Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 4 de 4
Filtrar
Mais filtros

Base de dados
Tipo de documento
Assunto da revista
País de afiliação
Intervalo de ano de publicação
1.
Bioorg Chem ; 82: 109-116, 2019 02.
Artigo em Inglês | MEDLINE | ID: mdl-30312865

RESUMO

Various 1,2,4 trisubstituted imidazolin-5-one derivatives were synthesized and evaluated for their inhibitory activity against p38 mitogen-activated protein kinase (p38MAPK) and carbonic anhydrase (CA) enzymes aiming to explore potential dual inhibitors. Results revealed that compounds 3c, 3g, 3h, 4a, 6c and 6d were the most effective derivatives against p38αMAPK (IC50 = 0.14, 0.14, 0.056, 0.14, 0.13 and 0.14 µM, respectively) compared to sorafenib (IC50 = 1.58 µM) as standard drug. On the other hand, compound 4a revealed the best inhibitory activity against all the tested carbonic anhydrase isoforms CA I, II, IV and IX with Ki values of 95.0, 0.83, 6.90 and 12.4 nM, respectively compared to acetazolamide with Ki values 250, 12.1, 74 and 12.8 nM, respectively. Therefore, compound 4a can be considered as a potent dual p38αMAPK/CA inhibitor.


Assuntos
Inibidores da Anidrase Carbônica/química , Imidazolinas/química , Inibidores de Proteínas Quinases/química , Sulfonamidas/química , Proteínas Quinases p38 Ativadas por Mitógeno/antagonistas & inibidores , Inibidores da Anidrase Carbônica/síntese química , Anidrases Carbônicas/metabolismo , Ensaios Enzimáticos , Humanos , Imidazolinas/síntese química , Isoenzimas/metabolismo , Estrutura Molecular , Inibidores de Proteínas Quinases/síntese química , Relação Estrutura-Atividade , Sulfonamidas/síntese química
2.
Spectrochim Acta A Mol Biomol Spectrosc ; 68(5): 1244-9, 2007 Dec 31.
Artigo em Inglês | MEDLINE | ID: mdl-17376736

RESUMO

A simple and rapid spectrophotometric method has been developed for the determination of tricyclic anti-depressant drugs such as trazodone (TZH), amineptine (APH) and amitriptyline (ATPH) hydrochlorides in pure form and in different pharmaceutical preparations. The charge transfer (CT) reaction between TZH, APH and ATPH as electron donors and TCNQ as electron acceptor was utilized for their spectrophotometric determination. The optimum experimental conditions, like time, temperature, stoichiometry, solvents, for the CT complex formation are established. The method permits the determination of TZH, APH and ATPH over a concentration range of 10-400, 10-440 and 10-300 microg ml(-1), respectively. The sensitivity (S) is found to be 0.09, 0.087 and 0.069 g cm(-2) for TZH, APH and ATPH, respectively. The SD values are found to be 0.146-0.293, 0.154-0.285 and 0.091-0.212 and RSD values are 0.142-1.92, 0.297-1.92 and 0.212-0.915 for TZH, APH and ATPH, respectively. The low values of the relative standard deviation indicate the high accuracy and precision of the method. The mean recovery values obtained together with a high correlation coefficient values, amount in the range 98-101.5, 98.7-102.9 and 93-101.9 for TZH, APH and ATPH, respectively. The method is applicable for the assay of the investigated drugs in different dosage forms and the results are in good agreement with those obtained by the official method.


Assuntos
Amitriptilina/análise , Antidepressivos Tricíclicos/análise , Dibenzocicloeptenos/análise , Nitrilas/química , Trazodona/análise , Amitriptilina/química , Antidepressivos Tricíclicos/química , Dibenzocicloeptenos/química , Preparações Farmacêuticas/química , Solventes , Espectrofotometria , Temperatura , Fatores de Tempo , Trazodona/química
3.
Artigo em Inglês | MEDLINE | ID: mdl-16527524

RESUMO

A simple and rapid extraction spectrophotometric procedure has been developed for the determination of tricyclic anti-depressant drugs such as trazodone (TZH), amineptine (APH) and amitriptyline (ATPH) hydrochlorides in pure form and in different dosage forms. The method involves the formation of intense yellow ion-pairs between these drugs under investigation and methyl orange (MO) and bromocresol green (BCG) reagents followed by their extraction with 1,2-dichloroethane and quantitative microdetermination at 420 and 410 nm using MO or BCG, respectively. The optimum experimental conditions for the ion-pairs formation are established. The method permits the determination of TZH, APH and ATPH over a concentration range of 2-50, 2-50 and 1-25 microg ml(-1) for TZH, APH and ATPH, using MO and 1-25 microg ml(-1) for TZH, APH and ATPH, using BCG, respectively. The Sandell sensitivity (S) is found to be 0.106, 0.1071 and 0.0907 g cm(-2) for TZH, APH and ATPH, respectively, using MO reagent and 0.0788, 0.0661 and 0.0494 g cm(-2) for TZH, APH and ATPH, respectively, using BCG. The method is applicable for the assay of the investigated drugs in different dosage forms and the results are in good agreement with those obtained by the official method.


Assuntos
Amitriptilina/química , Compostos Azo/química , Verde de Bromocresol/química , Dibenzocicloeptenos/química , Trazodona/química , Concentração de Íons de Hidrogênio , Indicadores e Reagentes/química , Estrutura Molecular , Preparações Farmacêuticas/química , Solventes/química , Espectrofotometria , Temperatura , Fatores de Tempo
4.
Artigo em Inglês | MEDLINE | ID: mdl-16829178

RESUMO

Extraction spectrophotometric method has been developed for the determination of tricyclic drugs such as trazodone (TZH), amineptine (APH) and amitriptyline (ATPH) hydrochlorides in pure form and in the dosage forms coming from different Egyptian markets. The method based on the formation of ion-pairs between these drugs under investigation and inorganic complex of Mo(V)-thiocyanate followed by its extraction with methylene chloride. The optimum conditions for the ion-pairs formation are established. The method permits the determination of TZH, APH and ATPH over the concentration range of 2-28, 2-32 and 1-30 microg ml(-1), respectively. The Sandell sensitivity (S) is found to be 0.105, 0.138 and 0.118 g cm(-2) for TZH, APH and ATPH, respectively. The SD is found to be 0.16-0.377, 0.12-0.259 and 0.091-0.286 and the R.S.D. are 0.14-0.55, 0.12-0.399 and 0.095-0.485 for TZH, APH and ATPH, respectively. The method is applicable for the assay of the investigated drugs in different dosage forms and the results are in good agreement with those obtained by the official method.


Assuntos
Amitriptilina/química , Dibenzocicloeptenos/química , Ácido Clorídrico/química , Molibdênio/química , Tiocianatos/química , Trazodona/química , Absorção/efeitos dos fármacos , Antidepressivos Tricíclicos/química , Ácido Ascórbico/farmacologia , Relação Dose-Resposta a Droga , Concentração de Íons de Hidrogênio , Modelos Biológicos , Molibdênio/farmacologia , Solventes/farmacologia , Espectrofotometria/métodos , Temperatura , Tiocianatos/farmacologia , Fatores de Tempo
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA