메뉴 건너뛰기




Volumn 5, Issue 3, 2009, Pages 190-200

Bringing down the wall of the Mycobacterium tuberculosis fortress: Old and new inhibitors of mycolic acid biosynthesis

Author keywords

Enoyl ACP reductase; Ethionamide; Isoniazid; Isoxyl; Mycolic acid biosynthesis; Thiacetazone; Tuberculosis

Indexed keywords

2,3 DIHYDRO 2 METHYL 6 NITRO 2 [4 [4 (4 TRIFLUOROMETHOXYPHENOXY) 1 PIPERIDINYL]PHENOXYMETHYL]IMIDAZO[2,1 B]OXAZOLE; 6,7 DIHYDRO 2 NITRO 6 (4 TRIFLUOROMETHOXYBENZYLOXY) 5H IMIDAZO[2,1 B][1,3]OXAZINE; ARABINOGALACTAN; BACTERIAL PROTEIN; DIHYDROFOLATE REDUCTASE; ENOYL ACYL CARRIER PROTEIN REDUCTASE (NADH); ETHA PROTEIN; ETHIONAMIDE; FATTY ACID SYNTHASE; FATTY ACID SYNTHETASE TYPE II; INHA PROTEIN; ISONIAZID; KATG PROTEIN; MYCOLIC ACID; NICOTINAMIDE ADENINE DINUCLEOTIDE; PEPTIDOGLYCAN; PYRAZINAMIDE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE; RIFAMPICIN; THIOACETAZONE; TIOCARLIDE; TRICLOSAN; TUBERCULOSTATIC AGENT; UNCLASSIFIED DRUG;

EID: 74849123475     PISSN: 1573398X     EISSN: None     Source Type: Journal    
DOI: 10.2174/157339809788922397     Document Type: Review
Times cited : (1)

References (150)
  • 1
    • 69949112474 scopus 로고    scopus 로고
    • World Health Organization. Global tuberculosis control: Surveillance, planning, financing
    • World Health Organization, WHO/HTM/TB/2008.393. 2009
    • World Health Organization. World Health Organization. Global tuberculosis control: surveillance, planning, financing: WHO report 2008. WHO/HTM/TB/2008.393. 2009.
    • WHO report 2008
  • 2
    • 0037928829 scopus 로고    scopus 로고
    • The role of DOTS in tuberculosis treatment and control
    • Davies PD. The role of DOTS in tuberculosis treatment and control. Am J Respir Med 2003; 2(3): 203-9.
    • (2003) Am J Respir Med , vol.2 , Issue.3 , pp. 203-209
    • Davies, P.D.1
  • 3
    • 0032512283 scopus 로고    scopus 로고
    • Prospects for worldwide tuberculosis control under the WHO DOTS strategy. Directly observed short-course therapy
    • Dye C, Garnett GP, Sleeman K, Williams BG. Prospects for worldwide tuberculosis control under the WHO DOTS strategy. Directly observed short-course therapy. Lancet 1998; 352(9144): 1886-91.
    • (1998) Lancet , vol.352 , Issue.9144 , pp. 1886-1891
    • Dye, C.1    Garnett, G.P.2    Sleeman, K.3    Williams, B.G.4
  • 5
    • 0037841362 scopus 로고    scopus 로고
    • The global situation of MDR-TB
    • Espinal MA. The global situation of MDR-TB. Tuberculosis (Edinb ) 2003; 83(1-3): 44-51.
    • (2003) Tuberculosis (Edinb , vol.83 , Issue.1-3 , pp. 44-51
    • Espinal, M.A.1
  • 6
    • 16344385633 scopus 로고    scopus 로고
    • Can DOTS control multidrug-resistant tuberculosis?
    • Espinal MA, Dye C. Can DOTS control multidrug-resistant tuberculosis? Lancet 2005; 365(9466): 1206-9.
    • (2005) Lancet , vol.365 , Issue.9466 , pp. 1206-1209
    • Espinal, M.A.1    Dye, C.2
  • 7
    • 33846995990 scopus 로고    scopus 로고
    • XDR tuberculosis-implications for global public health
    • Raviglione MC, Smith IM. XDR tuberculosis-implications for global public health. N Engl J Med 2007; 356(7): 656-9.
    • (2007) N Engl J Med , vol.356 , Issue.7 , pp. 656-659
    • Raviglione, M.C.1    Smith, I.M.2
  • 8
    • 66149099261 scopus 로고    scopus 로고
    • Epidemiology of antituberculosis drug resistance 2002-07: An updated analysis of the Global Project on Anti-Tuberculosis Drug Resistance Surveillance
    • Wright A, Zignol M, Van Deun A, et al. Epidemiology of antituberculosis drug resistance 2002-07: an updated analysis of the Global Project on Anti-Tuberculosis Drug Resistance Surveillance. Lancet 2009; 373(9678): 1861-73.
    • (2009) Lancet , vol.373 , Issue.9678 , pp. 1861-1873
    • Wright, A.1    Zignol, M.2    Van Deun, A.3
  • 9
    • 0036015838 scopus 로고    scopus 로고
    • The methylbranched fortifications of Mycobacterium tuberculosis
    • Minnikin DE, Kremer L, Dover LG, Besra GS. The methylbranched fortifications of Mycobacterium tuberculosis. Chem Biol 2002; 9(5): 545-53.
    • (2002) Chem Biol , vol.9 , Issue.5 , pp. 545-553
    • Minnikin, D.E.1    Kremer, L.2    Dover, L.G.3    Besra, G.S.4
  • 10
    • 0032452982 scopus 로고    scopus 로고
    • The envelope layers of mycobacteria with reference to their pathogenicity
    • Daffe M, Draper P. The envelope layers of mycobacteria with reference to their pathogenicity. Adv Microb Physiol 1998; 39: 131-203.
    • (1998) Adv Microb Physiol , vol.39 , pp. 131-203
    • Daffe, M.1    Draper, P.2
  • 11
    • 0025850991 scopus 로고
    • Mycobacterial cell wall and pathogenicity: A lipodologist's view
    • Laneelle G, Daffe M. Mycobacterial cell wall and pathogenicity: a lipodologist's view. Res Microbiol 1991; 142(4): 433-7.
    • (1991) Res Microbiol , vol.142 , Issue.4 , pp. 433-437
    • Laneelle, G.1    Daffe, M.2
  • 12
    • 0017839021 scopus 로고
    • Subunit structure of Mycobacterium smegmatis fatty acid synthetase. Evidence for identical multifunctional polypeptide chains
    • Wood WI, Peterson DO, Bloch K. Subunit structure of Mycobacterium smegmatis fatty acid synthetase. Evidence for identical multifunctional polypeptide chains. J Biol Chem 1978; 253(8): 2650-6.
    • (1978) J Biol Chem , vol.253 , Issue.8 , pp. 2650-2656
    • Wood, W.I.1    Peterson, D.O.2    Bloch, K.3
  • 13
    • 0016413224 scopus 로고
    • Fatty acid synthases from Mycobacterium phlei
    • Bloch K. Fatty acid synthases from Mycobacterium phlei. Methods Enzymol 1975; 35: 84-90.
    • (1975) Methods Enzymol , vol.35 , pp. 84-90
    • Bloch, K.1
  • 14
    • 65249124526 scopus 로고    scopus 로고
    • Identification of the polyketide synthase involved in the biosynthesis of the surface-exposed lipooligosaccharides in mycobacteria
    • Etienne G, Malaga W, Laval F, Lemassu A, Guilhot C, Daffe M. Identification of the polyketide synthase involved in the biosynthesis of the surface-exposed lipooligosaccharides in mycobacteria. J Bacteriol 2009; 191(8): 2613-21.
    • (2009) J Bacteriol , vol.191 , Issue.8 , pp. 2613-2621
    • Etienne, G.1    Malaga, W.2    Laval, F.3    Lemassu, A.4    Guilhot, C.5    Daffe, M.6
  • 15
    • 0037064003 scopus 로고    scopus 로고
    • Role of the pks15/1 gene in the biosynthesis of phenolglycolipids in the Mycobacterium tuberculosis complex. Evidence that all strains synthesize glycosylated p-hydroxybenzoic methyl esters and that strains devoid of phenolglycolipids harbor a frameshift mutation in the pks15/1 gene
    • Constant P, Perez E, Malaga W, et al. Role of the pks15/1 gene in the biosynthesis of phenolglycolipids in the Mycobacterium tuberculosis complex. Evidence that all strains synthesize glycosylated p-hydroxybenzoic methyl esters and that strains devoid of phenolglycolipids harbor a frameshift mutation in the pks15/1 gene. J Biol Chem 2002; 277(41): 38148-58.
    • (2002) J Biol Chem , vol.277 , Issue.41 , pp. 38148-38158
    • Constant, P.1    Perez, E.2    Malaga, W.3
  • 16
    • 33947662068 scopus 로고    scopus 로고
    • Versatile polyketide enzymatic machinery for the biosynthesis of complex mycobacterial lipids
    • Gokhale RS, Saxena P, Chopra T, Mohanty D. Versatile polyketide enzymatic machinery for the biosynthesis of complex mycobacterial lipids. Nat Prod Rep 2007; 24(2): 267-77.
    • (2007) Nat Prod Rep , vol.24 , Issue.2 , pp. 267-277
    • Gokhale, R.S.1    Saxena, P.2    Chopra, T.3    Mohanty, D.4
  • 17
    • 33847218318 scopus 로고    scopus 로고
    • Two polyketide-synthase-associated acyltransferases are required for sulfolipid biosynthesis in Mycobacterium tuberculosis
    • Bhatt K, Gurcha SS, Bhatt A, Besra GS, Jacobs WR, Jr. Two polyketide-synthase-associated acyltransferases are required for sulfolipid biosynthesis in Mycobacterium tuberculosis. Microbiology 2007; 153(Pt 2): 513-20.
    • (2007) Microbiology , vol.153 , Issue.PART 2 , pp. 513-520
    • Bhatt, K.1    Gurcha, S.S.2    Bhatt, A.3    Besra, G.S.4    Jacobs Jr., W.R.5
  • 18
    • 0036047931 scopus 로고    scopus 로고
    • Disruption of msl3 abolishes the synthesis of mycolipanoic and mycolipenic acids required for polyacyltrehalose synthesis in Mycobacterium tuberculosis H37Rv and causes cell aggregation
    • Dubey VS, Sirakova TD, Kolattukudy PE. Disruption of msl3 abolishes the synthesis of mycolipanoic and mycolipenic acids required for polyacyltrehalose synthesis in Mycobacterium tuberculosis H37Rv and causes cell aggregation. Mol Microbiol 2002; 45(5): 1451-9.
