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1.
Molecules ; 20(1): 974-86, 2015 Jan 08.
Artigo em Inglês | MEDLINE | ID: mdl-25580690

RESUMO

Imidazolidine derivatives, or hydantoins, are synthetic compounds with different therapeutic applications. Many imidazolidine derivatives have psychopharmacological properties, such as phenytoin, famous for its anticonvulsant efficacy, but also effective in the treatment of neuropathic pain. The hydantoin, 3-phenyl-5-(4-ethylphenyl)-imidazolidine-2,4-dione (IM-3), synthesized from the amino acid, glycine, was selected for psychopharmacological studies in mice on the basis of its chemical and structural similarity with phenytoin. The first step of this study was to define the LD50, which determined the doses of 50, 100 and 200 mg/kg for subsequent tests. The results obtained from the behavioral screening indicated that IM-3 produces decreased ambulation and analgesia in mice. Motor coordination and anxiety behavior were not affected by treatment with IM-3, as observed in the rotarod and elevated plus-maze tests, respectively. Regarding its antinociceptive properties, IM-3 showed efficacy in the acetic acid-induced writhing test by increasing the latency of the first writhe and reducing the number of writhes, as well as reducing the paw licking time in the second phase of the formalin test. The behavior of treated animals exposed to the hot plate test, however, did not differ from that of the control group. These data suggest that IM-3 has antinociceptive effects in mice, which is probably mediated by anti-inflammatory mechanisms.


Assuntos
Analgésicos/farmacologia , Hidantoínas/farmacologia , Ácido Acético , Animais , Comportamento Animal , Formaldeído , Hidantoínas/química , Masculino , Aprendizagem em Labirinto/efeitos dos fármacos , Camundongos , Teste de Desempenho do Rota-Rod , Testes de Toxicidade Aguda
3.
Molecules ; 17(5): 5095-107, 2012 May 03.
Artigo em Inglês | MEDLINE | ID: mdl-22555298

RESUMO

Five new 1-(2-(5-nitrofuran-2-yl)-5-(aryl)-1,3,4-oxadiazol-3-(2H)-yl) ethanone compounds 5a-e were synthesized by cyclization of N-acylhydrazones 4a-e with acetic anhydride under reflux conditions. Their structures were fully characterized by IR, ¹H-NMR, and ¹³C-NMR. Furthermore, evaluations of the antibacterial activity of the 1,3,4-oxadiazoles 5a-e and N-acylhydrazones 4a-e showed strong activity against several strains of Staphylococcus aureus, with MICs between 4 µg/mL to 32 µg/mL. In silico studies of the parameters of Lipinski's Rule of Five, as well as the topological polar surface area (TPSA), absorption percentage (% ABS), drug likeness and drug score indicate that these compounds, especially 4a and 5d, have potential to be new drug candidates.


Assuntos
Antibacterianos/síntese química , Hidrazonas/síntese química , Oxidiazóis/síntese química , Staphylococcus aureus/efeitos dos fármacos , Anidridos Acéticos/química , Antibacterianos/farmacologia , Simulação por Computador , Farmacorresistência Bacteriana Múltipla , Hidrazonas/farmacologia , Interações Hidrofóbicas e Hidrofílicas , Espectroscopia de Ressonância Magnética , Testes de Sensibilidade Microbiana , Modelos Moleculares , Oxidiazóis/farmacologia , Staphylococcus aureus/crescimento & desenvolvimento , Propriedades de Superfície
4.
Molecules ; 16(3): 2023-31, 2011 Feb 28.
Artigo em Inglês | MEDLINE | ID: mdl-21358591

RESUMO

Two salts of the mesoionic compounds 1,4-diphenyl-5-(5-nitro-2-furanyl)-1,3,4-thiadiazolium-2-thiol chloride (MC-1) and 4-phenyl-5-(5-nitro-2-furanyl)-1,3,4-thiadiazolium-2-phenylamine chloride (MC-2) were synthesized utilizing 1,4-diphenyl-thiosemicarbazide and 5-nitro-2-furoyl chloride as starting materials. Their structures were characterized by IR, ¹H-NMR, ¹³C-NMR and elemental analysis. These compounds were analyzed for their influence on the effectiveness of norfloxacin, tetracycline, and erythromycin (standard antibiotics) against resistant strains of Staphylococcus aureus. MC-1 and MC-2, at sub-inhibitory concentrations of 16 µg/mL, favourably modulated the antibiotic activity of tetracycline by 16- and 32-fold, respectively (MIC), and that of erythromycin by 4-fold.


Assuntos
Antibacterianos/farmacologia , Cloretos/farmacologia , Resistência Microbiana a Medicamentos , Staphylococcus aureus/efeitos dos fármacos , Antibacterianos/química , Cloretos/química , Espectroscopia de Ressonância Magnética , Testes de Sensibilidade Microbiana , Espectrofotometria Infravermelho
5.
Rev. bras. farmacogn ; 7/8(1): 41-47, 1998. tab, ilus
Artigo em Português | LILACS | ID: lil-534799

RESUMO

Neste trabalho foi verificado o teor de Óleos, sólidos e bixina em sementes de quatro variedades de Bixa orellana L. cultivadas na Paraíba: "Casca verde", "Casca vermelha", Bico de calango" e "Grão preto". Os melhores resultados foram obti­dos com os tipos "Casca verde" e "Casca vermelha" que apresentaram um rendimento em bixina pura, cristalina, de 1,3 e 1,1 por cento, respectivamente.


In this work it was verified the content of oils, solids and bixin in seeds of four varieties of Bixa orellana L. cultivated in Paraíba: "Casca verde", "Casca vermelha", Bico de calango" and "Grão preto". The best results were obtained with the types "Casca verde" and "Casca vermelha" that presented an yield in pure, crystalline bixina, of 1,3 and 1,1 percent, respectively.

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