QSAR evaluation of monoterpenoids' insecticidal activity

Journal of Agricultural and Food Chemistry

Volumn 50, Issue 16, 2002, Pages 4576-4580

  Grodnitzky, Justin A ^a   Coats, Joel R ^a  

^a IOWA STATE UNIVERSITY   (United States)

Author keywords

And electrotopological state; Insecticide; Monoterpenoid; Mulliken population; Quantitative structure activity relationship (QSAR); Quantum descriptor

Indexed keywords

ESTER; ETHER DERIVATIVE; INSECTICIDE; TERPENE; TERPENOID DERIVATIVE; THYMOL;

ANIMAL; ARTICLE; CHEMICAL COMPOSITION; CHEMICAL STRUCTURE; CHEMISTRY; GEOMETRY; HERBIVORY; HOUSE FLY; INSECTICIDAL ACTIVITY; LETHAL DOSE; METABOLISM; METABOLITE; MOLECULAR WEIGHT; PATHOGENESIS; PLANT; QUANTITATIVE STRUCTURE ACTIVITY RELATION; QUANTUM MECHANICS; SPECIES DIFFERENCE; STATISTICAL MODEL; SYNTHESIS; TOXICITY;

ANIMALIA; INSECTA; MUSCA DOMESTICA;

ANIMALS; ESTERS; ETHERS; HOUSEFLIES; INSECTICIDES; LINEAR MODELS; MOLECULAR STRUCTURE; QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIP; TERPENES; THYMOL;

EID: 0037205623     PISSN: 00218561     EISSN: None     Source Type: Journal    
DOI: 10.1021/jf0201475     Document Type: Article

References (16)

1. Starting from nature to make better insecticides
2. Monoterpenoid Biosynthesis in Glandular Trichomes of Labiate Plants
3. Insecticidal properties of monoterpenoid derivatives to the house fly (Diptera: Muscidae) and red flour beetle (Coleoptera: Tenebrionidae)
4. Structure/response correlations and similarity/diversity analysis by GETAWAY descriptors: I. Theory of the novel 3D molecular descriptors
5. Atom level electrotopological state indices in QSAR: Design and testing antithyroid agents
6. Application of the electrotopological state index in QSAR. Analysis of flavone derivatives as HIV-1 integrase inhibitors
7. QSAR modeling with the electrotopological state indices: Corticosteroids
8. Modeling the toxicity of amide herbicides using the electrotopological state
9. Monoterpenoids and their synthetic derivatives as leads for new insectcontrol agents
10. Trimmed Spearman-Karber method for estimating median lethal concentrations in toxicity bioassays
11. General Atomic and Molecular Electronic Structure System
12. Validation of QSAR's
13. Plant-insect coevolution and inhibition of acetylcholinesterase
14. α-thujone (the active component of absinthe): γ-aminobutyric acid type A receptor modulation and metabolic detoxification
15. Insecticidal activity of essential oils: Octopaminergic sites of action