    • (2002) Mol Microbiol , vol.45 , Issue.5 , pp. 1451-1459
    • Dubey, V.S.1    Sirakova, T.D.2    Kolattukudy, P.E.3
  • 19
    • 0028061607 scopus 로고
    • Mycobacterial cell wall: Structure and role in natural resistance to antibiotics
    • Jarlier V, Nikaido H. Mycobacterial cell wall: structure and role in natural resistance to antibiotics. FEMS Microbiol Lett 1994; 123(1-2): 11-8.
    • (1994) FEMS Microbiol Lett , vol.123 , Issue.1-2 , pp. 11-18
    • Jarlier, V.1    Nikaido, H.2
  • 20
    • 24144475288 scopus 로고    scopus 로고
    • Mycobacteria use their surface-exposed glycolipids to infect human macrophages through a receptor-dependent process
    • Villeneuve C, Gilleron M, Maridonneau-Parini I, Daffe M, starie-Dequeker C, Etienne G. Mycobacteria use their surface-exposed glycolipids to infect human macrophages through a receptor-dependent process. J Lipid Res 2005; 46(3): 475-83.
    • (2005) J Lipid Res , vol.46 , Issue.3 , pp. 475-483
    • Villeneuve, C.1    Gilleron, M.2    Maridonneau-Parini, I.3    Daffe, M.4    starie-Dequeker, C.5    Etienne, G.6
  • 21
    • 0001247792 scopus 로고    scopus 로고
    • Interaction of mycobacterial glycolipids with host cells
    • Vergne I, Daffe M. Interaction of mycobacterial glycolipids with host cells. Front Biosci 1998; 3: d865-d876.
    • (1998) Front Biosci , vol.3
    • Vergne, I.1    Daffe, M.2
  • 22
    • 0030070034 scopus 로고    scopus 로고
    • Identification of the surface-exposed lipids on the cell envelopes of Mycobacterium tuberculosis and other mycobacterial species
    • Ortalo-Magne A, Lemassu A, Laneelle MA, et al. Identification of the surface-exposed lipids on the cell envelopes of Mycobacterium tuberculosis and other mycobacterial species. J Bacteriol 1996; 178(2): 456-61.
    • (1996) J Bacteriol , vol.178 , Issue.2 , pp. 456-461
    • Ortalo-Magne, A.1    Lemassu, A.2    Laneelle, M.A.3
  • 23
    • 0024462240 scopus 로고
    • Glycolipids of recent clinical isolates of Mycobacterium tuberculosis: Chemical characterization and immunoreactivity
    • Daffe M, Papa F, Laszlo A, David HL. Glycolipids of recent clinical isolates of Mycobacterium tuberculosis: chemical characterization and immunoreactivity. J Gen Microbiol 1989; 135(10): 2759-66.
    • (1989) J Gen Microbiol , vol.135 , Issue.10 , pp. 2759-2766
    • Daffe, M.1    Papa, F.2    Laszlo, A.3    David, H.L.4
  • 24
    • 0037844364 scopus 로고    scopus 로고
    • Structure, function, and biogenesis of the cell wall of Mycobacterium tuberculosis
    • Brennan PJ. Structure, function, and biogenesis of the cell wall of Mycobacterium tuberculosis. Tuberculosis (Edinb ) 2003; 83(1-3): 91-7.
    • (2003) Tuberculosis (Edinb , vol.83 , Issue.1-3 , pp. 91-97
    • Brennan, P.J.1
  • 25
    • 0031315805 scopus 로고    scopus 로고
    • The mycobacterial cell wall: Structure, biosynthesis and sites of drug action
    • Chatterjee D. The mycobacterial cell wall: structure, biosynthesis and sites of drug action. Curr Opin Chem Biol 1997; 1(4): 579-88.
    • (1997) Curr Opin Chem Biol , vol.1 , Issue.4 , pp. 579-588
    • Chatterjee, D.1
  • 26
    • 0025773345 scopus 로고
    • Structure, function and biogenesis of the cell envelope of mycobacteria in relation to bacterial physiology, pathogenesis and drug resistance; some thoughts and possibilities arising from recent structural information
    • McNeil MR, Brennan PJ. Structure, function and biogenesis of the cell envelope of mycobacteria in relation to bacterial physiology, pathogenesis and drug resistance; some thoughts and possibilities arising from recent structural information. Res Microbiol 1991; 142(4): 451-63.
    • (1991) Res Microbiol , vol.142 , Issue.4 , pp. 451-463
    • McNeil, M.R.1    Brennan, P.J.2
  • 27
    • 0028911854 scopus 로고
    • A new interpretation of the structure of the mycolylarabinogalactan complex of Mycobacterium tuberculosis as revealed through characterization of oligoglycosylalditol fragments by fast-atom bombardment mass spectrometry and 1H nuclear magnetic resonance spectroscopy
    • Besra GS, Khoo KH, McNeil MR, Dell A, Morris HR, Brennan PJ. A new interpretation of the structure of the mycolylarabinogalactan complex of Mycobacterium tuberculosis as revealed through characterization of oligoglycosylalditol fragments by fast-atom bombardment mass spectrometry and 1H nuclear magnetic resonance spectroscopy. Biochemistry 1995; 34(13): 4257-66.
    • (1995) Biochemistry , vol.34 , Issue.13 , pp. 4257-4266
    • Besra, G.S.1    Khoo, K.H.2    McNeil, M.R.3    Dell, A.4    Morris, H.R.5    Brennan, P.J.6
  • 28
    • 0025129860 scopus 로고
    • Evidence for the nature of the link between the arabinogalactan and peptidoglycan of mycobacterial cell walls
    • McNeil M, Daffe M, Brennan PJ. Evidence for the nature of the link between the arabinogalactan and peptidoglycan of mycobacterial cell walls. J Biol Chem 1990; 265(30): 18200-6.
    • (1990) J Biol Chem , vol.265 , Issue.30 , pp. 18200-18206
    • McNeil, M.1    Daffe, M.2    Brennan, P.J.3
  • 29
    • 36749081671 scopus 로고    scopus 로고
    • Structure, function and biosynthesis of the Mycobacterium tuberculosis cell wall: Arabinogalactan and lipoarabinomannan assembly with a view to discovering new drug targets
    • Alderwick LJ, Birch HL, Mishra AK, Eggeling L, Besra GS. Structure, function and biosynthesis of the Mycobacterium tuberculosis cell wall: arabinogalactan and lipoarabinomannan assembly with a view to discovering new drug targets. Biochem Soc Trans 2007; 35(Pt 5): 1325-8.
    • (2007) Biochem Soc Trans , vol.35 , Issue.PART 5 , pp. 1325-1328
    • Alderwick, L.J.1    Birch, H.L.2    Mishra, A.K.3    Eggeling, L.4    Besra, G.S.5
  • 30
    • 34547110777 scopus 로고    scopus 로고
    • Targeting the formation of the cell wall core of M. tuberculosis
    • Barry CE, Crick DC, McNeil MR. Targeting the formation of the cell wall core of M. tuberculosis. Infect Disord Drug Targets 2007; 7(2): 182-202.
    • (2007) Infect Disord Drug Targets , vol.7 , Issue.2 , pp. 182-202
    • Barry, C.E.1    Crick, D.C.2    McNeil, M.R.3
  • 31
    • 0034770036 scopus 로고    scopus 로고
    • Biosynthesis of the arabinogalactan-peptidoglycan complex of Mycobacterium tuberculosis
    • Crick DC, Mahapatra S, Brennan PJ. Biosynthesis of the arabinogalactan-peptidoglycan complex of Mycobacterium tuberculosis. Glycobiology 2001; 11(9): 107R-18R.
    • (2001) Glycobiology , vol.11 , Issue.9
    • Crick, D.C.1    Mahapatra, S.2    Brennan, P.J.3
  • 32
    • 3242876593 scopus 로고    scopus 로고
    • Mycobacterial lipoarabinomannan and related lipoglycans: From biogenesis to modulation of the immune response
    • Briken V, Porcelli SA, Besra GS, Kremer L. Mycobacterial lipoarabinomannan and related lipoglycans: from biogenesis to modulation of the immune response. Mol Microbiol 2004; 53(2): 391-403.
    • (2004) Mol Microbiol , vol.53 , Issue.2 , pp. 391-403
    • Briken, V.1    Porcelli, S.A.2    Besra, G.S.3    Kremer, L.4
  • 33
    • 0025823104 scopus 로고
    • Structural features of the arabinan component of the lipoarabinomannan of Mycobacterium tuberculosis
    • Chatterjee D, Bozic CM, McNeil M, Brennan PJ. Structural features of the arabinan component of the lipoarabinomannan of Mycobacterium tuberculosis. J Biol Chem 1991; 266(15): 9652-60.
    • (1991) J Biol Chem , vol.266 , Issue.15 , pp. 9652-9660
    • Chatterjee, D.1    Bozic, C.M.2    McNeil, M.3    Brennan, P.J.4
  • 34
    • 1842588685 scopus 로고    scopus 로고
    • Mycobacterium tuberculosis lipomannan induces apoptosis and interleukin-12 production in macrophages
    • Dao DN, Kremer L, Guerardel Y, et al. Mycobacterium tuberculosis lipomannan induces apoptosis and interleukin-12 production in macrophages. Infect Immun 2004; 72(4): 2067-74.
    • (2004) Infect Immun , vol.72 , Issue.4 , pp. 2067-2074
    • Dao, D.N.1    Kremer, L.2    Guerardel, Y.3
  • 35
    • 33747068254 scopus 로고    scopus 로고
    • The role of trehalose dimycolate (cord factor) on morphology of virulent M. tuberculosis in vitro
    • Hunter RL, Venkataprasad N, Olsen MR. The role of trehalose dimycolate (cord factor) on morphology of virulent M. tuberculosis in vitro. Tuberculosis (Edinb ) 2006; 86(5): 349-56.
    • (2006) Tuberculosis (Edinb , vol.86 , Issue.5 , pp. 349-356
    • Hunter, R.L.1    Venkataprasad, N.2    Olsen, M.R.3
  • 36
    • 0033634971 scopus 로고    scopus 로고
    • A novel mycolic acid cyclopropane synthetase is required for cording, persistence, and virulence of Mycobacterium tuberculosis
    • Glickman MS, Cox JS, Jacobs WR, Jr. A novel mycolic acid cyclopropane synthetase is required for cording, persistence, and virulence of Mycobacterium tuberculosis. Mol Cell 2000; 5(4): 717-27.
