메뉴 건너뛰기




Volumn 4, Issue 7, 2018, Pages 1114-1120

Effects of the 1-N-(4-Amino-2 S-hydroxybutyryl) and 6′- N-(2-Hydroxyethyl) Substituents on Ribosomal Selectivity, Cochleotoxicity, and Antibacterial Activity in the Sisomicin Class of Aminoglycoside Antibiotics

Author keywords

aminoglycoside modifying enzymes; aminoglycosides; cell free translation assays; ribosomal methyltransferases; structure activity relationship

Indexed keywords

1 N BOC 4 AMINO 2 HYDROXYBUTYRIC ACID SISOMICIN; 6' (2 HYDROXYETHYL)SISOMICIN; AMINOGLYCOSIDE ANTIBIOTIC AGENT; APRAMYCIN; ARMA PROTEIN; GENTAMICIN C; METHYLTRANSFERASE; PLAZOMICIN; RIBOSOME PROTEIN; SISOMICIN; TOBRAMYCIN; UNCLASSIFIED DRUG; AMINOGLYCOSIDE; ANTIINFECTIVE AGENT;

EID: 85046537357     PISSN: None     EISSN: 23738227     Source Type: Journal    
DOI: 10.1021/acsinfecdis.8b00052     Document Type: Article
Times cited : (23)

References (74)
  • 3
    • 69549111337 scopus 로고    scopus 로고
    • Antibiotics for Emerging Pathogens
    • Fischbach, M. A. and Walsh, C. T. (2009) Antibiotics for Emerging Pathogens. Science 325, 1089-1093, 10.1126/science.1176667
    • (2009) Science , vol.325 , pp. 1089-1093
    • Fischbach, M.A.1    Walsh, C.T.2
  • 4
    • 84885183690 scopus 로고    scopus 로고
    • Combating Multidrug-Resistant Bacteria: Current Strategies for the Discovery of Novel Antibacterials
    • O'Connell, K. M. G., Hodgkinson, J. T., Sore, H. F., Welch, M., Salmond, G. P. C., and Spring, D. R. (2013) Combating Multidrug-Resistant Bacteria: Current Strategies for the Discovery of Novel Antibacterials. Angew. Chem., Int. Ed. 52, 10706-10733, 10.1002/anie.201209979
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 10706-10733
    • O'Connell, K.M.G.1    Hodgkinson, J.T.2    Sore, H.F.3    Welch, M.4    Salmond, G.P.C.5    Spring, D.R.6
  • 6
    • 84905994821 scopus 로고    scopus 로고
    • The Evolving Role of Chemical Synthesis in Antibacterial Drug Discovery
    • Wright, P. M., Seiple, I. B., and Myers, A. G. (2014) The Evolving Role of Chemical Synthesis in Antibacterial Drug Discovery. Angew. Chem., Int. Ed. 53, 8840-8863, 10.1002/anie.201310843
    • (2014) Angew. Chem., Int. Ed. , vol.53 , pp. 8840-8863
    • Wright, P.M.1    Seiple, I.B.2    Myers, A.G.3
  • 7
    • 84955300100 scopus 로고    scopus 로고
    • Endless Resistance. Endless Antibiotics?
