-
1
-
-
0028951636
-
The worldwide prevalence of methicillin-resistant Staphylococcus aureus
-
Voss, A.; Doebbeling, S. N. The worldwide prevalence of methicillin-resistant Staphylococcus aureus. Int. J. Antimicrob. Agents 1995, 5, 101-106.
-
(1995)
Int. J. Antimicrob. Agents
, vol.5
, pp. 101-106
-
-
Voss, A.1
Doebbeling, S.N.2
-
2
-
-
0033847734
-
The millennium bugs - The need for and development of new antibacterials
-
Bax, R.; Mullan, N.; Verhoef, J. The millennium bugs - The need for and development of new antibacterials. Int. J. Antimicrob. Agents 2000, 16 (1), 51-9.
-
(2000)
Int. J. Antimicrob. Agents
, vol.16
, Issue.1
, pp. 51-59
-
-
Bax, R.1
Mullan, N.2
Verhoef, J.3
-
3
-
-
0030923633
-
Current approaches to overcome bacterial resistance
-
Setti, E. L.; Quattrocchio, L.; Micetich, R. G. Current approaches to overcome bacterial resistance. Drugs Future 1997, 22, 271-284.
-
(1997)
Drugs Future
, vol.22
, pp. 271-284
-
-
Setti, E.L.1
Quattrocchio, L.2
Micetich, R.G.3
-
4
-
-
0036682463
-
Superbug' hurdles key drug barrier
-
Pearson, H. 'Superbug' hurdles key drug barrier. Nature 2002, 418, 469.
-
(2002)
Nature
, vol.418
, pp. 469
-
-
Pearson, H.1
-
6
-
-
0037339233
-
Novel antibacterial agents for the treatment of serious Gram-positive infections
-
Abbanat, D.; Macielag, M.; Bish, K. Novel antibacterial agents for the treatment of serious Gram-positive infections, Expert Opin. Invest. Drugs 2003, 12, 379-399.
-
(2003)
Expert Opin. Invest. Drugs
, vol.12
, pp. 379-399
-
-
Abbanat, D.1
Macielag, M.2
Bish, K.3
-
8
-
-
0035338328
-
Bacterial fatty-acid biosynthesis: A genomics-driven target for antibacterial drug discovery
-
Payne, D. J.; Warren, P. V.; Holmes, D. J.; Ji, Y.; Lonsdale, J. T. Bacterial fatty-acid biosynthesis: A genomics-driven target for antibacterial drug discovery. Drug Discovery Today 2001, 6 (10), 537-544.
-
(2001)
Drug Discovery Today
, vol.6
, Issue.10
, pp. 537-544
-
-
Payne, D.J.1
Warren, P.V.2
Holmes, D.J.3
Ji, Y.4
Lonsdale, J.T.5
-
9
-
-
0034804919
-
Lipid biosynthesis as a target for antibacterial agents
-
Heath, R. J.; White, S. W.; Rock, C. O. 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
-
10
-
-
0034780806
-
Bacterial fatty acid biosynthesis: Targets for antibacterial drug discovery
-
Campbell, J. W.; Cronan, J. E., Jr. Bacterial fatty acid biosynthesis: Targets for antibacterial drug discovery. Annu. Rev. Microbiol. 2001, 55, 305-32.
-
(2001)
Annu. Rev. Microbiol
, vol.55
, pp. 305-332
-
-
Campbell, J.W.1
Cronan Jr., J.E.2
-
11
-
-
0347065345
-
β-Ketoacyl-acyl carrier protein synthase III (FabH) is essential for bacterial fatty acid synthesis
-
Lai, C.-Y.; Cronan, J. E. β-Ketoacyl-acyl carrier protein synthase III (FabH) is essential for bacterial fatty acid synthesis. J. Biol. Chem. 2003, 278 (51), 51494-51503.
-
(2003)
J. Biol. Chem
, vol.278
, Issue.51
, pp. 51494-51503
-
-
Lai, C.-Y.1
Cronan, J.E.2
-
12
-
-
0035025631
-
-
Revill, W. P.; Bibb, M. J.; Scheu, A.-K.; Kieser, H. J.; Hopwood, D. A. β-Ketoacyl acyl carrier protein synthase III (FabH) is essential for fatty acid biosynthesis in Streptomyces coelicolor A3(2). J. Bacteriol. 2001, 183 (11), 3526-3530.
