-
1
-
-
84884597711
-
-
Centers for Disease Control and Prevention (), CDC, Atlanta, GA. Available Online
-
Centers for Disease Control and Prevention (2013) Antibiotic Resistance Threats in the United States, CDC, Atlanta, GA. Available Online: http://www.cdc.gov/drugresistance/threat-report-2013/pdf/ar-threats-2013-508.pdf.
-
(2013)
Antibiotic Resistance Threats in the United States
-
-
-
2
-
-
78751477224
-
Challenges of antibacterial discovery
-
Silver, L. L. (2011) Challenges of antibacterial discovery Clin. Microbiol. Rev. 24, 71-109
-
(2011)
Clin. Microbiol. Rev.
, vol.24
, pp. 71-109
-
-
Silver, L.L.1
-
3
-
-
34548108138
-
Targeting virulence: A new paradigm for antimicrobial therapy
-
Clatworthy, A. E., Pierson, E., and Hung, D. T. (2007) Targeting virulence: A new paradigm for antimicrobial therapy Nat. Chem. Biol. 3, 541-548
-
(2007)
Nat. Chem. Biol.
, vol.3
, pp. 541-548
-
-
Clatworthy, A.E.1
Pierson, E.2
Hung, D.T.3
-
4
-
-
84863220984
-
Fresh approaches to anti-infective therapies
-
Nathan, C. (2012) Fresh approaches to anti-infective therapies Sci. Transl. Med. 4, 140sr142
-
(2012)
Sci. Transl. Med.
, vol.4
, pp. 140sr142
-
-
Nathan, C.1
-
5
-
-
0033791468
-
Two-component signal transduction
-
Stock, A. M., Robinson, V. L., and Goudreau, P. N. (2000) Two-component signal transduction Annu. Rev. Biochem. 69, 183-215
-
(2000)
Annu. Rev. Biochem.
, vol.69
, pp. 183-215
-
-
Stock, A.M.1
Robinson, V.L.2
Goudreau, P.N.3
-
6
-
-
0025271478
-
Signal transduction in bacteria
-
Stock, J. B., Stock, A. M., and Mottonen, J. M. (1990) Signal transduction in bacteria Nature 344, 395-400
-
(1990)
Nature
, vol.344
, pp. 395-400
-
-
Stock, J.B.1
Stock, A.M.2
Mottonen, J.M.3
-
7
-
-
0033788637
-
Eukaryotic signal transduction via histidine-aspartate phosphorelay
-
Thomason, P. and Kay, R. (2000) Eukaryotic signal transduction via histidine-aspartate phosphorelay J. Cell Sci. 113, 3141-3150
-
(2000)
J. Cell Sci.
, vol.113
, pp. 3141-3150
-
-
Thomason, P.1
Kay, R.2
-
8
-
-
84455173453
-
Adaptation to environmental stimuli within the host: Two-component signal transduction systems of Mycobacterium tuberculosis
-
Bretl, D. J., Demetriadou, C., and Zahrt, T. C. (2011) Adaptation to environmental stimuli within the host: Two-component signal transduction systems of Mycobacterium tuberculosis Microbiol. Mol. Biol. R. 75, 566-582
-
(2011)
Microbiol. Mol. Biol. R.
, vol.75
, pp. 566-582
-
-
Bretl, D.J.1
Demetriadou, C.2
Zahrt, T.C.3
-
9
-
-
77949916499
-
Two-component signal transduction as potential drug targets in pathogenic bacteria
-
Gotoh, Y., Eguchi, Y., Watanabe, T., Okamoto, S., Doi, A., and Utsumi, R. (2010) Two-component signal transduction as potential drug targets in pathogenic bacteria Curr. Opin. Microbiol. 13, 232-239
-
(2010)
Curr. Opin. Microbiol.
, vol.13
, pp. 232-239
-
-
Gotoh, Y.1
Eguchi, Y.2
Watanabe, T.3
Okamoto, S.4
Doi, A.5
Utsumi, R.6
-
10
-
-
0035990926
-
Virulence- and antibiotic resistance-associated two-component signal transduction systems of Gram-positive pathogenic bacteria as targets for antimicrobial therapy
-
Stephenson, K. and Hoch, J. A. (2002) Virulence- and antibiotic resistance-associated two-component signal transduction systems of Gram-positive pathogenic bacteria as targets for antimicrobial therapy Pharmacol. Therapeut. 93, 293-305
-
(2002)
Pharmacol. Therapeut.