    • Fisher, J. F. and Mobashery, S. (2016) Endless Resistance. Endless Antibiotics?. MedChemComm 7, 37-49, 10.1039/C5MD00394F
    • (2016) MedChemComm , vol.7 , pp. 37-49
    • Fisher, J.F.1    Mobashery, S.2
  • 8
    • 0034699519 scopus 로고    scopus 로고
    • Functional Insights from the Structure of the 30S Ribosomal Subunit and Its Interactions with Antibiotics
    • Carter, A. P., Clemons, W. M., Brodersen, D. E., Morgan-Warren, R. J., Wimberly, B. T., and Ramakrishnan, V. (2000) Functional Insights from the Structure of the 30S Ribosomal Subunit and Its Interactions with Antibiotics. Nature 407, 340-348, 10.1038/35030019
    • (2000) Nature , vol.407 , pp. 340-348
    • Carter, A.P.1    Clemons, W.M.2    Brodersen, D.E.3    Morgan-Warren, R.J.4    Wimberly, B.T.5    Ramakrishnan, V.6
  • 11
    • 84927930436 scopus 로고    scopus 로고
    • The Structure of the Human Mitochondrial Ribosome
    • Amunts, A., Brown, A. D., Toots, J., Scheres, S. H. W., and Ramakrishnan, V. (2015) The Structure of the Human Mitochondrial Ribosome. Science 348, 95-98, 10.1126/science.aaa1193
    • (2015) Science , vol.348 , pp. 95-98
    • Amunts, A.1    Brown, A.D.2    Toots, J.3    Scheres, S.H.W.4    Ramakrishnan, V.5
  • 13
    • 0033965367 scopus 로고    scopus 로고
    • Aminoglycoside Antibiotics
    • Forge, A. and Schacht, J. (2000) Aminoglycoside Antibiotics. Audiol. Neuro-Otol. 5, 3-22, 10.1159/000013861
    • (2000) Audiol. Neuro-Otol. , vol.5 , pp. 3-22
    • Forge, A.1    Schacht, J.2
  • 14
    • 84865462505 scopus 로고    scopus 로고
    • Mechanisms of Aminoglycoside Ototoxicity and Targets of Hair Cell Protection
    • Huth, M. E., Ricci, A. J., and Cheng, A. G. (2011) Mechanisms of Aminoglycoside Ototoxicity and Targets of Hair Cell Protection. Int. J. Otolaryngol. 2011, 937861, 10.1155/2011/937861
    • (2011) Int. J. Otolaryngol. , vol.2011 , pp. 937861
    • Huth, M.E.1    Ricci, A.J.2    Cheng, A.G.3
  • 15
    • 84880577813 scopus 로고    scopus 로고
    • The Mitochondrion: A Perpetrator of Acquired Hearing Loss
    • Böttger, E. C. and Schacht, J. (2013) The Mitochondrion: A Perpetrator of Acquired Hearing Loss. Hear. Res. 303, 12-19, 10.1016/j.heares.2013.01.006
    • (2013) Hear. Res. , vol.303 , pp. 12-19
    • Böttger, E.C.1    Schacht, J.2
  • 16
    • 77951754356 scopus 로고    scopus 로고
    • The Future of Aminoglycosides: The End or Renaissance?
    • Houghton, J. L., Green, K. D., Chen, W., and Garneau-Tsodikova, S. (2010) The Future of Aminoglycosides: The End or Renaissance?. ChemBioChem 11, 880-902, 10.1002/cbic.200900779
    • (2010) ChemBioChem , vol.11 , pp. 880-902
    • Houghton, J.L.1    Green, K.D.2    Chen, W.3    Garneau-Tsodikova, S.4
  • 17
    • 84872533264 scopus 로고    scopus 로고
    • Aminoglycoside Antibiotics in the 21st Century
    • Becker, B. and Cooper, M. A. (2013) Aminoglycoside Antibiotics in the 21st Century. ACS Chem. Biol. 8, 105-115, 10.1021/cb3005116
    • (2013) ACS Chem. Biol. , vol.8 , pp. 105-115
    • Becker, B.1    Cooper, M.A.2
  • 19
    • 0016322891 scopus 로고
    • Structures and Syntheses of Aminoglycoside Antibiotics
    • Umezawa, S. (1974) Structures and Syntheses of Aminoglycoside Antibiotics. Adv. Carbohydr. Chem. Biochem. 30, 111-182, 10.1016/S0065-2318(08)60264-4
    • (1974) Adv. Carbohydr. Chem. Biochem. , vol.30 , pp. 111-182
    • Umezawa, S.1
  • 22
    • 84889359917 scopus 로고    scopus 로고
    • Design, Chemical Synthesis, and Antibacterial Activity of Kanamycin and Neomycin Class Aminoglycoside Antibiotics
    • (Ed.) Wiley: Hoboken, NJ
    • Wang, J., and Chang, C.-W. T. (2007) Design, Chemical Synthesis, and Antibacterial Activity of Kanamycin and Neomycin Class Aminoglycoside Antibiotics. In Aminoglycoside Antibiotics (Arya, D. P., Ed.) pp 141-180, Wiley: Hoboken, NJ.