    • (2000) Mol Cell , vol.5 , Issue.4 , pp. 717-727
    • Glickman, M.S.1    Cox, J.S.2    Jacobs Jr, W.R.3
  • 37
    • 45849136754 scopus 로고    scopus 로고
    • The Mycobacterium tuberculosis virulence factor trehalose dimycolate imparts desiccation resistance to model mycobacterial membranes
    • Harland CW, Rabuka D, Bertozzi CR, Parthasarathy R. The Mycobacterium tuberculosis virulence factor trehalose dimycolate imparts desiccation resistance to model mycobacterial membranes. Biophys J 2008; 94(12): 4718-24.
    • (2008) Biophys J , vol.94 , Issue.12 , pp. 4718-4724
    • Harland, C.W.1    Rabuka, D.2    Bertozzi, C.R.3    Parthasarathy, R.4
  • 38
    • 33645099315 scopus 로고    scopus 로고
    • Interferon-gamma independent formation of pulmonary granuloma in mice by injections with trehalose dimycolate (cord factor), lipoarabinomannan and phosphatidylinositol mannosides isolated from Mycobacterium tuberculosis
    • Takimoto H, Maruyama H, Shimada KI, Yakabe R, Yano I, Kumazawa Y. Interferon-gamma independent formation of pulmonary granuloma in mice by injections with trehalose dimycolate (cord factor), lipoarabinomannan and phosphatidylinositol mannosides isolated from Mycobacterium tuberculosis. Clin Exp Immunol 2006; 144(1): 134-41.
    • (2006) Clin Exp Immunol , vol.144 , Issue.1 , pp. 134-141
    • Takimoto, H.1    Maruyama, H.2    Shimada, K.I.3    Yakabe, R.4    Yano, I.5    Kumazawa, Y.6
  • 39
    • 0042424923 scopus 로고    scopus 로고
    • Cord factor trehalose 6,6'-dimycolate (TDM) mediates trafficking events during mycobacterial infection of murine macrophages
    • Indrigo J, Hunter RL, Jr., Actor JK. Cord factor trehalose 6,6'-dimycolate (TDM) mediates trafficking events during mycobacterial infection of murine macrophages. Microbiology 2003; 149(Pt 8): 2049-59.
    • (2003) Microbiology , vol.149 , Issue.PART 8 , pp. 2049-2059
    • Indrigo, J.1    Hunter Jr., R.L.2    Actor, J.K.3
  • 40
    • 1842281679 scopus 로고
    • Studies on the virulence of Tubercle bacilli; the effect of cord factor on murine tuberculosis
    • Bloch H, Noll H. Studies on the virulence of Tubercle bacilli; the effect of cord factor on murine tuberculosis. Br J Exp Pathol 1955; 36(1): 8-17.
    • (1955) Br J Exp Pathol , vol.36 , Issue.1 , pp. 8-17
    • Bloch, H.1    Noll, H.2
  • 41
    • 14244260489 scopus 로고    scopus 로고
    • Mycobacterium tuberculosis controls host innate immune activation through cyclopropane modification of a glycolipid effector molecule
    • Rao V, Fujiwara N, Porcelli SA, Glickman MS. Mycobacterium tuberculosis controls host innate immune activation through cyclopropane modification of a glycolipid effector molecule. J Exp Med 2005; 201(4): 535-43.
    • (2005) J Exp Med , vol.201 , Issue.4 , pp. 535-543
    • Rao, V.1    Fujiwara, N.2    Porcelli, S.A.3    Glickman, M.S.4
  • 42
    • 33745217856 scopus 로고    scopus 로고
    • Transcyclopropanation of mycolic acids on trehalose dimycolate suppresses Mycobacterium tuberculosis -induced inflammation and virulence
    • Rao V, Gao F, Chen B, Jacobs WR, Jr., Glickman MS. Transcyclopropanation of mycolic acids on trehalose dimycolate suppresses Mycobacterium tuberculosis -induced inflammation and virulence. J Clin Invest 2006; 116(6): 1660-7.
    • (2006) J Clin Invest , vol.116 , Issue.6 , pp. 1660-1667
    • Rao, V.1    Gao, F.2    Chen, B.3    Jacobs Jr., W.R.4    Glickman, M.S.5
  • 43
    • 0347091999 scopus 로고    scopus 로고
    • Gomez JE, McKinney JD. M. tuberculosis persistence, latency, and drug tolerance. Tuberculosis (Edinb ) 2004; 84(1-2): 29-44.
    • Gomez JE, McKinney JD. M. tuberculosis persistence, latency, and drug tolerance. Tuberculosis (Edinb ) 2004; 84(1-2): 29-44.
  • 44
    • 3242750587 scopus 로고    scopus 로고
    • Induction of a novel class of diacylglycerol acyltransferases and triacylglycerol accumulation in Mycobacterium tuberculosis as it goes into a dormancy-like state in culture
    • Daniel J, Deb C, Dubey VS, et al. Induction of a novel class of diacylglycerol acyltransferases and triacylglycerol accumulation in Mycobacterium tuberculosis as it goes into a dormancy-like state in culture. J Bacteriol 2004; 186(15): 5017-30.
    • (2004) J Bacteriol , vol.186 , Issue.15 , pp. 5017-5030
    • Daniel, J.1    Deb, C.2    Dubey, V.S.3
  • 45
    • 26844537406 scopus 로고    scopus 로고
    • The biosynthesis of mycolic acids in Mycobacterium tuberculosis relies on multiple specialized elongation complexes interconnected by specific protein-protein interactions
    • Veyron-Churlet R, Bigot S, Guerrini O, et al. The biosynthesis of mycolic acids in Mycobacterium tuberculosis relies on multiple specialized elongation complexes interconnected by specific protein-protein interactions. J Mol Biol 2005; 353(4): 847-58.
    • (2005) J Mol Biol , vol.353 , Issue.4 , pp. 847-858
    • Veyron-Churlet, R.1    Bigot, S.2    Guerrini, O.3
  • 46
    • 12844278679 scopus 로고    scopus 로고
    • Pathway to synthesis and processing of mycolic acids in Mycobacterium tuberculosis
    • Takayama K, Wang C, Besra GS. Pathway to synthesis and processing of mycolic acids in Mycobacterium tuberculosis. Clin Microbiol Rev 2005; 18(1): 81-101.
    • (2005) Clin Microbiol Rev , vol.18 , Issue.1 , pp. 81-101
    • Takayama, K.1    Wang, C.2    Besra, G.S.3
  • 47
    • 0001352336 scopus 로고
    • The chemical approach to the control of tuberculosis
    • Fox HH. The chemical approach to the control of tuberculosis. Science 1952; 116(3006): 129-34.
    • (1952) Science , vol.116 , Issue.3006 , pp. 129-134
    • Fox, H.H.1
  • 48
    • 33745098784 scopus 로고
    • Selective inhibition of nucleic acid synthesis in Mycobacterium tuberculosis by isoniazid
    • Gangadharam PR, Harold FM, Schaefer WB. Selective inhibition of nucleic acid synthesis in Mycobacterium tuberculosis by isoniazid. Nature 1963; 198: 712-4.
    • (1963) Nature , vol.198 , pp. 712-714
    • Gangadharam, P.R.1    Harold, F.M.2    Schaefer, W.B.3
  • 49
    • 0011910064 scopus 로고
    • Effect of isoniazid on the dehydrogenase activity of Mycobacterium tuberculosis
    • Schaefer WB. Effect of isoniazid on the dehydrogenase activity of Mycobacterium tuberculosis. J Bacteriol 1960; 79: 236-45.
    • (1960) J Bacteriol , vol.79 , pp. 236-245
    • Schaefer, W.B.1
  • 50
    • 0014118810 scopus 로고
    • Effects of isoniazid on the composition of mycobacteria, with particular reference to soluble carbohydrates and related substances
    • Winder FG, Brennan PJ, McDonnell I. Effects of isoniazid on the composition of mycobacteria, with particular reference to soluble carbohydrates and related substances. Biochem J 1967; 104(2): 385-93.
    • (1967) Biochem J , vol.104 , Issue.2 , pp. 385-393
    • Winder, F.G.1    Brennan, P.J.2    McDonnell, I.3
  • 51
    • 0014768948 scopus 로고
    • The effects of isoniazid on the carbohydrates of Mycobacterium tuberculosis BCG
    • Winder FG, Rooney SA. The effects of isoniazid on the carbohydrates of Mycobacterium tuberculosis BCG. Biochem J 1970; 117(2): 355-68.
    • (1970) Biochem J , vol.117 , Issue.2 , pp. 355-368
    • Winder, F.G.1    Rooney, S.A.2
  • 52
    • 0014841450 scopus 로고
    • Inhibition by isoniazid of synthesis of mycolic acids in Mycobacterium tuberculosis
    • Winder FG, Collins PB. Inhibition by isoniazid of synthesis of mycolic acids in Mycobacterium tuberculosis. J Gen Microbiol 1970; 63(1): 41-8.
    • (1970) J Gen Microbiol , vol.63 , Issue.1 , pp. 41-48
    • Winder, F.G.1    Collins, P.B.2
  • 53
    • 0016529811 scopus 로고
    • Site of inhibitory action of isoniazid in the synthesis of mycolic acids in Mycobacterium tuberculosis
    • Takayama K, Schnoes HK, Armstrong EL, Boyle RW. Site of inhibitory action of isoniazid in the synthesis of mycolic acids in Mycobacterium tuberculosis. J Lipid Res 1975; 16(4): 308-17.
    • (1975) J Lipid Res , vol.16 , Issue.4 , pp. 308-317
    • Takayama, K.1    Schnoes, H.K.2    Armstrong, E.L.3    Boyle, R.W.4
  • 54
    • 0015373050 scopus 로고
    • Effect of isoniazid on the in vivo mycolic acid synthesis, cell growth, and viability of Mycobacterium tuberculosis
    • Takayama K, Wang L, David HL. Effect of isoniazid on the in vivo mycolic acid synthesis, cell growth, and viability of Mycobacterium tuberculosis. Antimicrob Agents Chemother 1972; 2(1): 29-35.
    • (1972) Antimicrob Agents Chemother , vol.2 , Issue.1 , pp. 29-35
    • Takayama, K.1    Wang, L.2    David, H.L.3
  • 55
    • 74849089073 scopus 로고
    • Attenuation of isoniazid-resistant mutants of tubercle bacilli and host hypersensitivity to tuberculin
    • Middlebrook G, Cohn ML. Attenuation of isoniazid-resistant mutants of tubercle bacilli and host hypersensitivity to tuberculin. Proc Soc Exp Biol Med 1955; 88(4): 568-71.
