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1.
Bioorg Med Chem Lett ; 29(23): 126703, 2019 12 01.
Artigo em Inglês | MEDLINE | ID: mdl-31627993

RESUMO

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.


Assuntos
Antidepressivos/uso terapêutico , Piperazina/uso terapêutico , Piperidinas/uso terapêutico , Inibidores Seletivos de Recaptação de Serotonina/uso terapêutico , Antidepressivos/farmacologia , Humanos , Piperazina/farmacologia , Piperidinas/farmacologia , Inibidores Seletivos de Recaptação de Serotonina/farmacologia , Relação Estrutura-Atividade
2.
Bioorg Med Chem Lett ; 27(24): 5420-5423, 2017 12 15.
Artigo em Inglês | MEDLINE | ID: mdl-29138029

RESUMO

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.


Assuntos
Antidepressivos/síntese química , Piperazinas/química , Receptor 5-HT1A de Serotonina/metabolismo , Receptores de Serotonina/metabolismo , Inibidores Seletivos de Recaptação de Serotonina/síntese química , Animais , Antidepressivos/metabolismo , Antidepressivos/farmacologia , Células HEK293 , Meia-Vida , Humanos , Concentração Inibidora 50 , Camundongos , Microssomos Hepáticos/metabolismo , Atividade Motora/efeitos dos fármacos , Piperazinas/metabolismo , Piperazinas/farmacologia , Ratos , Receptor 5-HT1A de Serotonina/química , Receptores de Serotonina/química , Inibidores Seletivos de Recaptação de Serotonina/metabolismo , Inibidores Seletivos de Recaptação de Serotonina/farmacologia , Relação Estrutura-Atividade
3.
Chin Med Sci J ; 31(2): 89-94, 2016 Jun 20.
Artigo em Inglês | MEDLINE | ID: mdl-28031096

RESUMO

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.


Assuntos
Pressão Sanguínea , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Artérias , Criança , Feminino , Humanos , Aneurisma Intracraniano , Masculino , Pessoa de Meia-Idade , Prognóstico , Estudos Retrospectivos , Resultado do Tratamento , Adulto Jovem
4.
J Org Chem ; 79(12): 5806-11, 2014 Jun 20.
Artigo em Inglês | MEDLINE | ID: mdl-24869774

RESUMO

(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.


Assuntos
Benzimidazóis/química , Benzimidazóis/síntese química , Compostos Heterocíclicos/química , Imidazóis/química , Imidazóis/síntese química , Metano/análogos & derivados , Compostos Organometálicos/química , Paládio/química , Catálise , Ligação de Hidrogênio , Metano/química , Estrutura Molecular
5.
Eur J Med Chem ; 144: 701-715, 2018 Jan 20.
Artigo em Inglês | MEDLINE | ID: mdl-29291438

RESUMO

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.


Assuntos
Antidepressivos/farmacologia , Piperazinas/farmacologia , Receptor 5-HT1A de Serotonina/metabolismo , Receptores de Serotonina/metabolismo , Inibidores Seletivos de Recaptação de Serotonina/farmacologia , Animais , Antidepressivos/síntese química , Antidepressivos/química , Relação Dose-Resposta a Droga , Humanos , Masculino , Estrutura Molecular , Piperazina , Piperazinas/síntese química , Piperazinas/química , Ratos , Ratos Sprague-Dawley , Inibidores Seletivos de Recaptação de Serotonina/síntese química , Inibidores Seletivos de Recaptação de Serotonina/química , Relação Estrutura-Atividade
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