, vol.93
, pp. 293-305
-
-
Stephenson, K.1
Hoch, J.A.2
-
11
-
-
0034624047
-
The mechanism of action of inhibitors of bacterial two-component signal transduction systems
-
Stephenson, K., Yamaguchi, Y., and Hoch, J. A. (2000) The mechanism of action of inhibitors of bacterial two-component signal transduction systems J. Biol. Chem. 275, 38900-38904
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 38900-38904
-
-
Stephenson, K.1
Yamaguchi, Y.2
Hoch, J.A.3
-
12
-
-
84892980568
-
Small-molecule inhibition of bacterial two-component systems to combat antibiotic resistance and virulence
-
Worthington, R. J., Blackledge, M. S., and Melander, C. (2013) Small-molecule inhibition of bacterial two-component systems to combat antibiotic resistance and virulence Future Med. Chem. 5, 1265-1284
-
(2013)
Future Med. Chem.
, vol.5
, pp. 1265-1284
-
-
Worthington, R.J.1
Blackledge, M.S.2
Melander, C.3
-
14
-
-
7744220530
-
A signaling network reciprocally regulates genes associated with acute infection and chronic persistence in Pseudomonas aeruginosa
-
Goodman, A. L., Kulasekara, B., Rietsch, A., Boyd, D., Smith, R. S., and Lory, S. (2004) A signaling network reciprocally regulates genes associated with acute infection and chronic persistence in Pseudomonas aeruginosa Dev. Cell 7, 745-754
-
(2004)
Dev. Cell
, vol.7
, pp. 745-754
-
-
Goodman, A.L.1
Kulasekara, B.2
Rietsch, A.3
Boyd, D.4
Smith, R.S.5
Lory, S.6
-
15
-
-
46249116492
-
The GraRS regulatory system controls Staphylococcus aureus susceptibility to antimicrobial host defenses
-
Kraus, D., Herbert, S., Kristian, S. A., Khosravi, A., Nizet, V., Gotz, F., and Peschel, A. (2008) The GraRS regulatory system controls Staphylococcus aureus susceptibility to antimicrobial host defenses BMC Microbiol. 8, 85
-
(2008)
BMC Microbiol.
, vol.8
, pp. 85
-
-
Kraus, D.1
Herbert, S.2
Kristian, S.A.3
Khosravi, A.4
Nizet, V.5
Gotz, F.6
Peschel, A.7
-
16
-
-
73549110327
-
A novel signaling network essential for regulating Pseudomonas aeruginosa biofilm development
-
Petrova, O. E. and Sauer, K. (2009) A novel signaling network essential for regulating Pseudomonas aeruginosa biofilm development PLoS Pathog. 5, e1000668
-
(2009)
PLoS Pathog.
, vol.5
, pp. 1000668
-
-
Petrova, O.E.1
Sauer, K.2
-
17
-
-
2342501446
-
Signal transduction cascade between EvgA/EvgS and PhoP/PhoQ two-component systems of Escherichia coli
-
Eguchi, Y., Okada, T., Minagawa, S., Oshima, T., Mori, H., Yamamoto, K., Ishihama, A., and Utsumi, R. (2004) Signal transduction cascade between EvgA/EvgS and PhoP/PhoQ two-component systems of Escherichia coli J. Bacteriol. 186, 3006-3014
-
(2004)
J. Bacteriol.
, vol.186
, pp. 3006-3014
-
-
Eguchi, Y.1
Okada, T.2
Minagawa, S.3
Oshima, T.4
Mori, H.5
Yamamoto, K.6
Ishihama, A.7
Utsumi, R.8
-
18
-
-
0033985080
-
GHKL, an emergent ATPase/kinase superfamily
-
Dutta, R. and Inouye, M. (2000) GHKL, an emergent ATPase/kinase superfamily Trends Biochem. Sci. 25, 24-28
-
(2000)
Trends Biochem. Sci.
, vol.25
, pp. 24-28
-
-
Dutta, R.1
Inouye, M.2
-
19
-
-
42749090538
-
The Hsp90 inhibitor radicicol interacts with the ATP-binding pocket of bacterial sensor kinase PhoQ
-
Guarnieri, M. T., Zhang, L. D., Shen, J. P., and Zhao, R. (2008) The Hsp90 inhibitor radicicol interacts with the ATP-binding pocket of bacterial sensor kinase PhoQ J. Mol. Biol. 379, 82-93
-
(2008)
