-
1
-
-
77956307436
-
The antibiotics market
-
Hamad B. The antibiotics market. Nat Rev Drug Discov 2010; 9: 675-6.
-
(2010)
Nat Rev Drug Discov
, vol.9
, pp. 675-676
-
-
Hamad, B.1
-
2
-
-
57749107808
-
Bad bugs, no drugs: no ESKAPE! An update from the Infectious Diseases Society of America
-
Boucher HW, Talbot GH, Bradley JS et al. Bad bugs, no drugs: no ESKAPE! An update from the Infectious Diseases Society of America. Clin Infect Dis 2009; 48: 1-12.
-
(2009)
Clin Infect Dis
, vol.48
, pp. 1-12
-
-
Boucher, H.W.1
Talbot, G.H.2
Bradley, J.S.3
-
3
-
-
0242291985
-
Why is big Pharma getting out of antibacterial drug discovery?
-
Projan SJ. Why is big Pharma getting out of antibacterial drug discovery? Curr Opin Microbiol 2003; 6: 427-30.
-
(2003)
Curr Opin Microbiol
, vol.6
, pp. 427-430
-
-
Projan, S.J.1
-
4
-
-
0345320400
-
Efflux pumpmediated quinolone resistance in Staphylococcus aureus strains wild type for gyrA, gyrB, grlA, and norA
-
Munoz-Bellido JL, Manzanares MAA, Andres JAM et al. Efflux pumpmediated quinolone resistance in Staphylococcus aureus strains wild type for gyrA, gyrB, grlA, and norA. Antimicrob Agents Chemother 1999; 43: 354-6.
-
(1999)
Antimicrob Agents Chemother
, vol.43
, pp. 354-356
-
-
Munoz-Bellido, J.L.1
Manzanares, M.A.A.2
Andres, J.A.M.3
-
5
-
-
0033791727
-
Mechanism of quinolone resistance in Staphylococcus aureus
-
Tanaka M, Wang T, Onodera Y et al. Mechanism of quinolone resistance in Staphylococcus aureus. J Infect Chemother 2000; 6: 131-9.
-
(2000)
J Infect Chemother
, vol.6
, pp. 131-139
-
-
Tanaka, M.1
Wang, T.2
Onodera, Y.3
-
6
-
-
0027270540
-
Efflux-mediated fluoroquinolone resistance in Staphylococcus aureus
-
Kaatz GW, Seo SM, Ruble CA. Efflux-mediated fluoroquinolone resistance in Staphylococcus aureus. Antimicrob Agents Chemother 1993; 37: 1086-94.
-
(1993)
Antimicrob Agents Chemother
, vol.37
, pp. 1086-1094
-
-
Kaatz, G.W.1
Seo, S.M.2
Ruble, C.A.3
-
7
-
-
84857611419
-
The clinical significance of vancomycin minimum inhibitory concentration in Staphylococcus aureus infections: a systematic review and meta-analysis
-
Van Hal SJ, Lodise TP, Paterson DL. The clinical significance of vancomycin minimum inhibitory concentration in Staphylococcus aureus infections: a systematic review and meta-analysis. Clin Infect Dis 2012; 54: 755-71.
-
(2012)
Clin Infect Dis
, vol.54
, pp. 755-771
-
-
Van Hal, S.J.1
Lodise, T.P.2
Paterson, D.L.3
-
8
-
-
84878297844
-
Is it time to replace vancomycin in the treatment of methicillin-resistant Staphylococcus aureus infections?
-
Van Hal SJ, Fowler VG. Is it time to replace vancomycin in the treatment of methicillin-resistant Staphylococcus aureus infections? Clin Infect Dis 2013; 56: 1779-88.
-
(2013)
Clin Infect Dis
, vol.56
, pp. 1779-1788
-
-
Van Hal, S.J.1
Fowler, V.G.2
-
9
-
-
84861423745
-
Antibiotics: recover the lost art of drug discovery
-
Lewis K. Antibiotics: recover the lost art of drug discovery. Nature 2012; 485: 439-40.
-
(2012)
Nature
, vol.485
, pp. 439-440
-
-
Lewis, K.1
-
10
-
-
84879468910
-
New drugs for methicillin-resistant Staphylococcus aureus: an update
-
Kumar K, Chopra S. New drugs for methicillin-resistant Staphylococcus aureus: an update. J Antimicrob Chemother 2013; 68: 1465-70.
