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Volumn 3, Issue 3, 2010, Pages 679-701

2-Deoxystreptamine conjugates by truncation-derivatization of neomycin

Author keywords

Aminoglycosides; Aminopyridine; Aminoquinoline; Biosensor; Fluorescence; Hemocyanin; Morpholine

Indexed keywords

1 (AZIDOMETHYL) 2 METHOXYBENZENE; 1 (AZIDOMETHYL) 4 METHOXYBENZENE; 1 AZIDO 4 BROMOBENZENE; 1 AZIDO 4 METHOXYBENZENE; 1 BROMO 4 (AZIDOMETHYL)BROMOBENZENE; 2 (2 AMINOETHYLAMINO) 4 METHYLPYRIDINE; 2 (2 AMINOETHYLAMINO) 4 METHYLQUINOLINE; 2 (2 AMINOETHYLAMINO) 5 METHYLPYRIDINE; 2 DEOXYSTREPTAMINE; 5 O (BETA DEXTRO RIBOFURANOSYL) 2 DEOXYSTREPTAMINE; 5 O (N PROPYN 1 YL MORPHOLINO) 2 DEOXYSTREPTAMINE; 5 O [N PROPYN 1 YL 2 (METHYLAMINO N ETHYLAMINO N 4 METHYLPYRIDIN 2 YL)MORPHOLINO] 2 DEOXYSTREPTAMINE; 5 O [N PROPYN 1 YL 2 (METHYLAMINO N ETHYLAMINO N 5 METHYLPYRIDIN 2 YL)MORPHOLINO] 2 DEOXYSTREPTAMINE; 5 O [N PROPYN 1 YL 2 (METHYLAMINO N ETHYLAMINO N 5 METHYLQUINOLIN 2 YL)MORPHOLINO] 2 DEOXYSTREPTAMINE; AMINOGLYCOSIDE ANTIBIOTIC AGENT; AMINOPYRIDINE; AMINOQUINOLINE DERIVATIVE; ETHYLENEDIAMINE DERIVATIVE; HEMOCYANIN; KANAMYCIN; NEOMYCIN; REAGENT; UNCLASSIFIED DRUG;

EID: 77950452367     PISSN: None     EISSN: 14248247     Source Type: Journal    
DOI: 10.3390/ph3030679     Document Type: Article
Times cited : (3)

References (72)
  • 2
    • 0033152492 scopus 로고    scopus 로고
    • Basis for Prokaryotic Specificity of Action of Aminoglycoside Antibiotics
    • Recht, M.I.; Douthwaite, S.; Puglisi, J.D. Basis for Prokaryotic Specificity of Action of Aminoglycoside Antibiotics. EMBO J. 1999, 18, 3133-3138.
    • (1999) EMBO J. , vol.18 , pp. 3133-3138
    • Recht, M.I.1    Douthwaite, S.2    Puglisi, J.D.3
  • 3
    • 0028786856 scopus 로고
    • The role of aminoglycosides in Modern Therapy
    • Beaucaire, G. The role of aminoglycosides in Modern Therapy. J. Chemother. 1995, 7, 111-123.
    • (1995) J. Chemother. , vol.7 , pp. 111-123
    • Beaucaire, G.1
  • 4
    • 24044489584 scopus 로고    scopus 로고
    • Molecular Recognition of RNA by Neomycin and a Restricted Neomycin Derivative
    • Zhao, F.; Zhao, Q.; Blount, K.F.; Han, Q.; Tor, Y.; Hermann, T. Molecular Recognition of RNA by Neomycin and a Restricted Neomycin Derivative. Angew. Chem. Int. Ed. 2005, 44, 5329-5334.
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 5329-5334
    • Zhao, F.1    Zhao, Q.2    Blount, K.F.3    Han, Q.4    Tor, Y.5    Hermann, T.6
  • 5
    • 14844348264 scopus 로고    scopus 로고
    • Molecular Insights into Aminoglycoside Action and Resistance
    • Magnet, S.; Blanchard, J.S. Molecular Insights into Aminoglycoside Action and Resistance. Chem. Rev. 2005, 105, 477-497.