J. Mol. Biol.
, vol.379
, pp. 82-93
-
-
Guarnieri, M.T.1
Zhang, L.D.2
Shen, J.P.3
Zhao, R.4
-
20
-
-
0032487858
-
NMR structure of the histidine kinase domain of the E. Coli osmosensor EnvZ
-
Tanaka, T., Saha, S. K., Tomomori, C., Ishima, R., Liu, D., Tong, K. I., Park, H., Dutta, R., Qin, L., Swindells, M. B., Yamazaki, T., Ono, A. M., Kainosho, M., Inouye, M., and Ikura, M. (1998) NMR structure of the histidine kinase domain of the E. coli osmosensor EnvZ Nature 396, 88-92
-
(1998)
Nature
, vol.396
, pp. 88-92
-
-
Tanaka, T.1
Saha, S.K.2
Tomomori, C.3
Ishima, R.4
Liu, D.5
Tong, K.I.6
Park, H.7
Dutta, R.8
Qin, L.9
Swindells, M.B.10
Yamazaki, T.11
Ono, A.M.12
Kainosho, M.13
Inouye, M.14
Ikura, M.15
-
21
-
-
0035798570
-
Structural and mutational analysis of the PhoQ histidine kinase catalytic domain. Insight into the reaction mechanism
-
Marina, A., Mott, C., Auyzenberg, A., Hendrickson, W. A., and Waldburger, C. D. (2001) Structural and mutational analysis of the PhoQ histidine kinase catalytic domain. Insight into the reaction mechanism J. Biol. Chem. 276, 41182-41190
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 41182-41190
-
-
Marina, A.1
Mott, C.2
Auyzenberg, A.3
Hendrickson, W.A.4
Waldburger, C.D.5
-
22
-
-
78650662602
-
Structure of the cytoplasmic segment of histidine kinase receptor QseC, a key player in bacterial virulence
-
Xie, W., Dickson, C., Kwiatkowski, W., and Choe, S. (2010) Structure of the cytoplasmic segment of histidine kinase receptor QseC, a key player in bacterial virulence Protein Peptide Lett. 17, 1383-1391
-
(2010)
Protein Peptide Lett.
, vol.17
, pp. 1383-1391
-
-
Xie, W.1
Dickson, C.2
Kwiatkowski, W.3
Choe, S.4
-
23
-
-
84863235693
-
Thiazolidione derivatives targeting the histidine kinase YycG are effective against both planktonic and biofilm-associated Staphylococcus epidermidis
-
Huang, R. Z., Zheng, L. K., Liu, H. Y., Pan, B., Hu, J., Zhu, T., Wang, W., Jiang, D. B., Wu, Y., Wu, Y. C., Han, S. Q., and Qu, D. (2012) Thiazolidione derivatives targeting the histidine kinase YycG are effective against both planktonic and biofilm-associated Staphylococcus epidermidis Acta Pharmacol. Sin. 33, 418-425
-
(2012)
Acta Pharmacol. Sin.
, vol.33
, pp. 418-425
-
-
Huang, R.Z.1
Zheng, L.K.2
Liu, H.Y.3
Pan, B.4
Hu, J.5
Zhu, T.6
Wang, W.7
Jiang, D.B.8
Wu, Y.9
Wu, Y.C.10
Han, S.Q.11
Qu, D.12
-
24
-
-
34447544806
-
Structure-based discovery of inhibitors of the YycG histidine kinase: New chemical leads to combat Staphylococcus epidermidis infections
-
Qin, Z., Zhang, J., Xu, B., Chen, L., Wu, Y., Yang, X., Shen, X., Molin, S., Danchin, A., Jiang, H., and Qu, D. (2006) Structure-based discovery of inhibitors of the YycG histidine kinase: New chemical leads to combat Staphylococcus epidermidis infections BMC Microbiol. 6, 96
-
(2006)
BMC Microbiol.
, vol.6
, pp. 96
-
-
Qin, Z.1
Zhang, J.2
Xu, B.3
Chen, L.4
Wu, Y.5
Yang, X.6
Shen, X.7
Molin, S.8
Danchin, A.9
Jiang, H.10
Qu, D.11
-
25
-
-
68149144249
-
Discovery of novel inhibitors of Streptococcus pneumoniae based on the virtual screening with the homology-modeled structure of histidine kinase (VicK)
-
Li, N., Wang, F., Niu, S., Cao, J., Wu, K., Li, Y., Yin, N., Zhang, X., Zhu, W., and Yin, Y. (2009) Discovery of novel inhibitors of Streptococcus pneumoniae based on the virtual screening with the homology-modeled structure of histidine kinase (VicK) BMC Microbiol. 9, 129
-
(2009)
BMC Microbiol.
