Abstract | BACKGROUND:
Tuberculosis (TB) remains a leading cause of morbidity and mortality worldwide, yet no new drugs have been developed in the last 40 years. OBJECTIVE: The exceedingly lengthy TB chemotherapy and the increasing emergence of drug resistance complicated by HIV co-infection call for the development of new TB drugs. These problems are further compounded by a poor understanding of the biology of persister bacteria. METHODS: New molecular tools have offered insights into potential new drug targets, particularly the enzymes of the shikimate pathway, which is the focus of this review. RESULTS/CONCLUSION:
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Authors | Senta M Kapnick, Ying Zhang |
Journal | Expert opinion on drug discovery
(Expert Opin Drug Discov)
Vol. 3
Issue 5
Pg. 565-77
(May 2008)
ISSN: 1746-0441 [Print] England |
PMID | 23484927
(Publication Type: Journal Article)
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