Journal of Natural Products · 1998 · 35 citations · 8 references
Life SciencesEntomologyToxicologyInsect EcologyInsect ToxicologyStructure-activity RelationshipsInsecticide ToxicityPlant-insect Chemical InteractionsActive Compound IsolationActive Ingredient ExtractionBioactive Compound IsolationBioactivity ScreeningBioassay-guided FractionationBotanical BioassaysInsecticide ChemistryInsecticides From Botanical Extracts
Through insecticidal bioassay-guided fractionation and isolation, five isobutylamides 1-5 were isolated from n-hexane and EtOAc extracts of the aerial parts of Dinosperma erythrococca (Rutaceae). The structures of compounds 1-5 were established through 1D and 2D NMR. Compounds 1-3 were identified as erythrococcamides A-C and represent two novel classes of isobutylamide. Compounds 4-5 were identified as N-(2-hydroxy-2-methylpropyl)-6-phenyl-2(E), 4(E)-hexadienamide (4)1,2 and N-(2-methylpropyl)-6-phenyl-2(E), 4(E)-hexadienamide (5),1,3 respectively. Compound 1 showed lethal activity against the housefly (Musca domestica) (kill EC50 = 20.2 ppm) and the tobacco budworm (Heliothis virescens) (kill EC50 = 74.2 ppm). Compound 4 showed lethal activity against H. virescens at 500 ppm, while compound 5 showed lethal activity against M. domestica at 500 ppm.
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C. T. Bhunia · IETE Journal of Education · 1997 · 2.7K citations
Naturally Occurring Insecticides
Martin Jacobson, Donald G. Crosby, Andrew J. Forgash · Soil Science · 1972 · 548 citations
Chemical & Engineering News · 1989 · 383 citations · Full text
Choice Behavior in Rhesus Monkeys: Cocaine Versus Food
Thomas Aigner, Robert L. Balster · Science · 1978 · 160 citations