-
1
-
-
84871210454
-
-
World Health Organization: Fact Sheet No 104: tuberculosis. WHO Fact Sheets. Geneva: WHO
-
World Health Organization: Fact Sheet No 104: tuberculosis. WHO Fact Sheets. Geneva: WHO, 2002.
-
(2002)
-
-
-
2
-
-
25844434417
-
Tuberculosis control in the era of HIV
-
Nunn, P.; Williams, B.; Floyd, K.; Dye, C.; Elzinga, G.; Raviglione, M. Tuberculosis control in the era of HIV. Nat. Rev. Immunol., 2005, 5, 819-26.
-
(2005)
Nat. Rev. Immunol
, vol.5
, pp. 819-826
-
-
Nunn, P.1
Williams, B.2
Floyd, K.3
Dye, C.4
Elzinga, G.5
Raviglione, M.6
-
3
-
-
0034982047
-
Scientific blueprint for tuberculosis drug development
-
Global Alliance for Tuberculosis Drug Development. Tuberculosis
-
Global Alliance for Tuberculosis Drug Development. Tuberculosis. Scientific blueprint for tuberculosis drug development. Tuberculosis, 2001, 81(Suppl.), 1-52.
-
(2001)
Tuberculosis
, vol.81
, Issue.SUPPL.
, pp. 1-52
-
-
-
4
-
-
0025995304
-
Mycobacterium avium infection and AIDS: A therapeutic dilemma in rapid evolution
-
Ellner, J.J.; Goldberger, M.J.; Parenti, D.M. Mycobacterium avium infection and AIDS: a therapeutic dilemma in rapid evolution. J. Infect. Dis., 1991, 163, 1326-35.
-
(1991)
J. Infect. Dis
, vol.163
, pp. 1326-1335
-
-
Ellner, J.J.1
Goldberger, M.J.2
Parenti, D.M.3
-
5
-
-
0032508046
-
Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence
-
Cole, S.T.; Brosch, R.; Parkhill, J.; Garnier, T.; Churcher, C.; Harris, D.; Gordon, S.V.; Eiglmeier, K.; Gas, S.; Barry, C.E., 3rd; Tekaia, F.; Badcock, K.; Basham, D.; Brown, D.; Chillingworth, T.; Connor, R.; Davies, R.; Devlin, K.; Feltwell, T.; Gentles, S.; Hamlin, N.; Holroyd, S.; Hornsby, T.; Jagels, K.; Krogh, A.; McLean, J.; Moule, S.; Murphy, L.; Oliver, K.; Osborne, J.; Quail, M.A.; Rajandream, M.A.; Rogers, J.; Rutter, S.; Seeger, K.; Skelton, J.; Squares, R.; Squares, S.; Sulston, J.E.; Taylor, K.; Whitehead, S.; Barrell, B.G. Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence. Nature, 1998, 393, 537-44.
-
(1998)
Nature
, vol.393
, pp. 537-544
-
-
Cole, S.T.1
Brosch, R.2
Parkhill, J.3
Garnier, T.4
Churcher, C.5
Harris, D.6
Gordon, S.V.7
Eiglmeier, K.8
Gas, S.9
Barry III, C.E.10
Tekaia, F.11
Badcock, K.12
Basham, D.13
Brown, D.14
Chillingworth, T.15
Connor, R.16
Davies, R.17
Devlin, K.18
Feltwell, T.19
Gentles, S.20
Hamlin, N.21
Holroyd, S.22
Hornsby, T.23
Jagels, K.24
Krogh, A.25
McLean, J.26
Moule, S.27
Murphy, L.28
Oliver, K.29
Osborne, J.30
Quail, M.A.31
Rajandream, M.A.32
Rogers, J.33
Rutter, S.34
Seeger, K.35
Skelton, J.36
Squares, R.37
Squares, S.38
Sulston, J.E.39
Taylor, K.40
Whitehead, S.41
Barrell, B.G.42
more..
-
7
-
-
0029760189
-
Mycobacterium tuberculosis cell envelope
-
Lee, R.E.; Brennan, P.J.; Besra, G.S. Mycobacterium tuberculosis cell envelope. Curr. Top. Microbiol. Immunol., 1996, 215, 1-27.
-
(1996)
Curr. Top. Microbiol. Immunol
, vol.215
, pp. 1-27
-
-
Lee, R.E.1
Brennan, P.J.2
Besra, G.S.3
-
8
-
-
0036322591
-
Mycobacterium and the coat of many lipids
-
Russell, D.G.; Mwandumba, H.C.; Rhoades, E.E. Mycobacterium and the coat of many lipids. J. Cell. Biol., 2002, 158, 421-6.
-
(2002)
J. Cell. Biol
, vol.158
, pp. 421-426
-
-
Russell, D.G.1
Mwandumba, H.C.2
Rhoades, E.E.3
-
9
-
-
0029862802
-
Mycolic acid structure determines the fluidity of the mycobacterial cell wall
-
Liu, J.; Barry, C.E., 3rd; Besra, G.S.; Nikaido, H. Mycolic acid structure determines the fluidity of the mycobacterial cell wall. J. Biol. Chem., 1996, 271, 29545-51.
-
(1996)
J. Biol. Chem
, vol.271
, pp. 29545-29551
-
-
Liu, J.1
Barry III, C.E.2
Besra, G.S.3
Nikaido, H.4
-
10
-
-
0033966884
-
Another brick in the wall
-
Tonge, P.J. Another brick in the wall. Nat. Struct. Biol., 2000, 7, 94-6.
-
(2000)
Nat. Struct. Biol
, vol.7
, pp. 94-96
-
-
Tonge, P.J.1
-
11
-
-
0032126742
-
Mycolic acids: Structure, biosynthesis and physiological functions
-
Barry, C.E., III; Lee, R.E.; Mdluli, K.; Sampson, A.E.; Schroeder, B.G.; Slayden, R.A.; Yuan, Y. Mycolic acids: structure, biosynthesis and physiological functions. Prog. Lipid Res., 1998, 37, 143-79.
-
(1998)
Prog. Lipid Res
, vol.37
, pp. 143-179
-
-
Barry III, C.E.1
Lee, R.E.2
Mdluli, K.3
Sampson, A.E.4
Schroeder, B.G.5
Slayden, R.A.6
Yuan, Y.7
-
12
-
-
0035201541
-
An approach for the rational design of new antituberculosis agents
-
Pasqualoto, K.F.; Ferreira, E.I. An approach for the rational design of new antituberculosis agents. Curr. Drug Targets., 2001, 2, 427-37.
-
(2001)
Curr. Drug Targets
, vol.2
, pp. 427-437
-
-
Pasqualoto, K.F.1
Ferreira, E.I.2
-
13
-
-
0028156861
-
inhA, a gene encoding a target for isoniazid and ethionamide in Mycobacterium tuberculosis
-
Banerjee, A.; Dubnau, E.; Quemard, A.; Balasubramanian, V.; Um, K.S.; Wilson, T.; Collins, D.; de Lisle, G.; Jacobs, W.R. Jr. inhA, a gene encoding a target for isoniazid and ethionamide in Mycobacterium tuberculosis. Science, 1994, 263, 227-30.
-
(1994)
Science
, vol.263
, pp. 227-230
-
-
Banerjee, A.1
Dubnau, E.2
Quemard, A.3
Balasubramanian, V.4
Um, K.S.5
Wilson, T.6
Collins, D.7
de Lisle, G.8
Jacobs Jr., W.R.9
-
14
-
-
0028988237
-
Crystal structure and function of the isoniazid target of Mycobacterium tuberculosis
-
Dessen, A.; Quemard, A.; Blanchard, J.S.; Jacobs, W.R., Jr.; Sacchettini, J.C. Crystal structure and function of the isoniazid target of Mycobacterium tuberculosis. Science, 1995, 267, 1638-41.
-
(1995)
Science
, vol.267
, pp. 1638-1641
-
-
Dessen, A.1
Quemard, A.2
Blanchard, J.S.3
Jacobs Jr., W.R.4
Sacchettini, J.C.5
-
15
-
-
33746496066
-
Isoniazid is not a lead compound for its pyridyl ring derivatives, isonicotinoyl amides, hydrazides, and hydrazones: A critical review
-
Scior, T.; Garces-Eisele, S.J. Isoniazid is not a lead compound for its pyridyl ring derivatives, isonicotinoyl amides, hydrazides, and hydrazones: a critical review. Curr. Med. Chem., 2006, 13, 2205-19.