    • (1955) Proc Soc Exp Biol Med , vol.88 , Issue.4 , pp. 568-571
    • Middlebrook, G.1    Cohn, M.L.2
  • 56
    • 50449128872 scopus 로고
    • Isoniazid resistance
    • Middlebrook G, Dressler SH. Isoniazid resistance. Lancet 1955; 268(6865): 669-70.
    • (1955) Lancet , vol.268 , Issue.6865 , pp. 669-670
    • Middlebrook, G.1    Dressler, S.H.2
  • 57
    • 84959067587 scopus 로고
    • Studies on isoniazid and tubercle bacilli. III. The isolation, drug-susceptibility, and catalase-testing of tubercle bacilli from isoniazid-treated patients
    • Middlebrook G, Cohn ML, Schaefer WB. Studies on isoniazid and tubercle bacilli. III. The isolation, drug-susceptibility, and catalase-testing of tubercle bacilli from isoniazid-treated patients. Am Rev Tuberc 1954; 70(5): 852-72.
    • (1954) Am Rev Tuberc , vol.70 , Issue.5 , pp. 852-872
    • Middlebrook, G.1    Cohn, M.L.2    Schaefer, W.B.3
  • 58
    • 0026795159 scopus 로고
    • Isolation and characterization of isoniazid-resistant mutants of Mycobacterium smegmatis and M. aurum
    • Heym B, Cole ST. Isolation and characterization of isoniazid-resistant mutants of Mycobacterium smegmatis and M. aurum. Res Microbiol 1992; 143(7): 721-30.
    • (1992) Res Microbiol , vol.143 , Issue.7 , pp. 721-730
    • Heym, B.1    Cole, S.T.2
  • 59
    • 0032829623 scopus 로고    scopus 로고
    • The molecular basis of isoniazid resistance in Mycobacterium tuberculosis
    • Heym B, Saint-Joanis B, Cole ST. The molecular basis of isoniazid resistance in Mycobacterium tuberculosis. Tuber Lung Dis 1999; 79(4): 267-71.
    • (1999) Tuber Lung Dis , vol.79 , Issue.4 , pp. 267-271
    • Heym, B.1    Saint-Joanis, B.2    Cole, S.T.3
  • 60
    • 0028960179 scopus 로고
    • Missense mutations in the catalase-peroxidase gene, katG, are associated with isoniazid resistance in Mycobacterium tuberculosis
    • Heym B, Alzari PM, Honore N, Cole ST. Missense mutations in the catalase-peroxidase gene, katG, are associated with isoniazid resistance in Mycobacterium tuberculosis. Mol Microbiol 1995; 15(2): 235-45.
    • (1995) Mol Microbiol , vol.15 , Issue.2 , pp. 235-245
    • Heym, B.1    Alzari, P.M.2    Honore, N.3    Cole, S.T.4
  • 61
    • 0027248433 scopus 로고
    • Characterization of the katG gene encoding a catalase-peroxidase required for the isoniazid susceptibility of Mycobacterium tuberculosis
    • Heym B, Zhang Y, Poulet S, Young D, Cole ST. Characterization of the katG gene encoding a catalase-peroxidase required for the isoniazid susceptibility of Mycobacterium tuberculosis. J Bacteriol 1993; 175(13): 4255-9.
    • (1993) J Bacteriol , vol.175 , Issue.13 , pp. 4255-4259
    • Heym, B.1    Zhang, Y.2    Poulet, S.3    Young, D.4    Cole, S.T.5
  • 62
    • 0028156861 scopus 로고
    • inhA, a gene encoding a target for isoniazid and ethionamide in Mycobacterium tuberculosis
    • Banerjee A, Dubnau E, Quemard A, et al. inhA, a gene encoding a target for isoniazid and ethionamide in Mycobacterium tuberculosis. Science 1994; 263(5144): 227-30.
    • (1994) Science , vol.263 , Issue.5144 , pp. 227-230
    • Banerjee, A.1    Dubnau, E.2    Quemard, A.3
  • 63
    • 0032486197 scopus 로고    scopus 로고
    • Inhibition of a Mycobacterium tuberculosis beta-ketoacyl ACP synthase by isoniazid
    • Mdluli K, Slayden RA, Zhu Y, et al. Inhibition of a Mycobacterium tuberculosis beta-ketoacyl ACP synthase by isoniazid. Science 1998; 280(5369): 1607-10.
    • (1998) Science , vol.280 , Issue.5369 , pp. 1607-1610
    • Mdluli, K.1    Slayden, R.A.2    Zhu, Y.3
  • 64
    • 0033709606 scopus 로고    scopus 로고
    • Isoniazid affects multiple components of the type II fatty acid synthase system of Mycobacterium tuberculosis
    • Slayden RA, Lee RE, Barry CE, III. Isoniazid affects multiple components of the type II fatty acid synthase system of Mycobacterium tuberculosis. Mol Microbiol 2000; 38(3): 514-25.
    • (2000) Mol Microbiol , vol.38 , Issue.3 , pp. 514-525
    • Slayden, R.A.1    Lee, R.E.2    Barry III, C.E.3
  • 65
    • 0036448224 scopus 로고    scopus 로고
    • The role of KasA and KasB in the biosynthesis of meromycolic acids and isoniazid resistance in Mycobacterium tuberculosis
    • Slayden RA, Barry CE, III. The role of KasA and KasB in the biosynthesis of meromycolic acids and isoniazid resistance in Mycobacterium tuberculosis. Tuberculosis (Edinb) 2002; 82(4-5): 149-60.
    • (2002) Tuberculosis (Edinb) , vol.82 , Issue.4-5 , pp. 149-160
    • Slayden, R.A.1    Barry III, C.E.2
  • 66
    • 0031689089 scopus 로고    scopus 로고
    • Mechanisms of isoniazid resistance in Mycobacterium tuberculosis: Enzymatic characterization of enoyl reductase mutants identified in isoniazid-resistant clinical isolates
    • Basso LA, Zheng R, Musser JM, Jacobs WR, Jr., Blanchard JS. Mechanisms of isoniazid resistance in Mycobacterium tuberculosis: enzymatic characterization of enoyl reductase mutants identified in isoniazid-resistant clinical isolates. J Infect Dis 1998; 178(3): 769-75.
    • (1998) J Infect Dis , vol.178 , Issue.3 , pp. 769-775
    • Basso, L.A.1    Zheng, R.2    Musser, J.M.3    Jacobs Jr., W.R.4    Blanchard, J.S.5
  • 67
    • 0029153735 scopus 로고
    • Purification and characterization of the Mycobacterium smegmatis catalase-peroxidase involved in isoniazid activation
    • Marcinkeviciene JA, Magliozzo RS, Blanchard JS. Purification and characterization of the Mycobacterium smegmatis catalase-peroxidase involved in isoniazid activation. J Biol Chem 1995; 270(38): 22290-5.
    • (1995) J Biol Chem , vol.270 , Issue.38 , pp. 22290-22295
    • Marcinkeviciene, J.A.1    Magliozzo, R.S.2    Blanchard, J.S.3
  • 68
    • 0029000868 scopus 로고
    • Enzymatic characterization of the target for isoniazid in Mycobacterium tuberculosis
    • Quemard A, Sacchettini JC, Dessen A, et al. Enzymatic characterization of the target for isoniazid in Mycobacterium tuberculosis. Biochemistry 1995; 34(26): 8235-41.
    • (1995) Biochemistry , vol.34 , Issue.26 , pp. 8235-8241
    • Quemard, A.1    Sacchettini, J.C.2    Dessen, A.3
  • 69
    • 0028988237 scopus 로고
    • Crystal structure and function of the isoniazid target of Mycobacterium tuberculosis
    • Dessen A, Quemard A, Blanchard JS, Jacobs WR, Jr., Sacchettini JC. Crystal structure and function of the isoniazid target of Mycobacterium tuberculosis. Science 1995; 267(5204): 1638-41.
    • (1995) Science , vol.267 , Issue.5204 , pp. 1638-1641
    • Dessen, A.1    Quemard, A.2    Blanchard, J.S.3    Jacobs Jr., W.R.4    Sacchettini, J.C.5
  • 70
    • 33748469322 scopus 로고    scopus 로고
    • Transfer of a point mutation in Mycobacterium tuberculosis inhA resolves the target of isoniazid
    • Vilcheze C, Wang F, Arai M, et al. Transfer of a point mutation in Mycobacterium tuberculosis inhA resolves the target of isoniazid. Nat Med 2006; 12(9): 1027-9.
    • (2006) Nat Med , vol.12 , Issue.9 , pp. 1027-1029
    • Vilcheze, C.1    Wang, F.2    Arai, M.3
  • 71
    • 0038410325 scopus 로고    scopus 로고
    • Inactivation of the inhA-encoded fatty acid synthase II (FASII) enoyl-acyl carrier protein reductase induces accumulation of the FASI end products and cell lysis of Mycobacterium smegmatis
    • Vilcheze C, Morbidoni HR, Weisbrod TR, et al. Inactivation of the inhA-encoded fatty acid synthase II (FASII) enoyl-acyl carrier protein reductase induces accumulation of the FASI end products and cell lysis of Mycobacterium smegmatis. J Bacteriol 2000; 182(14): 4059-67.
    • (2000) J Bacteriol , vol.182 , Issue.14 , pp. 4059-4067
    • Vilcheze, C.1    Morbidoni, H.R.2    Weisbrod, T.R.3
  • 72
    • 0032472224 scopus 로고    scopus 로고
    • Modification of the NADH of the isoniazid target (InhA) from Mycobacterium tuberculosis
    • Rozwarski DA, Grant GA, Barton DH, Jacobs WR, Jr., Sacchettini JC. Modification of the NADH of the isoniazid target (InhA) from Mycobacterium tuberculosis. Science 1998; 279(5347): 98-102.
    • (1998) Science , vol.279 , Issue.5347 , pp. 98-102
    • Rozwarski, D.A.1    Grant, G.A.2    Barton, D.H.3    Jacobs Jr., W.R.4    Sacchettini, J.C.5
  • 73
    • 0028988237 scopus 로고
    • Crystal structure and function of the isoniazid target of Mycobacterium tuberculosis
    • Dessen A, Quemard A, Blanchard JS, Jacobs WR, Jr., Sacchettini JC. Crystal structure and function of the isoniazid target of Mycobacterium tuberculosis. Science 1995; 267(5204): 1638-41.