, vol.9
, pp. 129
-
-
Li, N.1
Wang, F.2
Niu, S.3
Cao, J.4
Wu, K.5
Li, Y.6
Yin, N.7
Zhang, X.8
Zhu, W.9
Yin, Y.10
-
26
-
-
80051498472
-
The effect of the potential PhoQ histidine kinase inhibitors on Shigella flexneri virulence
-
Cai, X., Zhang, J., Chen, M., Wu, Y., Wang, X., Chen, J., Zhang, J., Shen, X., Qu, D., and Jiang, H. (2011) The effect of the potential PhoQ histidine kinase inhibitors on Shigella flexneri virulence PLoS One 6, e23100
-
(2011)
PLoS One
, vol.6
, pp. 23100
-
-
Cai, X.1
Zhang, J.2
Chen, M.3
Wu, Y.4
Wang, X.5
Chen, J.6
Zhang, J.7
Shen, X.8
Qu, D.9
Jiang, H.10
-
27
-
-
84903608711
-
Efficacy of novel antibacterial compounds targeting histidine kinase YycG protein
-
Liu, H., Zhao, D., Chang, J., Yan, L., Zhao, F., Wu, Y., Xu, T., Gong, T., Chen, L., He, N., Wu, Y., Han, S., and Qu, D. (2014) Efficacy of novel antibacterial compounds targeting histidine kinase YycG protein Appl. Microbiol. Biot. 98, 6003-6013
-
(2014)
Appl. Microbiol. Biot.
, vol.98
, pp. 6003-6013
-
-
Liu, H.1
Zhao, D.2
Chang, J.3
Yan, L.4
Zhao, F.5
Wu, Y.6
Xu, T.7
Gong, T.8
Chen, L.9
He, N.10
Wu, Y.11
Han, S.12
Qu, D.13
-
28
-
-
79953216021
-
Development of an antivirulence drug against Streptococcus mutants: Repression of biofilm formation, acid tolerance, and competence by a histidine kinase inhibitor, Walkmycin C
-
Eguchi, Y., Kubo, N., Matsunaga, H., Igarashi, M., and Utsumi, R. (2011) Development of an antivirulence drug against Streptococcus mutants: Repression of biofilm formation, acid tolerance, and competence by a histidine kinase inhibitor, Walkmycin C Antimicrob. Agents Ch. 55, 1475-1484
-
(2011)
Antimicrob. Agents Ch.
, vol.55
, pp. 1475-1484
-
-
Eguchi, Y.1
Kubo, N.2
Matsunaga, H.3
Igarashi, M.4
Utsumi, R.5
-
29
-
-
28044469003
-
New class of competitive inhibitor of bacterial histidine kinases
-
Gilmour, R., Foster, J. E., Sheng, Q., McClain, J. R., Riley, A., Sun, P. M., Ng, W. L., Yan, D., Nicas, T. I., Henry, K., and Winkler, M. E. (2005) New class of competitive inhibitor of bacterial histidine kinases J. Bacteriol. 187, 8196-8200
-
(2005)
J. Bacteriol.
, vol.187
, pp. 8196-8200
-
-
Gilmour, R.1
Foster, J.E.2
Sheng, Q.3
McClain, J.R.4
Riley, A.5
Sun, P.M.6
Ng, W.L.7
Yan, D.8
Nicas, T.I.9
Henry, K.10
Winkler, M.E.11
-
30
-
-
0033277340
-
The histidine protein kinase superfamily
-
Grebe, T. W. and Stock, J. B. (1999) The histidine protein kinase superfamily Adv. Microb. Physiol. 41, 139-227
-
(1999)
Adv. Microb. Physiol.
, vol.41
, pp. 139-227
-
-
Grebe, T.W.1
Stock, J.B.2
-
31
-
-
0036400593
-
Histidine protein kinases: Key signal transducers outside the animal kingdom
-
Wolanin, P. M., Thomason, P. A., and Stock, J. B. (2002) Histidine protein kinases: Key signal transducers outside the animal kingdom Genome Biol. 3, 3013.1-3013.8
-
(2002)
Genome Biol.
, vol.3
, pp. 30131-30138
-
-
Wolanin, P.M.1
Thomason, P.A.2
Stock, J.B.3
-
32
-
-
70349795241
-
Structural insight into partner specificity and phosphoryl transfer in two-component signal transduction
-
Casino, P., Rubio, V., and Marina, A. (2009) Structural insight into partner specificity and phosphoryl transfer in two-component signal transduction Cell 139, 325-336
-
(2009)
Cell
, vol.139
, pp. 325-336
-
-
Casino, P.1
Rubio, V.2
Marina, A.3
-
33
-
-
29244433095
-
Structure of the entire cytoplasmic portion of a sensor histidine-kinase protein
-
Marina, A., Waldburger, C. D., and Hendrickson, W. A. (2005) Structure of the entire cytoplasmic portion of a sensor histidine-kinase protein EMBO J. 24, 4247-4259
-
(2005)
EMBO J.
