlure ; medfly ; Ceratitus capitata ; attractancy ; quantitative structure-activity relationship ; QSAR ; CHEM-X ; linear regression
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Trimedlure (tert-butyl 4- and 5-chloro-cis- andtrans-2-methylcyclohexane-1-carboxylate), a mixture of eight isomers, is used as an attractant for detecting and monitoring the male Mediterranean fruit fly. This paper reports the quantitative structure-activity relationship (QSAR), via CHEMX, of the eight purified isomers (racemic mixtures) of trimedlure. The relationship between structure and attractiveness is demonstrated by utilizing male medfly field catch on day 0 of the individual isomers vs. several molecular descriptors: volume, surface area, a torsion angle, and an interatomic distance.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical ecology 21 (1995), S. 69-79 
    ISSN: 1573-1561
    Keywords: Insecta ; Ceratitus capitata ; medfly ; trimedlure ; enantiomer ; attractant ; lure ; SAR ; VdW ; Chem-X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract tert-Butyl 4- (and 5-) chloro-trans-2-methylcyclohexane-1-carboxylate (TML), a mixture of four majortrans and four minorcis isomers, is used as an attractant for detecting and monitoring the male Mediterranean fruit fly (medfly),Ceratitis capitata (Wiedemann). The eight isomers (racemic mixtures) were isolated by HPLC, and their relative attractiveness in the field was determined. A quantitative structure-activity relationship (QSAR) was proposed that related a molecular measurement (Å3) of the TML structure to male medfly captures. More recently, thetrans-TML enantiomers were synthesized in sufficient quantities for field testing. This paper reports the computer-aided molecular modeling, via Chem-X, of thetrans-TML enantiomers and the staggered and superimposed fitting with the most attractive isomer, (1S,2S,4R)-TML-C, to determine common volumes and surface areas from Van der Waals (VdW) maps. Observations of structure-activity relationships (SAR) are reported for the staggered fittings.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
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