-
1
-
-
84874427385
-
-
Global Tuberculosis Report 2012, World Health Organization. (accessed January 22, 2013
-
Global Tuberculosis Report 2012, World Health Organization. http://apps.who.int/iris/bitstream/10665/75938/1/9789241564502-eng.pdf. (accessed January 22, 2013.
-
-
-
-
2
-
-
84874408991
-
-
Multidrug-Resistant Tuberculosis (MDR-TB), 2012 Update, World Health Organization. (accessed January 22, 2013
-
Multidrug-Resistant Tuberculosis (MDR-TB), 2012 Update, World Health Organization. http://www.who.int/tb/publications/MDRFactSheet2012.pdf (accessed January 22, 2013.
-
-
-
-
3
-
-
79251589638
-
The challenge of new drug discovery for tuberculosis
-
Koul, A.; Arnoult, E.; Lounis, N.; Guillemont, J.; Andries, K. The challenge of new drug discovery for tuberculosis Nature 2011, 469, 483-490
-
(2011)
Nature
, vol.469
, pp. 483-490
-
-
Koul, A.1
Arnoult, E.2
Lounis, N.3
Guillemont, J.4
Andries, K.5
-
4
-
-
50449104247
-
Developing new drugs for the treatment of drug-resistant tuberculosis: A regulatory perspective
-
Sacks, L. V.; Behrman, R. E. Developing new drugs for the treatment of drug-resistant tuberculosis: a regulatory perspective Tuberculosis 2008, 88, S93-100
-
(2008)
Tuberculosis
, vol.88
, pp. 93-100
-
-
Sacks, L.V.1
Behrman, R.E.2
-
5
-
-
77955331963
-
Syntheses and herbicidal activity of new triazolopyrimidine-2- sulfonamides as acetohydroxyacid synthase inhibitor
-
Chen, C. N.; Chen, Q.; Liu, Y. C.; Zhu, X. L.; Niu, C. W.; Xi, Z.; Yang, G. F. Syntheses and herbicidal activity of new triazolopyrimidine-2-sulfonamides as acetohydroxyacid synthase inhibitor Bioorg. Med. Chem. 2010, 18, 4897-4904
-
(2010)
Bioorg. Med. Chem.
, vol.18
, pp. 4897-4904
-
-
Chen, C.N.1
Chen, Q.2
Liu, Y.C.3
Zhu, X.L.4
Niu, C.W.5
Xi, Z.6
Yang, G.F.7
-
6
-
-
77952366796
-
Computational determination of fundamental pathway and activation barriers for acetohydroxyacid synthase-catalyzed condensation reactions of alpha-keto acids
-
Xiong, Y.; Liu, J.; Yang, G. F.; Zhan, C. G. Computational determination of fundamental pathway and activation barriers for acetohydroxyacid synthase-catalyzed condensation reactions of alpha-keto acids J. Comput. Chem. 2010, 31, 1592-1602
-
(2010)
J. Comput. Chem.
, vol.31
, pp. 1592-1602
-
-
Xiong, Y.1
Liu, J.2
Yang, G.F.3
Zhan, C.G.4
-
7
-
-
64049113738
-
Design and synthesis of N-2,6-difluorophenyl-5-methoxyl-1,2,4-triazolo[1, 5-a]-pyrimidine-2-sulfonamide as acetohydroxyacid synthase inhibitor
-
Chen, C. N.; Lv, L. L.; Ji, F. Q.; Chen, Q.; Xu, H.; Niu, C. W.; Xi, Z.; Yang, G. F. Design and synthesis of N-2,6-difluorophenyl-5-methoxyl-1,2,4- triazolo[1,5-a]-pyrimidine-2-sulfonamide as acetohydroxyacid synthase inhibitor Bioorg. Med. Chem. 2009, 17, 3011-3017
-
(2009)
Bioorg. Med. Chem.