, vol.24
, pp. 4247-4259
-
-
Marina, A.1
Waldburger, C.D.2
Hendrickson, W.A.3
-
34
-
-
84861864686
-
Activity-based probe for histidine kinase signaling
-
Wilke, K. E., Francis, S., and Carlson, E. E. (2012) Activity-based probe for histidine kinase signaling J. Am. Chem. Soc. 134, 9150-9153
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 9150-9153
-
-
Wilke, K.E.1
Francis, S.2
Carlson, E.E.3
-
35
-
-
84871747944
-
Mechanistic insight into inhibition of two-component system signaling
-
Francis, S., Wilke, K. E., Brown, D. E., and Carlson, E. E. (2013) Mechanistic insight into inhibition of two-component system signaling Med. Chem. Commun. 269-277
-
(2013)
Med. Chem. Commun.
, pp. 269-277
-
-
Francis, S.1
Wilke, K.E.2
Brown, D.E.3
Carlson, E.E.4
-
36
-
-
77951033959
-
Kinetic characterization of the WalRKSpn (VicRK) two-component system of Streptococcus pneumoniae: Dependence of WalKSpn (VicK) phosphatase activity on its PAS domain
-
Gutu, A. D., Wayne, K. J., Sham, L. T., and Winkler, M. E. (2010) Kinetic characterization of the WalRKSpn (VicRK) two-component system of Streptococcus pneumoniae: Dependence of WalKSpn (VicK) phosphatase activity on its PAS domain J. Bacteriol. 192, 2346-2358
-
(2010)
J. Bacteriol.
, vol.192
, pp. 2346-2358
-
-
Gutu, A.D.1
Wayne, K.J.2
Sham, L.T.3
Winkler, M.E.4
-
37
-
-
79957741036
-
Protein footprinting in a complex milieu: Identifying the interaction surfaces of the chemotaxis adaptor protein CheW
-
Underbakke, E. S., Zhu, Y., and Kiessling, L. L. (2011) Protein footprinting in a complex milieu: Identifying the interaction surfaces of the chemotaxis adaptor protein CheW J. Mol. Biol. 409, 483-495
-
(2011)
J. Mol. Biol.
, vol.409
, pp. 483-495
-
-
Underbakke, E.S.1
Zhu, Y.2
Kiessling, L.L.3
-
38
-
-
55949137666
-
Tearing down the wall: Peptidoglycan metabolism and the WalK/WalR (YycG/YycF) essential two-component system
-
in (Utsumi, R. Ed.), pp, Springer, New York
-
Dubrac, S. and Msadek, T. (2008) Tearing down the wall: Peptidoglycan metabolism and the WalK/WalR (YycG/YycF) essential two-component system, in Bacterial Signal Transduction: Networks and Drug Targets (Utsumi, R., Ed.), pp 214-228, Springer, New York.
-
(2008)
Bacterial Signal Transduction: Networks and Drug Targets
, pp. 214-228
-
-
Dubrac, S.1
Msadek, T.2
-
39
-
-
41949119968
-
Essentiality, bypass, and targeting of the YycFG (VicRK) two-component regulatory system in Gram-positive bacteria
-
Winkler, M. E. and Hoch, J. A. (2008) Essentiality, bypass, and targeting of the YycFG (VicRK) two-component regulatory system in Gram-positive bacteria J. Bacteriol. 190, 2645-2648
-
(2008)
J. Bacteriol.
, vol.190
, pp. 2645-2648
-
-
Winkler, M.E.1
Hoch, J.A.2
-
40
-
-
0035069228
-
Nucleotide binding by the histidine kinase CheA
-
Bilwes, A. M., Quezada, C. M., Croal, L. R., Crane, B. R., and Simon, M. I. (2001) Nucleotide binding by the histidine kinase CheA Nat. Struct. Biol. 8, 353-360
-
(2001)
Nat. Struct. Biol.
, vol.8
, pp. 353-360
-
-
Bilwes, A.M.1
Quezada, C.M.2
Croal, L.R.3
Crane, B.R.4
Simon, M.I.5
-
41
-
-
0032168668
-
TNP-ATP and TNP-ADP as probes of the nucleotide binding site of CheA, the histidine protein kinase in the chemotaxis signal transduction pathway of Escherichia coli
-
Stewart, R. C., VanBruggen, R., Ellefson, D. D., and Wolfe, A. J. (1998) TNP-ATP and TNP-ADP as probes of the nucleotide binding site of CheA, the histidine protein kinase in the chemotaxis signal transduction pathway of Escherichia coli Biochemistry 37, 12269-12279
-
(1998)
Biochemistry
, vol.37
, pp. 12269-12279
-
-
Stewart, R.C.1
Vanbruggen, R.2
Ellefson, D.D.3
Wolfe, A.J.4
-
42
-
-
84893827341
-
Visualizing autophosphorylation in histidine kinases
-
Casino, P., Miguel-Romero, L., and Marina, A. (2014) Visualizing autophosphorylation in histidine kinases Nature Commun. 5, 3258 10.1038/ncomms4258
-
(2014)
Nature Commun.
