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1.
Sci Rep ; 3: 2167, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23835605

RESUMEN

The phase transition of a nematic liquid crystal containing a push-pull azobenzene dye could be induced efficiently during irradiation with visible light. The dynamical disorganizing effect of the push-pull azobenzene dye on the liquid crystalline order through its trans-cis-trans photoisomerizaion cycle under visible light was contributed to the efficient phase transition. Then, the effects of light irradiation on the motion of small objects dispersed in the liquid crystals containing the push-pull azobenzene were explored, and the manipulation and assembly of those objects were successfully achieved in the nematic phase but also in the smectic phase. The combination of the photo-controlled dynamical change in the liquid crystalline order and the intrinsic self-assembly property of a liquid crystal is promising for use in technologies that require not only the organization of small objects but also the photo-driving of nano- and micro-sized mechanical materials.

2.
Bioorg Med Chem Lett ; 16(1): 142-5, 2006 Jan 01.
Artículo en Inglés | MEDLINE | ID: mdl-16236511

RESUMEN

For the systematic SAR study on mansonone F, a series of C6 and C9 analogs of mansonone F have been synthesized and their anti-MRSA activities were evaluated. Most of the analogs exhibited good or excellent anti-MRSA activities. In particular, the 6-n-butylmansonone F showed fourfold higher antibacterial activities compared to that of vancomycin.


Asunto(s)
Naftoquinonas/química , Quinonas/química , Sesquiterpenos/química , Antiinfecciosos/química , Antiinfecciosos/farmacología , Farmacorresistencia Bacteriana , Meticilina/farmacología , Modelos Químicos , Naftoquinonas/metabolismo , Sesquiterpenos/metabolismo , Infecciones Estafilocócicas/tratamiento farmacológico , Staphylococcus aureus/metabolismo , Relación Estructura-Actividad , Vancomicina/química
3.
Bioorg Med Chem Lett ; 14(17): 4519-23, 2004 Sep 06.
Artículo en Inglés | MEDLINE | ID: mdl-15357984

RESUMEN

Syntheses and excellent anti-MRSA activities of the mansonone F analogs are reported. In addition, the minimal structural requirements for its anti-MRSA activities as well as its structure-activity relationship including the C3 substituents effects on anti-MRSA activity are also described. In particular, this study revealed that both ortho-quinone and tricyclic systems of mansonone F are essential for anti-MRSA activities.


Asunto(s)
Antibacterianos/síntesis química , Resistencia a la Meticilina/efectos de los fármacos , Naftoquinonas/síntesis química , Naftoquinonas/farmacología , Sesquiterpenos/síntesis química , Sesquiterpenos/farmacología , Staphylococcus aureus/efectos de los fármacos , Antibacterianos/farmacología , Humanos , Resistencia a la Meticilina/fisiología , Pruebas de Sensibilidad Microbiana , Staphylococcus aureus/crecimiento & desarrollo , Relación Estructura-Actividad
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