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1.
Chem Biodivers ; 14(12)2017 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-29024401

RESUMO

Three new compounds, a bicyclogermacrene (1) and two 2,3-secoaromadendrane esters (2 and 3), together with (13S)-13-hydroxylabda-8,14-diene (4), fusicogigantone B (5), 3α,14-diacetoxy-2-hydoxybicyclogermacrene (6), fusicogigantone A (7), neofuranoplagiochilal (8), plagiochiline B (9), furanoplagiochilal (10), trans-nerolidol, spathulenol, α-tocopherol, and (+)-globulol were isolated from an Argentine collection of Plagiochila diversifolia. Their structures were elucidated by extensive mono and bidimensional NMR studies. Compounds 4, 5, and 6, incorporated to the larval diet at 100 µg per g of diet, reduced the larval growth of Spodoptera frugiperda (Lepidoptera: Noctuidae) by 70 ± 25, 57 ± 23, and 33 ± 16%, respectively. Compounds 4 and 5 produced 70% and 60% larval mortality at early instars. The latter also showed antifeedant properties in the Choice Test, with a feeding ratio of 0.54 ± 0.16.


Assuntos
Hepatófitas/química , Inseticidas/química , Animais , Argentina , Hepatófitas/metabolismo , Inseticidas/toxicidade , Larva/efeitos dos fármacos , Larva/crescimento & desenvolvimento , Espectroscopia de Ressonância Magnética , Conformação Molecular , Spodoptera/efeitos dos fármacos , Spodoptera/crescimento & desenvolvimento
2.
Nat Prod Commun ; 7(2): 245-8, 2012 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-22474971

RESUMO

The essential oil of an Argentine collection of the annual herb Acanthospermum hispidum DC. (Asteraceae), which contains the sesquiterpenoids beta-caryophyllene (35.2%), alpha-bisabolol (11.4%), and germacrene D (11.1%) as major constituents, displayed molluscicidal effects on an adult population of Biomphalaria peregrina Orbigny (LD50 37.8 microg/mL) and produced alteration of the feeding and oviposition behavior of the polyphagous insect Spodoptera frugiperda Smith when incorporated in the larval diet at 250 microg/g. In addition, a selective antibacterial activity was observed against pathogenic strains of Staphylococcus aureus and Enterococcus faecalis (MICs 62.5 and 125 microg/mL), but was inactive at 125 microg/mL against three beneficial lactic acid bacteria. Synergistic interactions were further validated by FIC index determination of the combination of the antibiotics oxacillin and gentamicin and the essential oil on the four pathogenic strains evaluated.


Assuntos
Antibacterianos/farmacologia , Asteraceae/química , Inseticidas/farmacologia , Moluscocidas/farmacologia , Óleos Voláteis/farmacologia , Óleos de Plantas/farmacologia , Animais , Antibacterianos/química , Bactérias/efeitos dos fármacos , Biomphalaria/efeitos dos fármacos , Dieta , Inseticidas/química , Larva/efeitos dos fármacos , Moluscocidas/química , Óleos Voláteis/química , Óleos de Plantas/química , Spodoptera/efeitos dos fármacos
3.
Chem Biodivers ; 7(7): 1855-61, 2010 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-20658675

RESUMO

The new 2,3-secoaromadendrane 1, together with the known compounds plagiochilines A and M (2 and 3, resp.), fusicogigantone A (4), and 1,4-dimethylazulene (5) were isolated from an Argentine collection of the liverwort Plagiochila bursata. Structures were elucidated by extensive 1D- and 2D-NMR studies. Compounds 2 and 4, incorporated to the larval diet at 100 microg per g of diet, reduced the larval growth of Spodoptera frugiperda (Lepidoptera: Noctuidae) by 66+/-29% and 25+/-8% and produced 55 and 75% larval mortality at early instars and 20 and 25% pupal mortality, respectively. Treatment with compound 2 also produced abdomen and wing malformation in adults leading to impossibility to mate.


Assuntos
Hepatófitas/química , Inseticidas/química , Inseticidas/farmacologia , Sesquiterpenos/química , Sesquiterpenos/farmacologia , Spodoptera/crescimento & desenvolvimento , Animais , Inseticidas/isolamento & purificação , Larva/crescimento & desenvolvimento , Pupa/crescimento & desenvolvimento , Sesquiterpenos/isolamento & purificação
4.
Nat Prod Res ; 21(3): 254-9, 2007 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-17365716

RESUMO

From an Argentine collection of the tropical tree Rollinia emarginata (Annonaceae), vomifoliol, dehydrovomifoliol, blumenol C, loliolide, 7-epiloliolide, vanillin, dihydroactinolide, as well as other common plant constituents were obtained, and identified by their NMR and MS features compared with authentic samples. Antifeedant and toxic actions were exerted to the polyphagous moth Spodoptera frugiperda by the ethanol extract of the plant, at 250 ppm in the larval diet. Additionally, in greenhouse studies, a 200 ppm aqueous solution of the extract produced a post-emergency herbicidal effect on the annual weed common lambsquarter (Chenopodium album).


