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1.
Biol Pharm Bull ; 25(11): 1436-41, 2002 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-12419955

RESUMEN

The anti-inflammatory activities of several novel oximes and O-acyl oximes that we synthesized have been reported based on carrageenan-induced rat foot-pad swelling assay and histamine-induced rat vascular permeability assay. A cyclooxygenase (COX)-1 inhibitory effect has also been reported for 4'-piperidinoacetophenone and 4'-morpholinoacetophenone oximes and their O-acyl derivatives. To further search for more effective non-steroidal anti-inflammatory or anti-allergic drugs, 1-hydroxylamino-1-(4'-piperidinophenyl) ethane (P-HA) and 1-hydroxylamino-1-(4'-morpholinophenyl) ethane (M-HA) were synthesized from the corresponding oximes with sodium cyanoborohydride, and N,O-diacetyl hydroxylamines (P-HA-Ac and M-HA-Ac) were prepared from these hydroxylamines using acetyl chloride. These hydroxylamines and N,O-diacetyl hydroxylamines clearly exhibited inhibitory effects on mouse carrageenan-induced foot-pad swelling induced by oral administration (150, 37.5 mg/kg). An oral dose of P-HA-Ac (150 mg/kg) significantly inhibited the mouse anaphylactic reaction to ovalbumin measured by the abdominal wall (AW) method. Percutaneous administration of P-HA and M-HA significantly inhibited 2,4-dinitrofluorobenzene (DNFB)-induced contact hypersensitivity reaction (type IV) in mice at a dose of 0.5 and 0.1 mg/ear, respectively. All tested hydroxylamines and N,O-diacetyl hydroxylamines clearly inhibited both COX-1 and COX-2 enzyme activities with IC(50) values of 1.9-28.7 and 1.6-2.9 micro M against COX-1 and COX-2, respectively. Hydroxylamines (P-HA and M-HA) also showed a 5-lipoxygenase inhibitory effect.


Asunto(s)
Antialérgicos/química , Antiinflamatorios no Esteroideos/química , Hidroxilamina/química , Hidroxilamina/farmacología , Animales , Antialérgicos/farmacología , Antialérgicos/uso terapéutico , Antiinflamatorios no Esteroideos/farmacología , Antiinflamatorios no Esteroideos/uso terapéutico , Edema/tratamiento farmacológico , Edema/fisiopatología , Hidroxilamina/uso terapéutico , Masculino , Ratones , Ratones Endogámicos BALB C , Dimensión del Dolor/efectos de los fármacos , Dimensión del Dolor/métodos , Ratas , Ratas Sprague-Dawley
2.
Chem Pharm Bull (Tokyo) ; 50(7): 996-1000, 2002 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-12130865

RESUMEN

Hydroxylamines gradually undergo oxidation to their oximes on being dissolved in organic solvent (e.g. methanol). This phenomenon was followed by (1)H-NMR and liquid chromatography-mass spectrometry (LC-MS). The oxidation rate was estimated from the peak area observed on the mass chromatogram at the protonated molecule or fragment ion on LC-atmospheric pressure chemical ionization (APCI)-MS. The results showed that the oxidation rate of hydroxylamines depended on the solvent type.


Asunto(s)
Hidroxilaminas/química , Calibración , Cloroformo , Cromatografía Liquida , Cetonas/química , Espectroscopía de Resonancia Magnética , Espectrometría de Masas , Oxidación-Reducción , Solventes
3.
Planta Med ; 68(3): 258-61, 2002 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-11914965

RESUMEN

The CHCl3-soluble part (HJ) of the MeOH extract from Hypericum japonicum afforded new bisxanthones, jacarelhyperols A (1) and B (2). The structures were elucidated by spectral methods. These compounds and HJ showed significant inhibitory effects against PAF-induced hypotension by an in vivo evaluation method, which can reveal the pharmacological action of the test material.


Asunto(s)
Presión Sanguínea/efectos de los fármacos , Hypericum , Hipotensión/tratamiento farmacológico , Xantenos/química , Xantenos/farmacología , Xantonas , Animales , Medicamentos Herbarios Chinos , Hipotensión/inducido químicamente , Espectroscopía de Resonancia Magnética , Masculino , Ratones , Ratones Endogámicos , Estructura Molecular , Éteres Fosfolípidos/farmacología , Extractos Vegetales/química , Extractos Vegetales/farmacología , Factor de Activación Plaquetaria/farmacología , Inhibidores de Agregación Plaquetaria/farmacología , Xantenos/aislamiento & purificación
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