    • (1995) Science , vol.267 , Issue.5204 , pp. 1638-1641
    • Dessen, A.1    Quemard, A.2    Blanchard, J.S.3    Jacobs Jr., W.R.4    Sacchettini, J.C.5
  • 74
    • 12944255779 scopus 로고    scopus 로고
    • Altered NADH/NAD+ ratio mediates coresistance to isoniazid and ethionamide in mycobacteria
    • Vilcheze C, Weisbrod TR, Chen B, et al. Altered NADH/NAD+ ratio mediates coresistance to isoniazid and ethionamide in mycobacteria. Antimicrob Agents Chemother 2005; 49(2): 708-20.
    • (2005) Antimicrob Agents Chemother , vol.49 , Issue.2 , pp. 708-720
    • Vilcheze, C.1    Weisbrod, T.R.2    Chen, B.3
  • 75
    • 33745094315 scopus 로고    scopus 로고
    • Mycobacterium tuberculosis dihydrofolate reductase is a target for isoniazid
    • Argyrou A, Vetting MW, Aladegbami B, Blanchard JS. Mycobacterium tuberculosis dihydrofolate reductase is a target for isoniazid. Nat Struct Mol Biol 2006; 13(5): 408-13.
    • (2006) Nat Struct Mol Biol , vol.13 , Issue.5 , pp. 408-413
    • Argyrou, A.1    Vetting, M.W.2    Aladegbami, B.3    Blanchard, J.S.4
  • 77
    • 0345306174 scopus 로고    scopus 로고
    • ethA, inhA, and katG loci of ethionamide-resistant clinical Mycobacterium tuberculosis isolates
    • Morlock GP, Metchock B, Sikes D, Crawford JT, Cooksey RC. ethA, inhA, and katG loci of ethionamide-resistant clinical Mycobacterium tuberculosis isolates. Antimicrob Agents Chemother 2003; 47(12): 3799-805.
    • (2003) Antimicrob Agents Chemother , vol.47 , Issue.12 , pp. 3799-3805
    • Morlock, G.P.1    Metchock, B.2    Sikes, D.3    Crawford, J.T.4    Cooksey, R.C.5
  • 78
    • 33847675813 scopus 로고    scopus 로고
    • EthA, a common activator of thiocarbamide-containing drugs acting on different mycobacterial targets
    • Dover LG, Alahari A, Gratraud P, et al. EthA, a common activator of thiocarbamide-containing drugs acting on different mycobacterial targets. Antimicrob Agents Chemother 2007; 51(3): 1055-63.
    • (2007) Antimicrob Agents Chemother , vol.51 , Issue.3 , pp. 1055-1063
    • Dover, L.G.1    Alahari, A.2    Gratraud, P.3
  • 79
    • 0034622924 scopus 로고    scopus 로고
    • Activation of the pro-drug ethionamide is regulated in mycobacteria
    • Baulard AR, Betts JC, Engohang-Ndong J, et al. Activation of the pro-drug ethionamide is regulated in mycobacteria. J Biol Chem 2000; 275(36): 28326-31.
    • (2000) J Biol Chem , vol.275 , Issue.36 , pp. 28326-28331
    • Baulard, A.R.1    Betts, J.C.2    Engohang-Ndong, J.3
  • 80
    • 0037066702 scopus 로고    scopus 로고
    • The antituberculosis drug ethionamide is activated by a flavoprotein monooxygenase
    • Vannelli TA, Dykman A, Ortiz de Montellano PR. The antituberculosis drug ethionamide is activated by a flavoprotein monooxygenase. J Biol Chem 2002; 277(15): 12824-9.
    • (2002) J Biol Chem , vol.277 , Issue.15 , pp. 12824-12829
    • Vannelli, T.A.1    Dykman, A.2    Ortiz de Montellano, P.R.3
  • 81
    • 0034662963 scopus 로고    scopus 로고
    • Ethionamide activation and sensitivity in multidrug-resistant Mycobacterium tuberculosis
    • DeBarber AE, Mdluli K, Bosman M, Bekker LG, Barry CE, III. Ethionamide activation and sensitivity in multidrug-resistant Mycobacterium tuberculosis. Proc Natl Acad Sci USA 2000; 97(17): 9677-82.
    • (2000) Proc Natl Acad Sci USA , vol.97 , Issue.17 , pp. 9677-9682
    • DeBarber, A.E.1    Mdluli, K.2    Bosman, M.3    Bekker, L.G.4    Barry III, C.E.5
  • 82
    • 33748681705 scopus 로고    scopus 로고
    • Selective intracellular accumulation of the major metabolite issued from the activation of the prodrug ethionamide in mycobacteria
    • Hanoulle X, Wieruszeski JM, Rousselot-Pailley P, et al. Selective intracellular accumulation of the major metabolite issued from the activation of the prodrug ethionamide in mycobacteria. J Antimicrob Chemother 2006; 58(4): 768-72.
    • (2006) J Antimicrob Chemother , vol.58 , Issue.4 , pp. 768-772
    • Hanoulle, X.1    Wieruszeski, J.M.2    Rousselot-Pailley, P.3
  • 83
    • 67349287483 scopus 로고    scopus 로고
    • Synthetic EthR inhibitors boost antituberculous activity of ethionamide
    • Willand N, Dirie B, Carette X, et al. Synthetic EthR inhibitors boost antituberculous activity of ethionamide. Nat Med 2009; 15(5): 537-44.
    • (2009) Nat Med , vol.15 , Issue.5 , pp. 537-544
    • Willand, N.1    Dirie, B.2    Carette, X.3
  • 84
    • 32444435597 scopus 로고    scopus 로고
    • Insights into mechanisms of induction and ligands recognition in the transcriptional repressor EthR from Mycobacterium tuberculosis
    • Frenois F, Baulard AR, Villeret V. Insights into mechanisms of induction and ligands recognition in the transcriptional repressor EthR from Mycobacterium tuberculosis. Tuberculosis (Edinb ) 2006; 86(2): 110-4.
    • (2006) Tuberculosis (Edinb , vol.86 , Issue.2 , pp. 110-114
    • Frenois, F.1    Baulard, A.R.2    Villeret, V.3
  • 85
    • 6344235517 scopus 로고    scopus 로고
    • Structure of EthR in a ligand bound conformation reveals therapeutic perspectives against tuberculosis
    • Frenois F, Engohang-Ndong J, Locht C, Baulard AR, Villeret V. Structure of EthR in a ligand bound conformation reveals therapeutic perspectives against tuberculosis. Mol Cell 2004; 16(2): 301-7.
    • (2004) Mol Cell , vol.16 , Issue.2 , pp. 301-307
    • Frenois, F.1    Engohang-Ndong, J.2    Locht, C.3    Baulard, A.R.4    Villeret, V.5
  • 86
    • 3242812945 scopus 로고    scopus 로고
    • Crystal structure of the TetR/CamR family repressor Mycobacterium tuberculosis EthR implicated in ethionamide resistance
    • Dover LG, Corsino PE, Daniels IR, et al. Crystal structure of the TetR/CamR family repressor Mycobacterium tuberculosis EthR implicated in ethionamide resistance. J Mol Biol 2004; 340(5):1095-105.
    • (2004) J Mol Biol , vol.340 , Issue.5 , pp. 1095-1105
    • Dover, L.G.1    Corsino, P.E.2    Daniels, I.R.3
  • 87
    • 0346964261 scopus 로고    scopus 로고
    • EthR, a repressor of the TetR/CamR family implicated in ethionamide resistance in mycobacteria, octamerizes cooperatively on its operator
    • Engohang-Ndong J, Baillat D, Aumercier M, et al. EthR, a repressor of the TetR/CamR family implicated in ethionamide resistance in mycobacteria, octamerizes cooperatively on its operator. Mol Microbiol 2004; 51(1):175-88.
    • (2004) Mol Microbiol , vol.51 , Issue.1 , pp. 175-188
    • Engohang-Ndong, J.1    Baillat, D.2    Aumercier, M.3
  • 88
    • 78650421645 scopus 로고    scopus 로고
    • Correlations of mutations in katG, oxyR-ahpC and inhA genes and in vitro susceptibility in Mycobacterium tuberculosis clinical strains segregated by spoligotype families from tuberculosis prevalent countries in South America
    • Dalla Costa ER, Ribeiro MO, Silva MS, et al. Correlations of mutations in katG, oxyR-ahpC and inhA genes and in vitro susceptibility in Mycobacterium tuberculosis clinical strains segregated by spoligotype families from tuberculosis prevalent countries in South America. BMC Microbiol 2009; 9: 39.
    • (2009) BMC Microbiol , vol.9 , pp. 39
    • Dalla Costa, E.R.1    Ribeiro, M.O.2    Silva, M.S.3
  • 89
    • 35848935866 scopus 로고    scopus 로고
    • The mechanism of isoniazid killing: Clarity through the scope of genetics
    • Vilcheze C, Jacobs WR, Jr. The mechanism of isoniazid killing: clarity through the scope of genetics. Annu Rev Microbiol 2007; 61: 35-50.
    • (2007) Annu Rev Microbiol , vol.61 , pp. 35-50
    • Vilcheze, C.1    Jacobs Jr., W.R.2
  • 90
    • 4344572019 scopus 로고    scopus 로고
    • Screening and characterization of mutations in isoniazid-resistant Mycobacterium tuberculosis isolates obtained in Brazil
    • Cardoso RF, Cooksey RC, Morlock GP, et al. Screening and characterization of mutations in isoniazid-resistant Mycobacterium tuberculosis isolates obtained in Brazil. Antimicrob Agents Chemother 2004; 48(9): 3373-81.
    • (2004) Antimicrob Agents Chemother , vol.48 , Issue.9 , pp. 3373-3381
    • Cardoso, R.F.1    Cooksey, R.C.2    Morlock, G.P.3
  • 91
    • 0036717879 scopus 로고    scopus 로고
    • Effect of katG mutations on the virulence of Mycobacterium tuberculosis and the implication for transmission in humans
    • Pym AS, Saint-Joanis B, Cole ST. Effect of katG mutations on the virulence of Mycobacterium tuberculosis and the implication for transmission in humans. Infect Immun 2002; 70(9): 4955-60.
    • (2002) Infect Immun , vol.70 , Issue.9 , pp. 4955-4960
    • Pym, A.S.1    Saint-Joanis, B.2    Cole, S.T.3
  • 92
    • 0036233717 scopus 로고    scopus 로고
    • High prevalence of KatG Ser315Thr substitution among isoniazid-resistant Mycobacterium tuberculosis clinical isolates from northwestern Russia, 1996 to 2001
    • Mokrousov I, Narvskaya O, Otten T, Limeschenko E, Steklova L, Vyshnevskiy B. High prevalence of KatG Ser315Thr substitution among isoniazid-resistant Mycobacterium tuberculosis clinical isolates from northwestern Russia, 1996 to 2001. Antimicrob Agents Chemother 2002; 46(5): 1417-24.