    • (2005) Chem. Rev. , vol.105 , pp. 477-497
    • Magnet, S.1    Blanchard, J.S.2
  • 7
    • 4744348954 scopus 로고    scopus 로고
    • Molecular Aspects of Renal Handling of Aminoglycoside and Strategies for Preventing the Nephrotoxicity
    • Nagai, J.; Takano, M. Molecular Aspects of Renal Handling of Aminoglycoside and Strategies for Preventing the Nephrotoxicity. Drug Metab. Pharmacokinet. 2004, 19, 159-170.
    • (2004) Drug Metab. Pharmacokinet. , vol.19 , pp. 159-170
    • Nagai, J.1    Takano, M.2
  • 8
    • 0030850832 scopus 로고    scopus 로고
    • Structure-activity Relationships of Hygromycin A and its Analogs: Protein Synthesis Inhibition Activity in a Cell-Free System
    • Hayashi, S.F.; Norcia, L.J.; Seibel, S.B.; Silvia, A.M. Structure-activity Relationships of Hygromycin A and its Analogs: Protein Synthesis Inhibition Activity in a Cell-Free System. J. Antibiot. 1997, 50, 514-521.
    • (1997) J. Antibiot. , vol.50 , pp. 514-521
    • Hayashi, S.F.1    Norcia, L.J.2    Seibel, S.B.3    Silvia, A.M.4
  • 9
    • 0029889142 scopus 로고    scopus 로고
    • Enzymatic 2'-N-Acetylation of Arbekacin and Antibiotic Activity of its Product
    • Hotta, K.; Zhu, C.B.; Ogata, T.; Sunada, A.; Ishikawa, J.; Mizuno, S.; Kondo, S. Enzymatic 2'-N-Acetylation of Arbekacin and Antibiotic Activity of its Product. J. Antibiot. 1996, 49, 458-464.
    • (1996) J. Antibiot. , vol.49 , pp. 458-464
    • Hotta, K.1    Zhu, C.B.2    Ogata, T.3    Sunada, A.4    Ishikawa, J.5    Mizuno, S.6    Kondo, S.7
  • 10
    • 0027478123 scopus 로고
    • Molecular Genetics of Aminoglycoside Resistance Genes and familial Relationships of the Aminoglycoside-Modifying Enzymes
    • Shaw, K.J.; Rather, P.N.; Hare, R.S.; Miller, G.H. Molecular Genetics of Aminoglycoside Resistance Genes and familial Relationships of the Aminoglycoside-Modifying Enzymes. Microbiol. Rev. 1993, 57, 138-163.
    • (1993) Microbiol. Rev. , vol.57 , pp. 138-163
    • Shaw, K.J.1    Rather, P.N.2    Hare, R.S.3    Miller, G.H.4
  • 11
    • 33644940301 scopus 로고    scopus 로고
    • Design and Synthesis of Pyrankacin: A Pyranmycin Class of Broad-Spectrum Aminoglycoside Antibiotic
    • Rai, R.; Chen, H.N.; Czyryca, P.G.; Li, J.; Chang, C.W.T. Design and Synthesis of Pyrankacin: A Pyranmycin Class of Broad-Spectrum Aminoglycoside Antibiotic. Org. Lett. 2006, 8, 887-889.
    • (2006) Org. Lett. , vol.8 , pp. 887-889
    • Rai, R.1    Chen, H.N.2    Czyryca, P.G.3    Li, J.4    Chang, C.W.T.5
  • 13
    • 0042074617 scopus 로고    scopus 로고
    • Design and Synthesis of Paromomycin-Related Heterocycle-Substituted Aminoglycoside Mimetics Based on a Mass Spectrometry RNA-Binding Assay
    • Ding, Y.; Hofstadler, S.A.; Swayze, E.E.; Risen, L.; Griffey, R.H. Design and Synthesis of Paromomycin-Related Heterocycle-Substituted Aminoglycoside Mimetics Based on a Mass Spectrometry RNA-Binding Assay. Angew. Chem. Int. Ed. 2003, 42, 3409-3412.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 3409-3412
    • Ding, Y.1    Hofstadler, S.A.2    Swayze, E.E.3    Risen, L.4    Griffey, R.H.5
  • 14
    • 33846540225 scopus 로고    scopus 로고
    • Synthesis of Paromomycin Derivatives Modified at C(5'') to Selectively Target Bacterial rRNA
    • Kudyba, I.; Fernandez, D.P.; Bottger, E.C.; Vasella, A. Synthesis of Paromomycin Derivatives Modified at C(5'') to Selectively Target Bacterial rRNA. Carbohydr. Res. 2007, 342, 499-519.
