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1.
J Med Entomol ; 46(4): 832-40, 2009 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-19645285

RESUMEN

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.


Asunto(s)
Aedes/efectos de los fármacos , Anopheles/efectos de los fármacos , Ciclopentanos/farmacología , Control de Insectos/métodos , Repelentes de Insectos/farmacología , Ixodes/efectos de los fármacos , Muscidae/efectos de los fármacos , Pironas/farmacología , Aedes/fisiología , Animales , Anopheles/fisiología , Monoterpenos Ciclopentánicos , Conducta Alimentaria/efectos de los fármacos , Humanos , Mordeduras y Picaduras de Insectos/prevención & control , Ixodes/fisiología , Muscidae/fisiología
2.
J Med Entomol ; 45(6): 1080-6, 2008 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-19058632

RESUMEN

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.


Asunto(s)
Aedes/efectos de los fármacos , Repelentes de Insectos/análisis , Nepeta/química , Aceites de Plantas/farmacología , Simuliidae/efectos de los fármacos , Administración Cutánea , Animales , Humanos , Repelentes de Insectos/administración & dosificación , Repelentes de Insectos/farmacología
3.
Bioorg Med Chem Lett ; 16(5): 1245-8, 2006 Mar 01.
Artículo en Inglés | MEDLINE | ID: mdl-16384703

RESUMEN

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.


Asunto(s)
Antibacterianos/síntesis química , Antibacterianos/farmacología , Peptoides/síntesis química , Peptoides/farmacología , Antibacterianos/química , Escherichia coli/efectos de los fármacos , Estructura Molecular , Peptoides/química
4.
J Org Chem ; 68(20): 7884-6, 2003 Oct 03.
Artículo en Inglés | MEDLINE | ID: mdl-14510571

RESUMEN

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.


Asunto(s)
Aminoácidos/síntesis química , Ciclopropanos/química , Rutenio/química , Aminoácidos/química , Catálisis , Cristalografía por Rayos X , Estructura Molecular , Compuestos Organometálicos/química , Estereoisomerismo
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