, vol.17
, pp. 3011-3017
-
-
Chen, C.N.1
Lv, L.L.2
Ji, F.Q.3
Chen, Q.4
Xu, H.5
Niu, C.W.6
Xi, Z.7
Yang, G.F.8
-
8
-
-
54449099215
-
Computational design and discovery of conformationally flexible inhibitors of acetohydroxyacid synthase to overcome drug resistance associated with the W586L mutation
-
Ji, F. Q.; Niu, C. W.; Chen, C. N.; Chen, Q.; Yang, G. F.; Xi, Z.; Zhan, C. G. Computational design and discovery of conformationally flexible inhibitors of acetohydroxyacid synthase to overcome drug resistance associated with the W586L mutation ChemMedChem 2008, 3, 1203-1206
-
(2008)
ChemMedChem
, vol.3
, pp. 1203-1206
-
-
Ji, F.Q.1
Niu, C.W.2
Chen, C.N.3
Chen, Q.4
Yang, G.F.5
Xi, Z.6
Zhan, C.G.7
-
9
-
-
37249033641
-
Rational design based on bioactive conformation analysis of pyrimidinylbenzoates as acetohydroxyacid synthase inhibitors by integrating molecular docking, CoMFA, CoMSIA, and DFT calculations
-
He, Y. Z.; Li, Y. X.; Zhu, X. L.; Xi, Z.; Niu, C.; Wan, J.; Zhang, L.; Yang, G. F. Rational design based on bioactive conformation analysis of pyrimidinylbenzoates as acetohydroxyacid synthase inhibitors by integrating molecular docking, CoMFA, CoMSIA, and DFT calculations J. Chem. Inf. Model. 2007, 47, 2335-2244
-
(2007)
J. Chem. Inf. Model.
, vol.47
, pp. 2335-2244
-
-
He, Y.Z.1
Li, Y.X.2
Zhu, X.L.3
Xi, Z.4
Niu, C.5
Wan, J.6
Zhang, L.7
Yang, G.F.8
-
10
-
-
33845678081
-
Design and syntheses of novel phthalazin-1(2H)-one derivatives as acetohydroxyacid synthase inhibitors
-
Li, Y. X.; Luo, Y. P.; Xi, Z.; Niu, C.; He, Y. Z.; Yang, G. F. Design and syntheses of novel phthalazin-1(2H)-one derivatives as acetohydroxyacid synthase inhibitors J. Agric. Food Chem. 2006, 54, 9135-9139
-
(2006)
J. Agric. Food Chem.
, vol.54
, pp. 9135-9139
-
-
Li, Y.X.1
Luo, Y.P.2
Xi, Z.3
Niu, C.4
He, Y.Z.5
Yang, G.F.6
-
11
-
-
33748543237
-
Development of a general quantum-chemical descriptor for steric effects: Density functional theory based QSAR study of herbicidal sulfonylurea analogues
-
Xi, Z.; Yu, Z.; Niu, C.; Ban, S.; Yang, G. Development of a general quantum-chemical descriptor for steric effects: Density functional theory based QSAR study of herbicidal sulfonylurea analogues J. Comput. Chem. 2006, 27, 1571-1576
-
(2006)
J. Comput. Chem.
, vol.27
, pp. 1571-1576
-
-
Xi, Z.1
Yu, Z.2
Niu, C.3
Ban, S.4
Yang, G.5
-
12
-
-
0033451875
-
QSAR and 3D-QSAR analysis of structurally diverse ALS inhibitors: Sulfonylureas and triazolopyrimidine-2-sulfonamides
-
Yang, G.; Liu, H.; Yang, H. QSAR and 3D-QSAR analysis of structurally diverse ALS inhibitors: Sulfonylureas and triazolopyrimidine-2-sulfonamides Pestic. Sci. 1999, 55, 1143-1150
-
(1999)
Pestic. Sci.