, vol.5
, pp. 3258
-
-
Casino, P.1
Miguel-Romero, L.2
Marina, A.3
-
43
-
-
0037061628
-
A common mechanism underlying promiscuous inhibitors from virtual and high-throughput screening
-
McGovern, S. L., Caselli, E., Grigorieff, N., and Shoichet, B. K. (2002) A common mechanism underlying promiscuous inhibitors from virtual and high-throughput screening J. Med. Chem. 45, 1712-1722
-
(2002)
J. Med. Chem.
, vol.45
, pp. 1712-1722
-
-
McGovern, S.L.1
Caselli, E.2
Grigorieff, N.3
Shoichet, B.K.4
-
44
-
-
0028097839
-
A controlled trial of riluzole in amyotrophic-lateral-sclerosis
-
Bensimon, G., Lacomblez, L., Meininger, V., Bouche, P., Delwaide, C., Couratier, P., Blin, O., Viader, F., Peyrostpaul, H., David, J., Maloteaux, J. M., Hugon, J., Laterre, E. C., Rascol, A., Clanet, M., Vallat, J. M., Dumas, A., Serratrice, G., Lechevallier, B., Peuch, A. J., Nguyen, T., Shu, C., Bastien, P., Papillon, C., Durrleman, S., Louvel, E., Guillet, P., Ledoux, L., Orvoenfrija, E., and Dib, M. (1994) A controlled trial of riluzole in amyotrophic-lateral-sclerosis N. Engl. J. Med. 330, 585-591
-
(1994)
N. Engl. J. Med.
, vol.330
, pp. 585-591
-
-
Bensimon, G.1
Lacomblez, L.2
Meininger, V.3
Bouche, P.4
Delwaide, C.5
Couratier, P.6
Blin, O.7
Viader, F.8
Peyrostpaul, H.9
David, J.10
Maloteaux, J.M.11
Hugon, J.12
Laterre, E.C.13
Rascol, A.14
Clanet, M.15
Vallat, J.M.16
Dumas, A.17
Serratrice, G.18
Lechevallier, B.19
Peuch, A.J.20
Nguyen, T.21
Shu, C.22
Bastien, P.23
Papillon, C.24
Durrleman, S.25
Louvel, E.26
Guillet, P.27
Ledoux, L.28
Orvoenfrija, E.29
Dib, M.30
more..
-
45
-
-
62749165351
-
Distribution and biological activities of the flavonoid luteolin
-
Lopez-Lázaro, M. (2009) Distribution and biological activities of the flavonoid luteolin Mini-Rev. Med. Chem. 9, 31-59
-
(2009)
Mini-Rev. Med. Chem.
, vol.9
, pp. 31-59
-
-
Lopez-Lázaro, M.1
-
46
-
-
0021351568
-
Novel antibiotic hypersensitive mutants of Escherichia coli. Genetic mapping and chemical characterization
-
Clark, D. (1984) Novel antibiotic hypersensitive mutants of Escherichia coli. Genetic mapping and chemical characterization FEMS Microbiol. Lett. 21, 189-195
-
(1984)
FEMS Microbiol. Lett.
, vol.21
, pp. 189-195
-
-
Clark, D.1
-
47
-
-
0026764121
-
Genistein inhibits protein histidine kinase
-
Huang, J., Nasr, M., Kim, Y., and Matthews, H. R. (1992) Genistein inhibits protein histidine kinase J. Biol. Chem. 267, 15511-15515
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 15511-15515
-
-
Huang, J.1
Nasr, M.2
Kim, Y.3
Matthews, H.R.4
-
48
-
-
84901257251
-
Hsp90 inhibitors: Current development and potential in cancer therapy
-
Sidera, K. and Patsavoudi, E. (2014) Hsp90 inhibitors: Current development and potential in cancer therapy Recent Pat. Anti-Cancer Drug Discovery 9, 1-20
-
(2014)
Recent Pat. Anti-Cancer Drug Discovery
, vol.9
, pp. 1-20
-
-
Sidera, K.1
Patsavoudi, E.2
-
49
-
-
33746914732
-
Structural and quantum chemical studies of 8-aryl-sulfanyl adenine class Hsp90 inhibitors
-
Immormino, R. M., Kang, Y., Choisis, G., and Gewirth, D. T. (2006) Structural and quantum chemical studies of 8-aryl-sulfanyl adenine class Hsp90 inhibitors J. Med. Chem. 49, 4953-4960
-
(2006)