-
(2006)
Curr. Med. Chem
, vol.13
, pp. 2205-2219
-
-
Scior, T.1
Garces-Eisele, S.J.2
-
16
-
-
17644436310
-
Inhibition of InhA, the enoyl reductase from Mycobacterium tuberculosis, by triclosan and isoniazid
-
Parikh, S.L.; Xiao, G.; Tonge, P.J. Inhibition of InhA, the enoyl reductase from Mycobacterium tuberculosis, by triclosan and isoniazid. Biochemistry, 2000, 39, 7645-50.
-
(2000)
Biochemistry
, vol.39
, pp. 7645-7650
-
-
Parikh, S.L.1
Xiao, G.2
Tonge, P.J.3
-
17
-
-
0345133299
-
The isoniazid-NAD adduct is a slow, tight-binding inhibitor of InhA, the Mycobacterium tuberculosis enoyl reductase: Adduct affinity and drug resistance
-
Rawat, R.; Whitty, A.; Tonge, P.J. The isoniazid-NAD adduct is a slow, tight-binding inhibitor of InhA, the Mycobacterium tuberculosis enoyl reductase: adduct affinity and drug resistance. Proc. Natl. Acad. Sci. USA, 2003, 100, 13881-6.
-
(2003)
Proc. Natl. Acad. Sci. USA
, vol.100
, pp. 13881-13886
-
-
Rawat, R.1
Whitty, A.2
Tonge, P.J.3
-
18
-
-
33947651030
-
Development of modern InhA inhibitors to combat drug resistant strains of Mycobacterium tuberculosis
-
Tong, P.J.; Kisker C.; Slayden, R.A. Development of modern InhA inhibitors to combat drug resistant strains of Mycobacterium tuberculosis. Curr. Top. Med. Chem., 2007, 7, 489-98.
-
(2007)
Curr. Top. Med. Chem
, vol.7
, pp. 489-498
-
-
Tong, P.J.1
Kisker, C.2
Slayden, R.A.3
-
19
-
-
0038757566
-
Targeting tuberculosis and malaria through inhibition of Enoyl reductase: Compound activity and structural data
-
Kuo, M.R.; Morbidoni, H.R.; Alland, D.; Sneddon, S.F.; Gourlie, B.B.; Staveski, M.M.; Leonard, M.; Gregory, J.S.; Janjigian, A.D.; Yee, C.; Musser, J.M.; Kreiswirth, B.; Iwamoto, H.; Perozzo, R.; Jacobs, W.R., Jr.; Sacchettini, J.C.; Fidock, D.A. Targeting tuberculosis and malaria through inhibition of Enoyl reductase: compound activity and structural data. J. Biol. Chem., 2003, 278, 20851-9.
-
(2003)
J. Biol. Chem
, vol.278
, pp. 20851-20859
-
-
Kuo, M.R.1
Morbidoni, H.R.2
Alland, D.3
Sneddon, S.F.4
Gourlie, B.B.5
Staveski, M.M.6
Leonard, M.7
Gregory, J.S.8
Janjigian, A.D.9
Yee, C.10
Musser, J.M.11
Kreiswirth, B.12
Iwamoto, H.13
Perozzo, R.14
Jacobs Jr., W.R.15
Sacchettini, J.C.16
Fidock, D.A.17
-
20
-
-
33750111588
-
Pyrrolidine carboxamides as a novel class of inhibitors of enoyl acyl carrier protein reductase from Mycobacterium tuberculosis
-
He, X.; Alian, A.; Stroud, R.; Ortiz de Montellano, P.R. Pyrrolidine carboxamides as a novel class of inhibitors of enoyl acyl carrier protein reductase from Mycobacterium tuberculosis. J. Med. Chem., 2006, 49, 6308-23.
-
(2006)
J. Med. Chem
, vol.49
, pp. 6308-6323
-
-
He, X.1
Alian, A.2
Stroud, R.3
de Montellano, O.P.R.4
-
21
-
-
34548526629
-
Inhibition of the Mycobacterium tuberculosis enoyl acyl carrier protein reductase InhA by arylamides
-
He, X.; Alian, A.; Ortiz de Montellano, P.R. Inhibition of the Mycobacterium tuberculosis enoyl acyl carrier protein reductase InhA by arylamides. Bioorg. Med. Chem., 2007, 15, 6649-58.
-
(2007)
Bioorg. Med. Chem
, vol.15
, pp. 6649-6658
-
-
He, X.1
Alian, A.2
de Montellano, O.P.R.3
-
22
-
-
34247347420
-
Evaluation of N-(phenylmethyl)-4-[5-(phenylmethyl)-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]p yridin-4-yl]benzamide inhibitors of Mycobacterium tuberculosis growth
-
Wall, M.D.; Oshin, M.; Chung, G.A.; Parkhouse, T.; Gore, A.; Herreros, E.; Cox, B.; Duncan, K.; Evans, B.; Everett, M.; Mendoza, A. Evaluation of N-(phenylmethyl)-4-[5-(phenylmethyl)-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]p yridin-4-yl]benzamide inhibitors of Mycobacterium tuberculosis growth. Bioorg. Med. Chem. Lett., 2007, 17, 2740-4.
-
(2007)
Bioorg. Med. Chem. Lett
, vol.17
, pp. 2740-2744
-
-
Wall, M.D.1
Oshin, M.2
Chung, G.A.3
Parkhouse, T.4
Gore, A.5
Herreros, E.6
Cox, B.7
Duncan, K.8
Evans, B.9
Everett, M.10
Mendoza, A.11
-
23
-
-
0001352336
-
The chemical approach to the control of tuberculosis
-
Fox, H.H. The chemical approach to the control of tuberculosis. Science, 1952, 116, 129-34.
-
(1952)
Science
, vol.116
, pp. 129-134
-
-
Fox, H.H.1
-
24
-
-
0001206572
-
In vitro studies on isonicotinic acid hydrazide
-
Pansy, F.; Stander, H.; Donovick, R. In vitro studies on isonicotinic acid hydrazide. Am. Rev. Tuberc., 1952, 65, 761-4.
-
(1952)
Am. Rev. Tuberc
, vol.65
, pp. 761-764
-
-
Pansy, F.1
Stander, H.2
Donovick, R.3
-
25
-
-
0026705772
-
The catalaseperoxidase gene and isoniazid resistance of Mycobacterium tuberculosis
-
Zhang, Y.; Heym, B.; Allen, B.; Young, D.; Cole, S. The catalaseperoxidase gene and isoniazid resistance of Mycobacterium tuberculosis. Nature, 1992, 358, 591-3.
-
(1992)
Nature
, vol.358
, pp. 591-593
-
-
Zhang, Y.1
Heym, B.2
Allen, B.3
Young, D.4
Cole, S.5
-
26
-
-
25444522967
-
Correlation between isoniazid resistance and superoxide reactivity in Mycobacterium tuberculosis KatG
-
Ghiladi, R.A.; Medzihradszky, K.F.; Rusnak, F.M.; Ortiz de Montellano, P.R. Correlation between isoniazid resistance and superoxide reactivity in Mycobacterium tuberculosis KatG. J. Am. Chem. Soc., 2005, 127, 13428-42.
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 13428-13442
-
-
Ghiladi, R.A.1
Medzihradszky, K.F.2
Rusnak, F.M.3
de Montellano, O.P.R.4
-
27
-
-
0027993499
-
Mechanistic Studies of the Oxidation of Isoniazid by the Catalase Peroxidase from Mycobacterium tuberculosis
-
Johnsson, K.; Schultz, P.G. Mechanistic Studies of the Oxidation of Isoniazid by the Catalase Peroxidase from Mycobacterium tuberculosis. J. Am. Chem. Soc., 1994, 116, 7425-6.
-
(1994)
J. Am. Chem. Soc
, vol.116
, pp. 7425-7426
-
-
Johnsson, K.1
Schultz, P.G.2
-
28
-
-
0029042636
-
Studies on the mechanism of action of isoniazid and ethionamide in the chemotherapy of tuberculosis
-
Johnsson, K.; King, D.S.; Schultz, P.G. Studies on the mechanism of action of isoniazid and ethionamide in the chemotherapy of tuberculosis. J. Am. Chem. Soc., 1995, 117, 5009-10.
-
(1995)
J. Am. Chem. Soc
, vol.117
, pp. 5009-5010
-
-
Johnsson, K.1
King, D.S.2
Schultz, P.G.3
-
29
-
-
0029860774
-
Kinetics of Inactivation of WT and C243S Mutant of Mycobacterium tuberculosis Enoyl Reductase by Activated Isoniazid
-
Basso, L.A.; Zheng, R.J.; Blanchard, J.S. Kinetics of Inactivation of WT and C243S Mutant of Mycobacterium tuberculosis Enoyl Reductase by Activated Isoniazid. J. Am. Chem. Soc., 1996, 118, 11301-2.
-
(1996)
J. Am. Chem. Soc
, vol.118
, pp. 11301-11302
-
-
Basso, L.A.1
Zheng, R.J.2
Blanchard, J.S.3
-
30
-
-
0036461031
-
Antitubercular isoniazid and drug resistance of Mycobacterium tuberculosis--a review
-
Scior, T.; Meneses Morales, I.; Garces Eisele, S.J.; Domeyer, D.; Laufer, S. Antitubercular isoniazid and drug resistance of Mycobacterium tuberculosis--a review. Arch. Pharm. Pharm. Med. Chem., 2002, 355, 511-25.
-
(2002)
Arch. Pharm. Pharm. Med. Chem
, vol.355
, pp. 511-525
-
-
Scior, T.1
Meneses, M.I.2
Garces, E.S.J.3
Domeyer, D.4
Laufer, S.5
-
31
-
-
0032472224
-
Modification of the NADH of the isoniazid target (InhA) from Mycobacterium tuberculosis
-
Rozwarski, D.A.; Grant, G.A.; Barton, D.H.; Jacobs, W.R., Jr.; Sacchettini, J.C. Modification of the NADH of the isoniazid target (InhA) from Mycobacterium tuberculosis. Science, 1998, 279, 98-102.
-
(1998)
Science
, vol.279
, pp. 98-102
-
-
Rozwarski, D.A.1
Grant, G.A.2
Barton, D.H.3
Jacobs Jr., W.R.4
Sacchettini, J.C.5
-
32
-
-
0034723345
-
Action mechanism of antitubercular isoniazid. Activation by Mycobacterium tuberculosis KatG, isolation, and characterization of inha inhibitor
-
Lei, B.; Wei, C.J.; Tu, S.C. Action mechanism of antitubercular isoniazid. Activation by Mycobacterium tuberculosis KatG, isolation, and characterization of inha inhibitor. J. Biol. Chem., 2000, 275, 2520-6.
-
(2000)
J. Biol. Chem
, vol.275
, pp. 2520-2526
-
-
Lei, B.1
Wei, C.J.2
Tu, S.C.3
-
33
-
-
55949093998
-
Binding of the tautomeric forms of isoniazid-NAD adducts to the active site of the Mycobacterium tuberculosis enoyl-ACP reductase (InhA): A theoretical approach
-
Stigliani, J.L.; Arnaud, P.; Delaine, T.; Bernardes-Genisson, V.; Meunier, B.; Bernadou, J. Binding of the tautomeric forms of isoniazid-NAD adducts to the active site of the Mycobacterium tuberculosis enoyl-ACP reductase (InhA): a theoretical approach. J. Mol. Graph. Model., 2008, 27, 536-45.
-
(2008)
J. Mol. Graph. Model
, vol.27
, pp. 536-545
-
-
Stigliani, J.L.1
Arnaud, P.2
Delaine, T.3
Bernardes-Genisson, V.4
Meunier, B.5
Bernadou, J.6
-
34
-
-
0027282748
-
Catalase-peroxidase gene sequences in isoniazid-sensitive and -resistant strains of Mycobacterium tuberculosis from New York City
-
Stoeckle, M.Y.; Guan, L.; Riegler, N.; Weitzman, I.; Kreiswirth, B.; Kornblum, J.; Laraque, F.; Riley, L.W. Catalase-peroxidase gene sequences in isoniazid-sensitive and -resistant strains of Mycobacterium tuberculosis from New York City. J. Infect. Dis., 1993, 168, 1063-5.
-
(1993)
J. Infect. Dis
, vol.168
, pp. 1063-1065
-
-
Stoeckle, M.Y.1
Guan, L.2
Riegler, N.3
Weitzman, I.4
Kreiswirth, B.5
Kornblum, J.6
Laraque, F.7
Riley, L.W.8
-
35
-
-
0030042509
-
Characterization of the catalaseperoxidase gene (katG) and inhA locus in isoniazid-resistant and -susceptible strains of Mycobacterium tuberculosis by automated DNA sequencing: Restricted array of mutations associated with drug resistance
-
Musser, J.M.; Kapur, V.; Williams, D.L.; Kreiswirth, B.N.; van Soolingen, D.; van Embden, J.D. Characterization of the catalaseperoxidase gene (katG) and inhA locus in isoniazid-resistant and -susceptible strains of Mycobacterium tuberculosis by automated DNA sequencing: restricted array of mutations associated with drug resistance. J. Infect. Dis., 1996, 173, 196-202.
-
(1996)
J. Infect. Dis
, vol.173
, pp. 196-202
-
-
Musser, J.M.1
Kapur, V.2
Williams, D.L.3
Kreiswirth, B.N.4
van Soolingen, D.5
van Embden, J.D.6
-
36
-
-
0037378059
-
Single nucleotide polymorphisms in genes associated with isoniazid resistance in Mycobacterium tuberculosis
-
Ramaswamy, S.V.; Reich, R.; Dou, S.J.; Jasperse, L.; Pan, X.; Wanger, A.; Quitugua, T.; Graviss, E.A. Single nucleotide polymorphisms in genes associated with isoniazid resistance in Mycobacterium tuberculosis. Antimicrob. Agents Chemother., 2003, 47, 1241-50.
-
(2003)
Antimicrob. Agents Chemother
, vol.47
, pp. 1241-1250
-
-
Ramaswamy, S.V.1
Reich, R.2
Dou, S.J.3
Jasperse, L.4
Pan, X.5
Wanger, A.6
Quitugua, T.7
Graviss, E.A.8
-
37
-
-
33645551821
-
Hydrogen peroxide-mediated isoniazid activation catalyzed by Mycobacterium tuberculosis catalase-peroxidase (KatG) and its S315T mutant
-
Zhao, X.; Yu, H.; Yu, S.; Wang, F.; Sacchettini, J.C.; Magliozzo, R.S. Hydrogen peroxide-mediated isoniazid activation catalyzed by Mycobacterium tuberculosis catalase-peroxidase (KatG) and its S315T mutant. Biochemistry, 2006, 45, 4131-40.
-
(2006)
Biochemistry
, vol.45
, pp. 4131-4140
-
-
Zhao, X.1
Yu, H.2
Yu, S.3
Wang, F.4
Sacchettini, J.C.5
Magliozzo, R.S.6
-
38
-
-
0031689089
-
Mechanisms of isoniazid resistance in Mycobacterium tuberculosis: Enzymatic characterization of enoyl reductase mutants identified in isoniazid-resistant clinical isolates
-
Basso, L.A.; Zheng, R.; Musser, J.M.; Jacobs, W.R., Jr.; Blanchard, J.S. Mechanisms of isoniazid resistance in Mycobacterium tuberculosis: enzymatic characterization of enoyl reductase mutants identified in isoniazid-resistant clinical isolates. J. Infect. Dis., 1998, 178, 769-75.
-
(1998)
J. Infect. Dis
, vol.178
, pp. 769-775
-
-
Basso, L.A.1
Zheng, R.2
Musser, J.M.3
Jacobs Jr., W.R.4
Blanchard, J.S.5
-
39
-
-
0032486197
-
Inhibition of a Mycobacterium tuberculosis beta-ketoacyl ACP synthase by isoniazid
-
Mdluli, K.; Slayden, R.A.; Zhu, Y.; Ramaswamy, S.; Pan, X.; Mead, D.; Crane, D.D.; Musser, J.M.; Barry, C.E., 3rd. Inhibition of a Mycobacterium tuberculosis beta-ketoacyl ACP synthase by isoniazid. Science, 1998, 280, 1607-10.
-
(1998)
Science
, vol.280
, pp. 1607-1610
-
-
Mdluli, K.1
Slayden, R.A.2
Zhu, Y.3
Ramaswamy, S.4
Pan, X.5
Mead, D.6
Crane, D.D.7
Musser, J.M.8
Barry III, C.E.9
-
40
-
-
33748469322
-
Transfer of a point mutation in Mycobacterium tuberculosis inhA resolves the target of isoniazid
-
Vilcheze, C.; Wang, F.; Arai, M.; Hazbon, M.H.; Colangeli, R.; Kremer, L.; Weisbrod, T.R.; Alland, D.; Sacchettini, J.C.; Jacobs, W.R., Jr. Transfer of a point mutation in Mycobacterium tuberculosis inhA resolves the target of isoniazid. Nat. Med., 2006, 12, 1027-9.
