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1.
Bioorg Med Chem Lett ; 29(23): 126703, 2019 12 01.
Artículo en Inglés | MEDLINE | ID: mdl-31627993

RESUMEN

A series of novel aralkyl piperazine and piperidine derivatives were synthesized, and evaluated for their serotonin reuptake inhibitory and 5-HT1A/5-HT7 receptors affinities activity. Antidepressant activities in vivo of the selective compound were screened using the forced swimming test (FST) and tail suspension test (TST). The results indicated that compound 19a exhibited high affinities for the 5-HT1A/5-HT7 receptors (5-HT1A, Ki = 12 nM; 5-HT7, Ki = 3.2 nM) coupled with potent serotonin reuptake inhibition (IC50 = 14 nM) and showed a marked antidepressant-like effect in the FST and TST models.


Asunto(s)
Antidepresivos/uso terapéutico , Piperazina/uso terapéutico , Piperidinas/uso terapéutico , Inhibidores Selectivos de la Recaptación de Serotonina/uso terapéutico , Antidepresivos/farmacología , Humanos , Piperazina/farmacología , Piperidinas/farmacología , Inhibidores Selectivos de la Recaptación de Serotonina/farmacología , Relación Estructura-Actividad
2.
Bioorg Med Chem Lett ; 27(24): 5420-5423, 2017 12 15.
Artículo en Inglés | MEDLINE | ID: mdl-29138029

RESUMEN

A series of arylalkanol and aralkyl piperazine derivatives have been synthesized and evaluated for 5-HT reuptake inhibitory abilities and binding affinities at the 5-HT1A/5-HT7 receptors. Antidepressant activities of the compounds in vivo were screened using the forced swimming test (FST). The results indicated that the compound 8j exhibited high affinities for the 5-HT1A/5-HT7 receptors (5-HT1A, ki = 0.84 nM; 5-HT7, ki = 12 nM) coupling with moderate 5-HT reuptake inhibitory activity (RUI, IC50 = 100 nM) and showed a marked antidepressant-like activity in the FST model.


Asunto(s)
Antidepresivos/síntesis química , Piperazinas/química , Receptor de Serotonina 5-HT1A/metabolismo , Receptores de Serotonina/metabolismo , Inhibidores Selectivos de la Recaptación de Serotonina/síntesis química , Animales , Antidepresivos/metabolismo , Antidepresivos/farmacología , Células HEK293 , Semivida , Humanos , Concentración 50 Inhibidora , Ratones , Microsomas Hepáticos/metabolismo , Actividad Motora/efectos de los fármacos , Piperazinas/metabolismo , Piperazinas/farmacología , Ratas , Receptor de Serotonina 5-HT1A/química , Receptores de Serotonina/química , Inhibidores Selectivos de la Recaptación de Serotonina/metabolismo , Inhibidores Selectivos de la Recaptación de Serotonina/farmacología , Relación Estructura-Actividad
3.
Chin Med Sci J ; 31(2): 89-94, 2016 Jun 20.
Artículo en Inglés | MEDLINE | ID: mdl-28031096