Assuntos
Rollinia/química , Animais , Artemia , Dieta , Ensaios de Seleção de Medicamentos Antitumorais , Ingestão de Alimentos/efeitos dos fármacos , Etanol , Cromatografia Gasosa-Espectrometria de Massas , Herbicidas/isolamento & purificação , Herbicidas/farmacologia , Inseticidas/isolamento & purificação , Inseticidas/farmacologia , Larva , Extratos Vegetais/farmacologia , Extratos Vegetais/toxicidade , Solventes , Glycine max , Spodoptera
5.
Chem Biodivers ; 3(1): 21-6, 2006 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-17193211

RESUMO

The phagodepression activity of five coumarins (= 2H-1-benzopyran-2-ones), 6-hydroxy-7-isoprenyloxycoumarin (1), 6-methoxy-7-isoprenyloxycoumarin (2), 6,7-methylenedioxycoumarin (3), 5-methoxy-6,7-methylenedioxycoumarin (4), and 6-methoxy-7-(2-hydroxyethoxy)coumarin (5), from the Argentine native herb Pterocaulon polystachyum, was tested against Spodoptera frugiperda (Lepidoptera: Noctuidae) larvae. Two analogs, scopoletin (6) and 2-methoxy-2-methyl-3,4,5,6,7,8-hexahydro-3H-chromen-5-one (7), synthesized in our laboratory, were also evaluated for comparison. The compounds were added to an artificial diet at doses ranging from 50 to 200 microg per g of diet. Natural coumarins induced 100% of phagodepression when 200 microg were added per g of diet. Binary equimolar mixtures of the natural coumarins were phagodepressors against S. frugiperda surpassing the expected additive responses, indicating that these compounds can act synergistically against S. frugiperda larvae. Compounds 1 and 3 (non-methoxylated coumarins), and the equimolar mixture of both, displayed the strongest phagodepression. Additionally, 50 microg/g of 1 and 3 incorporated to the larval diet caused 80 and 50% of pupal mortality, respectively, while a 100 microg/g dose of compounds 2, 4, 6, and 7 produced 60, 50, 10, and 80% pupal mortality, respectively. Larval growing rate during the early larval instars was significantly reduced by treatments with the methylenedioxycoumarins 3 and 4. Coincidentally, the larval period duration was significantly increased by the latter compounds.


Assuntos
Cumarínicos/toxicidade , Comportamento Alimentar/efeitos dos fármacos , Spodoptera/efeitos dos fármacos , Animais , Comportamento de Escolha/efeitos dos fármacos , Comportamento de Escolha/fisiologia , Cumarínicos/química , Cumarínicos/isolamento & purificação , Sinergismo Farmacológico , Comportamento Alimentar/fisiologia , Flores , Larva/efeitos dos fármacos , Larva/fisiologia , Extratos Vegetais/química , Extratos Vegetais/isolamento & purificação , Extratos Vegetais/toxicidade , Folhas de Planta , Preparações de Plantas/química , Preparações de Plantas/isolamento & purificação , Preparações de Plantas/toxicidade , Spodoptera/fisiologia
6.
J Nat Prod ; 68(4): 554-8, 2005 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-15844947

RESUMO

Two new norditerpenoids, 4beta-hydroxy-19-normanoyl oxide (1) and 4alpha-hydroxy-18-normanoyl oxide (2), the new 18-O-alpha-l-arabinopyranosylmanoyl oxide (3a), and the known diterpenoids jhanol (4) and 18-hydroxy-13-epi-manoyl oxide (5) were isolated, together with other common plant constituents from an Argentine collection of Grindelia scorzonerifolia. The structures of the new compounds were established by extensive 1D and 2D NMR techniques and chemical transformations. Structural features of compounds 2 and 4 were verified by X-ray crystallographic analyses. The insecticidal effect of compound 3a was evaluated against the polyphagous pest Spodoptera frugiperda. Pupal and adult malformations leading to death occurred when 3a was incorporated in a larval diet at a concentration of 100 ppm.


Assuntos
Diterpenos/isolamento & purificação , Grindelia/química , Inseticidas/isolamento & purificação , Plantas Medicinais/química , Spodoptera/efeitos dos fármacos , Animais , Argentina , Cristalografia por Raios X , Diterpenos/química , Diterpenos/farmacologia , Comportamento Alimentar/efeitos dos fármacos , Inseticidas/química , Inseticidas/farmacologia , Larva/efeitos dos fármacos , Conformação Molecular , Estrutura Molecular
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