, vol.55
, pp. 1143-1150
-
-
Yang, G.1
Liu, H.2
Yang, H.3
-
13
-
-
0031718499
-
Inhibitors of branched-chain amino acid biosynthesis as potential antituberculosis agents
-
Grandoni, J. A.; Marta, P. T.; Schloss, J. V. Inhibitors of branched-chain amino acid biosynthesis as potential antituberculosis agents J. Antimicrob. Chemother. 1998, 42, 475-482
-
(1998)
J. Antimicrob. Chemother.
, vol.42
, pp. 475-482
-
-
Grandoni, J.A.1
Marta, P.T.2
Schloss, J.V.3
-
14
-
-
78650758054
-
Biochemical and transcription analysis of acetohydroxyacid synthase isoforms in Mycobacterium tuberculosis identifies these enzymes as potential targets for drug development
-
Singh, V.; Chandra, D.; Srivastava, B. S.; Srivastava, R. Biochemical and transcription analysis of acetohydroxyacid synthase isoforms in Mycobacterium tuberculosis identifies these enzymes as potential targets for drug development Microbiology 2011, 157, 29-37
-
(2011)
Microbiology
, vol.157
, pp. 29-37
-
-
Singh, V.1
Chandra, D.2
Srivastava, B.S.3
Srivastava, R.4
-
15
-
-
0032537483
-
Biosynthesis of 2-aceto-2-hydroxy acids: Acetolactate synthases and acetohydroxyacid synthases
-
Chipman, D.; Barak, Z.; Schloss, J. V. Biosynthesis of 2-aceto-2-hydroxy acids: Acetolactate synthases and acetohydroxyacid synthases Biochim. Biophys. Acta 1998, 1385, 401-419
-
(1998)
Biochim. Biophys. Acta
, vol.1385
, pp. 401-419
-
-
Chipman, D.1
Barak, Z.2
Schloss, J.V.3
-
17
-
-
37049182338
-
Acetolactate synthase is the site of action of two sulfonylurea herbicides in higher plants
-
Chaleff, R. S.; Mauvais, C. J. Acetolactate synthase is the site of action of two sulfonylurea herbicides in higher plants Science 1984, 224, 1443-1445
-
(1984)
Science
, vol.224
, pp. 1443-1445
-
-
Chaleff, R.S.1
Mauvais, C.J.2
-
18
-
-
84957869700
-
Imidazolinones: Potent inhibitors of acetohydroxyacid synthase
-
Shaner, D. L; Anderson, P. C.; Stidham, M. A. Imidazolinones: potent inhibitors of acetohydroxyacid synthase Plant Physiol. 1984, 76, 545-546
-
(1984)
Plant Physiol.
, vol.76
, pp. 545-546
-
-
Shaner, D.L.1
Anderson, P.C.2
Stidham, M.A.3
-
19
-
-
43549126424
-
In vitro and ex vivo activity of new derivatives of acetohydroxyacid synthase inhibitors against Mycobacterium tuberculosis and non-tuberculous mycobacteria
-
Sohn, H.; Lee, K. S.; Ko, Y. K.; Ryu, J. W.; Woo, J. C.; Koo, D. W.; Shin, S. J.; Ahn, S. J.; Shin, A. R.; Song, C. H.; Jo, E. K.; Park, J. K.; Kim, H. J. In vitro and ex vivo activity of new derivatives of acetohydroxyacid synthase inhibitors against Mycobacterium tuberculosis and non-tuberculous mycobacteria Int. J. Antimicrob. Agents 2008, 31, 567-571
-
(2008)
Int. J. Antimicrob. Agents
, vol.31
, pp. 567-571
-
-
Sohn, H.1
Lee, K.S.2
Ko, Y.K.3
Ryu, J.W.4
Woo, J.C.5
Koo, D.W.6
Shin, S.J.7
Ahn, S.J.8
Shin, A.R.9
Song, C.H.10
Jo, E.K.11
Park, J.K.12
Kim, H.J.13
-
20
-
-
24044548711
-
Characterization of acetohydroxyacid synthase from Mycobacterium tuberculosis and the identification of its new inhibitor from the screening of a chemical library
-
Choi, K. J.; Yu, Y. G.; Hahn, H. G.; Choi, J. D.; Yoon, M. Y. Characterization of acetohydroxyacid synthase from Mycobacterium tuberculosis and the identification of its new inhibitor from the screening of a chemical library FEBS Lett. 2005, 579, 4903-4910
-
(2005)
FEBS Lett.
, vol.579
, pp. 4903-4910
-
-
Choi, K.J.1
Yu, Y.G.2
Hahn, H.G.3
Choi, J.D.4
Yoon, M.Y.5
-
21
-
-
0043123259
-
Acetohydroxyacid synthase from Mycobacterium avium and its inhibition by sulfonylureas and imidazolinones
-
Zohar, Y.; Einav, M.; Chipman, D. M.; Barak, Z. Acetohydroxyacid synthase from Mycobacterium avium and its inhibition by sulfonylureas and imidazolinones Biochim. Biophys. Acta 2003, 1649, 97-105
-
(2003)
Biochim. Biophys. Acta
, vol.1649
, pp. 97-105
-
-
Zohar, Y.1
Einav, M.2
Chipman, D.M.3
Barak, Z.4
-
22
-
-
84862822242
-
Synthesis and evaluation of novel monosubstituted sulfonylurea derivatives as antituberculosis agents
-
Pan, L.; Jiang, Y.; Liu, Z.; Liu, X. H.; Wang, G.; Li, Z. M.; Wang, D. Synthesis and evaluation of novel monosubstituted sulfonylurea derivatives as antituberculosis agents Eur. J. Med. Chem. 2012, 50, 18-26
-
(2012)
Eur. J. Med. Chem.
, vol.50
, pp. 18-26
-
-
Pan, L.1
Jiang, Y.2
Liu, Z.3
Liu, X.H.4
Wang, G.5
Li, Z.M.6
Wang, D.7
-
23
-
-
49649083784
-
Molecular modelling of Mycobacterium tuberculosis acetolactate synthase catalytic subunit and its molecular docking study with inhibitors
-
Souza, T. C. S.; Josa, D.; Ramalho, T. C.; Caetano, M. S.; da Cunha, E. F. F. Molecular modelling of Mycobacterium tuberculosis acetolactate synthase catalytic subunit and its molecular docking study with inhibitors Mol. Simulat. 2008, 34, 707-713
-
(2008)
Mol. Simulat.
, vol.34
, pp. 707-713
-
-
Souza, T.C.S.1
Josa, D.2
Ramalho, T.C.3
Caetano, M.S.4
Da Cunha, E.F.F.5
-
24
-
-
0037470165
-
Molecular basis of sulfonylurea herbicide inhibition of acetohydroxyacid synthase
-
Pang, S. S.; Guddat, L. W.; Duggleby, R. G. Molecular basis of sulfonylurea herbicide inhibition of acetohydroxyacid synthase J. Biol. Chem. 2003, 278, 7639-7644
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 7639-7644
-
-
Pang, S.S.1
Guddat, L.W.2
Duggleby, R.G.3
-
25
-
-
0000243829
-
PROCHECK: A program to check the stereochemical quality of protein structures
-
Laskowski, R. A.; MacArthur, M. W.; Moss, D. S.; Thornton, J. M. PROCHECK: A program to check the stereochemical quality of protein structures J. App. Cryst. 1993, 26, 283-291
-
(1993)
J. App. Cryst.
, vol.26
, pp. 283-291
-
-
Laskowski, R.A.1
MacArthur, M.W.2
Moss, D.S.3
Thornton, J.M.4
-
26
-
-
34547566446
-
ProSA-web: Interactive web service for the recognition of errors in three-dimensional structures of proteins
-
Wiederstein, M.; Sippl, M. J. ProSA-web: interactive web service for the recognition of errors in three-dimensional structures of proteins Nucleic Acids Res. 2007, 35, W407-410
-
(2007)
Nucleic Acids Res.
, vol.35
, pp. 407-410
-
-
Wiederstein, M.1
Sippl, M.J.2
-
27
-
-
0032212916
-
Mutagenesis of Escherichia coli acetohydroxyacid synthase isoenzyme II and characterization of three herbicide-insensitive forms
-
Hill, C. M.; Duggleby, R. G. Mutagenesis of Escherichia coli acetohydroxyacid synthase isoenzyme II and characterization of three herbicide-insensitive forms Biochem. J. 1998, 335, 653-661
-
(1998)
Biochem. J.
