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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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Published in: | Journal of sulfur chemistry 2008-04, Vol.29 (2), p.145-149 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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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. |
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ISSN: | 1741-5993 1741-6000 |
DOI: | 10.1080/17415990701845963 |