Recent advances in the design and synthesis of heterocycles as anti-tubercular agents

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dc.contributor.author Sunduru, Naresh
dc.contributor.author Sharma, Moni
dc.contributor.author Chauhan, P M S
dc.date.accessioned 2011-05-13T09:11:24Z
dc.date.available 2011-05-13T09:11:24Z
dc.date.issued 2010
dc.identifier.citation Future Medicinal Chemistry, 2(9), 2010, 1469-1500 en
dc.identifier.uri http://hdl.handle.net/123456789/665
dc.description.abstract Due to the unusual structure and chemical composition of the mycobacterial cell wall, effective TB treatment is difficult, which makes many antibiotics ineffective and hinders the entry of drugs. With approximately 33% of infection, tuberculosis is still the second most imperative infectious disease worldwide. The most important reason for this is drug resistant TB (MDR, XDR), persistent infection (latent TB) and synergism of TB with HIV; furthermore no any new chemical entity has come in picture in last 40 years. New data available from the recently sequenced genome of the mycobacterium and the application of methods of modern drug design promise to bring significant development in the fight against this disease. In present review we discussed brief introduction of tuberculosis followed en
dc.format.extent 1979276 bytes
dc.format.mimetype application/pdf
dc.language.iso en en
dc.relation.ispartofseries cdricommunicationno.7951 en
dc.subject XDR-TB en
dc.subject G+C Gram-positive bacteria en
dc.subject Aminoglycoside en
dc.subject Macrolide antibiotics en
dc.subject Serum half life en
dc.subject CFU en
dc.title Recent advances in the design and synthesis of heterocycles as anti-tubercular agents en
dc.type Article en


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