-
(2006)
Nat. Med
, vol.12
, pp. 1027-1029
-
-
Vilcheze, C.1
Wang, F.2
Arai, M.3
Hazbon, M.H.4
Colangeli, R.5
Kremer, L.6
Weisbrod, T.R.7
Alland, D.8
Sacchettini, J.C.9
Jacobs Jr., W.R.10
-
41
-
-
33646893263
-
Crystallographic and pre-steady-state kinetics studies on binding of NADH to wild-type and isoniazid-resistant enoyl-ACP(CoA) reductase enzymes from Mycobacterium tuberculosis
-
Oliveira, J.S.; Pereira, J.H.; Canduri, F.; Rodrigues, N.C.; de Souza, O.N.; de Azevedo, W.F., Jr.; Basso, L.A.; Santos, D.S. Crystallographic and pre-steady-state kinetics studies on binding of NADH to wild-type and isoniazid-resistant enoyl-ACP(CoA) reductase enzymes from Mycobacterium tuberculosis. J. Mol. Biol., 2006, 359, 646-66.
-
(2006)
J. Mol. Biol
, vol.359
, pp. 646-666
-
-
Oliveira, J.S.1
Pereira, J.H.2
Canduri, F.3
Rodrigues, N.C.4
de Souza, O.N.5
de Azevedo Jr., W.F.6
Basso, L.A.7
Santos, D.S.8
-
42
-
-
34548335105
-
Crystallographic studies on the binding of isonicotinyl-NAD adduct to wild-type and isoniazid resistant 2-trans-enoyl-ACP (CoA) reductase from Mycobacterium tuberculosis
-
Dias, M.V.; Vasconcelos, I.B.; Prado, A.M.; Fadel, V.; Basso, L.A.; de Azevedo, W.F., Jr.; Santos, D.S. Crystallographic studies on the binding of isonicotinyl-NAD adduct to wild-type and isoniazid resistant 2-trans-enoyl-ACP (CoA) reductase from Mycobacterium tuberculosis. J. Struct. Biol., 2007, 159, 369-80.
-
(2007)
J. Struct. Biol
, vol.159
, pp. 369-380
-
-
Dias, M.V.1
Vasconcelos, I.B.2
Prado, A.M.3
Fadel, V.4
Basso, L.A.5
de Azevedo Jr., W.F.6
Santos, D.S.7
-
43
-
-
34547576168
-
Probing mechanisms of resistance to the tuberculosis drug isoniazid: Conformational changes caused by inhibition of InhA, the enoyl reductase from Mycobacterium tuberculosis
-
Kruh, N.A.; Rawat, R.; Ruzsicska, B.P.; Tonge, P.J. Probing mechanisms of resistance to the tuberculosis drug isoniazid: Conformational changes caused by inhibition of InhA, the enoyl reductase from Mycobacterium tuberculosis. Protein Sci., 2007, 16, 1617-27.
-
(2007)
Protein Sci
, vol.16
, pp. 1617-1627
-
-
Kruh, N.A.1
Rawat, R.2
Ruzsicska, B.P.3
Tonge, P.J.4
-
44
-
-
0023229665
-
Therapeutic implications of inhibition versus killing of Mycobacterium avium complex by antimicrobial agents
-
Yajko, D.M.; Nassos, P.S.; Hadley, W.K. Therapeutic implications of inhibition versus killing of Mycobacterium avium complex by antimicrobial agents. Antimicrob. Agents Chemother., 1987, 31, 117-20.
-
(1987)
Antimicrob. Agents Chemother
, vol.31
, pp. 117-120
-
-
Yajko, D.M.1
Nassos, P.S.2
Hadley, W.K.3
-
45
-
-
33645964027
-
A clinical trial of ethionamide and prothionamide for treatment of lepromatous leprosy
-
Fajardo, T.T.; Guinto, R.S.; Cellona, R.V.; Abalos, R.M.; Dela Cruz, E.C.; Gelber, R.H. A clinical trial of ethionamide and prothionamide for treatment of lepromatous leprosy. Am. J. Trop. Med. Hyg., 2006, 74, 457-61.
-
(2006)
Am. J. Trop. Med. Hyg
, vol.74
, pp. 457-461
-
-
Fajardo, T.T.1
Guinto, R.S.2
Cellona, R.V.3
Abalos, R.M.4
Dela, C.E.C.5
Gelber, R.H.6
-
46
-
-
33746571948
-
Emergence of Mycobacterium tuberculosis with extensive resistance to second-line drugs
-
Centers for Disease Control and Prevention
-
Centers for Disease Control and Prevention. Emergence of Mycobacterium tuberculosis with extensive resistance to second-line drugs. Ann. Pharmacother., 2006, 40, 1007-8.
-
(2006)
Ann. Pharmacother
, vol.40
, pp. 1007-1008
-
-
-
47
-
-
0015373050
-
Effect of isoniazid on the in vivo mycolic acid synthesis, cell growth, and viability of Mycobacterium tuberculosis
-
Takayama, K.; Wang, L.; David, H.L. Effect of isoniazid on the in vivo mycolic acid synthesis, cell growth, and viability of Mycobacterium tuberculosis. Antimicrob. Agents Chemother., 1972, 2, 29-35.
-
(1972)
Antimicrob. Agents Chemother
, vol.2
, pp. 29-35
-
-
Takayama, K.1
Wang, L.2
David, H.L.3
-
48
-
-
0015075116
-
Effects of ethionamide and isoxyl on mycolic acid synthesis in Mycobacterium tuberculosis BCG
-
Winder, F.G.; Collins, P.B.; Whelan, D. Effects of ethionamide and isoxyl on mycolic acid synthesis in Mycobacterium tuberculosis BCG. J. Gen. Microbiol., 1971, 66, 379-80.
-
(1971)
J. Gen. Microbiol
, vol.66
, pp. 379-380
-
-
Winder, F.G.1
Collins, P.B.2
Whelan, D.3
-
49
-
-
0345306174
-
ethA, inhA, and katG loci of ethionamide-resistant clinical Mycobacterium tuberculosis isolates
-
Morlock, G.P.; Metchock, B.; Sikes, D.; Crawford, J.T.; Cooksey, R.C. ethA, inhA, and katG loci of ethionamide-resistant clinical Mycobacterium tuberculosis isolates. Antimicrob. Agents Chemother., 2003, 47, 3799-805.
-
(2003)
Antimicrob. Agents Chemother.
, vol.47
, pp. 3799-3805
-
-
Morlock, G.P.1
Metchock, B.2
Sikes, D.3
Crawford, J.T.4
Cooksey, R.C.5
-
50
-
-
0033393147
-
Activity of 16 antimicrobial agents against drug-resistant strains of Mycobacterium tuberculosis
-
Fattorini, L.; Iona, E.; Ricci, M.L.; Thoresen, O.F.; Orru, G.; Oggioni, M.R.; Tortoli, E.; Piersimoni, C.; Chiaradonna, P.; Tronci, M.; Pozzi, G.; Orefici, G. Activity of 16 antimicrobial agents against drug-resistant strains of Mycobacterium tuberculosis. Microb. Drug Resist., 1999, 5, 265-70.
-
(1999)
Microb. Drug Resist
, vol.5
, pp. 265-270
-
-
Fattorini, L.1
Iona, E.2
Ricci, M.L.3
Thoresen, O.F.4
Orru, G.5
Oggioni, M.R.6
Tortoli, E.7
Piersimoni, C.8
Chiaradonna, P.9
Tronci, M.10
Pozzi, G.11
Orefici, G.12
-
51
-
-
0034662963
-
Ethionamide activation and sensitivity in multidrugresistant Mycobacterium tuberculosis
-
DeBarber, A.E.; Mdluli, K.; Bosman, M.; Bekker, L.G.; Barry, C.E., 3rd. Ethionamide activation and sensitivity in multidrugresistant Mycobacterium tuberculosis. Proc. Natl. Acad. Sci. USA, 2000, 97, 9677-82.
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 9677-9682
-
-
Debarber, A.E.1
Mdluli, K.2
Bosman, M.3
Bekker, L.G.4
Barry III, C.E.5
-
52
-
-
0034622924
-
Activation of the pro-drug ethionamide is regulated in mycobacteria
-
Baulard, A.R.; Betts, J.C.; Engohang-Ndong, J.; Quan, S.; McAdam, R.A.; Brennan, P.J.; Locht, C.; Besra, G.S. Activation of the pro-drug ethionamide is regulated in mycobacteria. J. Biol. Chem., 2000, 275, 28326-31.
-
(2000)
J. Biol. Chem
, vol.275
, pp. 28326-28331
-
-
Baulard, A.R.1
Betts, J.C.2
Engohang-Ndong, J.3
Quan, S.4
McAdam, R.A.5
Brennan, P.J.6
Locht, C.7
Besra, G.S.8
-
53
-
-
33846446699
-
Mechanism of thioamide drug action against tuberculosis and leprosy
-
Wang, F.; Langley, R.; Gulten, G.; Dover, L.G.; Besra, G.S.; Jacobs, W.R., Jr.; Sacchettini, J.C. Mechanism of thioamide drug action against tuberculosis and leprosy. J. Exp. Med., 2007, 204, 73-8.