    • (2007) Aminoglycoside Antibiotics , pp. 141-180
    • Wang, J.1    Chang, C.-W.T.2    Arya, D.P.3
  • 24
    • 14844348264 scopus 로고    scopus 로고
    • Molecular Insights into Aminoglycoside Action and Resistance
    • Magnet, S. and Blanchard, J. S. (2005) Molecular Insights into Aminoglycoside Action and Resistance. Chem. Rev. 105, 477-497, 10.1021/cr0301088
    • (2005) Chem. Rev. , vol.105 , pp. 477-497
    • Magnet, S.1    Blanchard, J.S.2
  • 25
    • 84864070915 scopus 로고    scopus 로고
    • Aminoglycosides and Gram-Negative Bacteria
    • (Eds.) ASM Press, Washington, DC
    • Lambert, T. (2010) Aminoglycosides and Gram-Negative Bacteria. In Antibiogram (Courvalin, P., Leclercq, R., and Rice, L. B., Eds.) pp 225-242, ASM Press, Washington, DC.
    • (2010) Antibiogram , pp. 225-242
    • Lambert, T.1    Courvalin, P.2    Leclercq, R.3    Rice, L.B.4
  • 26
    • 84864070915 scopus 로고    scopus 로고
    • Aminoglycosides and Gram-Positive Bacteria
    • (Eds.) ASM Press, Washington, DC
    • Bismuth, R., and Courvalin, P. (2010) Aminoglycosides and Gram-Positive Bacteria. In Antibiogram (Courvalin, P., Leclercq, R., and Rice, L. B., Eds.) pp 213-224, ASM Press, Washington, DC.
    • (2010) Antibiogram , pp. 213-224
    • Bismuth, R.1    Courvalin, P.2    Courvalin, P.3    Leclercq, R.4    Rice, L.B.5
  • 27
    • 84955323086 scopus 로고    scopus 로고
    • Drug-Target Networks in Aminoglycoside Resistance: Hierarchy of Priority in Structural Drug Design
    • Bacot-Davis, V. R., Bassenden, A. V., and Berghuis, I. M. (2016) Drug-Target Networks in Aminoglycoside Resistance: Hierarchy of Priority in Structural Drug Design. MedChemComm 7, 103-113, 10.1039/C5MD00384A
    • (2016) MedChemComm , vol.7 , pp. 103-113
    • Bacot-Davis, V.R.1    Bassenden, A.V.2    Berghuis, I.M.3
  • 28
    • 84955245868 scopus 로고    scopus 로고
    • Mechanisms of Resistance to Aminoglycoside Antibiotics: Overview and Perspectives
    • Garneau-Tsodikova, S. and Labby, K. J. (2016) Mechanisms of Resistance to Aminoglycoside Antibiotics: Overview and Perspectives. MedChemComm 7, 11-27, 10.1039/C5MD00344J
    • (2016) MedChemComm , vol.7 , pp. 11-27
    • Garneau-Tsodikova, S.1    Labby, K.J.2
  • 30
    • 0016378450 scopus 로고
    • Effect of Structural Modifications on the Biological Properties of Aminoglycoside Antibiotics Containing 2-Deoxystreptamine
    • Price, K. E., Godfrey, J. C., and Kawaguchi, H. (1974) Effect of Structural Modifications on the Biological Properties of Aminoglycoside Antibiotics Containing 2-Deoxystreptamine. Adv. Appl. Microbiol. 18, 191-307, 10.1016/S0065-2164(08)70572-0
    • (1974) Adv. Appl. Microbiol. , vol.18 , pp. 191-307
    • Price, K.E.1    Godfrey, J.C.2    Kawaguchi, H.3
  • 31
    • 78649909618 scopus 로고    scopus 로고
    • Development of Aminoglycoside Antibiotics Effective against Resistant Bacterial Strains
    • Yang, L. and Ye, X. S. (2010) Development of Aminoglycoside Antibiotics Effective against Resistant Bacterial Strains. Curr. Top. Med. Chem. 10, 1898-1926, 10.2174/156802610793176684
    • (2010) Curr. Top. Med. Chem. , vol.10 , pp. 1898-1926
    • Yang, L.1    Ye, X.S.2
  • 38
    • 58549117857 scopus 로고    scopus 로고
    • Genetic Analysis of Interactions with Eukaryotic rRNA Identify the Mitoribosome as Target in Aminoglycoside Ototoxicity