-
Revill, W. P.; Bibb, M. J.; Scheu, A.-K.; Kieser, H. J.; Hopwood, D. A. β-Ketoacyl acyl carrier protein synthase III (FabH) is essential for fatty acid biosynthesis in Streptomyces coelicolor A3(2). J. Bacteriol. 2001, 183 (11), 3526-3530.
-
-
-
-
13
-
-
0035026139
-
Response of Bacillus subtilis to cerulenin and acquisition of resistance
-
Schujman, G. E.; Choi, K.-H.; Altabe, S.; Rock, C. O.; Mendoza, D. DE. Response of Bacillus subtilis to cerulenin and acquisition of resistance. J. Bacteriol. 2001, 183 (10), 3032-40.
-
(2001)
J. Bacteriol
, vol.183
, Issue.10
, pp. 3032-3040
-
-
Schujman, G.E.1
Choi, K.-H.2
Altabe, S.3
Rock, C.O.4
Mendoza, D.D.5
-
14
-
-
0036952586
-
β-Ketoacyl acyl carrier protein reductase (FabG) activity of the fatty acid biosynthetic pathway is a determining factor of 3-oxo-homoserine lactone acyl chain lengths
-
Hoang, T. T.; Sullivan, S. A.; Cusick, J. K.; Schweizer, H. P. β-Ketoacyl acyl carrier protein reductase (FabG) activity of the fatty acid biosynthetic pathway is a determining factor of 3-oxo-homoserine lactone acyl chain lengths. Microbiol. 2002, 148, 3849-3856.
-
(2002)
Microbiol
, vol.148
, pp. 3849-3856
-
-
Hoang, T.T.1
Sullivan, S.A.2
Cusick, J.K.3
Schweizer, H.P.4
-
15
-
-
33744819176
-
Inhibition of Plasmodium falciparum fatty acid biosynthesis: Evaluation of FabG, FabZ, and FabI as drug targets for flavonoids
-
Tasdemir, D.; Lack, G.; Brun, R. Rüedi, P.; Scapozza, L.; Perozzo, R. Inhibition of Plasmodium falciparum fatty acid biosynthesis: Evaluation of FabG, FabZ, and FabI as drug targets for flavonoids. J. Med. Chem. 2006, 49 (17), 3345-3353.
-
(2006)
J. Med. Chem
, vol.49
, Issue.17
, pp. 3345-3353
-
-
Tasdemir, D.1
Lack, G.2
Brun, R.3
Rüedi, P.4
Scapozza, L.5
Perozzo, R.6
-
16
-
-
10644295401
-
The structure of (3R)-hydroxyacyl-acyl carrier protein dehydratase (FabZ) from Pseudomonas aeruginosa
-
Kimber, M. S.; Martin, F.; Lu, Y.; Houston, S.; Vedadi, M.; Dharamsi, A.; Fiebig, K. M.; Schmid, M.; Rock, C. O. The structure of (3R)-hydroxyacyl-acyl carrier protein dehydratase (FabZ) from Pseudomonas aeruginosa. J. Biol. Chem. 2004, 279 (50), 52593-52602.
-
(2004)
J. Biol. Chem
, vol.279
, Issue.50
, pp. 52593-52602
-
-
Kimber, M.S.1
Martin, F.2
Lu, Y.3
Houston, S.4
Vedadi, M.5
Dharamsi, A.6
Fiebig, K.M.7
Schmid, M.8
Rock, C.O.9
-
17
-
-
4544303329
-
Functional replacement of the FabA and FabB proteins of Escherichia coli fatty acid synthesis by Enterococcus faecalis FabZ and FabF homologues
-
Wang, H.; Cronan, J. E. Functional replacement of the FabA and FabB proteins of Escherichia coli fatty acid synthesis by Enterococcus faecalis FabZ and FabF homologues. J. Biol. Chem. 2004, 279 (33), 34489-34495.