-
(2007)
J. Exp. Med
, vol.204
, pp. 73-78
-
-
Wang, F.1
Langley, R.2
Gulten, G.3
Dover, L.G.4
Besra, G.S.5
Jacobs Jr., W.R.6
Sacchettini, J.C.7
-
54
-
-
0035984784
-
Mn(III) pyrophosphate as an efficient tool for studying the mode of action of isoniazid on the InhA protein of Mycobacterium tuberculosis
-
Nguyen, M.; Quémard, A.; Broussy, S.; Bernadou, J.; Meunier, B. Mn(III) pyrophosphate as an efficient tool for studying the mode of action of isoniazid on the InhA protein of Mycobacterium tuberculosis. Antimicrob. Agents Chemother., 2002, 46, 2137-44.
-
(2002)
Antimicrob. Agents Chemother
, vol.46
, pp. 2137-2144
-
-
Nguyen, M.1
Quémard, A.2
Broussy, S.3
Bernadou, J.4
Meunier, B.5
-
55
-
-
28744445549
-
The first chemical synthesis of the core structure of the benzoylhydrazine-NAD adduct, a competitive inhibitor of the Mycobacterium tuberculosis enoyl reductase
-
Broussy, S.; Bernardes-Genisson, V.; Quemard, A.; Meunier, B.; Bernadou, J. The first chemical synthesis of the core structure of the benzoylhydrazine-NAD adduct, a competitive inhibitor of the Mycobacterium tuberculosis enoyl reductase. J. Org. Chem., 2005, 70, 10502-10.
-
(2005)
J. Org. Chem
, vol.70
, pp. 10502-10510
-
-
Broussy, S.1
Bernardes-Genisson, V.2
Quemard, A.3
Meunier, B.4
Bernadou, J.5
-
56
-
-
34547729339
-
New insight into the mechanism of action of and resistance to isoniazid: Interaction of Mycobacterium tuberculosis enoyl-ACP reductase with INHNADP
-
Argyrou, A.; Vetting, M.W.; Blanchard, J.S. New insight into the mechanism of action of and resistance to isoniazid: interaction of Mycobacterium tuberculosis enoyl-ACP reductase with INHNADP. J. Am. Chem. Soc., 2007, 129, 9582-3.
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 9582-9583
-
-
Argyrou, A.1
Vetting, M.W.2
Blanchard, J.S.3
-
57
-
-
33846214785
-
Synthesis of the isonicotinoylnicotinamide scaffolds of the naturally occurring isoniazid-NAD(P) adducts
-
Delaine, T.; Bernardes-Genisson, V.; Meunier, B.; Bernadou, J. Synthesis of the isonicotinoylnicotinamide scaffolds of the naturally occurring isoniazid-NAD(P) adducts. J. Org. Chem., 2007, 72, 675-8.
-
(2007)
J. Org. Chem
, vol.72
, pp. 675-678
-
-
Delaine, T.1
Bernardes-Genisson, V.2
Meunier, B.3
Bernadou, J.4
-
58
-
-
0035804160
-
A fast and efficient metal-mediated oxidation of isoniazid and identification of isoniazid-NAD(H) adducts
-
Nguyen, M.; Claparols, C.; Bernadou, J.; Meunier, B. A fast and efficient metal-mediated oxidation of isoniazid and identification of isoniazid-NAD(H) adducts. ChemBioChem, 2001, 2, 877-83.
-
(2001)
ChemBioChem
, vol.2
, pp. 877-883
-
-
Nguyen, M.1
Claparols, C.2
Bernadou, J.3
Meunier, B.4
-
59
-
-
0033520469
-
Spontaneous Formation of the Bioactive Form of the Tuberculosis Drug Isoniazid
-
Wilming, M.; Johnsson, K. Spontaneous Formation of the Bioactive Form of the Tuberculosis Drug Isoniazid. Angew. Chem. Int. Ed. Engl., 1999, 38, 2588-90.
-
(1999)
Angew. Chem. Int. Ed. Engl
, vol.38
, pp. 2588-2590
-
-
Wilming, M.1
Johnsson, K.2
-
60
-
-
0038814033
-
13C NMR characterization of hemiamidal isoniazid-NAD(H) adducts as possible inhibitors of InhA reductase of Mycobacterium tuberculosis
-
13C NMR characterization of hemiamidal isoniazid-NAD(H) adducts as possible inhibitors of InhA reductase of Mycobacterium tuberculosis. Chemistry, 2003, 9, 2034-8.
-
(2003)
Chemistry
, vol.9
, pp. 2034-2038
-
-
Broussy, S.1
Coppel, Y.2
Nguyen, M.3
Bernadou, J.4
Meunier, B.5
-
61
-
-
34447336119
-
Synthesis of 4-phenoxybenzamide adenine dinucleotide as NAD analogue with inhibitory activity against enoyl-ACP reductase (InhA) of Mycobacterium tuberculosis
-
Bonnac, L.; Gao, G.Y.; Chen, L.; Felczak, K.; Bennett, E.M.; Xu, H.; Kim, T.; Liu, N.; Oh, H.; Tonge, P.J.; Pankiewicz, K.W. Synthesis of 4-phenoxybenzamide adenine dinucleotide as NAD analogue with inhibitory activity against enoyl-ACP reductase (InhA) of Mycobacterium tuberculosis. Bioorg. Med. Chem. Lett., 2007, 17, 4588-91.
-
(2007)
Bioorg. Med. Chem. Lett
, vol.17
, pp. 4588-4591
-
-
Bonnac, L.1
Gao, G.Y.2
Chen, L.3
Felczak, K.4
Bennett, E.M.5
Xu, H.6
Kim, T.7
Liu, N.8
Oh, H.9
Tonge, P.J.10
Pankiewicz, K.W.11
-
62
-
-
0029894336
-
Chemical synthesis of benzamide adenine dinucleotide: Inhibition of inosine monophosphate dehydrogenase (types I and II)
-
Zatorski, A.; Watanabe, K.A.; Carr, S.F.; Goldstein, B.M.; Pankiewicz, K.W. Chemical synthesis of benzamide adenine dinucleotide: inhibition of inosine monophosphate dehydrogenase (types I and II). J. Med. Chem., 1996, 39, 2422-6.
-
(1996)
J. Med. Chem
, vol.39
, pp. 2422-2426
-
-
Zatorski, A.1
Watanabe, K.A.2
Carr, S.F.3
Goldstein, B.M.4
Pankiewicz, K.W.5
-
63
-
-
0030907934
-
The practical synthesis of a methylenebisphosphonate analogue of benzamide adenine dinucleotide: Inhibition of human inosine monophosphate dehydrogenase (type I and II)
-
Pankiewicz, K.W.; Lesiak, K.; Zatorski, A.; Goldstein, B.M.; Carr, S.F.; Sochacki, M.; Majumdar, A.; Seidman, M.; Watanabe, K.A. The practical synthesis of a methylenebisphosphonate analogue of benzamide adenine dinucleotide: inhibition of human inosine monophosphate dehydrogenase (type I and II). J. Med. Chem., 1997, 40, 1287-91.
-
(1997)
J. Med. Chem
, vol.40
, pp. 1287-1291
-
-
Pankiewicz, K.W.1
Lesiak, K.2
Zatorski, A.3
Goldstein, B.M.4
Carr, S.F.5
Sochacki, M.6
Majumdar, A.7
Seidman, M.8
Watanabe, K.A.9
-
64
-
-
0037204010
-
Novel mycophenolic adenine bis(phosphonate) analogues as potential differentiation agents against human leukemia
-
Pankiewicz, K.W.; Lesiak-Watanabe, K.B.; Watanabe, K.A.; Patterson, S.E.; Jayaram, H.N.; Yalowitz, J.A.; Miller, M.D.; Seidman, M.; Majumdar, A.; Prehna, G.; Goldstein, B.M. Novel mycophenolic adenine bis(phosphonate) analogues as potential differentiation agents against human leukemia. J. Med. Chem., 2002, 45, 703-12.
-
(2002)
J. Med. Chem
, vol.45
, pp. 703-712
-
-
Pankiewicz, K.W.1
Lesiak-Watanabe, K.B.2
Watanabe, K.A.3
Patterson, S.E.4
Jayaram, H.N.5
Yalowitz, J.A.6
Miller, M.D.7
Seidman, M.8
Majumdar, A.9
Prehna, G.10
Goldstein, B.M.11
-
65
-
-
0032490937
-
Triclosan targets lipid synthesis
-
McMurry, L.M.; Oethinger, M.; Levy, S.B. Triclosan targets lipid synthesis. Nature, 1998, 394, 531-2.