    • Hobbie, S. N., Akshay, S., Kalapala, S. K., Bruell, C., Shcherbakov, D., and Böttger, E. C. (2008) Genetic Analysis of Interactions with Eukaryotic rRNA Identify the Mitoribosome as Target in Aminoglycoside Ototoxicity. Proc. Natl. Acad. Sci. U. S. A. 105, 20888-20893, 10.1073/pnas.0811258106
    • (2008) Proc. Natl. Acad. Sci. U. S. A. , vol.105 , pp. 20888-20893
    • Hobbie, S.N.1    Akshay, S.2    Kalapala, S.K.3    Bruell, C.4    Shcherbakov, D.5    Böttger, E.C.6
  • 43
    • 85027946616 scopus 로고    scopus 로고
    • Importance of the 6′-Hydroxy Group and Its Configuration for Apramycin Activity
    • Mandhapati, A. R., Shcherbakov, D., Duscha, S., Vasella, A., Böttger, E. C., and Crich, D. (2014) Importance of the 6′-Hydroxy Group and Its Configuration for Apramycin Activity. ChemMedChem 9, 2074-2083, 10.1002/cmdc.201402146
    • (2014) ChemMedChem , vol.9 , pp. 2074-2083
    • Mandhapati, A.R.1    Shcherbakov, D.2    Duscha, S.3    Vasella, A.4    Böttger, E.C.5    Crich, D.6
  • 44
    • 84904818868 scopus 로고    scopus 로고
    • Synthesis, Antiribosomal and Antibacterial Activity of 4′- O-Glycopyranosyl Paromomycin Aminoglycoside Antibiotics
    • Chen, W., Matsushita, T., Shcherbakov, D., Boukari, H., Vasella, A., Böttger, E. C., and Crich, D. (2014) Synthesis, Antiribosomal and Antibacterial Activity of 4′- O-Glycopyranosyl Paromomycin Aminoglycoside Antibiotics. MedChemComm 5, 1179-1187, 10.1039/C4MD00119B
    • (2014) MedChemComm , vol.5 , pp. 1179-1187
    • Chen, W.1    Matsushita, T.2    Shcherbakov, D.3    Boukari, H.4    Vasella, A.5    Böttger, E.C.6    Crich, D.7
  • 46
    • 84966427974 scopus 로고    scopus 로고
    • Synthesis and Antiribosomal Activities of 4′- O-, 6′- O-, 4″- O-, 4′,6′- O- and 4″,6″- O-Derivatives in the Kanamycin Series Indicate Differing Target Selectivity Patterns between the 4,5- and 4,6-Series of Disubstituted 2-Deoxystreptamine Aminoglycoside Antibiotics
    • Kato, T., Yang, G., Teo, Y., Juskeviciene, R., Perez-Fernandez, D., Shinde, H. M., Salian, S., Bernet, B., Vasella, A., Böttger, E. C., and Crich, D. (2015) Synthesis and Antiribosomal Activities of 4′- O-, 6′- O-, 4″- O-, 4′,6′- O- and 4″,6″- O-Derivatives in the Kanamycin Series Indicate Differing Target Selectivity Patterns between the 4,5- and 4,6-Series of Disubstituted 2-Deoxystreptamine Aminoglycoside Antibiotics. ACS Infect. Dis. 1, 479-486, 10.1021/acsinfecdis.5b00069
    • (2015) ACS Infect. Dis. , vol.1 , pp. 479-486
    • Kato, T.1    Yang, G.2    Teo, Y.3    Juskeviciene, R.4    Perez-Fernandez, D.5    Shinde, H.M.6    Salian, S.7    Bernet, B.8    Vasella, A.9    Böttger, E.C.10    Crich, D.11
  • 47
    • 85019181591 scopus 로고    scopus 로고
    • N6′, N6', and O4′-Modifications to Neomycin Affect Ribosomal Selectivity without Compromising Antibacterial Activity
    • Sati, G. C., Shcherbakov, D., Hobbie, S., Vasella, A., Böttger, E. C., and Crich, D. (2017) N6′, N6', and O4′-Modifications to Neomycin Affect Ribosomal Selectivity without Compromising Antibacterial Activity. ACS Infect. Dis. 3, 368-376, 10.1021/acsinfecdis.6b00214
    • (2017) ACS Infect. Dis. , vol.3 , pp. 368-376
    • Sati, G.C.1    Shcherbakov, D.2    Hobbie, S.3    Vasella, A.4    Böttger, E.C.5    Crich, D.6
  • 48
    • 85031716627 scopus 로고    scopus 로고
