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Synthesis and antimicrobial activities of 5-arylidene-thiazolidine-2,4-dione derivatives
- Source :
- Repositório Institucional da Universidade Federal do Ceará (UFC), Universidade Federal do Ceará (UFC), instacron:UFC, BioMed Research International, Vol 2014 (2014), BioMed Research International
- Publication Year :
- 2014
- Publisher :
- BioMed Research International, 2014.
-
Abstract
- Antibiotic resistance is considered one of the world's major public health concerns. The main cause of bacterial resistance is the improper and repeated use of antibiotics. To alleviate this problem, new chemical substances against microorganisms are being synthesized and tested. Thiazolidines are compounds having many pharmacological activities including antimicrobial activities. For this purpose some thiazolidine derivatives substituted at position 5 in the thiazolidine nucleus were synthesized and tested against several microorganisms. Using a disc diffusion method, antimicrobial activity was verified against Gram-positive, Gram-negative, and alcohol acid resistant bacteria and yeast. The minimum inhibition concentrations (MIC) and minimum bactericidal concentrations (MBC) were determined. All derivatives showed antimicrobial activity mainly against Gram-positive bacteria, with MIC values ranging from 2 to 16 µg/mL.
- Subjects :
- Article Subject
Cell Survival
medicine.drug_class
Microorganism
Antibiotics
Thiazolidine
lcsh:Medicine
Biology
Bacterial Physiological Phenomena
General Biochemistry, Genetics and Molecular Biology
Microbiology
Lethal Dose 50
chemistry.chemical_compound
Antibiotic resistance
Anti-Infective Agents
medicine
Tiazolidinas
Dose-Response Relationship, Drug
General Immunology and Microbiology
Thiazolidines
lcsh:R
Resistência a Medicamentos
General Medicine
Antimicrobial
biology.organism_classification
Combinatorial chemistry
Yeast
chemistry
Bacteria
Research Article
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Journal :
- Repositório Institucional da Universidade Federal do Ceará (UFC), Universidade Federal do Ceará (UFC), instacron:UFC, BioMed Research International, Vol 2014 (2014), BioMed Research International
- Accession number :
- edsair.doi.dedup.....e763fe712639f3e7287faf9772f9c620