    • (2007) Carbohydr. Res. , vol.342 , pp. 499-519
    • Kudyba, I.1    Fernandez, D.P.2    Bottger, E.C.3    Vasella, A.4
  • 16
    • 0142106443 scopus 로고    scopus 로고
    • A New Class of Branched Aminoglycosides: Pseudo-Pentasaccharide Derivatives of Neomycin B
    • Fridman, M.; Blakhov, V.; Yaron, S.; Baasov, T. A New Class of Branched Aminoglycosides: Pseudo-Pentasaccharide Derivatives of Neomycin B. Org. Lett. 2003, 5, 3575-3578.
    • (2003) Org. Lett. , vol.5 , pp. 3575-3578
    • Fridman, M.1    Blakhov, V.2    Yaron, S.3    Baasov, T.4
  • 17
    • 0028882807 scopus 로고
    • Mechanism-based Inactivation of Bacterial Aminoglycoside 3' Phosphotransferases
    • Roestamadji, J.; Grapsas, I.; Mobashery, S. Mechanism-based Inactivation of Bacterial Aminoglycoside 3' Phosphotransferases. J. Am. Chem. Soc. 1995, 117, 80-84.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 80-84
    • Roestamadji, J.1    Grapsas, I.2    Mobashery, S.3
  • 18
    • 0037429028 scopus 로고    scopus 로고
    • Tobramycin Analouges with C-5 Aminoalkyl Ether Chains Intended to Mimic Rings III and IV of Paromomycin
    • Hanessian, S.; Tremblay, M.; Swayze, E.E. Tobramycin Analouges with C-5 Aminoalkyl Ether Chains Intended to Mimic Rings III and IV of Paromomycin. Tetrahedron 2003, 59, 983-993.
    • (2003) Tetrahedron , vol.59 , pp. 983-993
    • Hanessian, S.1    Tremblay, M.2    Swayze, E.E.3
  • 19
    • 12344323881 scopus 로고    scopus 로고
    • Dual Effect of Synthetic Aminoglycosides: Antibacterial Activity Against Bacillus Anthracis and Inhibition of Anthrax Lethal Factor
    • Fridman, M.; Blakhov, V.; Lee, L.V.; Liang, F.S.; Wong, C.H.; Baasov, T. Dual Effect of Synthetic Aminoglycosides: Antibacterial Activity Against Bacillus Anthracis and Inhibition of Anthrax Lethal Factor. Angew. Chem. Int. Ed. 2005, 44, 447-452.
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 447-452
    • Fridman, M.1    Blakhov, V.2    Lee, L.V.3    Liang, F.S.4    Wong, C.H.5    Baasov, T.6
  • 20
    • 0036257684 scopus 로고    scopus 로고
    • Aminoglycoside Mimetics as Small-molecule Drugs Targeting RNA
    • Ye, X.S.; Zhang, L.H. Aminoglycoside Mimetics as Small-molecule Drugs Targeting RNA. Curr. Med. Chem. 2002, 9, 929-939.
    • (2002) Curr. Med. Chem. , vol.9 , pp. 929-939
    • Ye, X.S.1    Zhang, L.H.2
  • 21
    • 84889359917 scopus 로고    scopus 로고
    • Design, Chemical Synthesis and Antibacterial Activity of Kanamycin and Neomycin Class Aminoglycoside Antibiotics
    • Wiley: New Jersey, USA
    • Arya, D.P. Design, Chemical Synthesis and Antibacterial Activity of Kanamycin and Neomycin Class Aminoglycoside Antibiotics. In Aminoglycoside Antibiotics: From Chemical Biology to Drug Discovery; Wiley: New Jersey, USA, 2007.
