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1.
J Med Entomol ; 46(4): 832-40, 2009 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-19645285

RESUMO

The essential oil of catmint, Nepeta cataria L., contains nepetalactones, that, on hydrogenation, yield the corresponding dihydronepetalactone (DHN) diastereomers. The DHN diastereomer (4R,4aR,7S,7aS)-4,7-dimethylhexahydrocyclopenta[c]pyran-1(3H)-one, DHN 1) was evaluated as mosquito repellent, as was the mixture of diastereomers {mostly (4S,4aR,7S,7aR)-4,7-dimethylhexahydrocyclopenta[c]pyran-1(3H)-one, DHN 2} present after hydrogenation of catmint oil itself. The repellency of these materials to Aedes aegypti L. and Anopheles albimanus Wiedemann mosquitoes was tested in vitro and found to be comparable to that obtained with the well-known insect repellent active ingredient N,N-diethyl-3-methylbenzamide (DEET). DHN 1 and DHN 2 also repelled the stable fly, Stomoxys calcitrans L., in this study. DHN 1, DHN 2, and p-menthane-3,8-diol (PMD), another natural monoterpenoid repellent, gave comparable levels of repellency against An. albimanus and S. calcitrans. Laboratory testing of DHN 1 and DHN 2 using human subjects with An. albimanus mosquitoes was carried out. Both DHN 1 and DHN 2 at 10% (wt:vol) conferred complete protection from bites for significant periods of time (3.5 and 5 h, respectively), with DHN2 conferring protection statistically equivalent to DEET. The DHN 1 and DHN 2 diastereomers were also efficaceous against black-legged tick (Ixodes scapularis Say) nymphs.


Assuntos
Aedes/efeitos dos fármacos , Anopheles/efeitos dos fármacos , Ciclopentanos/farmacologia , Controle de Insetos/métodos , Repelentes de Insetos/farmacologia , Ixodes/efeitos dos fármacos , Muscidae/efeitos dos fármacos , Pironas/farmacologia , Aedes/fisiologia , Animais , Anopheles/fisiologia , Monoterpenos Ciclopentânicos , Comportamento Alimentar/efeitos dos fármacos , Humanos , Mordeduras e Picadas de Insetos/prevenção & controle , Ixodes/fisiologia , Muscidae/fisiologia
2.
J Med Entomol ; 45(6): 1080-6, 2008 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-19058632

RESUMO

The essential oil of catmint, Nepeta cataria L., was hydrogenated to yield an oil enriched in dihydronepetalactone (DHN) diastereomers, termed. This material was used for the preparation of liquid alcohol-based and lotion formulations. The efficacy of these formulations as repellents was tested after application to human test subjects at two locations in the United States: Maine and Florida. In Maine, data on repellency of the hydrogenated catmint oil formulations toward black flies (Simulium decorum Walker) and mosquitoes (primarily Aedes intrudens Dyar) were obtained. In these tests, protection from black flies was conferred for 6 h or more with all formulations, and both liquid and lotion formulations at 15 wt% active ingredient gave complete protection for 7.5 h. All formulations conferred protection from mosquitoes for >4 h, with the best (15 wt% lotion) giving >8 h of complete protection. In Florida, data on repellency toward a mixed population of mosquitoes indicated that all formulations conferred protection for >4 h, with the 15 wt% lotion giving >6 h complete protection from bites.


Assuntos
Aedes/efeitos dos fármacos , Repelentes de Insetos/análise , Nepeta/química , Óleos de Plantas/farmacologia , Simuliidae/efeitos dos fármacos , Administração Cutânea , Animais , Humanos , Repelentes de Insetos/administração & dosagem , Repelentes de Insetos/farmacologia
3.
Bioorg Med Chem Lett ; 16(5): 1245-8, 2006 Mar 01.
Artigo em Inglês | MEDLINE | ID: mdl-16384703

RESUMO

Antimicrobial peptides and their mimetics offer a potential new disinfective tool. beta-Peptoids (oligo-N-substituted beta-alanines) were synthesized and investigated for antimicrobial activity. A block approach whereby di- and tri-beta-peptoids were first prepared and then ligated via amide bond formation to synthesize larger beta-peptoids was developed. The beta-peptoids were found to possess moderate activity in an Escheridchia coli assay.


Assuntos
Antibacterianos/síntese química , Antibacterianos/farmacologia , Peptoides/síntese química , Peptoides/farmacologia , Antibacterianos/química , Escherichia coli/efeitos dos fármacos , Estrutura Molecular , Peptoides/química
4.
J Org Chem ; 68(20): 7884-6, 2003 Oct 03.
Artigo em Inglês | MEDLINE | ID: mdl-14510571

RESUMO

trans-Cyclopropyl beta-amino acid derivatives can be synthesized in five steps with excellent enantioselectivities using a chiral (Salen)Ru(II) cyclopropanation catalyst in the key asymmetry-induction step. This facile synthesis proceeds with high overall yield and can be used to prepare a number of carbamate-protected (Cbz and Boc are demonstrated) beta-amino acid derivatives.


Assuntos
Aminoácidos/síntese química , Ciclopropanos/química , Rutênio/química , Aminoácidos/química , Catálise , Cristalografia por Raios X , Estrutura Molecular , Compostos Organometálicos/química , Estereoisomerismo
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