, vol.335
, pp. 653-661
-
-
Hill, C.M.1
Duggleby, R.G.2
-
28
-
-
77957726864
-
Prevalence of multidrug and extensively drug-resistant tuberculosis in Beijing, China: A hospital-based retrospective study
-
Wang, D.; Yang, C.; Kuang, T.; Lei, H.; Meng, X.; Tong, A.; He, J. F.; Jiang, Y.; Guo, F.; Dong, M. Prevalence of multidrug and extensively drug-resistant tuberculosis in Beijing, China: A hospital-based retrospective study Jpn. J. Infect. Dis. 2010, 63, 368-371
-
(2010)
Jpn. J. Infect. Dis.
, vol.63
, pp. 368-371
-
-
Wang, D.1
Yang, C.2
Kuang, T.3
Lei, H.4
Meng, X.5
Tong, A.6
He, J.F.7
Jiang, Y.8
Guo, F.9
Dong, M.10
-
29
-
-
0021195869
-
The sulfonylurea herbicide sulfometuron methyl is an extremely potent and selective inhibitor of acetolactate synthase in Salmonella typhimurium
-
LaRossa, R. A.; Schloss, J. V. The sulfonylurea herbicide sulfometuron methyl is an extremely potent and selective inhibitor of acetolactate synthase in Salmonella typhimurium J. Biol. Chem. 1984, 259, 8753-8757
-
(1984)
J. Biol. Chem.
, vol.259
, pp. 8753-8757
-
-
Larossa, R.A.1
Schloss, J.V.2
-
30
-
-
33747135959
-
Acetohydroxyacid synthase and its role in the biosynthetic pathway for branched-chain amino acids
-
McCourt, J. A.; Duggleby, R. G. Acetohydroxyacid synthase and its role in the biosynthetic pathway for branched-chain amino acids Amino Acids 2006, 31, 173-210
-
(2006)
Amino Acids
, vol.31
, pp. 173-210
-
-
McCourt, J.A.1
Duggleby, R.G.2
-
31
-
-
69949184894
-
Inactivation of the ilvB1 gene in Mycobacterium tuberculosis leads to branched-chain amino acid auxotrophy and attenuation of virulence in mice
-
Awasthy, D.; Gaonkar, S.; Shandil, R. K.; Yadav, R.; Bharath, S.; Marcel, N.; Subbulakshmi, V.; Sharma, U. Inactivation of the ilvB1 gene in Mycobacterium tuberculosis leads to branched-chain amino acid auxotrophy and attenuation of virulence in mice Microbiology 2009, 155, 2978-2987
-
(2009)
Microbiology
, vol.155
, pp. 2978-2987
-
-
Awasthy, D.1
Gaonkar, S.2
Shandil, R.K.3
Yadav, R.4
Bharath, S.5
Marcel, N.6
Subbulakshmi, V.7
Sharma, U.8
-
32
-
-
0028922586
-
LIGPLOT: A program to generate schematic diagrams of protein-ligand interactions
-
Wallace, A. C.; Laskowski, R. A.; Thornton, J. M. LIGPLOT: A program to generate schematic diagrams of protein-ligand interactions Protein Eng. 1995, 8, 127-134
-
(1995)
Protein Eng.
, vol.8
, pp. 127-134
-
-
Wallace, A.C.1
Laskowski, R.A.2
Thornton, J.M.3
-
33
-
-
0027968068
-
CLUSTAL W: Improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice
-
Thompson, J. D.; Higgins, D. G.; Gibson, T. J. CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice Nucleic Acids Res. 1994, 22, 4673-4680
-
(1994)
Nucleic Acids Res.
, vol.22
, pp. 4673-4680
-
-
Thompson, J.D.1
Higgins, D.G.2
Gibson, T.J.3
-
34
-
-
33644580916
-
-
version 2005; Accelrys: San Diego, CA
-
Insight II, version 2005; Accelrys: San Diego, CA, 2005.
