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. 2012 Jun 28;5(7):690-718.
doi: 10.3390/ph5070690.

Chemotherapeutic interventions against tuberculosis

Affiliations

Chemotherapeutic interventions against tuberculosis

Neeraj Shakya et al. Pharmaceuticals (Basel). .

Abstract

Tuberculosis is the second leading cause of infectious deaths globally. Many effective conventional antimycobacterial drugs have been available, however, emergence of multidrug-resistant tuberculosis (MDR-TB) and extensively drug-resistant tuberculosis (XDR-TB) has overshadowed the effectiveness of the current first and second line drugs. Further, currently available agents are complicated by serious side effects, drug interactions and long-term administration. This has prompted urgent research efforts in the discovery and development of new anti-tuberculosis agent(s). Several families of compounds are currently being explored for the treatment of tuberculosis. This review article presents an account of the existing chemotherapeutics and highlights the therapeutic potential of emerging molecules that are at different stages of development for the management of tuberculosis disease.

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Figures

Figure 1
Figure 1
First line anti-tuberculosis drugs.
Figure 2
Figure 2
Pyrimidine nucleosides as anti-tuberculosis agents.
Figure 3
Figure 3
Acyclic pyrimidine nucleosides as anti-tuberculosis agents.
Figure 4
Figure 4
Some recent pyrimidine nucleosides as anti-tuberculosis agents.
Figure 5
Figure 5
Purine nucleosides as anti-tuberculosis agents.
Figure 6
Figure 6
Carbohydrate derivatives as anti-tuberculosis agents.
Figure 7
Figure 7
Fluoroquinolones as anti-tuberculosis agents.
Figure 8
Figure 8
Quinoxaline-2-carboxylate 1,4-dioxide derivatives as anti-tuberculosis agents.
Figure 9
Figure 9
1,4-di-N-oxide-3-phenylquinoxalines as anti-tuberculosis agents.
Figure 10
Figure 10
Some other quinoline derivatives as anti-tuberculosis agents.
Figure 11
Figure 11
Pyrimidine and Purine analogs as anti-tuberculosis agents.
Figure 12
Figure 12
Azole analogs as anti-tuberculosis agents.
Figure 13
Figure 13
N-Aryl-C-nitroazoles as anti-tuberculosis agents.
Figure 14
Figure 14
Azines as anti-tuberculosis agents.
Figure 15
Figure 15
INH analogs as anti-tuberculosis agents.
Figure 16
Figure 16
Artemisinin analog as anti-tuberculosis agents.
Figure 17
Figure 17
Macrolide as anti-tuberculosis agents.
Figure 18
Figure 18
Structure of thiolactomycin.
Figure 19
Figure 19
Structure of CPZEN-45.
Figure 20
Figure 20
Structure of DC-159a.
Figure 21
Figure 21
Structure of SQ609.
Figure 22
Figure 22
Structure of SQ-641.
Figure 23
Figure 23
Structure of BTZ-043.
Figure 24
Figure 24
Structure of tryptanthrin.
Figure 25
Figure 25
Structure of PNU-100480.
Figure 26
Figure 26
Structure of LL3858.
Figure 27
Figure 27
Structure of SQ109.
Figure 28
Figure 28
Structure of PA-824.
Figure 29
Figure 29
Structure of OPC-67683.
Figure 30
Figure 30
Structure of TMC-207.
Figure 31
Figure 31
Structure of linezolid.
Figure 32
Figure 32
Structure of rifapentine.
Figure 33
Figure 33
Structures of moxifloxacin and gatifloxacin.

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