    • Structure-Based Design and Synthesis of Apramycin-Paromomycin Analogues. Importance of the Configuration at the 6′-Position and Differences between the 6′-Amino and Hydroxy Series
    • Mandhapati, A. R., Yang, G., Kato, T., Shcherbakov, D., Hobbie, S. N., Vasella, A., Böttger, E. C., and Crich, D. (2017) Structure-Based Design and Synthesis of Apramycin-Paromomycin Analogues. Importance of the Configuration at the 6′-Position and Differences between the 6′-Amino and Hydroxy Series. J. Am. Chem. Soc. 139, 14611-14619, 10.1021/jacs.7b07754
    • (2017) J. Am. Chem. Soc. , vol.139 , pp. 14611-14619
    • Mandhapati, A.R.1    Yang, G.2    Kato, T.3    Shcherbakov, D.4    Hobbie, S.N.5    Vasella, A.6    Böttger, E.C.7    Crich, D.8
  • 49
    • 84939786412 scopus 로고    scopus 로고
    • Selective Protection of Secondary Amines as the N-Phenyl Triazenes. Application to Aminoglycoside Antibiotics
    • Sonousi, A. and Crich, D. (2015) Selective Protection of Secondary Amines as the N-Phenyl Triazenes. Application to Aminoglycoside Antibiotics. Org. Lett. 17, 4006-4009, 10.1021/acs.orglett.5b01902
    • (2015) Org. Lett. , vol.17 , pp. 4006-4009
    • Sonousi, A.1    Crich, D.2
  • 51
    • 0017863105 scopus 로고
    • Semisynthetic Aminoglycoside Antibacterials. 6. Synthesis of Sisomicin, Antibiotic G-52, and Novel 6′-Substituted Analogues of Sisomicin from Aminoglycoside 66-40C
    • Davies, D. H., Mallams, A. K., Counelis, M., Loebenberg, D., Moss, E. L., Jr., and Waitz, J. A. (1978) Semisynthetic Aminoglycoside Antibacterials. 6. Synthesis of Sisomicin, Antibiotic G-52, and Novel 6′-Substituted Analogues of Sisomicin from Aminoglycoside 66-40C. J. Med. Chem. 21, 189-193, 10.1021/jm00200a009
    • (1978) J. Med. Chem. , vol.21 , pp. 189-193
    • Davies, D.H.1    Mallams, A.K.2    Counelis, M.3    Loebenberg, D.4    Moss, E.L.5    Waitz, J.A.6
  • 52
    • 61449241846 scopus 로고    scopus 로고
    • Synthesis and Comparative Antibacterial Activity of Verdamicin C2 and C2a. A New Oxidation of Primary Allylic Azides in Dihydro[2 H]pyrans
    • This oxidation mimics one previously reported by the Hanessian lab with related N3″-Fmoc or acetamido derivatives. See: Hanessian, S., Szychowski, J., and Maianti, J. P. (2009) Synthesis and Comparative Antibacterial Activity of Verdamicin C2 and C2a. A New Oxidation of Primary Allylic Azides in Dihydro[2 H]pyrans. Org. Lett. 11, 429-432, 10.1021/ol802421d
    • (2009) Org. Lett. , vol.11 , pp. 429-432
    • Hanessian, S.1    Szychowski, J.2    Maianti, J.P.3
  • 56
    • 84861224930 scopus 로고    scopus 로고
    • A High pH Based Reversed-Phase High Performance Liquid Chromatographic Method for the Analysis of Aminoglycoside Plazomicin and Its Impurities
    • Tan, L., Wlasichuk, K. B., Schmidt, D. E., Campbell, R. L., Hirtzer, P., Cheng, L., and Karr, D. E. (2012) A High pH Based Reversed-Phase High Performance Liquid Chromatographic Method for the Analysis of Aminoglycoside Plazomicin and Its Impurities. J. Pharm. Biomed. Anal. 66, 75-84, 10.1016/j.jpba.2012.03.003
    • (2012) J. Pharm. Biomed. Anal. , vol.66 , pp. 75-84
    • Tan, L.1    Wlasichuk, K.B.2    Schmidt, D.E.3    Campbell, R.L.4    Hirtzer, P.5    Cheng, L.6    Karr, D.E.7
  • 57
    • 0037424873 scopus 로고    scopus 로고
    • Total Synthesis of the Cytotoxic Cyclopeptide Mollamide, Isolated from the Sea Squirt Didemnum Molle
