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Synthesis and characterization of n-hydroxyalkyl and oxazolinyl ethionamide derivatives

Multidrug-resistant tuberculosis (MDR-TB) is a serious problem worldwide, especially in people living with human immunodeficiency virus. In considering the MDR-TB problem, ethionamide (ETH) is a structural analog of isoniazid that is typically used when the patient exhibits resistance to the front-l...

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Bibliographic Details
Published in:Journal of sulfur chemistry 2008-04, Vol.29 (2), p.145-149
Main Authors: Cardoso, Sílvia H., Vieira De Almeida, Mauro, Vitor De Assis, João, Diniz, Renata, Speziali, Nivaldo L., De Souza, Marcus V.N.
Format: Article
Language:English
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Summary:Multidrug-resistant tuberculosis (MDR-TB) is a serious problem worldwide, especially in people living with human immunodeficiency virus. In considering the MDR-TB problem, ethionamide (ETH) is a structural analog of isoniazid that is typically used when the patient exhibits resistance to the front-line drugs, being one of the most frequently used drugs, for the treatment of drug-resistant tuberculosis. Due to the importance of ETH in TB treatment, the aim of our work was the synthesis and characterization of oxazolinyl (1,2) and N-hydroxyalkyl (3-5) ETH derivatives.
ISSN:1741-5993
1741-6000
DOI:10.1080/17415990701845963