    • (2002) Antimicrob Agents Chemother , vol.46 , Issue.5 , pp. 1417-1424
    • Mokrousov, I.1    Narvskaya, O.2    Otten, T.3    Limeschenko, E.4    Steklova, L.5    Vyshnevskiy, B.6
  • 93
    • 0034599481 scopus 로고    scopus 로고
    • Isoniazid-related copper(II) and nickel(II) complexes with antimycobacterial in vitro activity. Part 9
    • Bottari B, Maccari R, Monforte F, Ottana R, Rotondo E, Vigorita MG. Isoniazid-related copper(II) and nickel(II) complexes with antimycobacterial in vitro activity. Part 9. Bioorg Med Chem Lett 2000; 10(7): 657-60.
    • (2000) Bioorg Med Chem Lett , vol.10 , Issue.7 , pp. 657-660
    • Bottari, B.1    Maccari, R.2    Monforte, F.3    Ottana, R.4    Rotondo, E.5    Vigorita, M.G.6
  • 94
    • 0034896782 scopus 로고    scopus 로고
    • Nickel(II) 2,6-diacetylpyridine bis(isonicotinoylhydrazonate) and bis(benzoylhydrazonate) complexes: Structure and antimycobacterial evaluation. Part XI
    • Bottari B, Maccari R, Monforte F, et al. Nickel(II) 2,6-diacetylpyridine bis(isonicotinoylhydrazonate) and bis(benzoylhydrazonate) complexes: structure and antimycobacterial evaluation. Part XI. Bioorg Med Chem 2001; 9(8): 2203-11.
    • (2001) Bioorg Med Chem , vol.9 , Issue.8 , pp. 2203-2211
    • Bottari, B.1    Maccari, R.2    Monforte, F.3
  • 95
    • 30444439708 scopus 로고    scopus 로고
    • Synthesis, antitubercular activity and pharmacokinetic studies of some Schiff bases derived from 1-alkylisatin and isonicotinic acid hydrazide (INH)
    • Aboul-Fadl T, Mohammed FA, Hassan EA. Synthesis, antitubercular activity and pharmacokinetic studies of some Schiff bases derived from 1-alkylisatin and isonicotinic acid hydrazide (INH). Arch Pharm Res 2003; 26(10): 778-84.
    • (2003) Arch Pharm Res , vol.26 , Issue.10 , pp. 778-784
    • Aboul-Fadl, T.1    Mohammed, F.A.2    Hassan, E.A.3
  • 97
    • 0000284564 scopus 로고
    • Synthesis and anti-tubercular activity of isonicotinoyl and cyanoacetyl hydrazones
    • Chakravarty D, Bose A, Bose S. Synthesis and anti-tubercular activity of isonicotinoyl and cyanoacetyl hydrazones. J Pharm Sci 1964; 53: 1036-9.
    • (1964) J Pharm Sci , vol.53 , pp. 1036-1039
    • Chakravarty, D.1    Bose, A.2    Bose, S.3
  • 98
    • 44449126631 scopus 로고    scopus 로고
    • Synthesis and anti-mycobacterial activity of (E)-N'- (monosubstituted-benzylidene)isonicotinohydrazide derivatives
    • Lourenco MC, Ferreira ML, de Souza MV, Peralta MA, Vasconcelos TR, Henriques MG. Synthesis and anti-mycobacterial activity of (E)-N'- (monosubstituted-benzylidene)isonicotinohydrazide derivatives. Eur J Med Chem 2008; 43(6): 1344-7.
    • (2008) Eur J Med Chem , vol.43 , Issue.6 , pp. 1344-1347
    • Lourenco, M.C.1    Ferreira, M.L.2    de Souza, M.V.3    Peralta, M.A.4    Vasconcelos, T.R.5    Henriques, M.G.6
  • 99
    • 0036146574 scopus 로고    scopus 로고
    • In vitro antimycobacterial activities of 2'-monosubstituted isonicotinohydrazides and their cyanoborane adducts
    • Maccari R, Ottana R, Monforte F, Vigorita MG. In vitro antimycobacterial activities of 2'-monosubstituted isonicotinohydrazides and their cyanoborane adducts. Antimicrob Agents Chemother 2002; 46(2): 294-9.
    • (2002) Antimicrob Agents Chemother , vol.46 , Issue.2 , pp. 294-299
    • Maccari, R.1    Ottana, R.2    Monforte, F.3    Vigorita, M.G.4
  • 100
    • 46049088103 scopus 로고    scopus 로고
    • Synthesis and in vitro antimycobacterial activity of 3-substituted 5-hydroxy-5- trifluoro[chloro]methyl-4,5-dihydro-1H-1-(isonicotinoyl) pyrazoles
    • Almeida da Silva PE, Ramos DF, Bonacorso HG, et al. Synthesis and in vitro antimycobacterial activity of 3-substituted 5-hydroxy-5- trifluoro[chloro]methyl-4,5-dihydro-1H-1-(isonicotinoyl) pyrazoles. Int J Antimicrob Agents 2008; 32(2): 139-44.
    • (2008) Int J Antimicrob Agents , vol.32 , Issue.2 , pp. 139-144
    • Almeida da Silva, P.E.1    Ramos, D.F.2    Bonacorso, H.G.3
  • 101
    • 3142581371 scopus 로고    scopus 로고
    • Rational design of new antituberculosis agents: Receptor-independent four-dimensional quantitative structure-activity relationship analysis of a set of isoniazid derivatives
    • Pasqualoto KF, Ferreira EI, Santos-Filho OA, Hopfinger AJ. Rational design of new antituberculosis agents: receptor-independent four-dimensional quantitative structure-activity relationship analysis of a set of isoniazid derivatives. J Med Chem 2004; 47(15): 3755-64.
    • (2004) J Med Chem , vol.47 , Issue.15 , pp. 3755-3764
    • Pasqualoto, K.F.1    Ferreira, E.I.2    Santos-Filho, O.A.3    Hopfinger, A.J.4
  • 102
    • 24344459482 scopus 로고    scopus 로고
    • Synthesis and in vitro and in vivo antimycobacterial activity of isonicotinoyl hydrazones
    • Sriram D, Yogeeswari P, Madhu K. Synthesis and in vitro and in vivo antimycobacterial activity of isonicotinoyl hydrazones. Bioorg Med Chem Lett 2005; 15(20): 4502-5.
    • (2005) Bioorg Med Chem Lett , vol.15 , Issue.20 , pp. 4502-4505
    • Sriram, D.1    Yogeeswari, P.2    Madhu, K.3
  • 103
    • 59649116165 scopus 로고    scopus 로고
    • 5-Nitrofuran-2-yl derivatives: Synthesis and inhibitory activities against growing and dormant mycobacterium species
    • Sriram D, Yogeeswari P, Dhakla P, Senthilkumar P, Banerjee D, Manjashetty TH. 5-Nitrofuran-2-yl derivatives: synthesis and inhibitory activities against growing and dormant mycobacterium species. Bioorg Med Chem Lett 2009; 19(4): 1152-4.
    • (2009) Bioorg Med Chem Lett , vol.19 , Issue.4 , pp. 1152-1154
    • Sriram, D.1    Yogeeswari, P.2    Dhakla, P.3    Senthilkumar, P.4    Banerjee, D.5    Manjashetty, T.H.6
  • 104
    • 58049140164 scopus 로고    scopus 로고
    • Antimycobacterial activity of novel N-(substituted)-2-isonicotinoylhydrazinocarbothioamide endowed with high activity towards isoniazid resistant tuberculosis
    • Sriram D, Yogeeswari P, Yelamanchili PD. Antimycobacterial activity of novel N-(substituted)-2-isonicotinoylhydrazinocarbothioamide endowed with high activity towards isoniazid resistant tuberculosis. Biomed Pharmacother 2009; 63(1): 36-9.
    • (2009) Biomed Pharmacother , vol.63 , Issue.1 , pp. 36-39
    • Sriram, D.1    Yogeeswari, P.2    Yelamanchili, P.D.3
  • 105
    • 74849128171 scopus 로고
    • Isonicotinoyl hydrazine derivatives and their activity against Mycobacterium tuberculosis in the mouse
    • Strube RE, Stern KF. Isonicotinoyl hydrazine derivatives and their activity against Mycobacterium tuberculosis in the mouse. J Am Pharm Assoc Am Pharm Assoc (Baltim) 1957; 46(12): 738-41.
    • (1957) J Am Pharm Assoc Am Pharm Assoc (Baltim) , vol.46 , Issue.12 , pp. 738-741
    • Strube, R.E.1    Stern, K.F.2
  • 106
    • 33847412751 scopus 로고    scopus 로고
    • Synthesis of isonicotinoylhydrazones from anacardic acid and their in vitro activity against Mycobacterium smegmatis
    • Swamy BN, Suma TK, Rao GV, Reddy GC. Synthesis of isonicotinoylhydrazones from anacardic acid and their in vitro activity against Mycobacterium smegmatis. Eur J Med Chem 2007; 42(3): 420-4.
    • (2007) Eur J Med Chem , vol.42 , Issue.3 , pp. 420-424
    • Swamy, B.N.1    Suma, T.K.2    Rao, G.V.3    Reddy, G.C.4
  • 107
    • 33746496066 scopus 로고    scopus 로고
    • Isoniazid is not a lead compound for its pyridyl ring derivatives, isonicotinoyl amides, hydrazides, and hydrazones: A critical review
    • Scior T, Garces-Eisele SJ. Isoniazid is not a lead compound for its pyridyl ring derivatives, isonicotinoyl amides, hydrazides, and hydrazones: a critical review. Curr Med Chem 2006; 13(18): 2205-19.
    • (2006) Curr Med Chem , vol.13 , Issue.18 , pp. 2205-2219
    • Scior, T.1    Garces-Eisele, S.J.2
  • 108
    • 33847779109 scopus 로고    scopus 로고
    • Enoyl reductases as targets for the development of anti-tubercular and anti-malarial agents
    • Oliveira JS, Vasconcelos IB, Moreira IS, Santos DS, Basso LA. Enoyl reductases as targets for the development of anti-tubercular and anti-malarial agents. Curr Drug Targets 2007; 8(3): 399-411.