-
(1998)
Nature
, vol.394
, pp. 531-532
-
-
McMurry, L.M.1
Oethinger, M.2
Levy, S.B.3
-
66
-
-
0033607650
-
Crystallographic analysis of triclosan bound to enoyl reductase
-
Roujeinikova, A.; Levy, C.W.; Rowsell, S.; Sedelnikova, S.; Baker, P.J.; Minshull, C.A.; Mistry, A.; Colls, J.G.; Camble, R.; Stuitje, A.R.; Slabas, A.R.; Rafferty, J.B.; Pauptit, R.A.; Viner, R.; Rice, D.W. Crystallographic analysis of triclosan bound to enoyl reductase. J. Mol. Biol., 1999, 294, 527-35.
-
(1999)
J. Mol. Biol
, vol.294
, pp. 527-535
-
-
Roujeinikova, A.1
Levy, C.W.2
Rowsell, S.3
Sedelnikova, S.4
Baker, P.J.5
Minshull, C.A.6
Mistry, A.7
Colls, J.G.8
Camble, R.9
Stuitje, A.R.10
Slabas, A.R.11
Rafferty, J.B.12
Pauptit, R.A.13
Viner, R.14
Rice, D.W.15
-
67
-
-
0033119057
-
Molecular basis of triclosan activity
-
Levy, C.W.; Roujeinikova, A.; Sedelnikova, S.; Baker, P.J.; Stuitje, A.R.; Slabas, A.R.; Rice, D.W.; Rafferty, J.B. Molecular basis of triclosan activity. Nature, 1999, 398, 383-4.
-
(1999)
Nature
, vol.398
, pp. 383-384
-
-
Levy, C.W.1
Roujeinikova, A.2
Sedelnikova, S.3
Baker, P.J.4
Stuitje, A.R.5
Slabas, A.R.6
Rice, D.W.7
Rafferty, J.B.8
-
68
-
-
0033592365
-
Kinetic and structural characteristics of the inhibition of enoyl (acyl carrier protein) reductase by triclosan
-
Ward, W.H.; Holdgate, G.A.; Rowsell, S.; McLean, E.G.; Pauptit, R.A.; Clayton, E.; Nichols, W.W.; Colls, J.G.; Minshull, C.A.; Jude, D.A.; Mistry, A.; Timms, D.; Camble, R.; Hales, N.J.; Britton, C.J.; Taylor, I.W. Kinetic and structural characteristics of the inhibition of enoyl (acyl carrier protein) reductase by triclosan. Biochemistry, 1999, 38, 12514-25.
-
(1999)
Biochemistry
, vol.38
, pp. 12514-12525
-
-
Ward, W.H.1
Holdgate, G.A.2
Rowsell, S.3
McLean, E.G.4
Pauptit, R.A.5
Clayton, E.6
Nichols, W.W.7
Colls, J.G.8
Minshull, C.A.9
Jude, D.A.10
Mistry, A.11
Timms, D.12
Camble, R.13
Hales, N.J.14
Britton, C.J.15
Taylor, I.W.16
-
69
-
-
0033574422
-
Mechanism of triclosan inhibition of bacterial fatty acid synthesis
-
Heath, R.J.; Rubin, J.R.; Holland, D.R.; Zhang, E.; Snow, M.E.; Rock, C.O. Mechanism of triclosan inhibition of bacterial fatty acid synthesis. J. Biol. Chem., 1999, 274, 11110-4.
-
(1999)
J. Biol. Chem
, vol.274
, pp. 11110-11114
-
-
Heath, R.J.1
Rubin, J.R.2
Holland, D.R.3
Zhang, E.4
Snow, M.E.5
Rock, C.O.6
-
70
-
-
38949097460
-
Inhibitors of FabI, an enzyme drug target in the bacterial fatty acid biosynthesis pathway
-
Lu, H.; Tonge, P.J. Inhibitors of FabI, an enzyme drug target in the bacterial fatty acid biosynthesis pathway. Acc. Chem. Res., 2008, 41, 11-20.
-
(2008)
Acc. Chem. Res
, vol.41
, pp. 11-20
-
-
Lu, H.1
Tonge, P.J.2
-
71
-
-
0030452311
-
A mechanism of drug action revealed by structural studies of enoyl reductase
-
Baldock, C.; Rafferty, J.B.; Sedelnikova, S.E.; Baker, P.J.; Stuitje, A.R.; Slabas, A.R.; Hawkes, T.R.; Rice, D.W. A mechanism of drug action revealed by structural studies of enoyl reductase. Science, 1996, 274, 2107-10.
-
(1996)
Science
, vol.274
, pp. 2107-2110
-
-
Baldock, C.1
Rafferty, J.B.2
Sedelnikova, S.E.3
Baker, P.J.4
Stuitje, A.R.5
Slabas, A.R.6
Hawkes, T.R.7
Rice, D.W.8
-
72
-
-
0035946935
-
A study of the structure-activity relationship for diazaborine inhibition of Escherichia coli enoyl-ACP reductase
-
Levy, C.W.; Baldock, C.; Wallace, A.J.; Sedelnikova, S.; Viner, R.C.; Clough, J.M.; Stuitje, A.R.; Slabas, A.R.; Rice, D.W.; Rafferty, J.B. A study of the structure-activity relationship for diazaborine inhibition of Escherichia coli enoyl-ACP reductase. J. Mol. Biol., 2001, 309, 171-80.
-
(2001)
J. Mol. Biol
, vol.309
, pp. 171-180
-
-
Levy, C.W.1
Baldock, C.2
Wallace, A.J.3
Sedelnikova, S.4
Viner, R.C.5
Clough, J.M.6
Stuitje, A.R.7
Slabas, A.R.8
Rice, D.W.9
Rafferty, J.B.10
-
73
-
-
33750036420
-
Novel diphenyl ethers: Design, docking studies, synthesis and inhibition of enoyl ACP reductase of Plasmodium falciparum and Escherichia coli
-
Chhibber, M.; Kumar, G.; Parasuraman, P.; Ramya, T.N.; Surolia, N.; Surolia, A. Novel diphenyl ethers: design, docking studies, synthesis and inhibition of enoyl ACP reductase of Plasmodium falciparum and Escherichia coli. Bioorg. Med. Chem., 2006, 14, 8086-98.
-
(2006)
Bioorg. Med. Chem
, vol.14
, pp. 8086-8098
-
-
Chhibber, M.1
Kumar, G.2
Parasuraman, P.3
Ramya, T.N.4
Surolia, N.5
Surolia, A.6
-
74
-
-
0037130227
-
Discovery of aminopyridine-based inhibitors of bacterial enoyl-ACP reductase (FabI)
-
Miller, W.H.; Seefeld, M.A.; Newlander, K.A.; Uzinskas, I.N.; Burgess, W.J.; Heerding, D.A.; Yuan, C.C.K.; Head, M.S.; Payne, D.J.; Rittenhouse, S.F.; Moore, T.D.; Pearson, S.C.; Berry, V.; DeWolf, W.E., Jr.; Keller, P.M.; Polizzi, B.J.; Qiu, X.; Janson, C.A.; Huffman, W.F. Discovery of aminopyridine-based inhibitors of bacterial enoyl-ACP reductase (FabI). J. Med. Chem., 2002, 45, 3246-56.
-
(2002)
J. Med. Chem
, vol.45
, pp. 3246-3256
-
-
Miller, W.H.1
Seefeld, M.A.2
Newlander, K.A.3
Uzinskas, I.N.4
Burgess, W.J.5
Heerding, D.A.6
Yuan, C.C.K.7
Head, M.S.8
Payne, D.J.9
Rittenhouse, S.F.10
Moore, T.D.11
Pearson, S.C.12
Berry, V.13
Dewolf Jr., W.E.14
Keller, P.M.15
Polizzi, B.J.16
Qiu, X.17
Janson, C.A.18
Huffman, W.F.19
-
75
-
-
17944379321
-
Inhibitors of bacterial enoyl acyl carrier protein reductase (FabI): 2,9-disubstituted 1,2,3,4-tetrahydropyrido[3,4-b]indoles as potential antibacterial agents
-
Seefeld, M.A.; Miller, W.H.; Newlander, K.A.; Burgess, W.J.; Payne, D.J.; Rittenhouse, S.F.; Moore, T.D.; DeWolf, W.E., Jr.; Keller, P.M.; Qiu, X.; Janson, C.A.; Vaidya, K.; Fosberry, A.P.; Smyth, M.G.; Jaworski, D.D.; Slater-Radosti, C.; Huffman, W.F. Inhibitors of bacterial enoyl acyl carrier protein reductase (FabI): 2,9-disubstituted 1,2,3,4-tetrahydropyrido[3,4-b]indoles as potential antibacterial agents. Bioorg. Med. Chem. Lett., 2001, 11, 2241-4.
