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1.
J Chem Ecol ; 47(8-9): 732-739, 2021 Sep.
Article in English | MEDLINE | ID: mdl-34347234

ABSTRACT

The pine brown tail moth, Euproctis terminalis (Walker 1855), is a periodic pest in pine plantations in South Africa. The larvae feed on pine needles and can cause severe defoliation when population densities are high. Population densities fluctuate temporally and spatially, complicating the prediction of potential growth loss and tree mortality. The aim of this study was to identify the sex pheromone of the pine brown tail moth to provide stakeholders with a tool for monitoring it. Gas chromatography-electroantennogram detection and gas chromatography/mass spectrometry analyses of female pheromone gland extracts identified the major component as (Z,Z,Z,Z)-7,13,16,19-docosatetraen-1-ol isobutyrate. Traps baited with (Z,Z,Z,Z)-7,13,16,19-docosatetraen-1-ol isobutyrate caught more males than unbaited traps. A delta trap was shown to be a superior design compared to a bucket funnel trap. This pheromone can now be used for monitoring E. terminalis in pine plantations.


Subject(s)
Moths/physiology , Sex Attractants/analysis , Animals , DNA/chemistry , Electron Transport Complex IV/genetics , Female , Gas Chromatography-Mass Spectrometry , Isobutyrates/analysis , Isobutyrates/pharmacology , Larva/growth & development , Male , Moths/chemistry , Moths/growth & development , Pinus/parasitology , Sequence Analysis, DNA , Sex Attractants/pharmacology , Sexual Behavior, Animal/drug effects
2.
J Nat Prod ; 83(8): 2483-2489, 2020 08 28.
Article in English | MEDLINE | ID: mdl-32786879

ABSTRACT

Phytochemical investigation of extracts of the stems of Hypoestes aristata led to the isolation of nine lignans that included four known compounds, namely, hinokinin (1), savinin (2), medioresinol (3), and two cubebins (8a,b), three new butyrolactone lignans (4-6), and butyrolactol lignans 7a-c. The structures of the new compounds were established using 1D and 2D NMR and HRESIMS data. The absolute configurations of the new lignans were determined from their ECD data and the Mosher's ester method. This is the first unequivocal assignment of the absolute configuration at C-7 and C-7' of 7- and 7'-hydroxybutyrolactone lignans. The compounds were screened for inhibition of an HIV-1 protease enzyme, and compounds 1 and 6 exhibited moderate activity in this regard.


Subject(s)
Acanthaceae/chemistry , Lignans/pharmacology , Chromatography, Liquid/methods , Lignans/isolation & purification , Plant Components, Aerial/chemistry , Solid Phase Extraction , Spectrum Analysis/methods
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