    • (2007) Aminoglycoside Antibiotics: From Chemical Biology to Drug Discovery
    • Arya, D.P.1
  • 22
    • 0034624435 scopus 로고    scopus 로고
    • Neomycin-Acridine Conjugate: A Potent Inhibitor of Rev-RRE Binding
    • Kirk, S.R.; Luedtke, N.W.; Tor, Y. Neomycin-Acridine Conjugate: A Potent Inhibitor of Rev-RRE Binding. J. Am. Chem. Soc. 2000, 122, 980-981.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 980-981
    • Kirk, S.R.1    Luedtke, N.W.2    Tor, Y.3
  • 23
    • 32344443375 scopus 로고    scopus 로고
    • Aminoglycoside-quinacridine Conjugates: Towards Recognition of the P6.1 Element of Telomerase RNA
    • Kaiser, M.; Sainlos, M.; Lehn, J.; Bombard, S.; Teulade-Fichou, M. Aminoglycoside-quinacridine Conjugates: Towards Recognition of the P6.1 Element of Telomerase RNA. Chem. Bio. Chem. 2006, 7, 321-329.
    • (2006) Chem. Bio. Chem. , vol.7 , pp. 321-329
    • Kaiser, M.1    Sainlos, M.2    Lehn, J.3    Bombard, S.4    Teulade-Fichou, M.5
  • 24
    • 33749669210 scopus 로고    scopus 로고
    • A Tale of Two Targets: Differential RNA Selectivity of Nucleobase-Aminoglycoside Conjugates
    • Blount, K.F.; Tor, Y. A Tale of Two Targets: Differential RNA Selectivity of Nucleobase-Aminoglycoside Conjugates. Chem. Bio. Chem. 2006, 7, 1612-1621.
    • (2006) Chem. Bio. Chem. , vol.7 , pp. 1612-1621
    • Blount, K.F.1    Tor, Y.2
  • 25
    • 33846463039 scopus 로고    scopus 로고
    • Sequence-specific Targeting of RNA with an Oligonuleotide-Neomycin Conjugate
    • Charles, I.; Xi, H.; Arya, D.P. Sequence-specific Targeting of RNA with an Oligonuleotide-Neomycin Conjugate. Bioconjug. Chem. 2007, 18, 160-169.
    • (2007) Bioconjug. Chem. , vol.18 , pp. 160-169
    • Charles, I.1    Xi, H.2    Arya, D.P.3
  • 26
    • 12844268189 scopus 로고    scopus 로고
    • Library Construction of Neomycin-dipeptide Heteroconjugates and Selection Against RRE RNA
    • Ahn, D.; Yu, J. Library Construction of Neomycin-dipeptide Heteroconjugates and Selection Against RRE RNA. Bioorg. Med. Chem. 2005, 13, 1177-1183.
    • (2005) Bioorg. Med. Chem. , vol.13 , pp. 1177-1183
    • Ahn, D.1    Yu, J.2
  • 27
    • 33746832437 scopus 로고    scopus 로고
    • A Strategy for the Design of Selective RNA Binding Agents, Preparations and RRE RNA Binding Affinities of a Neomycin-peptide Nucleic Acid Heteroconjugate Library. Bioorg. Med
    • Hyun, S.; Lee, K.H.; Yu, J. A Strategy for the Design of Selective RNA Binding Agents, Preparations and RRE RNA Binding Affinities of a Neomycin-peptide Nucleic Acid Heteroconjugate Library. Bioorg. Med. Chem. Lett. 2006, 16, 4757-4759.