-
(2001)
Bioorg. Med. Chem. Lett
, vol.11
, pp. 2241-2244
-
-
Seefeld, M.A.1
Miller, W.H.2
Newlander, K.A.3
Burgess, W.J.4
Payne, D.J.5
Rittenhouse, S.F.6
Moore, T.D.7
Dewolf Jr., W.E.8
Keller, P.M.9
Qiu, X.10
Janson, C.A.11
Vaidya, K.12
Fosberry, A.P.13
Smyth, M.G.14
Jaworski, D.D.15
Slater-Radosti, C.16
Huffman, W.F.17
-
76
-
-
0037464456
-
Indole naphthyridinones as inhibitors of bacterial enoyl-ACP reductases FabI and FabK
-
Seefeld, M.A.; Miller, W.H.; Newlander, K.A.; Burgess, W.J.; DeWolf, W.E., Jr.; Elkins, P.A.; Head, M.S.; Jakas, D.R.; Janson, C.A.; Keller, P.M.; Manley, P.J.; Moore, T.D.; Payne, D.J.; Pearson, S.; Polizzi, B.J.; Qiu, X.; Rittenhouse, S.F.; Uzinskas, I.N.; Wallis, N.G.; Huffman, W.F. Indole naphthyridinones as inhibitors of bacterial enoyl-ACP reductases FabI and FabK. J. Med. Chem., 2003, 46, 1627-35.
-
(2003)
J. Med. Chem
, vol.46
, pp. 1627-1635
-
-
Seefeld, M.A.1
Miller, W.H.2
Newlander, K.A.3
Burgess, W.J.4
Dewolf Jr., W.E.5
Elkins, P.A.6
Head, M.S.7
Jakas, D.R.8
Janson, C.A.9
Keller, P.M.10
Manley, P.J.11
Moore, T.D.12
Payne, D.J.13
Pearson, S.14
Polizzi, B.J.15
Qiu, X.16
Rittenhouse, S.F.17
Uzinskas, I.N.18
Wallis, N.G.19
Huffman, W.F.20
more..
-
77
-
-
0036783668
-
Discovery of a novel and potent class of FabI-directed antibacterial agents
-
Payne, D.J.; Miller, W.H.; Berry, V.; Brosky, J.; Burgess, W.J.; Chen, E.; DeWolf Jr, W.E., Jr.; Fosberry, A.P.; Greenwood, R.; Head, M.S.; Heerding, D.A.; Janson, C.A.; Jaworski, D.D.; Keller, P.M.; Manley, P.J.; Moore, T.D.; Newlander, K.A.; Pearson, S.; Polizzi, B.J.; Qiu, X.; Rittenhouse, S.F.; Slater-Radosti, C.; Salyers, K.L.; Seefeld, M.A.; Smyth, M.G.; Takata, D.T.; Uzinskas, I.N.; Vaidya, K.; Wallis, N.G.; Winram, S.B.; Yuan, C.C.; Huffman, W.F. Discovery of a novel and potent class of FabI-directed antibacterial agents. Antimicrob. Agents Chemother., 2002, 46, 3118-24.
-
(2002)
Antimicrob. Agents Chemother
, vol.46
, pp. 3118-3124
-
-
Payne, D.J.1
Miller, W.H.2
Berry, V.3
Brosky, J.4
Burgess, W.J.5
Chen, E.6
Dewolf Jr., W.E.7
Fosberry, A.P.8
Greenwood, R.9
Head, M.S.10
Heerding, D.A.11
Janson, C.A.12
Jaworski, D.D.13
Keller, P.M.14
Manley, P.J.15
Moore, T.D.16
Newlander, K.A.17
Pearson, S.18
Polizzi, B.J.19
Qiu, X.20
Rittenhouse, S.F.21
Slater-Radosti, C.22
Salyers, K.L.23
Seefeld, M.A.24
Smyth, M.G.25
Takata, D.T.26
Uzinskas, I.N.27
Vaidya, K.28
Wallis, N.G.29
Winram, S.B.30
Yuan, C.C.31
Huffman, W.F.32
more..
-
78
-
-
34848874500
-
CG400462, a new bacterial enoyl-acyl carrier protein reductase (FabI) inhibitor
-
Park, H.S.; Yoon, Y.M.; Jung, S.J.; Yun, I.N.; Kim, C.M.; Kim, J.M.; Kwak, J.H. CG400462, a new bacterial enoyl-acyl carrier protein reductase (FabI) inhibitor. Int. J. Antimicrob. Agents, 2007, 30, 446-51.
-
(2007)
Int. J. Antimicrob. Agents
, vol.30
, pp. 446-451
-
-
Park, H.S.1
Yoon, Y.M.2
Jung, S.J.3
Yun, I.N.4
Kim, C.M.5
Kim, J.M.6
Kwak, J.H.7
-
79
-
-
11144356444
-
Identification and characterization of inhibitors of bacterial enoyl-acyl carrier protein reductase
-
Ling, L.L.; Xian, J.; Ali, S.; Geng, B.; Fan, J.; Mills, D.M.; Arvanites, A.C.; Orgueira, H.; Ashwell, M.A.; Carmel, G.; Xiang, Y.; Moir, D.T. Identification and characterization of inhibitors of bacterial enoyl-acyl carrier protein reductase. Antimicrob. Agents Chemother., 2004, 48, 1541-7.
-
(2004)
Antimicrob. Agents Chemother
, vol.48
, pp. 1541-1547
-
-
Ling, L.L.1
Xian, J.2
Ali, S.3
Geng, B.4
Fan, J.5
Mills, D.M.6
Arvanites, A.C.7
Orgueira, H.8
Ashwell, M.A.9
Carmel, G.10
Xiang, Y.11
Moir, D.T.12
-
80
-
-
33845298658
-
4-Pyridone derivatives as new inhibitors of bacterial enoyl-ACP reductase FabI
-
Kitagawa, H.; Kumura, K.; Takahata, S.; Iida, M.; Atsumi, K. 4-Pyridone derivatives as new inhibitors of bacterial enoyl-ACP reductase FabI. Bioorg. Med. Chem., 2007, 15, 1106-16.
-
(2007)
Bioorg. Med. Chem
, vol.15
, pp. 1106-1116
-
-
Kitagawa, H.1
Kumura, K.2
Takahata, S.3
Iida, M.4
Atsumi, K.5
-
81
-
-
34447263022
-
In vitro activities of CG400549, a novel FabI inhibitor, against recently isolated clinical staphylococcal strains in Korea
-
Yum, J.H.; Kim, C.K.; Yong, D.; Lee, K.; Chong, Y.; Kim, C.M.; Kim, J.M.; Ro, S.; Cho, J.M. In vitro activities of CG400549, a novel FabI inhibitor, against recently isolated clinical staphylococcal strains in Korea. Antimicrob. Agents Chemother., 2007, 51, 2591-3.
-
(2007)
Antimicrob. Agents Chemother
, vol.51
, pp. 2591-2593
-
-
Yum, J.H.1
Kim, C.K.2
Yong, D.3
Lee, K.4
Chong, Y.5
Kim, C.M.6
Kim, J.M.7
Ro, S.8
Cho, J.M.9
-
82
-
-
0033055847
-
Genetic evidence that InhA of Mycobacterium smegmatis is a target for triclosan
-
McMurry, L.M.; McDermott, P.F.; Levy, S.B. Genetic evidence that InhA of Mycobacterium smegmatis is a target for triclosan. Antimicrob. Agents Chemother., 1999, 43, 711-3.
-
(1999)
Antimicrob. Agents Chemother
, vol.43
, pp. 711-713
-
-
McMurry, L.M.1
McDermott, P.F.2
Levy, S.B.3
-
83
-
-
0040017633
-
Crystal structure of the Mycobacterium tuberculosis enoyl-ACP reductase, InhA, in complex with NAD+ and a C16 fatty acyl substrate
-
Rozwarski, D.A.; Vilcheze, C.; Sugantino, M.; Bittman, R.; Sacchettini, J.C. Crystal structure of the Mycobacterium tuberculosis enoyl-ACP reductase, InhA, in complex with NAD+ and a C16 fatty acyl substrate. J. Biol. Chem., 1999, 274, 15582-9.
-
(1999)
J. Biol. Chem
, vol.274
, pp. 15582-15589
-
-
Rozwarski, D.A.1
Vilcheze, C.2
Sugantino, M.3
Bittman, R.4
Sacchettini, J.C.5
-
84
-
-
33750048012
-
High affinity InhA inhibitors with activity against drug-resistant strains of Mycobacterium tuberculosis
-
Sullivan, T.J.; Truglio, J.J.; Boyne, M.E.; Novichenok, P.; Zhang, X.; Stratton, C.F.; Li, H.J.; Kaur, T.; Amin, A.; Johnson, F.; Slayden, R.A.; Kisker, C.; Tonge, P.J. High affinity InhA inhibitors with activity against drug-resistant strains of Mycobacterium tuberculosis. ACS. Chem. Biol., 2006, 1, 43-53.
