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1.
Mol Biol Rep ; 48(7): 5497-5502, 2021 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-34291393

RESUMO

BACKGROUND: A cluster of many risk factors for type 2 diabetes and cardiovascular disease is used to describe the metabolic syndrome (MetS). Moreover, genetic differences associated with metabolic syndrome play a key role in its prevalence and side effects. This study aims to investigate the expression of DYRK1B and its association with metabolic syndrome in a small cohort of Egyptian. MATERIALS AND METHODS: A total of 100 adult Egyptians (50 with MetS and 50 healthy control subjects) were included to this study. Clinical, biochemical and anthropometric analysis were assessed. Relative gene expressions of DYRK1B were compared between two groups of subjects using real time PCR. RESULTS: We observed marked overexpression in DYRK1B (p < 0.05) in MetS subjects when compared with the healthy control subjects. CONCLUSION: This is the first study to provide evidence that DYRK1B is highly expressed among the MetS subjects.


Assuntos
Expressão Gênica , Síndrome Metabólica/etiologia , Síndrome Metabólica/metabolismo , Proteínas Serina-Treonina Quinases/genética , Proteínas Tirosina Quinases/genética , Biomarcadores , Pesos e Medidas Corporais , Estudos de Casos e Controles , Estudos de Coortes , Egito , Feminino , Humanos , Lipídeos/sangue , Masculino , Síndrome Metabólica/diagnóstico , Quinases Dyrk
2.
Arch Pharm (Weinheim) ; 335(6): 251-61, 2002 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-12210767

RESUMO

Condensation of carbohydrazide derivatives Ia, b with dimethyl acetylenedicarboxylate and acetylenedicarboxylic acid yielded benzofuran derivatives II a-d. Reaction of Ib with aromatic aldehydes formed products III a-d. Treatment of compounds III a-d with mercaptoacetic acid yielded the cyclocondensation products (IVa-d). Phthalic anhydride reacted with compounds (Ia, b)to form products (Va, b). It has been found that both khellin and visnagin (VIa, b)react with aromatic aldehydes to give arylidene derivatives (VIIa-e). Condensation of diphenyl nitrilamine with 2-arylidene furochromones VII derivatives afforded cyclo-adducts (VIII a-i). The antibacterial activities of the selected compounds were tested against Staphylococcus aureus, B. subtilis, E. coli, Pseudomonas, Salmonella and Erwinia with good results.


Assuntos
Antibacterianos/síntese química , Antibacterianos/farmacologia , Bactérias/efeitos dos fármacos , Oxazóis/síntese química , Oxazóis/farmacologia , Ftalimidas/síntese química , Ftalimidas/farmacologia , Tiazóis/síntese química , Tiazóis/farmacologia , Fenômenos Químicos , Físico-Química , Indicadores e Reagentes , Quelina/química , Espectroscopia de Ressonância Magnética , Testes de Sensibilidade Microbiana , Espectrofotometria Infravermelho
3.
Arch Pharm (Weinheim) ; 324(1): 35-7, 1991 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-2043040

RESUMO

Cycloaddition reactions of the nitrilimines 4-6 with N-arylmaleimides 7 and acrylamide (11) yield the pyrrolopyrazole derivatives 8-10 and 2-pyrazolines 12, respectively, in excellent yield. The regioselectivity and biological activities of some of the new compounds were investigated.


Assuntos
Antibacterianos/síntese química , Pirazóis/síntese química , Pirróis/síntese química , Antibacterianos/farmacologia , Bactérias/efeitos dos fármacos , Testes de Sensibilidade Microbiana , Pirazóis/farmacologia , Pirróis/farmacologia
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