-
(2005)
Insight II
-
-
-
35
-
-
84874439054
-
-
version 6.8; Tripos Associates: St. Louis, MO
-
SYBYL, version 6.8; Tripos Associates: St. Louis, MO, 2001.
-
(2001)
SYBYL
-
-
-
36
-
-
0029011701
-
A second generation force field for the simulation of proteins, nucleic acids, and organic molecules
-
Cornell, W. D.; Cieplak, P.; Bayly, C. I.; Gould, I. R.; Merz, K. M.; Ferguson, D. M.; Spellmeyer, D. C.; Fox, T.; Caldwell, J. W.; Kollman, P. A. A second generation force field for the simulation of proteins, nucleic acids, and organic molecules J. Am. Chem. Soc. 1995, 117, 5179-5197
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 5179-5197
-
-
Cornell, W.D.1
Cieplak, P.2
Bayly, C.I.3
Gould, I.R.4
Merz, K.M.5
Ferguson, D.M.6
Spellmeyer, D.C.7
Fox, T.8
Caldwell, J.W.9
Kollman, P.A.10
-
37
-
-
84874449692
-
-
version 7.5.112; Schrödinger: Portland, OR
-
Maestro, version 7.5.112; Schrödinger: Portland, OR, 2000.
-
(2000)
Maestro
-
-
-
38
-
-
33750991346
-
Benchmarking sets for molecular docking
-
Huang, N.; Shoichet, B. K.; Irwin, J. J. Benchmarking sets for molecular docking J. Med. Chem. 2006, 49, 6789-6801
-
(2006)
J. Med. Chem.
, vol.49
, pp. 6789-6801
-
-
Huang, N.1
Shoichet, B.K.2
Irwin, J.J.3
-
39
-
-
37249062877
-
-
version 2.1; Accelrys: San Diego, CA
-
Discovery Studio, version 2.1; Accelrys: San Diego, CA, 2008.
-
(2008)
Discovery Studio
-
-
-
40
-
-
12944249776
-
A discussion of the solution for the best rotation to relate two sets of vectors
-
Kabsch, W. A discussion of the solution for the best rotation to relate two sets of vectors Acta Crystallogr. 1978, A34, 827-828
-
(1978)
Acta Crystallogr.
, vol.34
, pp. 827-828
-
-
Kabsch, W.1
-
41
-
-
0034663485
-
Mutagenesis studies on the sensitivity of Escherichia coli acetohydroxyacid synthase II to herbicides and valine
-
Lee, Y. T.; Duggleby, R. G. Mutagenesis studies on the sensitivity of Escherichia coli acetohydroxyacid synthase II to herbicides and valine Biochem. J. 2000, 350, 69-73
-
(2000)
Biochem. J.
, vol.350
, pp. 69-73
-
-
Lee, Y.T.1
Duggleby, R.G.2
-
42
-
-
33644504841
-
Structure-activity relationships for a new family of sulfonylurea herbicides
-
Wang, J. G.; Li, Z. M.; Ma, N.; Wang, B. L.; Jiang, L.; Pang, S. S.; Lee, Y. T.; Guddat, L. W.; Duggleby, R. G. Structure-activity relationships for a new family of sulfonylurea herbicides J. Comput.-Aided Mol. Des. 2005, 19, 801-820
-
(2005)
J. Comput.-Aided Mol. Des.
, vol.19
, pp. 801-820
-
-
Wang, J.G.1
Li, Z.M.2
Ma, N.3
Wang, B.L.4
Jiang, L.5
Pang, S.S.6
Lee, Y.T.7
Guddat, L.W.8
Duggleby, R.G.9
-
43
-
-
84874438430
-
-
version 1.3r1 edu; DeLano Scientific: Palo Alto, CA
-
PyMOL, version 1.3r1 edu; DeLano Scientific: Palo Alto, CA, 2010.
-
(2010)
PyMOL
-
-
|