-
(2006)
ACS. Chem. Biol
, vol.1
, pp. 43-53
-
-
Sullivan, T.J.1
Truglio, J.J.2
Boyne, M.E.3
Novichenok, P.4
Zhang, X.5
Stratton, C.F.6
Li, H.J.7
Kaur, T.8
Amin, A.9
Johnson, F.10
Slayden, R.A.11
Kisker, C.12
Tonge, P.J.13
-
85
-
-
0037461276
-
Structure-activity studies of the inhibition of FabI, the enoyl reductase from Escherichia coli, by triclosan: Kinetic analysis of mutant FabIs
-
Sivaraman, S.; Zwahlen, J.; Bell, A.F.; Hedstrom, L.; Tonge, P.J. Structure-activity studies of the inhibition of FabI, the enoyl reductase from Escherichia coli, by triclosan: kinetic analysis of mutant FabIs. Biochemistry, 2003, 42, 4406-13.
-
(2003)
Biochemistry
, vol.42
, pp. 4406-4413
-
-
Sivaraman, S.1
Zwahlen, J.2
Bell, A.F.3
Hedstrom, L.4
Tonge, P.J.5
-
86
-
-
34948861094
-
Targeting fatty acid biosynthesis for the development of novel chemotherapeutics against Mycobacterium tuberculosis: Evaluation of A-ring-modified diphenyl ethers as highaffinity InhA inhibitors
-
Boyne, M.E.; Sullivan, T.J.; amEnde, C.W.; Lu, H.; Gruppo, V.; Heaslip, D.; Amin, A.G.; Chatterjee, D.; Lenaerts, A.; Tonge, P.J.; Slayden, R.A. Targeting fatty acid biosynthesis for the development of novel chemotherapeutics against Mycobacterium tuberculosis: evaluation of A-ring-modified diphenyl ethers as highaffinity InhA inhibitors. Antimicrob. Agents Chemother., 2007, 51, 3562-7.
-
(2007)
Antimicrob. Agents Chemother
, vol.51
, pp. 3562-3567
-
-
Boyne, M.E.1
Sullivan, T.J.2
Amende, C.W.3
Lu, H.4
Gruppo, V.5
Heaslip, D.6
Amin, A.G.7
Chatterjee, D.8
Lenaerts, A.9
Tonge, P.J.10
Slayden, R.A.11
-
87
-
-
43549103754
-
Synthesis and in vitro antimycobacterial activity of B-ring modified diaryl ether InhA inhibitors
-
am Ende, C.W.; Kundson, S.E.; Liu, N.; Childs, J.; Sullivan, T.J.; Boyne, M.; Xu, H.; Knudson, D.L.; Johnson, F.; Peloquin, C.A.; Slayden, R.A.; Tonge, P.J. Synthesis and in vitro antimycobacterial activity of B-ring modified diaryl ether InhA inhibitors. Bioorg. Med. Chem. Lett., 2008, 18, 3029-33.
-
(2008)
Bioorg. Med. Chem. Lett
, vol.18
, pp. 3029-3033
-
-
am Ende, C.W.1
Kundson, S.E.2
Liu, N.3
Childs, J.4
Sullivan, T.J.5
Boyne, M.6
Xu, H.7
Knudson, D.L.8
Johnson, F.9
Peloquin, C.A.10
Slayden, R.A.11
Tonge, P.J.12
-
88
-
-
60149091036
-
Synthesis, antitubercular activity and docking study of novel cyclic azole substituted diphenyl ether derivatives
-
Kini, S.G.; Bhat, A.R.; Bryant, B.; Williamson, J.S.; Dayan, F.E. Synthesis, antitubercular activity and docking study of novel cyclic azole substituted diphenyl ether derivatives. Eur. J. Med. Chem., 2009, 44, 492-500.
-
(2009)
Eur. J. Med. Chem
, vol.44
, pp. 492-500
-
-
Kini, S.G.1
Bhat, A.R.2
Bryant, B.3
Williamson, J.S.4
Dayan, F.E.5
-
89
-
-
0142119368
-
Rapid diversity-oriented synthesis in microtiter plates for in situ screening: Discovery of potent and selective alpha-fucosidase inhibitors
-
Wu, C.Y.; Chang, C.F.; Chen, J.S.; Wong, C.H.; Lin, C.H. Rapid diversity-oriented synthesis in microtiter plates for in situ screening: discovery of potent and selective alpha-fucosidase inhibitors. Angew. Chem. Int. Ed. Engl., 2003, 42, 4661-4.
-
(2003)
Angew. Chem. Int. Ed. Engl
, vol.42
, pp. 4661-4664
-
-
Wu, C.Y.1
Chang, C.F.2
Chen, J.S.3
Wong, C.H.4
Lin, C.H.5
-
90
-
-
0001684124
-
Some 4-Aryl-4,5,6,7-tetrahydroimidazo[4,5-c]pyridines Derived from Histamine
-
Stocker, F.B.; Fordice, M.W.; Larson, J.K.; Thorstenson, J.H. Some 4-Aryl-4,5,6,7-tetrahydroimidazo[4,5-c]pyridines Derived from Histamine. J. Org. Chem., 1966, 31, 2380-3.
-
(1966)
J. Org. Chem
, vol.31
, pp. 2380-2383
-
-
Stocker, F.B.1
Fordice, M.W.2
Larson, J.K.3
Thorstenson, J.H.4
-
91
-
-
0025310708
-
Synthesis of 6-aryl-4,5-dibenzamido-1,2,3,6-tetrahydropyridines
-
Stocker, F.B.; Evans, A.J. Synthesis of 6-aryl-4,5-dibenzamido-1,2,3,6-tetrahydropyridines. J. Org. Chem., 1990, 55, 3370-3.
-
(1990)
J. Org. Chem
, vol.55
, pp. 3370-3373
-
-
Stocker, F.B.1
Evans, A.J.2
-
92
-
-
50349087804
-
CoMFA based de novo design of pyrrolidine carboxamides as inhibitors of enoyl acyl carrier protein reductase from Mycobacterium tuberculosis
-
Kumar, A.; Siddiqi, M.I. CoMFA based de novo design of pyrrolidine carboxamides as inhibitors of enoyl acyl carrier protein reductase from Mycobacterium tuberculosis. J. Mol. Model., 2008, 14, 923-35.
-
(2008)
J. Mol. Model
, vol.14
, pp. 923-935
-
-
Kumar, A.1
Siddiqi, M.I.2
-
93
-
-
54249105397
-
Structure-based design of a novel class of potent inhibitors of InhA, the enoyl acyl carrier protein reductase from Mycobacterium tuberculosis: A computer modelling approach
-
Subba Rao, G.; Vijayakrishnan, R.; Kumar, M. Structure-based design of a novel class of potent inhibitors of InhA, the enoyl acyl carrier protein reductase from Mycobacterium tuberculosis: a computer modelling approach. Chem. Biol. Drug Des., 2008, 72, 444-9.
-
(2008)
Chem. Biol. Drug Des
, vol.72
, pp. 444-449
-
-
Subba, R.G.1
Vijayakrishnan, R.2
Kumar, M.3
-
94
-
-
40049105721
-
Essential factors for successful virtual screening
-
Seifert, M.H.; Lang, M. Essential factors for successful virtual screening. Mini-Rev. Med. Chem., 2008, 7, 63-72.
-
(2008)
Mini-Rev. Med. Chem
, vol.7
, pp. 63-72
-
-
Seifert, M.H.1
Lang, M.2
-
96
-
-
0031552362
-
Development and validation of a genetic algorithm for flexible docking
-
Jones, G.; Willett, P.; Glen, R.C.; Leach, A.R.; Taylor, R. Development and validation of a genetic algorithm for flexible docking. J. Mol. Biol., 1997, 267, 727-48.
-
(1997)
J. Mol. Biol
, vol.267
, pp. 727-748
-
-
Jones, G.1
Willett, P.2
Glen, R.C.3
Leach, A.R.4
Taylor, R.5
-
97
-
-
0035289779
-
Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
-
Lipinski, C.A.; Lombardo, F.; Dominy, B.W.; Feeney, P.J. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv. Drug Deliv. Rev., 2001, 46, 3-26.
-
(2001)
Adv. Drug Deliv. Rev
, vol.46
, pp. 3-26
-
-
Lipinski, C.A.1
Lombardo, F.2
Dominy, B.W.3
Feeney, P.J.4
|