-
(2004)
J. Biol. Chem
, vol.279
, Issue.33
, pp. 34489-34495
-
-
Wang, H.1
Cronan, J.E.2
-
18
-
-
0030431493
-
The enoyl-[acyl-carrier-protein] reductase (FabI) of Escherichia coli, which catalyzes a key regulatory step in fatty acid biosynthesis, accepts NADH and NADPH as cofactors and is inhibited by palmitoyl-CoA
-
Bergler, H.; Fuchsbichler, S.; Högenauer, G.; Turnowsky, F. The enoyl-[acyl-carrier-protein] reductase (FabI) of Escherichia coli, which catalyzes a key regulatory step in fatty acid biosynthesis, accepts NADH and NADPH as cofactors and is inhibited by palmitoyl-CoA. Eur. J. Biochem. 1996, 242, 689-694.
-
(1996)
Eur. J. Biochem
, vol.242
, pp. 689-694
-
-
Bergler, H.1
Fuchsbichler, S.2
Högenauer, G.3
Turnowsky, F.4
-
19
-
-
0034681329
-
Inhibition of the Staphylococcus aureus NADPH-dependent enoyl-acyl carrier protein reductase by triclosan and hexachlorophene
-
Heath, R. J.; Li, J.; Roland, G. E.; Rock, C. O. Inhibition of the Staphylococcus aureus NADPH-dependent enoyl-acyl carrier protein reductase by triclosan and hexachlorophene. J. Biol. Chem. 2000, 275 (7), 4654-4659.
-
(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
-
20
-
-
0030033704
-
Regulation of fatty acid elongation and initiation by acyl-acyl carrier protein in Escherichia coli
-
Heath, R. J.; Rock, C. O. Regulation of fatty acid elongation and initiation by acyl-acyl carrier protein in Escherichia coli. J. Biol. Chem. 1996, 271 (4), 1833-1836.
-
(1996)
J. Biol. Chem
, vol.271
, Issue.4
, pp. 1833-1836
-
-
Heath, R.J.1
Rock, C.O.2
-
21
-
-
17544367317
-
Inhibition of β-ketoacyl-acyl carrier protein synthase III (FabH) by acyl-acyl carrier protein in Escherichia coli
-
Heath, R. J.; Rock, C. O. Inhibition of β-ketoacyl-acyl carrier protein synthase III (FabH) by acyl-acyl carrier protein in Escherichia coli. J. Biol. Chem. 1996, 271 (18), 10996-11000.
-
(1996)
J. Biol. Chem
, vol.271
, Issue.18
, pp. 10996-11000
-
-
Heath, R.J.1
Rock, C.O.2
-
22
-
-
0028070318
-
Protein envM is the NADH-dependent enoyl-ACP reductase fabI of Escherichia coli
-
Bergler, H.; Wallner, P.; Ebeling, A.; leitinger, B.; Fuchsbichler, S.; Aschauer, H.; Kollenz, G.; Högenauer, G.; Turnowsky, F. Protein envM is the NADH-dependent enoyl-ACP reductase fabI of Escherichia coli. J. Biol. Chem. 1994, 269, 5493-5496.
-
(1994)
J. Biol. Chem
, vol.269
, pp. 5493-5496
-
-
Bergler, H.1
Wallner, P.2
Ebeling, A.3
leitinger, B.4
Fuchsbichler, S.5
Aschauer, H.6
Kollenz, G.7
Högenauer, G.8
Turnowsky, F.9
-
23
-
-
0028855972
-
Enoyl-acyl carrier protein reductase (fabI) plays a determinant role in completing cycles of fatty acid elongation in Escherichia coli
-
Heath, R. J.; Rock, C. O. Enoyl-acyl carrier protein reductase (fabI) plays a determinant role in completing cycles of fatty acid elongation in Escherichia coli. J. Biol. Chem. 1995, 270, 26538-26542.
-
(1995)
J. Biol. Chem
, vol.270
, pp. 26538-26542
-
-
Heath, R.J.1
Rock, C.O.2
-
24
-
-
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 (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
-
25
-
-
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 (5295), 2107-10.
-
(1996)
Science
, vol.274
, Issue.5295
, 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
-
26
-
-
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 (1), 171-80.