    • (2006) Chem. Lett. , vol.16 , pp. 4757-4759
    • Hyun, S.1    Lee, K.H.2    Yu, J.3
  • 28
    • 1242319523 scopus 로고    scopus 로고
    • An Approach to Enhance Specificity Against RNA Targets Using Heteroconjugates of Aminoglycosides and Chloramphenicol (or Linezolid)
    • Lee, J.; Kwon, M.; Lee, K.H.; Jeong, S.; Hyun, S.; Shin, K.J.; Yu, J. An Approach to Enhance Specificity Against RNA Targets Using Heteroconjugates of Aminoglycosides and Chloramphenicol (or Linezolid). J. Am. Chem. Soc. 2004, 126, 1956-1957.
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 1956-1957
    • Lee, J.1    Kwon, M.2    Lee, K.H.3    Jeong, S.4    Hyun, S.5    Shin, K.J.6    Yu, J.7
  • 29
    • 0029905917 scopus 로고    scopus 로고
    • Rapid Combinatorial Synthesis of Aminoglycoside Antibiotics Mimetics: Use of a Polyethylene glycol-linked Amine and Neamine Derived Aldehyde in Multicomponent Condensation as a Strategy for the Discovery of New Inhibitors of the HIV RNA Rev Response Element
    • Park, W.K.C.; Auer, M.; Jaksche, H.; Wong, C.H. Rapid Combinatorial Synthesis of Aminoglycoside Antibiotics Mimetics: Use of a Polyethylene glycol-linked Amine and Neamine Derived Aldehyde in Multicomponent Condensation as a Strategy for the Discovery of New Inhibitors of the HIV RNA Rev Response Element. J. Am. Chem. Soc.1996, 118, 10150-10155.
    • (1996) , vol.118 , pp. 10150-10155
    • Park, W.K.C.1    Auer, M.2    Jaksche, H.3    Wong, C.H.4
  • 30
    • 0033591922 scopus 로고    scopus 로고
    • Design and Synthesis of New Aminoglycoside Antibiotics Containing Neamine as an Optimal Core: Correlation of Antibiotic Activity with in Vitro Inhibition of Translation
    • Greenberg, W.A.; Priestley, E.S.; Sears, P.S.; Alper, P.B.; Rosenbohn, C.; Hendrix, M.; Hung, S.C.; Wong, C.H. Design and Synthesis of New Aminoglycoside Antibiotics Containing Neamine as an Optimal Core: Correlation of Antibiotic Activity with in Vitro Inhibition of Translation. J. Am. Chem. Soc. 1999, 121, 6527-6541.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 6527-6541
    • Greenberg, W.A.1    Priestley, E.S.2    Sears, P.S.3    Alper, P.B.4    Rosenbohn, C.5    Hendrix, M.6    Hung, S.C.7    Wong, C.H.8
  • 31
    • 0033601437 scopus 로고    scopus 로고
    • Synthesis of Neamine Libraries for RNA Recognition Using Solution Phase Chemistry
    • Nunns, C.L.; Spence, L.A.; Slater, M.J.; Berrisford, D.J. Synthesis of Neamine Libraries for RNA Recognition Using Solution Phase Chemistry. Tetrahedron Lett. 1999, 40, 9341-9345.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 9341-9345
    • Nunns, C.L.1    Spence, L.A.2    Slater, M.J.3    Berrisford, D.J.4
  • 32
    • 0037430542 scopus 로고    scopus 로고
    • Synthesis of (+), (-) Neamine and Their Positional Isomers as Potential Antibiotics
    • Ryu, D.H.; Tan, C.H.; Rando, R.R. Synthesis of (+), (-) Neamine and Their Positional Isomers as Potential Antibiotics. Bioorg. Med. Chem. Lett. 2003, 13, 901-903.
    • (2003) Bioorg. Med. Chem. Lett. , vol.13 , pp. 901-903
    • Ryu, D.H.1    Tan, C.H.2    Rando, R.R.3
  • 35
    • 0030838564 scopus 로고    scopus 로고
    • Dimeric Aminoglycosides: Design, Synthesis and RNA Binding
    • Wang, H.; Tor, Y. Dimeric Aminoglycosides: Design, Synthesis and RNA Binding. Bioorg. Med. Chem. Lett. 1997, 7, 1951-1956.