-
(2013)
J Antimicrob Chemother
, vol.68
, pp. 1465-1470
-
-
Kumar, K.1
Chopra, S.2
-
11
-
-
3442887705
-
The antibiotic pipeline: challenges, costs, and values
-
Wenzel RP. The antibiotic pipeline: challenges, costs, and values. N Engl J Med 2004; 351: 523-6.
-
(2004)
N Engl J Med
, vol.351
, pp. 523-526
-
-
Wenzel, R.P.1
-
12
-
-
84255201091
-
The oxazolidinones: past, present, and future
-
Shaw KJ, Barbachyn MR. The oxazolidinones: past, present, and future. Ann N Y Acad Sci 2011; 1241: 48-70.
-
(2011)
Ann N Y Acad Sci
, vol.1241
, pp. 48-70
-
-
Shaw, K.J.1
Barbachyn, M.R.2
-
13
-
-
84857770864
-
Daptomycin: a review of properties, clinical use, drug delivery and resistance
-
Vilhena C, Bettencourt A. Daptomycin: a review of properties, clinical use, drug delivery and resistance. Mini Rev Med Chem 2012; 12: 202-9.
-
(2012)
Mini Rev Med Chem
, vol.12
, pp. 202-209
-
-
Vilhena, C.1
Bettencourt, A.2
-
14
-
-
77956261728
-
Daptomycin, a bacterial lipopeptide synthesized by a nonribosomal machinery
-
Robbel L, Marahiel MA. Daptomycin, a bacterial lipopeptide synthesized by a nonribosomal machinery. J Biol Chem 2010; 285: 27501-8.
-
(2010)
J Biol Chem
, vol.285
, pp. 27501-27508
-
-
Robbel, L.1
Marahiel, M.A.2
-
15
-
-
84872858655
-
Mechanisms of daptomycin resistance in Staphylococcus aureus: role of the cell membrane and cell wall
-
Bayer AS, Schneider T, Sahl H-G. Mechanisms of daptomycin resistance in Staphylococcus aureus: role of the cell membrane and cell wall. Ann N Y Acad Sci 2013; 1277: 139-58.
-
(2013)
Ann N Y Acad Sci
, vol.1277
, pp. 139-158
-
-
Bayer, A.S.1
Schneider, T.2
Sahl, H.-G.3
-
16
-
-
84856068450
-
Resistance to linezolid caused by modifications at its binding site on the ribosome
-
Long KS, Vester B. Resistance to linezolid caused by modifications at its binding site on the ribosome. Antimicrob Agents Chemother 2012; 56: 603-12.
-
(2012)
Antimicrob Agents Chemother
, vol.56
, pp. 603-612
-
-
Long, K.S.1
Vester, B.2
-
17
-
-
27844463013
-
Indole alkaloid marine natural products: an established source of cancer drug leads with considerable promise for the control of parasitic, neurological and other diseases
-
Gul W, Hamann MT. Indole alkaloid marine natural products: an established source of cancer drug leads with considerable promise for the control of parasitic, neurological and other diseases. Life Sci 2005; 78: 442-53.
-
(2005)
Life Sci
, vol.78
, pp. 442-453
-
-
Gul, W.1
Hamann, M.T.2
-
18
-
-
84930523013
-
Chimie des nitrones: applications en synthèse organique et à la synthèse de composés bio-actifs
-
PhD Thesis. Université Joseph Fourier, Grenoble, France
-
Guinchard X. Chimie des nitrones: applications en synthèse organique et à la synthèse de composés bio-actifs. PhD Thesis. Université Joseph Fourier, Grenoble, France, 2006.
-
(2006)
-
-
Guinchard, X.1
-
19
-
-
33645241103
-
Antimicrobial activity and cytotoxicity of bis(indole) alkaloids from the sponge Spongosorites sp
-
Oh K-B, Mar W, Kim S et al. Antimicrobial activity and cytotoxicity of bis(indole) alkaloids from the sponge Spongosorites sp. Biol Pharm Bull 2006; 29: 570-3.
-
(2006)
Biol Pharm Bull
, vol.29
, pp. 570-573
-
-
Oh, K.-B.1
Mar, W.2
Kim, S.3
-
20
-
-
34848874052
-
Total syntheses of brominated marine sponge alkaloids
-
Guinchard X, Vallée Y, Denis J-N. Total syntheses of brominated marine sponge alkaloids. Org Lett 2007; 9: 3761-4.