-
(2001)
J. Mol. Biol
, vol.309
, Issue.1
, 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
-
27
-
-
0032490937
-
Triclosan targets lipid synthesis
-
McMurry, L. M.; Oethinger, M.; Levy, S. B. Triclosan targets lipid synthesis. Nature 1998, 394 (6693), 531-532.
-
(1998)
Nature
, vol.394
, Issue.6693
, pp. 531-532
-
-
McMurry, L.M.1
Oethinger, M.2
Levy, S.B.3
-
28
-
-
0032515066
-
Broad spectrum antimicrobial biocides target the FabI component of fatty acid synthesis
-
Heath, R. J.; Yu, Y.-T.; Shapiro, M. A.; Olson, E.; Rock, C. O. Broad spectrum antimicrobial biocides target the FabI component of fatty acid synthesis. J. Biol. Chem. 1998, 273, 30316-30320.
-
(1998)
J. Biol. Chem
, vol.273
, pp. 30316-30320
-
-
Heath, R.J.1
Yu, Y.-T.2
Shapiro, M.A.3
Olson, E.4
Rock, C.O.5
-
29
-
-
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 (6726), 383-384.
-
(1999)
Nature
, vol.398
, Issue.6726
, 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
-
30
-
-
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, 711-713.
-
(1999)
Antimicrob. Agents. Chemother
, vol.43
, pp. 711-713
-
-
McMurry, L.M.1
McDermott, P.F.2
Levy, S.B.3
-
31
-
-
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 (38), 12514-25.
-
(1999)
Biochemistry
, vol.38
, Issue.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
-
32
-
-
0032775211
-
Structural basis and mechanism of enoyl reductase inhibition by triclosan
-
Stewart, M. J.; Parikh, S.; Xiao, G.; Tonge, P. J.; Kisker, C. Structural basis and mechanism of enoyl reductase inhibition by triclosan. J. Mol. Biol. 1999, 290 (4), 859-865.
-
(1999)
J. Mol. Biol
, vol.290
, Issue.4
, pp. 859-865
-
-
Stewart, M.J.1
Parikh, S.2
Xiao, G.3
Tonge, P.J.4
Kisker, C.5
-
33
-
-
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 (9), 1627-1635.
-
(2003)
J. Med. Chem
, vol.46
, Issue.9
, 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..
-
34
-
-
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.; 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 (15), 3246-3256.
-
(2002)
J. Med. Chem
, vol.45
, Issue.15
, 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.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
-
35
-
-
17944379321
-
-
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 (17), 2241-2244.
-
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 (17), 2241-2244.
-
-
-
-
36
-
-
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 (5), 1541-1547.
-
(2004)
Antimicrob. Agents. Chemother
, vol.48
, Issue.5
, 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
-
37
-
-
0034644010
-
A triclosan-resistant bacterial enzyme
-
Heath, R. J.; Rock, C. O. A triclosan-resistant bacterial enzyme. Nature 2000, 406 (6792), 145-6.
-
(2000)
Nature
, vol.406
, Issue.6792
, pp. 145-146
-
-
Heath, R.J.1
Rock, C.O.2
-
38
-
-
0037444822
-
Characterization of Streptococcus pneumoniae enoyl-(acyl-carrier protein) reductase (FabK)
-
Marrakchi, H.; Dewolf, W. E., Jr.; Quinn, C.; West, J.; Polizzi, B. J.; So, C. Y.; Holmes, D. J.; Reed, S. L.; Heath, R. J.; Payne, D. J.; Rock, C. O.; Wallis, N. G. Characterization of Streptococcus pneumoniae enoyl-(acyl-carrier protein) reductase (FabK). Biochem. J. 2003, 370, 1055-62.
-
(2003)
Biochem. J
, vol.370
, pp. 1055-1062
-
-
Marrakchi, H.1
Dewolf Jr., W.E.2
Quinn, C.3
West, J.4
Polizzi, B.J.5
So, C.Y.6
Holmes, D.J.7
Reed, S.L.8
Heath, R.J.9
Payne, D.J.10
Rock, C.O.11
Wallis, N.G.12
-
39
-
-
0036783668
-
-
Payne, D. J.; Miller, W. H.; Berry, V.; Brosky, J.; Burgess, W. J.; Chen, E.; DeWolf, W. E.; Jr, Fosberry, A. P., Jr.; 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 (10), 3118-24.