    • (1997) Bioorg. Med. Chem. Lett. , vol.7 , pp. 1951-1956
    • Wang, H.1    Tor, Y.2
  • 36
    • 0034738144 scopus 로고    scopus 로고
    • Sears. P.; Wright, G.D.; Wong, C.H. Design of Bifunctional Antibiotics that Target Bacterial rRNA and Inhibit Resistance-causing Enzymes
    • Sucheck, S.J.; Wong, A.L.; Koeller, K.M.; Boehr, D.D.; Draker, K.A.; Sears. P.; Wright, G.D.; Wong, C.H. Design of Bifunctional Antibiotics that Target Bacterial rRNA and Inhibit Resistance-causing Enzymes. J. Am. Chem. Soc. 2000, 122, 5230-5231.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 5230-5231
    • Sucheck, S.J.1    Wong, A.L.2    Koeller, K.M.3    Boehr, D.D.4    Draker, K.A.5
  • 37
    • 0034679859 scopus 로고    scopus 로고
    • Enhanced Binding of Aminoglycoside Dimer to a "Dimerized" A-site rRNA Construct
    • Tok, J.B.H.; Huffman, G.R. Enhanced Binding of Aminoglycoside Dimer to a "Dimerized" A-site rRNA Construct. Bioorg. Med. Chem. Lett. 2000, 10, 1593-1595.
    • (2000) Bioorg. Med. Chem. Lett. , vol.10 , pp. 1593-1595
    • Tok, J.B.H.1    Huffman, G.R.2
  • 38
    • 0035821413 scopus 로고    scopus 로고
    • Binding of Dimeric Aminoglycosides to the HIV-1 Rev Response Element (RRE) RNA Construct
    • Tok, J.B.H.; Dunn, L.J.; Des Jean, R.C. Binding of Dimeric Aminoglycosides to the HIV-1 Rev Response Element (RRE) RNA Construct. Bioorg. Med. Chem. Lett. 2001, 11, 1127-1131.
    • (2001) , vol.11 , pp. 1127-1131
    • Tok, J.B.H.1    Dunn, L.J.2    des Jean, R.C.3
  • 39
    • 0035914615 scopus 로고    scopus 로고
    • Novel Synthesis and RNA-binding Properties of Aminoglycoside Dimers Conjugated via a Naphthalene diimide-based Intercalator
    • Tok, J.B.H.; Fenker J. Novel Synthesis and RNA-binding Properties of Aminoglycoside Dimers Conjugated via a Naphthalene diimide-based Intercalator. Bioorg. Med. Chem. Lett. 2001, 11, 2987-2991.
    • (2001) Bioorg. Med. Chem. Lett. , vol.11 , pp. 2987-2991
    • Tok, J.B.H.1    Fenker, J.2
  • 40
    • 0141483331 scopus 로고    scopus 로고
    • RNA-ligand Interactions: Affinity and Specificity of Aminoglycoside Dimers and Acridine Conjugates to the HIV-1 Rev Response Element
    • Leudtke, N.W.; Liu, Q.; Tor, Y. RNA-ligand Interactions: Affinity and Specificity of Aminoglycoside Dimers and Acridine Conjugates to the HIV-1 Rev Response Element. Biochemistry 2003, 42, 11391-11403.
    • (2003) , vol.42 , pp. 11391-11403
    • Leudtke, N.W.1    Liu, Q.2    Tor, Y.3
  • 43
    • 67649370762 scopus 로고    scopus 로고
    • Selective Deprotection of the Cbz Amine Protecting Group for the Facile Synthesis of Kanamycin A Dimers Linked at N-3'' Position
    • Chen, G.H.; Pan, P.; Chen, Y.; Meng, X.B.; Li, Z.J. Selective Deprotection of the Cbz Amine Protecting Group for the Facile Synthesis of Kanamycin A Dimers Linked at N-3'' Position. Tetrahedron 2009, 65, 5922-5927.
