Academic Journal

Synthesis, anti-toxoplasma gondii and antimicrobial activities of 2-hydrazolyl-3-phenyl-5-(4-nitrobenzylidene)-4-thiazolidinone substituted derivatives

التفاصيل البيبلوغرافية
العنوان: Synthesis, anti-toxoplasma gondii and antimicrobial activities of 2-hydrazolyl-3-phenyl-5-(4-nitrobenzylidene)-4-thiazolidinone substituted derivatives
المؤلفون: Góes, Alexandre J. S., Melo, Edésio J.T., Alves, Antonio J., Lima, José G., Araújo, Janete M., Faria, Antônio R., Alves, Anselmo Q., Lima, Vânia T., Carvalho, Cristiane S., Spacov, Isabel C.G., Nascimento, André A.P.L., Aquino, Thiago M.
سنة النشر: 2011
المجموعة: Universidad Nacional de La Plata (UNLP): SeDiCI (Servicio de Difusión de la Creación Intelectual)
مصطلحات موضوعية: Farmacia, antimicrobial activity, anti-toxoplasma gondii activity, 4-thiazolidinone, thiosemicarbazone
الوصف: A novel series of 2-hydrazolyl-3-phenyl-5-(4-nitrobenzylidene)-4-thiazolidinone substituted (3a-p) has been synthesized. The intermediates 2-hydrazolyl-3-phenyl-4-thiazolidinone substituted (2a-p) were prepared by condensation of benzaldehyde 4-phenyl-3-thiosemicarbazone substituted (1a-p) with ethyl chloroacetate. Theses intermediates were submitted to reaction with ethyl 2-cyano-3-(4-nitrophenyl)-acetate to give the title compounds. The 4-thiazolidinones were screened for their anti-Toxoplasma gondii, and all derivatives promoted decrease of percentage of infection of Vero cells, with elimination of intracellular tachyzoites. The LD50 ranged around 0.5 mM for the intracellular parasites and were higher than 10 mM for Vero cells. According to results of antimicrobial activity, only two compounds showed significant inhibition against M. luteus, but demonstrated higher values of MIC and MBC when compared with standard drug. ; Colegio de Farmacéuticos de la Provincia de Buenos Aires
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf; 1567-1573
اللغة: English
Relation: http://sedici.unlp.edu.ar/handle/10915/8340
الاتاحة: http://sedici.unlp.edu.ar/handle/10915/8340
رقم الانضمام: edsbas.69B1E739
قاعدة البيانات: BASE