    • McKeever, B. and Pattenden, G. (2003) Total Synthesis of the Cytotoxic Cyclopeptide Mollamide, Isolated from the Sea Squirt Didemnum Molle. Tetrahedron 59, 2701-2712, 10.1016/S0040-4020(03)00293-X
    • (2003) Tetrahedron , vol.59 , pp. 2701-2712
    • McKeever, B.1    Pattenden, G.2
  • 58
    • 0035806208 scopus 로고    scopus 로고
    • Selective Reactions of Reactive Amino Groups in Polyamino Compounds by Metal-Chelated or -Mediated Methods
    • Lee, S. H. and Cheong, C. S. (2001) Selective Reactions of Reactive Amino Groups in Polyamino Compounds by Metal-Chelated or -Mediated Methods. Tetrahedron 57, 4801-4815, 10.1016/S0040-4020(01)00297-6
    • (2001) Tetrahedron , vol.57 , pp. 4801-4815
    • Lee, S.H.1    Cheong, C.S.2
  • 59
    • 78650822243 scopus 로고    scopus 로고
    • Tandem Ugi MCR/Mitsunobu Cyclization as a Short, Protecting-Group-Free Route to Benzoxazinones with Four Diversity Points
    • Banfi, L., Basso, A., Giardini, L., Riva, R., Rocca, V., and Guanti, G. (2011) Tandem Ugi MCR/Mitsunobu Cyclization as a Short, Protecting-Group-Free Route to Benzoxazinones with Four Diversity Points. Eur. J. Org. Chem. 2011, 100-109, 10.1002/ejoc.201001077
    • (2011) Eur. J. Org. Chem. , vol.2011 , pp. 100-109
    • Banfi, L.1    Basso, A.2    Giardini, L.3    Riva, R.4    Rocca, V.5    Guanti, G.6
  • 60
    • 0016165420 scopus 로고
    • The Use of N-Hydroxy-5-Norbornene-2,3-Dicarboximide Active Esters in Peptide Synthesis
    • Fujino, M., Kobayashi, S., Obayashi, M., Fukuda, T., Shinagawa, S., and Nishimura, O. (1974) The Use of N-Hydroxy-5-Norbornene-2,3-Dicarboximide Active Esters in Peptide Synthesis. Chem. Pharm. Bull. 22, 1857-1863, 10.1248/cpb.22.1857
    • (1974) Chem. Pharm. Bull. , vol.22 , pp. 1857-1863
    • Fujino, M.1    Kobayashi, S.2    Obayashi, M.3    Fukuda, T.4    Shinagawa, S.5    Nishimura, O.6
  • 61
    • 0000844109 scopus 로고    scopus 로고
    • Reductive Amination of Aldehydes and Ketones with Sodium Triacetoxyborohydride. Studies on Direct and Indirect Reductive Amination Procedures
    • Abdel-Magid, A. F., Carson, K. G., Harris, B. D., Maryanoff, C. A., and Shah, R. D. (1996) Reductive Amination of Aldehydes and Ketones with Sodium Triacetoxyborohydride. Studies on Direct and Indirect Reductive Amination Procedures. J. Org. Chem. 61, 3849-3862, 10.1021/jo960057x
    • (1996) J. Org. Chem. , vol.61 , pp. 3849-3862
    • Abdel-Magid, A.F.1    Carson, K.G.2    Harris, B.D.3    Maryanoff, C.A.4    Shah, R.D.5
  • 62
    • 84864919962 scopus 로고    scopus 로고
    • An Efficient Method for Reductive Amination of Carbonyl Compounds under Nonacidic Conditions
    • Hudson, J. A. and Sweeney, J. B. (2012) An Efficient Method for Reductive Amination of Carbonyl Compounds under Nonacidic Conditions. Synlett 23, 2176-2178, 10.1055/s-0032-1316683
    • (2012) Synlett , vol.23 , pp. 2176-2178
    • Hudson, J.A.1    Sweeney, J.B.2
  • 63
    • 84994229434 scopus 로고    scopus 로고
    • Evaluation of Apramycin Activity against Carbapenem-Resistant and -Susceptible Strains of Enterobacteriaceae
    • Smith, K. P. and Kirby, J. E. (2016) Evaluation of Apramycin Activity against Carbapenem-Resistant and -Susceptible Strains of Enterobacteriaceae. Diagn. Microbiol. Infect. Dis. 86, 439-441, 10.1016/j.diagmicrobio.2016.09.002
    • (2016) Diagn. Microbiol. Infect. Dis. , vol.86 , pp. 439-441
