Abstract
Annual Review of Pharmacology and Toxicology
Vol. 45:
529-564
(Volume publication date February 2005)
(doi:10.1146/annurev.pharmtox.45.120403.100120)
First published online as a Review in Advance on October 7, 2004THE MAGIC BULLETS AND TUBERCULOSIS DRUG TARGETS Ying ZhangDepartment of Molecular Microbiology and Immunology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland 21205; email: yzhang@jhsph.edu ▪ Abstract Modern chemotherapy has played a major role in our control of tuberculosis. Yet tuberculosis still remains a leading infectious disease worldwide, largely owing to persistence of tubercle bacillus and inadequacy of the current chemotherapy. The increasing emergence of drug-resistant tuberculosis along with the HIV pandemic threatens disease control and highlights both the need to understand how our current drugs work and the need to develop new and more effective drugs. This review provides a brief historical account of tuberculosis drugs, examines the problem of current chemotherapy, discusses the targets of current tuberculosis drugs, focuses on some promising new drug candidates, and proposes a range of novel drug targets for intervention. Finally, this review addresses the problem of conventional drug screens based on inhibition of replicating bacilli and the challenge to develop drugs that target nonreplicating persistent bacilli. A new generation of drugs that target persistent bacilli is needed for more effective treatment of tuberculosis. Mutational, inhibitory and microcalorimetric analyses of Plasmodium falciparum TMP kinase. Implications for drug discovery Parasitology 136(01):11 (2009) Alginate-based sustained release drug delivery systems for tuberculosis Expert Opinion on Drug Delivery 5(12):1323-1334 (2009) Synthesis and Antituberculosis Activity of New Hydrazide Derivatives Archiv der Pharmazie 341(11):721-724 (2008) Enhancement of the antituberculosis activity of weak acids by inhibitors of energy metabolism but not by anaerobiosis suggests that weak acids act differently from the front-line tuberculosis drug pyrazinamide Journal of Medical Microbiology 57(9):1129-1134 (2008) Exploring Acyclic Nucleoside Analogues as Inhibitors of
Mycobacterium tuberculosis
Thymidylate Kinase ChemMedChem 3(7):1083-1093 (2008)
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