RESUMEN

Objective In cerebral aneurysm clipping and embolization, blood pressure control and temporary parent artery blocking are common methods to prevent aneurysm rupture. Their influence on the prognosis is uncertain. In this study, we try to find out the association between methods above and prognostic indicators.Methods We held a retrospective analysis on patients' medical records of cerebral aneurysms surgical clipping and endovascular coiling , and recorded gender, age, diagnosis, Hunt-Hess grade, Glasgow coma scale score, treatment methods, a history of hypertension, preoperative systolic blood pressure, with or without controlled hypotension, systolic blood pressure difference before and after controlled hypotension, with or without temporary artery blocking, with or without hypertension after treated aneurysm, prognostic indicators including mortality after 1 month, intensive care unit (ICU) stay time of survivors, discharged Glasgow outcome scale (GOS) score. Prognostic indicators were regarded as dependent variable, all the factors were regarded as independent variable, and the strength analysis of influence factors on prognostic indicators was made by binary logistic regression.Results Total cases were 165, including 68 males and 97 females, with an average age of 56 (12-85) years. The mortality after 1 month was 10.9% (18 cases). The ICU stay time of survivors was 7.35 (0-67) days. GOS score at discharge was 1-3 in 40 (24.2%) patients and 4-5 in 125 (75.8%) patients. Systolic blood pressure difference before and after controlled hypotension was an independent factor influencing mortality (t=2.273, P=0.024), and the greater the difference was, the higher the mortality would be. Timely hypertension after aneurysm treated was an independent factor affecting ICU stay time of survivors and patients with hypertension had shorter ICU stay time (χ2=10.017, P=0.001). Blood pressure control (χ2=0.088, P=0.767) and temporary blocking (χ2=1.307, P=0.253) did not show significant influence on GOS score at discharge.Conclusions Timely controlled hypertension after aneurysm clipping and embolization can significantly shorten the stay time in ICU. The degree of controlled hypotension associates with postoperative mortality, the greater systolic blood pressure difference before and after antihypertensive treatment is, the higher the mortality will be.


Asunto(s)
Presión Sanguínea , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Arterias , Niño , Femenino , Humanos , Aneurisma Intracraneal , Masculino , Persona de Mediana Edad , Pronóstico , Estudios Retrospectivos , Resultado del Tratamiento , Adulto Joven
4.
J Org Chem ; 79(12): 5806-11, 2014 Jun 20.
Artículo en Inglés | MEDLINE | ID: mdl-24869774

RESUMEN

(Benz)imidazoles can be efficiently functionalized by (hetero)aryl chlorides via direct C-H bond arylation in the presence of a well-defined NHC-Pd(II)-Im complex. Under the optimal conditions, various activated, unactivated, and deactivated (hetero)aryl chlorides were successfully applied as the arylating reagents to achieve the 2-(hetero)aryl (benz)imidazoles in acceptable to high yields, giving a facile and alternative methodology for the direct C-H bond arylation of (benz)imidazoles.


Asunto(s)
Bencimidazoles/química , Bencimidazoles/síntesis química , Compuestos Heterocíclicos/química , Imidazoles/química , Imidazoles/síntesis química , Metano/análogos & derivados , Compuestos Organometálicos/química , Paladio/química , Catálisis , Enlace de Hidrógeno , Metano/química , Estructura Molecular
5.
Eur J Med Chem ; 144: 701-715, 2018 Jan 20.
Artículo en Inglés | MEDLINE | ID: mdl-29291438

RESUMEN

A series of novel aralkyl piperazine derivatives were synthesized, and evaluated for their serotonin reuptake inhibitory and 5-HT1A/5-HT7 receptors affinities activity. Antidepressant activities in vivo of the compounds were screened using the forced swimming test (FST) and tail suspension test (TST). The results indicated that compounds 21k (RUI, IC50 = 31 nM; 5-HT1A, 5-HT7, ki = 62, 12 nM) and 21n (RUI, IC50 = 25 nM; 5-HT1A, 5-HT7, ki = 28, 3.3 nM) exhibited high affinities for the 5-HT1A/5-HT7 receptors coupled with potent serotonin reuptake inhibition. Specifically, the most promising compound 21n possessed a good oral pharmacokinetic properties and an acceptable hERG profile, and showed potent antidepressant-like effect in the FST and TST models.


Asunto(s)
Antidepresivos/farmacología , Piperazinas/farmacología , Receptor de Serotonina 5-HT1A/metabolismo , Receptores de Serotonina/metabolismo , Inhibidores Selectivos de la Recaptación de Serotonina/farmacología , Animales , Antidepresivos/síntesis química , Antidepresivos/química , Relación Dosis-Respuesta a Droga , Humanos , Masculino , Estructura Molecular , Piperazina , Piperazinas/síntesis química , Piperazinas/química , Ratas , Ratas Sprague-Dawley , Inhibidores Selectivos de la Recaptación de Serotonina/síntesis química , Inhibidores Selectivos de la Recaptación de Serotonina/química , Relación Estructura-Actividad
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