-
(2007)
Org Lett
, vol.9
, pp. 3761-3764
-
-
Guinchard, X.1
Vallée, Y.2
Denis, J.-N.3
-
21
-
-
34248595120
-
Total synthesis of marine sponge bis(indole) alkaloids of the topsentin class
-
Guinchard X, Vallée Y, Denis J-N. Total synthesis of marine sponge bis(indole) alkaloids of the topsentin class. J Org Chem 2007; 72: 3972-5.
-
(2007)
J Org Chem
, vol.72
, pp. 3972-3975
-
-
Guinchard, X.1
Vallée, Y.2
Denis, J.-N.3
-
22
-
-
79956191508
-
Synthesis and evaluation of 1-(1H-indol-3-yl)ethanamine derivatives as new antibacterial agents
-
Burchak ON, Pihive EL, Maigre L et al. Synthesis and evaluation of 1-(1H-indol-3-yl)ethanamine derivatives as new antibacterial agents. Bioorg Med Chem 2011; 19: 3204-15.
-
(2011)
Bioorg Med Chem
, vol.19
, pp. 3204-3215
-
-
Burchak, O.N.1
Pihive, E.L.2
Maigre, L.3
-
23
-
-
84903820842
-
1-(1H-Indol-3-yl)ethanamine derivatives as potent Staphylococcus aureus NorA efflux pump inhibitors
-
Hequet A, Burchak ON, Jeanty M et al. 1-(1H-Indol-3-yl)ethanamine derivatives as potent Staphylococcus aureus NorA efflux pump inhibitors. ChemMedChem 2014; 9: 1534-45.
-
(2014)
ChemMedChem
, vol.9
, pp. 1534-1545
-
-
Hequet, A.1
Burchak, O.N.2
Jeanty, M.3
-
24
-
-
84930523014
-
Synthesis of new indole derivatives, their preparation processes, and their antibacterial uses
-
September, WO 2008110690 A2 20080918
-
Denis J-N, Guinchard X, Moreau N et al. Synthesis of new indole derivatives, their preparation processes, and their antibacterial uses. September 2008. PCT Int Appl, WO 2008110690 A2 20080918.
-
(2008)
PCT Int Appl
-
-
Denis, J.-N.1
Guinchard, X.2
Moreau, N.3
-
25
-
-
84930523015
-
Preparation of novel bis-indolic derivatives antibacterial drugs and a process for preparing them
-
January, WO 2013014102 A1 20130131
-
Denis J-N, Jolivalt C, Maurin M et al. Preparation of novel bis-indolic derivatives antibacterial drugs and a process for preparing them. January 2013. PCT Int Appl, WO 2013014102 A1 20130131.
-
(2013)
PCT Int Appl
-
-
Denis, J.-N.1
Jolivalt, C.2
Maurin, M.3
-
26
-
-
84930523016
-
Preparation of bis-indole derivatives useful as antibacterials
-
January, WO 2013014104 A1 20130131
-
Denis J-N, Jolivalt C, Maurin M et al. Preparation of bis-indole derivatives useful as antibacterials. January 2013. PCT Int Appl, WO 2013014104 A1 20130131.
-
(2013)
PCT Int Appl
-
-
Denis, J.-N.1
Jolivalt, C.2
Maurin, M.3
-
27
-
-
79951727258
-
Species identification of staphylococci by amplification and sequencing of the tuf gene compared to the gap gene and by matrix-assisted laser desorption ionization timeof- flightmass spectrometry
-
Bergeron M, Dauwalder O, Gouy M et al. Species identification of staphylococci by amplification and sequencing of the tuf gene compared to the gap gene and by matrix-assisted laser desorption ionization timeof- flightmass spectrometry. Eur J ClinMicrobiol Infect Dis 2011; 30: 343-54.
-
(2011)
Eur J ClinMicrobiol Infect Dis
, vol.30
, pp. 343-354
-
-
Bergeron, M.1
Dauwalder, O.2
Gouy, M.3
-
28
-
-
80051910934
-
Evolution from a natural flavones nucleus to obtain 2-(4-propoxyphenyl)quinoline derivatives as potent inhibitors of the S. aureus NorA efflux pump
-
Sabatini S, Gosetto F, Manfroni G et al. Evolution from a natural flavones nucleus to obtain 2-(4-propoxyphenyl)quinoline derivatives as potent inhibitors of the S. aureus NorA efflux pump. J Med Chem 2011; 54: 5722-36.