J. Med. Chem.
, vol.49
, pp. 4953-4960
-
-
Immormino, R.M.1
Kang, Y.2
Choisis, G.3
Gewirth, D.T.4
-
50
-
-
84905111606
-
Fragment-based hit discovery and structure-based optimization of aminotriazoloquinazolines as novel Hsp90 inhibitors
-
Casale, E., Amboldi, N., Brasca, M. G., Caronni, D., Colombo, N., Dalvit, C., Felder, E. R., Fogliatto, G., Galvani, A., Isacchi, A., Polucci, P., Riceputi, L., Sola, F., Visco, C., Zuccotto, F., and Casuscelli, F. (2014) Fragment-based hit discovery and structure-based optimization of aminotriazoloquinazolines as novel Hsp90 inhibitors Bioorgan. Med. Chem. 22, 4135-4150
-
(2014)
Bioorgan. Med. Chem.
, vol.22
, pp. 4135-4150
-
-
Casale, E.1
Amboldi, N.2
Brasca, M.G.3
Caronni, D.4
Colombo, N.5
Dalvit, C.6
Felder, E.R.7
Fogliatto, G.8
Galvani, A.9
Isacchi, A.10
Polucci, P.11
Riceputi, L.12
Sola, F.13
Visco, C.14
Zuccotto, F.15
Casuscelli, F.16
-
51
-
-
84893648853
-
Thiazolopyridone ureas as DNA gyrase B inhibitors: Optimization of antitubercular activity and efficacy
-
Kale, R. R., Kale, M. G., Waterson, D., Raichurkar, A., Hameed, S. P., Manjunatha, M. R., Kishore Reddy, B. K., Malolanarasimhan, K., Shinde, V., Koushik, K., Jena, L. K., Menasinakai, S., Humnabadkar, V., Madhavapeddi, P., Basavarajappa, H., Sharma, S., Nandishaiah, R., Mahesh Kumar, K. N., Ganguly, S., Ahuja, V., Gaonkar, S., Naveen Kumar, C. N., Ogg, D., Boriack-Sjodin, P. A., Sambandamurthy, V. K., de Sousa, S. M., and Ghorpade, S. R. (2014) Thiazolopyridone ureas as DNA gyrase B inhibitors: Optimization of antitubercular activity and efficacy Bioorg. Med. Chem. Lett. 24, 870-879
-
(2014)
Bioorg. Med. Chem. Lett.
, vol.24
, pp. 870-879
-
-
Kale, R.R.1
Kale, M.G.2
Waterson, D.3
Raichurkar, A.4
Hameed, S.P.5
Manjunatha, M.R.6
Kishore Reddy, B.K.7
Malolanarasimhan, K.8
Shinde, V.9
Koushik, K.10
Jena, L.K.11
Menasinakai, S.12
Humnabadkar, V.13
Madhavapeddi, P.14
Basavarajappa, H.15
Sharma, S.16
Nandishaiah, R.17
Mahesh Kumar, K.N.18
Ganguly, S.19
Ahuja, V.20
Gaonkar, S.21
Naveen Kumar, C.N.22
Ogg, D.23
Boriack-Sjodin, P.A.24
Sambandamurthy, V.K.25
De Sousa, S.M.26
Ghorpade, S.R.27
more..
-
52
-
-
84887882612
-
Fragment-to-hit-to-lead discovery of a novel pyridylurea scaffold of ATP competitive dual targeting type II topoisomerase inhibiting antibacterial agents
-
Basarab, G. S., Manchester, J. I., Bist, S., Boriack-Sjodin, P. A., Dangel, B., Illingworth, R., Sherer, B. A., Sriram, S., Uria-Nickelsen, M., and Eakin, A. E. (2013) Fragment-to-hit-to-lead discovery of a novel pyridylurea scaffold of ATP competitive dual targeting type II topoisomerase inhibiting antibacterial agents J. Med. Chem. 56, 8712-8735
-
(2013)
J. Med. Chem.
, vol.56
, pp. 8712-8735
-
-
Basarab, G.S.1
Manchester, J.I.2
Bist, S.3
Boriack-Sjodin, P.A.4
Dangel, B.5
Illingworth, R.6
Sherer, B.A.7
Sriram, S.8
Uria-Nickelsen, M.9
Eakin, A.E.10
-
53
-
-
51849112827
-
Novel dual-targeting benzimidazole urea inhibitors of DNA gyrase and topoisomerase IV possessing potent antibacterial activity: Intelligent design and evolution through the judicious use of structure-guided design and stucture-activity relationships
-
Charifson, P. S., Grillot, A.-L., Grossman, T. H., Parsons, J. D., Badia, M., Bellon, S., Deininger, D. D., Drumm, J. E., Gross, C. H., LeTiran, A., Liao, Y., Mani, N., Nicolau, D. P., Perola, E., Ronkin, S., Shannon, D., Swenson, L. L., Tang, Q., Tessier, P. R., Tian, S.-K., Trudeau, M., Wang, T., Wei, Y., Zhang, H., and Stamos, D. (2008) Novel dual-targeting benzimidazole urea inhibitors of DNA gyrase and topoisomerase IV possessing potent antibacterial activity: Intelligent design and evolution through the judicious use of structure-guided design and stucture-activity relationships J. Med. Chem. 51, 5243-5263
-
(2008)