    • (2007) Curr Drug Targets , vol.8 , Issue.3 , pp. 399-411
    • Oliveira, J.S.1    Vasconcelos, I.B.2    Moreira, I.S.3    Santos, D.S.4    Basso, L.A.5
  • 109
    • 1342324175 scopus 로고    scopus 로고
    • An inorganic iron complex that inhibits wild-type and an isoniazid-resistant mutant 2-transenoyl-ACP (CoA) reductase from Mycobacterium tuberculosis
    • Oliveira JS, Sousa EH, Basso LA, et al. An inorganic iron complex that inhibits wild-type and an isoniazid-resistant mutant 2-transenoyl-ACP (CoA) reductase from Mycobacterium tuberculosis. Chem Commun (Camb) 2004; (3): 312-3.
    • (2004) Chem Commun (Camb) , vol.3 , pp. 312-313
    • Oliveira, J.S.1    Sousa, E.H.2    Basso, L.A.3
  • 110
    • 0036348258 scopus 로고    scopus 로고
    • Use of antimicrobial agents in consumer products
    • Tan L, Nielsen NH, Young DC, Trizna Z. Use of antimicrobial agents in consumer products. Arch Dermatol 2002; 138(8): 1082-6.
    • (2002) Arch Dermatol , vol.138 , Issue.8 , pp. 1082-1086
    • Tan, L.1    Nielsen, N.H.2    Young, D.C.3    Trizna, Z.4
  • 111
    • 0034007314 scopus 로고    scopus 로고
    • Triclosan: A review of effectiveness and safety in health care settings
    • Jones RD, Jampani HB, Newman JL, Lee AS. Triclosan: a review of effectiveness and safety in health care settings. Am J Infect Control 2000; 28(2): 184-96.
    • (2000) Am J Infect Control , vol.28 , Issue.2 , pp. 184-196
    • Jones, R.D.1    Jampani, H.B.2    Newman, J.L.3    Lee, A.S.4
  • 112
    • 0035822555 scopus 로고    scopus 로고
    • Triclosan: A widely used biocide and its link to antibiotics
    • Schweizer HP. Triclosan: a widely used biocide and its link to antibiotics. FEMS Microbiol Lett 2001; 202(1): 1-7.
    • (2001) FEMS Microbiol Lett , vol.202 , Issue.1 , pp. 1-7
    • Schweizer, H.P.1
  • 113
    • 0032529948 scopus 로고    scopus 로고
    • Overexpression of marA, soxS, or acrAB produces resistance to triclosan in laboratory and clinical strains of Escherichia coli
    • McMurry LM, Oethinger M, Levy SB. Overexpression of marA, soxS, or acrAB produces resistance to triclosan in laboratory and clinical strains of Escherichia coli. FEMS Microbiol Lett 1998; 166(2): 305-9.
    • (1998) FEMS Microbiol Lett , vol.166 , Issue.2 , pp. 305-309
    • McMurry, L.M.1    Oethinger, M.2    Levy, S.B.3
  • 114
    • 0032490937 scopus 로고    scopus 로고
    • Triclosan targets lipid synthesis
    • McMurry LM, Oethinger M, Levy SB. Triclosan targets lipid synthesis. Nature 1998; 394(6693): 531-2.
    • (1998) Nature , vol.394 , Issue.6693 , pp. 531-532
    • McMurry, L.M.1    Oethinger, M.2    Levy, S.B.3
  • 115
    • 0034681329 scopus 로고    scopus 로고
    • Inhibition of the Staphylococcus aureus NADPH-dependent enoyl-acyl carrier protein reductase by triclosan and hexachlorophene
    • Heath RJ, Li J, Roland GE, Rock CO. Inhibition of the Staphylococcus aureus NADPH-dependent enoyl-acyl carrier protein reductase by triclosan and hexachlorophene. J Biol Chem 2000; 275(7): 4654-9.
    • (2000) J Biol Chem , vol.275 , Issue.7 , pp. 4654-4659
    • Heath, R.J.1    Li, J.2    Roland, G.E.3    Rock, C.O.4
  • 116
    • 0033055847 scopus 로고    scopus 로고
    • Genetic evidence that InhA of Mycobacterium smegmatis is a target for triclosan
    • McMurry LM, McDermott PF, Levy SB. Genetic evidence that InhA of Mycobacterium smegmatis is a target for triclosan. Antimicrob Agents Chemother 1999; 43(3): 711-3.
    • (1999) Antimicrob Agents Chemother , vol.43 , Issue.3 , pp. 711-713
    • McMurry, L.M.1    McDermott, P.F.2    Levy, S.B.3
  • 117
    • 0034804919 scopus 로고    scopus 로고
    • Lipid biosynthesis as a target for antibacterial agents
    • Heath RJ, White SW, Rock CO. Lipid biosynthesis as a target for antibacterial agents. Prog Lipid Res 2001; 40(6): 467-97.
    • (2001) Prog Lipid Res , vol.40 , Issue.6 , pp. 467-497
    • Heath, R.J.1    White, S.W.2    Rock, C.O.3
  • 118
    • 0036247948 scopus 로고    scopus 로고
    • Inhibitors of fatty acid synthesis as antimicrobial chemotherapeutics
    • Heath RJ, White SW, Rock CO. Inhibitors of fatty acid synthesis as antimicrobial chemotherapeutics. Appl Microbiol Biotechnol 2002; 58(6): 695-703.
    • (2002) Appl Microbiol Biotechnol , vol.58 , Issue.6 , pp. 695-703
    • Heath, R.J.1    White, S.W.2    Rock, C.O.3
  • 119
    • 3042764816 scopus 로고    scopus 로고
    • Fatty acid biosynthesis as a target for novel antibacterials
    • Heath RJ, Rock CO. Fatty acid biosynthesis as a target for novel antibacterials. Curr Opin Investig Drugs 2004; 5(2): 146-53.
    • (2004) Curr Opin Investig Drugs , vol.5 , Issue.2 , pp. 146-153
    • Heath, R.J.1    Rock, C.O.2
  • 120
    • 12344300344 scopus 로고    scopus 로고
    • The reductase steps of the type II fatty acid synthase as antimicrobial targets
    • Zhang YM, Lu YJ, Rock CO. The reductase steps of the type II fatty acid synthase as antimicrobial targets. Lipids 2004; 39(11): 1055-60.
    • (2004) Lipids , vol.39 , Issue.11 , pp. 1055-1060
    • Zhang, Y.M.1    Lu, Y.J.2    Rock, C.O.3
  • 121
    • 4143138567 scopus 로고    scopus 로고
    • Location and orientation of Triclosan in phospholipid model membranes
    • Guillen J, Bernabeu A, Shapiro S, Villalain J. Location and orientation of Triclosan in phospholipid model membranes. Eur Biophys J 2004; 33(5): 448-53.
    • (2004) Eur Biophys J , vol.33 , Issue.5 , pp. 448-453
    • Guillen, J.1    Bernabeu, A.2    Shapiro, S.3    Villalain, J.4
  • 123
    • 17644436310 scopus 로고    scopus 로고
    • Inhibition of InhA, the enoyl reductase from Mycobacterium tuberculosis, by triclosan and isoniazid
    • Parikh SL, Xiao G, Tonge PJ. Inhibition of InhA, the enoyl reductase from Mycobacterium tuberculosis, by triclosan and isoniazid. Biochemistry 2000; 39(26): 7645-50.
    • (2000) Biochemistry , vol.39 , Issue.26 , pp. 7645-7650
    • Parikh, S.L.1    Xiao, G.2    Tonge, P.J.3
  • 124
    • 0038757566 scopus 로고    scopus 로고
    • Targeting tuberculosis and malaria through inhibition of Enoyl reductase: Compound activity and structural data
    • Kuo MR, Morbidoni HR, Alland D, et al. Targeting tuberculosis and malaria through inhibition of Enoyl reductase: compound activity and structural data. J Biol Chem 2003; 278(23): 20851-9.
    • (2003) J Biol Chem , vol.278 , Issue.23 , pp. 20851-20859
    • Kuo, M.R.1    Morbidoni, H.R.2    Alland, D.3
  • 125
    • 34948861094 scopus 로고    scopus 로고
    • Targeting fatty acid biosynthesis for the development of novel chemotherapeutics against Mycobacterium tuberculosis: Evaluation of A-ring-modified diphenyl ethers as high-affinity InhA inhibitors
    • Boyne ME, Sullivan TJ, amEnde CW, et al. Targeting fatty acid biosynthesis for the development of novel chemotherapeutics against Mycobacterium tuberculosis: evaluation of A-ring-modified diphenyl ethers as high-affinity InhA inhibitors. Antimicrob Agents Chemother 2007; 51(10): 3562-7.
    • (2007) Antimicrob Agents Chemother , vol.51 , Issue.10 , pp. 3562-3567
    • Boyne, M.E.1    Sullivan, T.J.2    amEnde, C.W.3
  • 126
    • 33750048012 scopus 로고    scopus 로고
    • High affinity InhA inhibitors with activity against drug-resistant strains of Mycobacterium tuberculosis. ACS
    • Sullivan TJ, Truglio JJ, Boyne ME, et al. High affinity InhA inhibitors with activity against drug-resistant strains of Mycobacterium tuberculosis. ACS Chem Biol 2006; 1(1): 43-53.
    • (2006) Chem Biol , vol.1 , Issue.1 , pp. 43-53
    • Sullivan, T.J.1    Truglio, J.J.2    Boyne, M.E.3
  • 127
    • 60849124512 scopus 로고    scopus 로고
    • Triclosan derivatives: Towards potent inhibitors of drug-sensitive and drug-resistant Mycobacterium tuberculosis
    • Freundlich JS, Wang F, Vilcheze C, et al. Triclosan derivatives: towards potent inhibitors of drug-sensitive and drug-resistant Mycobacterium tuberculosis. ChemMedChem 2009; 4(2): 241-8.
    • (2009) ChemMedChem , vol.4 , Issue.2 , pp. 241-248
    • Freundlich, J.S.1    Wang, F.2    Vilcheze, C.3
  • 128
    • 0014886269 scopus 로고
    • Isoxyl monotherapy
    • Dormer BA. Isoxyl monotherapy. Antibiot Chemother 1970; 16: 105-7.
    • (1970) Antibiot Chemother , vol.16 , pp. 105-107
    • Dormer, B.A.1
  • 129
    • 0014886221 scopus 로고
    • Isoxyl: A review of the results of its use over a five-year period in the tuberculosis field service of a large urban area
    • Gallen CS. Isoxyl: a review of the results of its use over a five-year period in the tuberculosis field service of a large urban area. Antibiot Chemother 1970; 16: 139-48.
    • (1970) Antibiot Chemother , vol.16 , pp. 139-148
    • Gallen, C.S.1
  • 131
    • 0014886148 scopus 로고
    • Clinical experience with thiocarlide (Isoxyl)
    • Urbancik B. Clinical experience with thiocarlide (Isoxyl). Antibiot Chemother 1970; 16: 117-23.