-
(2011)
J Med Chem
, vol.54
, pp. 5722-5736
-
-
Sabatini, S.1
Gosetto, F.2
Manfroni, G.3
-
30
-
-
0029922030
-
Drug-protein binding studies new trends in analytical and experimental methodology
-
Oravcova J, Böhs B, Lindner W. Drug-protein binding studies new trends in analytical and experimental methodology. J Chromatogr B Biomed Sci App 1996; 677: 1-28.
-
(1996)
J Chromatogr B Biomed Sci App
, vol.677
, pp. 1-28
-
-
Oravcova, J.1
Böhs, B.2
Lindner, W.3
-
31
-
-
0034929926
-
oct) from gradient RP-HPLC retention and a hydrogen bond acidity term (Sigma alpha2H)
-
oct) from gradient RP-HPLC retention and a hydrogen bond acidity term (Sigma alpha2H). Curr Med Chem 2001; 8: 1137-46.
-
(2001)
Curr Med Chem
, vol.8
, pp. 1137-1146
-
-
Valko, K.1
Du, C.2
Bevan, C.3
-
32
-
-
79951860177
-
Management of serious meticillinresistant Staphylococcus aureus infections: what are the limits?
-
Gould IM, Cauda R, Esposito S et al. Management of serious meticillinresistant Staphylococcus aureus infections: what are the limits? Int J Antimicrob Agents 2011; 37: 202-9.
-
(2011)
Int J Antimicrob Agents
, vol.37
, pp. 202-209
-
-
Gould, I.M.1
Cauda, R.2
Esposito, S.3
-
33
-
-
33847082059
-
Bisindole alkaloids of the topsentin and hamacanthin classes from a marine sponge Spongosorites sp
-
Bao B, Sun Q, Yao X et al. Bisindole alkaloids of the topsentin and hamacanthin classes from a marine sponge Spongosorites sp. J Nat Prod 2007; 70: 2-8.
-
(2007)
J Nat Prod
, vol.70
, pp. 2-8
-
-
Bao, B.1
Sun, Q.2
Yao, X.3
-
34
-
-
0034098001
-
New bisindole alkaloids of the topsentin and hamacanthin classes from the Mediterranean marine sponge Rhaphisia lacazei
-
Casapullo A, Bifulco G, Bruno I et al. New bisindole alkaloids of the topsentin and hamacanthin classes from the Mediterranean marine sponge Rhaphisia lacazei. J Nat Prod 2000; 63: 447-51.
-
(2000)
J Nat Prod
, vol.63
, pp. 447-451
-
-
Casapullo, A.1
Bifulco, G.2
Bruno, I.3
-
35
-
-
0027948295
-
Hamacanthins A and B, new antifungal bis indole alkaloids from the deep-water marine sponge, Hamacantha sp
-
Gunasekera SP, McCarthy PJ, Kelly-Borges M. Hamacanthins A and B, new antifungal bis indole alkaloids from the deep-water marine sponge, Hamacantha sp. J Nat Prod 1994; 57: 1437-41.
-
(1994)
J Nat Prod
, vol.57
, pp. 1437-1441
-
-
Gunasekera, S.P.1
McCarthy, P.J.2
Kelly-Borges, M.3
-
36
-
-
20444432777
-
Cytotoxic bisindole alkaloids from a marine sponge Spongosorites sp
-
Bao B, Sun Q, Yao X et al. Cytotoxic bisindole alkaloids from a marine sponge Spongosorites sp. J Nat Prod 2005; 68: 711-5.
-
(2005)
J Nat Prod
, vol.68
, pp. 711-715
-
-
Bao, B.1
Sun, Q.2
Yao, X.3
-
37
-
-
0026669966
-
A new bis-(indole) alkaloid from a deep-water marine sponge of the genus Spongosorites
-
Wright AE, Pomponi SA, Cross SS et al. A new bis-(indole) alkaloid from a deep-water marine sponge of the genus Spongosorites. J Org Chem 1992; 57: 4772-5.
-
(1992)
J Org Chem
, vol.57
, pp. 4772-4775
-
-
Wright, A.E.1
Pomponi, S.A.2
Cross, S.S.3
-
38
-
-
84455192535
-
Methicillin-resistant Staphylococcus aureus (MRSA) pyruvate kinase as a target for bis-indole alkaloids with antibacterial activities
-
Zoraghi R, Worrall L, See RH et al. Methicillin-resistant Staphylococcus aureus (MRSA) pyruvate kinase as a target for bis-indole alkaloids with antibacterial activities. J Biol Chem 2011; 286: 44716-25.