    • Smith, K.P.1    Kirby, J.E.2
  • 64
    • 85015803622 scopus 로고    scopus 로고
    • In vitro Apramycin Activity against Multidrug-Resistant Acinetobacter Baumannii and Pseudomonas Aeruginosa
    • Kang, A. D., Smith, K. P., Eliopoulos, G. M., Berg, A. H., McCoy, C., and Kirby, J. E. (2017) In vitro Apramycin Activity against Multidrug-Resistant Acinetobacter Baumannii and Pseudomonas Aeruginosa. Diagn. Microbiol. Infect. Dis. 88, 188-191, 10.1016/j.diagmicrobio.2017.03.006
    • (2017) Diagn. Microbiol. Infect. Dis. , vol.88 , pp. 188-191
    • Kang, A.D.1    Smith, K.P.2    Eliopoulos, G.M.3    Berg, A.H.4    McCoy, C.5    Kirby, J.E.6
  • 65
    • 79953195147 scopus 로고    scopus 로고
    • In vitro Efficacy of the Novel Aminoglycoside ACHN-490 in Murine Infection Models
    • Reyes, N., Aggen, J. B., and Kostrub, C. F. (2011) In vitro Efficacy of the Novel Aminoglycoside ACHN-490 in Murine Infection Models. Antimicrob. Agents Chemother. 55, 1728-1733, 10.1128/AAC.00862-10
    • (2011) Antimicrob. Agents Chemother. , vol.55 , pp. 1728-1733
    • Reyes, N.1    Aggen, J.B.2    Kostrub, C.F.3
  • 67
    • 84898640237 scopus 로고    scopus 로고
    • In vitro Activity of Plazomicin against 5,105 Gram-Negative and Gram-Positive Clinical Isolates from Patients in Canadian Hospitals as Part of the Canward Study, 2011-2012
    • Walkty, A., Adam, H., Baxter, M., Denisuik, A., Lagacé-Wiens, P., Karlowsky, J. A., Hoban, D. J., and Zhanel, G. G. (2014) In vitro Activity of Plazomicin against 5,105 Gram-Negative and Gram-Positive Clinical Isolates from Patients in Canadian Hospitals as Part of the Canward Study, 2011-2012. Antimicrob. Agents Chemother. 58, 2554-2563, 10.1128/AAC.02744-13
    • (2014) Antimicrob. Agents Chemother. , vol.58 , pp. 2554-2563
    • Walkty, A.1    Adam, H.2    Baxter, M.3    Denisuik, A.4    Lagacé-Wiens, P.5    Karlowsky, J.A.6    Hoban, D.J.7    Zhanel, G.G.8
  • 71
    • 34250839342 scopus 로고    scopus 로고
    • 16S Ribosomal RNA Methylation: Emerging Resistance Mechanism against Aminoglycosides
    • Doi, Y. and Arakawa, Y. (2007) 16S Ribosomal RNA Methylation: Emerging Resistance Mechanism against Aminoglycosides. Clin. Infect. Dis. 45, 88-94, 10.1086/518605
    • (2007) Clin. Infect. Dis. , vol.45 , pp. 88-94
    • Doi, Y.1    Arakawa, Y.2
  • 72
    • 84862638890 scopus 로고    scopus 로고
    • Exogenously Acquired 16S rRNA Methyltransferases Found in Aminoglycoside-Resistant Pathogenic Gram-Negative Bacteria: An Update
    • Wachino, J.-i. and Arakawa, Y. (2012) Exogenously Acquired 16S rRNA Methyltransferases Found in Aminoglycoside-Resistant Pathogenic Gram-Negative Bacteria: An Update. Drug Resist. Updates 15, 133-148, 10.1016/j.drup.2012.05.001
    • (2012) Drug Resist. Updates , vol.15 , pp. 133-148
    • Wachino, J.-I.1    Arakawa, Y.2
  • 73
    • 0018098260 scopus 로고
    • Ototoxicity of Tobramycin, Gentamicin, Amikacin and Sisomicin in the Guinea Pig
    • Brummett, R. E., Fox, K. E., Bendrick, T. W., and Himes, D. L. (1978) Ototoxicity of Tobramycin, Gentamicin, Amikacin and Sisomicin in the Guinea Pig. J. Antimicrob. Chemother. 4 (Suppl. A), 73-83, 10.1093/jac/4.suppl-A.73
    • (1978) J. Antimicrob. Chemother. , vol.4 , pp. 73-83
    • Brummett, R.E.1    Fox, K.E.2    Bendrick, T.W.3    Himes, D.L.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.