    • (1970) Antibiot Chemother , vol.16 , pp. 117-123
    • Urbancik, B.1
  • 132
    • 33847675813 scopus 로고    scopus 로고
    • EthA, a common activator of thiocarbamide-containing drugs acting on different mycobacterial targets
    • Dover LG, Alahari A, Gratraud P, et al. EthA, a common activator of thiocarbamide-containing drugs acting on different mycobacterial targets. Antimicrob Agents Chemother 2007; 51(3): 1055-63.
    • (2007) Antimicrob Agents Chemother , vol.51 , Issue.3 , pp. 1055-1063
    • Dover, L.G.1    Alahari, A.2    Gratraud, P.3
  • 133
    • 0015075116 scopus 로고
    • Effects of ethionamide and isoxyl on mycolic acid synthesis in Mycobacterium tuberculosis BCG
    • Winder FG, Collins PB, Whelan D. Effects of ethionamide and isoxyl on mycolic acid synthesis in Mycobacterium tuberculosis BCG. J Gen Microbiol 1971; 66(3): 379-80.
    • (1971) J Gen Microbiol , vol.66 , Issue.3 , pp. 379-380
    • Winder, F.G.1    Collins, P.B.2    Whelan, D.3
  • 134
    • 0032930265 scopus 로고    scopus 로고
    • Antimycobacterial activities of isoxyl and new derivatives through the inhibition of mycolic acid synthesis
    • Phetsuksiri B, Baulard AR, Cooper AM, et al. Antimycobacterial activities of isoxyl and new derivatives through the inhibition of mycolic acid synthesis. Antimicrob Agents Chemother 1999; 43(5): 1042-51.
    • (1999) Antimicrob Agents Chemother , vol.43 , Issue.5 , pp. 1042-1051
    • Phetsuksiri, B.1    Baulard, A.R.2    Cooper, A.M.3
  • 135
    • 9144238713 scopus 로고    scopus 로고
    • Unique mechanism of action of the thiourea drug isoxyl on Mycobacterium tuberculosis
    • Phetsuksiri B, Jackson M, Scherman H, et al. Unique mechanism of action of the thiourea drug isoxyl on Mycobacterium tuberculosis. J Biol Chem 2003; 278(52): 53123-30.
    • (2003) J Biol Chem , vol.278 , Issue.52 , pp. 53123-53130
    • Phetsuksiri, B.1    Jackson, M.2    Scherman, H.3
  • 136
    • 33747025717 scopus 로고    scopus 로고
    • Symmetrical and unsymmetrical analogues of isoxyl; active agents against Mycobacterium tuberculosis
    • Bhowruth V, Brown AK, Reynolds RC, et al. Symmetrical and unsymmetrical analogues of isoxyl; active agents against Mycobacterium tuberculosis. Bioorg Med Chem Lett 2006; 16(18): 4743-7.
    • (2006) Bioorg Med Chem Lett , vol.16 , Issue.18 , pp. 4743-4747
    • Bhowruth, V.1    Brown, A.K.2    Reynolds, R.C.3
  • 137
    • 0014266865 scopus 로고
    • Thiacetazone toxicity: A general review
    • Miller AB. Thiacetazone toxicity: a general review. Tubercle 1968; 49(Suppl): 54-6.
    • (1968) Tubercle , vol.49 , Issue.SUPPL. , pp. 54-56
    • Miller, A.B.1
  • 138
    • 0027432118 scopus 로고
    • Thiacetazone--avoid like poison or use with care?
    • Nunn P, Porter J, Winstanley P. Thiacetazone--avoid like poison or use with care? Trans R Soc Trop Med Hyg 1993; 87(5): 578-82.
    • (1993) Trans R Soc Trop Med Hyg , vol.87 , Issue.5 , pp. 578-582
    • Nunn, P.1    Porter, J.2    Winstanley, P.3
  • 139
    • 0031243354 scopus 로고    scopus 로고
    • Risk factors for adverse drug reactions during thiacetazone treatment of pulmonary tuberculosis in human immunodeficiency virus infected adults
    • Okwera A, Johnson JL, Vjecha MJ, et al. Risk factors for adverse drug reactions during thiacetazone treatment of pulmonary tuberculosis in human immunodeficiency virus infected adults. Int J Tuberc Lung Dis 1997; 1(5): 441-5.
    • (1997) Int J Tuberc Lung Dis , vol.1 , Issue.5 , pp. 441-445
    • Okwera, A.1    Johnson, J.L.2    Vjecha, M.J.3
  • 140
    • 0018227679 scopus 로고
    • Thiacetazone toxicity in the treatment of tuberculosis patients in Nigeria
    • Pearson CA. Thiacetazone toxicity in the treatment of tuberculosis patients in Nigeria. J Trop Med Hyg 1978; 81(12): 238-42.
    • (1978) J Trop Med Hyg , vol.81 , Issue.12 , pp. 238-242
    • Pearson, C.A.1
  • 141
    • 43249131427 scopus 로고    scopus 로고
    • Thiacetazone, an antitubercular drug that inhibits cyclopropanation of cell wall mycolic acids in mycobacteria
    • Alahari A, Trivelli X, Guerardel Y, et al. Thiacetazone, an antitubercular drug that inhibits cyclopropanation of cell wall mycolic acids in mycobacteria. PLoS ONE 2007; 2(12): e1343.
    • (2007) PLoS ONE , vol.2 , Issue.12
    • Alahari, A.1    Trivelli, X.2    Guerardel, Y.3
  • 142
    • 60649090254 scopus 로고    scopus 로고
    • Mycolic acid methyltransferase, MmaA4, is necessary for thiacetazone susceptibility in Mycobacterium tuberculosis
    • Alahari A, Alibaud L, Trivelli X, et al. Mycolic acid methyltransferase, MmaA4, is necessary for thiacetazone susceptibility in Mycobacterium tuberculosis. Mol Microbiol 2009; 71(5): 1263-77.
    • (2009) Mol Microbiol , vol.71 , Issue.5 , pp. 1263-1277
    • Alahari, A.1    Alibaud, L.2    Trivelli, X.3
  • 143
    • 54549121616 scopus 로고    scopus 로고
    • A microbiological assessment of novel nitrofuranylamides as anti-tuberculosis agents
    • Hurdle JG, Lee RB, Budha NR, et al. A microbiological assessment of novel nitrofuranylamides as anti-tuberculosis agents. J Antimicrob Chemother 2008; 62(5): 1037-45.
    • (2008) J Antimicrob Chemother , vol.62 , Issue.5 , pp. 1037-1045
    • Hurdle, J.G.1    Lee, R.B.2    Budha, N.R.3
  • 144
    • 38349010517 scopus 로고    scopus 로고
    • Comparison of the sterilising activities of the nitroimidazopyran PA-824 and moxifloxacin against persisting Mycobacterium tuberculosis
    • Hu Y, Coates AR, Mitchison DA. Comparison of the sterilising activities of the nitroimidazopyran PA-824 and moxifloxacin against persisting Mycobacterium tuberculosis. Int J Tuberc Lung Dis 2008; 12(1): 69-73.
    • (2008) Int J Tuberc Lung Dis , vol.12 , Issue.1 , pp. 69-73
    • Hu, Y.1    Coates, A.R.2    Mitchison, D.A.3
  • 145
    • 64349096833 scopus 로고    scopus 로고
    • Structure-Activity Relationships of Antitubercular Nitroimidazoles. 1. Structural Features Associated with Aerobic and Anaerobic Activities of 4- and 5-Nitroimidazoles
    • Kim P, Zhang L, Manjunatha UH, et al. Structure-Activity Relationships of Antitubercular Nitroimidazoles. 1. Structural Features Associated with Aerobic and Anaerobic Activities of 4- and 5-Nitroimidazoles. J Med Chem 2009; 52(5): 1329-44.
    • (2009) J Med Chem , vol.52 , Issue.5 , pp. 1329-1344
    • Kim, P.1    Zhang, L.2    Manjunatha, U.H.3
  • 146
    • 34247515586 scopus 로고    scopus 로고
    • Expression, purification and crystallization of native and selenomethionine labeled Mycobacterium tuberculosis FGD1 (Rv0407) using a Mycobacterium smegmatis expression system
    • Bashiri G, Squire CJ, Baker EN, Moreland NJ. Expression, purification and crystallization of native and selenomethionine labeled Mycobacterium tuberculosis FGD1 (Rv0407) using a Mycobacterium smegmatis expression system. Protein Expr Purif 2007; 54(1): 38-44.
    • (2007) Protein Expr Purif , vol.54 , Issue.1 , pp. 38-44
    • Bashiri, G.1    Squire, C.J.2    Baker, E.N.3    Moreland, N.J.4
  • 147
    • 47749152561 scopus 로고    scopus 로고
    • Crystal structures of F420-dependent glucose-6-phosphate dehydrogenase FGD1 involved in the activation of the anti-tuberculosis drug candidate PA-824 reveal the basis of coenzyme and substrate binding
    • Bashiri G, Squire CJ, Moreland NJ, Baker EN. Crystal structures of F420-dependent glucose-6-phosphate dehydrogenase FGD1 involved in the activation of the anti-tuberculosis drug candidate PA-824 reveal the basis of coenzyme and substrate binding. J Biol Chem 2008; 283(25): 17531-41.
    • (2008) J Biol Chem , vol.283 , Issue.25 , pp. 17531-17541
    • Bashiri, G.1    Squire, C.J.2    Moreland, N.J.3    Baker, E.N.4
  • 149
    • 57149099588 scopus 로고    scopus 로고
    • PA-824 kills nonreplicating Mycobacterium tuberculosis by intracellular NO release
    • Singh R, Manjunatha U, Boshoff HI, et al. PA-824 kills nonreplicating Mycobacterium tuberculosis by intracellular NO release. Science 2008; 322(5906): 1392-5.
    • (2008) Science , vol.322 , Issue.5906 , pp. 1392-1395
    • Singh, R.1    Manjunatha, U.2    Boshoff, H.I.3
  • 150
    • 33845323336 scopus 로고    scopus 로고
    • OPC-67683, a nitro-dihydro-imidazooxazole derivative with promising action against tuberculosis in vitro and in mice
    • Matsumoto M, Hashizume H, Tomishige T, et al. OPC-67683, a nitro-dihydro-imidazooxazole derivative with promising action against tuberculosis in vitro and in mice. PLoS Med 2006; 3(11): e466.
    • (2006) PLoS Med , vol.3 , Issue.11
    • Matsumoto, M.1    Hashizume, H.2    Tomishige, T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.