-
(2011)
J Biol Chem
, vol.286
, pp. 44716-44725
-
-
Zoraghi, R.1
Worrall, L.2
See, R.H.3
-
39
-
-
70349328445
-
Novel broad-spectrum bis-(imidazolinylindole) derivatives with potent antibacterial activities against antibioticresistant strains
-
Panchal RG, Ulrich RL, Lane D et al. Novel broad-spectrum bis-(imidazolinylindole) derivatives with potent antibacterial activities against antibioticresistant strains. Antimicrob Agents Chemother 2009; 53: 4283-91.
-
(2009)
Antimicrob Agents Chemother
, vol.53
, pp. 4283-4291
-
-
Panchal, R.G.1
Ulrich, R.L.2
Lane, D.3
-
40
-
-
77956120372
-
Comparative in vitro activity profiles of novel bis-indole antibacterials against Gram-positive and Gram-negative clinical isolates
-
Butler MM, Williams JD, Peet NP et al. Comparative in vitro activity profiles of novel bis-indole antibacterials against Gram-positive and Gram-negative clinical isolates. Antimicrob Agents Chemother 2010; 54: 3974-7.
-
(2010)
Antimicrob Agents Chemother
, vol.54
, pp. 3974-3977
-
-
Butler, M.M.1
Williams, J.D.2
Peet, N.P.3
-
41
-
-
84873821215
-
Bis-imidazolinylindoles are active against methicillin-resistant Staphylococcus aureus and multidrug-resistant Mycobacterium tuberculosis
-
Panchal RG, Lane D, Boshoff HI et al. Bis-imidazolinylindoles are active against methicillin-resistant Staphylococcus aureus and multidrug-resistant Mycobacterium tuberculosis. J Antibiot (Tokyo) 2013; 66: 47-9.
-
(2013)
J Antibiot (Tokyo)
, vol.66
, pp. 47-49
-
-
Panchal, R.G.1
Lane, D.2
Boshoff, H.I.3
-
42
-
-
78649910297
-
Novel bis-indole agents active against multidrug-resistant Acinetobacter baumannii
-
Jacobs MR, Bajaksouzian S, Good CE et al. Novel bis-indole agents active against multidrug-resistant Acinetobacter baumannii. Diagn Microbiol Infect Dis 2011; 69: 114-6.
-
(2011)
Diagn Microbiol Infect Dis
, vol.69
, pp. 114-116
-
-
Jacobs, M.R.1
Bajaksouzian, S.2
Good, C.E.3
-
43
-
-
84867815898
-
An efficient one pot syntheses of aryl-3,3′-bis(indolyl)methanes and studies on their spectral characteristics, DPPH radical scavenging-, antimicrobial-, cytotoxicity-, and antituberculosis activity
-
Kumar GS, Kumaresan S, Muthu Prabhu AA et al. An efficient one pot syntheses of aryl-3,3′-bis(indolyl)methanes and studies on their spectral characteristics, DPPH radical scavenging-, antimicrobial-, cytotoxicity-, and antituberculosis activity. Spectrochim Acta A Mol Biomol Spectrosc 2013; 101: 254-63.
-
(2013)
Spectrochim Acta A Mol Biomol Spectrosc
, vol.101
, pp. 254-263
-
-
Kumar, G.S.1
Kumaresan, S.2
Muthu Prabhu, A.A.3
-
44
-
-
84898048769
-
Synthesis and biological activity of novel bis-indole inhibitors of bacterial transcription initiation complex formation
-
Mielczarek M, Devakaram RV, Ma C et al. Synthesis and biological activity of novel bis-indole inhibitors of bacterial transcription initiation complex formation. Org Biomol Chem 2014; 12: 2882-94.
-
(2014)
Org Biomol Chem
, vol.12
, pp. 2882-2894
-
-
Mielczarek, M.1
Devakaram, R.V.2
Ma, C.3
-
45
-
-
25844457688
-
Bis(indole) alkaloids as sortase A inhibitors from the sponge Spongosorites sp
-
Oh K-B, Mar W, Kim S et al. Bis(indole) alkaloids as sortase A inhibitors from the sponge Spongosorites sp. Bioorg Med Chem Lett 2005; 15: 4927-31.