J. Med. Chem.
, vol.51
, pp. 5243-5263
-
-
Charifson, P.S.1
Grillot, A.-L.2
Grossman, T.H.3
Parsons, J.D.4
Badia, M.5
Bellon, S.6
Deininger, D.D.7
Drumm, J.E.8
Gross, C.H.9
Letiran, A.10
Liao, Y.11
Mani, N.12
Nicolau, D.P.13
Perola, E.14
Ronkin, S.15
Shannon, D.16
Swenson, L.L.17
Tang, Q.18
Tessier, P.R.19
Tian, S.-K.20
Trudeau, M.21
Wang, T.22
Wei, Y.23
Zhang, H.24
Stamos, D.25
more..
-
54
-
-
84894127873
-
Structure-guided development of specific pyruvate dehydrogenase kinase inhibitors targeting the ATP-binding pocket
-
Tso, S. C., Qi, X., Gui, W. J., Wu, C. Y., Chuang, J. L., Wernstedt-Asterholm, I., Morlock, L. K., Owens, K. R., Scherer, P. E., Williams, N. S., Tambar, U. K., Wynn, R. M., and Chuang, D. T. (2014) Structure-guided development of specific pyruvate dehydrogenase kinase inhibitors targeting the ATP-binding pocket J. Biol. Chem. 289, 4432-4443
-
(2014)
J. Biol. Chem.
, vol.289
, pp. 4432-4443
-
-
Tso, S.C.1
Qi, X.2
Gui, W.J.3
Wu, C.Y.4
Chuang, J.L.5
Wernstedt-Asterholm, I.6
Morlock, L.K.7
Owens, K.R.8
Scherer, P.E.9
Williams, N.S.10
Tambar, U.K.11
Wynn, R.M.12
Chuang, D.T.13
-
55
-
-
0041935939
-
-
U.S. National Institutes of Health, Bethesda, MD
-
Rasband, W. S. (1997-2014) ImageJ; U.S. National Institutes of Health, Bethesda, MD.
-
(1997)
ImageJ
-
-
Rasband, W.S.1
-
56
-
-
79952385103
-
Analysis of protein-ligand interactions by fluorescence polarization
-
Rossi, A. M. and Taylor, C. W. (2011) Analysis of protein-ligand interactions by fluorescence polarization Nat. Protoc. 6, 365-387
-
(2011)
Nat. Protoc.
, vol.6
, pp. 365-387
-
-
Rossi, A.M.1
Taylor, C.W.2
-
57
-
-
84921757196
-
Receptor binding assays for HTS and drug discovery
-
in (Sittampalam, S. Ed.), Eli Lilly & Company, Indianapolis, IN
-
Auld, D. S., Farmen, M. W., Kahl, S. D., Kriauciunas, A., McKnight, K. L., Montrose, C., and Weidner, J. R. (2012) Receptor binding assays for HTS and drug discovery, in Assay Guidance Manual (Sittampalam, S., Ed.), Eli Lilly & Company, Indianapolis, IN.
-
(2012)
Assay Guidance Manual
-
-
Auld, D.S.1
Farmen, M.W.2
Kahl, S.D.3
Kriauciunas, A.4
McKnight, K.L.5
Montrose, C.6
Weidner, J.R.7
-
58
-
-
0034924241
-
Determination of minimum inhibitory concentrations
-
Andrews, J. M. (2001) Determination of minimum inhibitory concentrations J. Antimicrob. Chemoth. 48 (Suppl. SI) 5-16
-
(2001)
J. Antimicrob. Chemoth.
, vol.48
, pp. 5-16
-
-
Andrews, J.M.1
-
59
-
-
39449086721
-
Agar and broth dilution methods to determine the minimal inhibitory concentration (MIC) of antimicrobial substances
-
Wiegand, I., Hilpert, K., and Hancock, R. E. (2008) Agar and broth dilution methods to determine the minimal inhibitory concentration (MIC) of antimicrobial substances Nat. Protoc. 3, 163-175
-
(2008)
Nat. Protoc.
, vol.3
, pp. 163-175
-
-
Wiegand, I.1
Hilpert, K.2
Hancock, R.E.3
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