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1.
Anal Bioanal Chem ; 406(22): 5521-6, 2014 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-24972875

RESUMEN

A simple, sensitive, and reliable liquid chromatography tandem mass spectrometry (LC-MS/MS) method has been developed for determination of pyraoxystrobin in rat plasma and applied to a toxicokinetics study. The separation was performed by gradient elution on a Luna 5 µ C18 (2) 100 Å column (50 × 4.6 mm I.D., 5 µm) with mobile phase: water (0.1 % formic acid, v/v)/acetonitrile (0.1 % formic acid, v/v), followed by quantification with a mass detector in multiple reaction monitoring (MRM) mode using ESI as an interface. The calibration curve was linear over a concentration range of 1.00-200 ng/mL. The recovery for pyraoxystrobin ranged from 101.4 to 108.2 %. The intraday bias and precision ranged from -9.3 to 8.1 % and from 0.7 to 8.4 %, respectively, and the interday bias and precision ranged from -0.3 to 4.0 % and from 4.4 to 7.2 %, respectively. The toxicokinetics of pyraoxystrobin after single 100 and 1,000 mg/kg oral doses were studied in rats.


Asunto(s)
Acrilatos/sangre , Antifúngicos/sangre , Cromatografía Líquida de Alta Presión/métodos , Pirazoles/sangre , Espectrometría de Masas en Tándem/métodos , Acrilatos/química , Administración Oral , Animales , Antifúngicos/química , Calibración , Masculino , Pirazoles/química , Control de Calidad , Ratas , Ratas Sprague-Dawley , Reproducibilidad de los Resultados , Medición de Riesgo , Sensibilidad y Especificidad , Toxicocinética
2.
Bioorg Med Chem Lett ; 19(19): 5737-40, 2009 Oct 01.
Artículo en Inglés | MEDLINE | ID: mdl-19700322

RESUMEN

Three new humulane-type sesquiterpenes, 8-O-(p-coumaroyl)-5beta-hydroperoxy-1(10)E,4(15)-humuladien-8alpha-ol (1), 8-O-(3-nitro-p-coumaroyl)-1(10)E,4(15)-humuladien-5beta,8alpha-diol (2) and 8-O-(p-coumaroyl)-1(10)E,4(5)E-humuladien-8-ol (3), and a new copaborneol derivative, 1-O-p-coumaroyl-copaborneol (4), have been isolated from the methanol extract of Pileacavaleriei Lévl. subsp. crenata C. J. Chen. Their structures were elucidated using spectroscopic methods. Cytotoxic and antimicrobial activities of the isolated compounds were evaluated.


Asunto(s)
Antibacterianos/química , Antineoplásicos Fitogénicos/química , Sesquiterpenos/química , Urticaceae/química , Antibacterianos/aislamiento & purificación , Antibacterianos/farmacología , Antineoplásicos Fitogénicos/aislamiento & purificación , Antineoplásicos Fitogénicos/farmacología , Línea Celular Tumoral , Ensayos de Selección de Medicamentos Antitumorales , Humanos , Pruebas de Sensibilidad Microbiana , Conformación Molecular , Extractos Vegetales/química , Sesquiterpenos/aislamiento & purificación , Sesquiterpenos/farmacología
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