-
(2005)
Bioorg Med Chem Lett
, vol.15
, pp. 4927-4931
-
-
Oh, K.-B.1
Mar, W.2
Kim, S.3
-
46
-
-
79955533411
-
Identification of pyruvate kinase in methicillin-resistant Staphylococcus aureus as a novel antimicrobial drug target
-
Zoraghi R, See RH, Axerio-Cilies P et al. Identification of pyruvate kinase in methicillin-resistant Staphylococcus aureus as a novel antimicrobial drug target. Antimicrob Agents Chemother 2011; 55: 2042-53.
-
(2011)
Antimicrob Agents Chemother
, vol.55
, pp. 2042-2053
-
-
Zoraghi, R.1
See, R.H.2
Axerio-Cilies, P.3
-
47
-
-
84857557642
-
Cheminformatics-driven discovery of selective, nanomolar inhibitors for staphylococcal pyruvate kinase
-
Axerio-Cilies P, See RH, Zoraghi R et al. Cheminformatics-driven discovery of selective, nanomolar inhibitors for staphylococcal pyruvate kinase. ACS Chem Biol 2012; 7: 350-9.
-
(2012)
ACS Chem Biol
, vol.7
, pp. 350-359
-
-
Axerio-Cilies, P.1
See, R.H.2
Zoraghi, R.3
-
48
-
-
84896698945
-
Discovery and optimization of a new class of pyruvate kinase inhibitors as potential therapeutics for the treatment of methicillin-resistant Staphylococcus aureus infections
-
Kumar NS, Dullaghan EM, Finlay BB et al. Discovery and optimization of a new class of pyruvate kinase inhibitors as potential therapeutics for the treatment of methicillin-resistant Staphylococcus aureus infections. Bioorg Med Chem 2014; 22: 1708-25.
-
(2014)
Bioorg Med Chem
, vol.22
, pp. 1708-1725
-
-
Kumar, N.S.1
Dullaghan, E.M.2
Finlay, B.B.3
-
49
-
-
84870064229
-
Optimization and structure-activity relationships of a series of potent inhibitors of methicillin-resistant Staphylococcus aureus (MRSA) pyruvate kinase as novel antimicrobial agents
-
Kumar NS, Amandoron EA, Cherkasov A et al. Optimization and structure-activity relationships of a series of potent inhibitors of methicillin-resistant Staphylococcus aureus (MRSA) pyruvate kinase as novel antimicrobial agents. Bioorg Med Chem 2012; 20: 7069-82.
-
(2012)
Bioorg Med Chem
, vol.20
, pp. 7069-7082
-
-
Kumar, N.S.1
Amandoron, E.A.2
Cherkasov, A.3
-
50
-
-
84897923568
-
Bis-indolic compounds as potential new therapeutic alternatives for tularaemia
-
Caspar Y, Sutera V, Boisset S et al. Bis-indolic compounds as potential new therapeutic alternatives for tularaemia. Front Cell Infect Microbiol 2014; 4: 24.
-
(2014)
Front Cell Infect Microbiol
, vol.4
, pp. 24
-
-
Caspar, Y.1
Sutera, V.2
Boisset, S.3
-
51
-
-
0032871136
-
Multiple novel inhibitors of the NorA multidrug transporter of Staphylococcus aureus
-
Markham PN, Westhaus E, Klyachko K et al. Multiple novel inhibitors of the NorA multidrug transporter of Staphylococcus aureus. Antimicrob Agents Chemother 1999; 43: 2404-8.
-
(1999)
Antimicrob Agents Chemother
, vol.43
, pp. 2404-2408
-
-
Markham, P.N.1
Westhaus, E.2
Klyachko, K.3
-
52
-
-
80054939368
-
Exploring the contribution of efflux on the resistance to fluoroquinolones in clinical isolates of Staphylococcus aureus
-
Costa SS, Falcão C, Viveiros M et al. Exploring the contribution of efflux on the resistance to fluoroquinolones in clinical isolates of Staphylococcus aureus. BMC Microbiol 2011; 11: 241.
-
(2011)
BMC Microbiol
, vol.11
, pp. 241
-
-
Costa, S.S.1
Falcão, C.2
Viveiros, M.3
-
53
-
-
65549100031
-
Antibacterial activity of berberine-NorA pump inhibitor hybrids with a methylene ether linking group
-
Samosorn S, Tanwirat B, Muhamad N et al. Antibacterial activity of berberine-NorA pump inhibitor hybrids with a methylene ether linking group. Bioorg Med Chem 2009; 17: 3866-72.
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(2009)
Bioorg Med Chem
, vol.17
, pp. 3866-3872
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Samosorn, S.1
Tanwirat, B.2
Muhamad, N.3
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