-
Payne, D. J.; Miller, W. H.; Berry, V.; Brosky, J.; Burgess, W. J.; Chen, E.; DeWolf, W. E.; Jr, Fosberry, A. P., Jr.; 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 (10), 3118-24.
-
-
-
-
40
-
-
33845298658
-
4-Pyridone derivatives as new inhibitors of bacterial enoyl-ACP reductase Fabl
-
Kitagawa, H.; Kumura, K.; Takahata, S.; Iida, M.; Atsumi, K. 4-Pyridone derivatives as new inhibitors of bacterial enoyl-ACP reductase Fabl. Bioorg. Med. Chem. 2007, 15, 1106-1116.
-
(2007)
Bioorg. Med. Chem
, vol.15
, pp. 1106-1116
-
-
Kitagawa, H.1
Kumura, K.2
Takahata, S.3
Iida, M.4
Atsumi, K.5
-
41
-
-
34547553734
-
Phenylimidazole derivatives as new inhibitors of bacterial enoyl-ACP reductase FabK
-
in press
-
Kitagawa, H.; Ozawa, T.; Takahata, S.; Iida, M. Phenylimidazole derivatives as new inhibitors of bacterial enoyl-ACP reductase FabK. Bioorg. Med Chem. Lett. 2007, in press.
-
(2007)
Bioorg. Med Chem. Lett
-
-
Kitagawa, H.1
Ozawa, T.2
Takahata, S.3
Iida, M.4
-
42
-
-
33746892678
-
-
Takahata, S.; Iida, M; Osaki, Y.; Saito, J.; Kitagawa, H.; Ozawa, T.; Yoshida, T., Hoshiko, S. AG205, a novel agent directed against FabK of Streptococcus pneumoniae. Antimicrob. Agents. Chemother. 2006, 50 (8), 2869-2871.
-
Takahata, S.; Iida, M; Osaki, Y.; Saito, J.; Kitagawa, H.; Ozawa, T.; Yoshida, T., Hoshiko, S. AG205, a novel agent directed against FabK of Streptococcus pneumoniae. Antimicrob. Agents. Chemother. 2006, 50 (8), 2869-2871.
-
-
-
-
43
-
-
33745127323
-
Crystallization and preliminary X-ray analysis of enoyl-acyl carrier protein reductase (FabK) from Streptococcus pneumoniae
-
Saito, J.; Yamada, M.; Watanabe, T.; Kitagawa, H.; Takeuchi, Y. Crystallization and preliminary X-ray analysis of enoyl-acyl carrier protein reductase (FabK) from Streptococcus pneumoniae. Acta Crystallogr. 2006, F62, 576-578.
-
(2006)
Acta Crystallogr
, vol.F62
, pp. 576-578
-
-
Saito, J.1
Yamada, M.2
Watanabe, T.3
Kitagawa, H.4
Takeuchi, Y.5
-
44
-
-
33749348168
-
A novel synthesis of 2,3-disubstituted-4-pyridones from 4-methoxypyridine
-
Kitagawa, H.; Kumura, K.; Atsumi, K. A novel synthesis of 2,3-disubstituted-4-pyridones from 4-methoxypyridine. Chem. Lett. 2006, 35, 712.
-
(2006)
Chem. Lett
, vol.35
, pp. 712
-
-
Kitagawa, H.1
Kumura, K.2
Atsumi, K.3
-
45
-
-
34249739592
-
Discovery of 4-pyridone derivatives as specific inhibitors of enoyl-acyl carrier protein reductase (FabI) with antibacterial activity against Staphylococcus aureus
-
Takahata, S.; Iida, M.; Yoshida, T.; Kumura, K.; Kitagawa, H.; Hoshiko, S. Discovery of 4-pyridone derivatives as specific inhibitors of enoyl-acyl carrier protein reductase (FabI) with antibacterial activity against Staphylococcus aureus. J. Antibiot. (Tokyo). 2007, 60, 123-128.
-
(2007)
J. Antibiot. (Tokyo)
, vol.60
, pp. 123-128
-
-
Takahata, S.1
Iida, M.2
Yoshida, T.3
Kumura, K.4
Kitagawa, H.5
Hoshiko, S.6
|