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1.
Rev Med Chir Soc Med Nat Iasi ; 117(2): 558-64, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-24340546

RESUMEN

Sulfonamides and their different derivatives are extensively used in therapy due to their pharmacological properties. Sulfa drugs were amongst the oldest synthesized antimicrobial agents and are still widely used today to treat different microbial infections. Clinical treatment with sulfonamides has regained confidence with the use of a combination of sulfamethoxazole and trimethoprim to treat urinary tract bacterial infections. Today, they are widely used as antimicrobial agents, chiefly because of their low cost, low toxicity and excellent activity against bacterial diseases. Over the course of time, the application of sulfonamides has been extended from their use as antimicrobial agents to anticancer agents, antiglaucoma agents, inhibitors of gamma-secretase, cyclooxgenase-2 and lipoxygenase, anticonvulsivant agents, hypoglycemic agents.


Asunto(s)
Antiinfecciosos/uso terapéutico , Infecciones Bacterianas/tratamiento farmacológico , Sulfonamidas/uso terapéutico , Antiinfecciosos/economía , Infecciones Bacterianas/economía , Quimioterapia/economía , Quimioterapia/tendencias , Humanos , Rumanía , Sulfonamidas/economía , Combinación Trimetoprim y Sulfametoxazol/uso terapéutico , Infecciones Urinarias/tratamiento farmacológico
2.
Rev Med Chir Soc Med Nat Iasi ; 117(1): 238-43, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-24505922

RESUMEN

UNLABELLED: Infections caused by bacterial species are common in immunocompromised patients and carry significant treatment costs and mortality. The emerging resistance of microorganisms to some synthetic antimicrobial agents makes it necessary to continue the research for new antimicrobial drugs. AIM: To design new sulphonamide compounds with potential antibacterial and antioxidant activity. MATERIAL AND METHODS: New N-hydrazino acetyl-sulphonamides were prepared by condensation of some sulphonamides with chloroacetyl chloride and amination of intermediate compounds with hydrazine hydrate. RESULTS: The synthesized compounds were screened for their antibacterial activity against Gram positive (Klebsiellapneumoniae. Proteus vulgaris, Citrobacter freundii, Enterobacter cloacae, Staphylococcus aureus, Staphylococcus epidermidis, Enterococcus faecalis) and Gram negative bacterial strains (Pseudomonas aeruginosa, Escherichia coli). Some of them were found to have good antibacterial activity. The antioxidant activity of these compounds was also tested using different methods: total antioxidant capacity, reducing power, and DPPH radical scavenging activity. CONCLUSIONS: Chemical modulations performed on sulphonamide structure have a good influence on the biological activity of the synthesized compounds, especially on their antioxidant effects.


Asunto(s)
Acetatos/química , Antiinfecciosos/síntesis química , Antioxidantes/síntesis química , Hidrazinas/síntesis química , Solventes/química , Sulfonamidas/síntesis química , Aminación , Antiinfecciosos/química , Antiinfecciosos/farmacología , Antioxidantes/farmacología , Bacterias Gramnegativas/efectos de los fármacos , Bacterias Grampositivas/efectos de los fármacos , Humanos , Hidrazinas/química , Hidrazinas/farmacología , Pruebas de Sensibilidad Microbiana , Sulfonamidas/química , Sulfonamidas/farmacología
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