    • (2009) Tetrahedron , vol.65 , pp. 5922-5927
    • Chen, G.H.1    Pan, P.2    Chen, Y.3    Meng, X.B.4    Li, Z.J.5
  • 44
    • 17244378938 scopus 로고    scopus 로고
    • 2-Deoxystreptamine: Central Scaffold of Aminoglycoside Antibiotics
    • Busscher, G.F.; Rutjes, F.P.J.T.; van Delft, F.L. 2-Deoxystreptamine: Central Scaffold of Aminoglycoside Antibiotics. Chem. Rev. 2005, 205, 775-792.
    • (2005) Chem. Rev. , vol.205 , pp. 775-792
    • Busscher, G.F.1    Rutjes, F.P.J.T.2    van Delft, F.L.3
  • 45
    • 1842686343 scopus 로고    scopus 로고
    • Synthesis of a Protected Enantiomerically Pure 2-Deoxystreptamine Derivative from D-Allylglycine
    • Busscher, G.F.; Rutjes, F.P.J.T.; van Delft, F.L. Synthesis of a Protected Enantiomerically Pure 2-Deoxystreptamine Derivative from D-Allylglycine. Tetrahedron Lett. 2004, 69, 3629-3632.
    • (2004) Tetrahedron Lett. , vol.69 , pp. 3629-3632
    • Busscher, G.F.1    Rutjes, F.P.J.T.2    van Delft, F.L.3
  • 46
    • 3042781848 scopus 로고    scopus 로고
    • Efficient Preparation of a 1,3-Diazidocyclitol as a Versatile 2-Deoxystreptamine Precursor
    • Busscher, G.F.; Groothuys, S.; de Gelder, R.; Rutjes, F.P.J.T.; van Delft, F.L. Efficient Preparation of a 1,3-Diazidocyclitol as a Versatile 2-Deoxystreptamine Precursor. J. Org. Chem. 2004, 69, 4477-4481.
    • (2004) J. Org. Chem. , vol.69 , pp. 4477-4481
    • Busscher, G.F.1    Groothuys, S.2    de Gelder, R.3    Rutjes, F.P.J.T.4    van Delft, F.L.5
  • 49
    • 0033007592 scopus 로고    scopus 로고
    • Enhanced RNA-Binding of Dimerized Aminoglycosides
    • Michael, K.; Wang, H.; Tor, Y. Enhanced RNA-Binding of Dimerized Aminoglycosides. Bioorg. Med. Chem. 1999, 7, 1361-1371.
    • (1999) Bioorg. Med. Chem. , vol.7 , pp. 1361-1371
    • Michael, K.1    Wang, H.2    Tor, Y.3
  • 50
    • 0037448895 scopus 로고    scopus 로고
    • Discovery of Aminoglycoside Mimetics by NMR-based Screening of Escherichia Coli A-site RNA
    • Yu, L.; Oost, T.K.; Schkeryantz, J.M.; Yang, J.; Janowick, D.; Fesik, S.W. Discovery of Aminoglycoside Mimetics by NMR-based Screening of Escherichia Coli A-site RNA. J. Am. Chem. Soc. 2003, 125, 4444-4450.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 4444-4450
    • Yu, L.1    Oost, T.K.2    Schkeryantz, J.M.3    Yang, J.4    Janowick, D.5    Fesik, S.W.6
  • 51
    • 0033538635 scopus 로고    scopus 로고
    • Selective Oxidation of Primary Silyl Ethers and its Application to the Synthesis of Natural Products
    • Rodriguez, A.; Nomen, M.; Spur, B.W.; Godfroid, J.J. Selective Oxidation of Primary Silyl Ethers and its Application to the Synthesis of Natural Products. Tetrahedron Lett. 1999, 40, 5161-5164.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 5161-5164
    • Rodriguez, A.1    Nomen, M.2    Spur, B.W.3    Godfroid, J.J.4
  • 52
    • 0037940081 scopus 로고    scopus 로고
    • Trichloroisocynauric/TEMPO Oxidation of Alcohols under Mild Conditions: A Close Investigation
    • Luca, L.D.; Giacomelli, G.; Masala, S.; Porcheddu, A. Trichloroisocynauric/TEMPO Oxidation of Alcohols under Mild Conditions: A Close Investigation. J. Org. Chem. 2003, 68, 4999-5001.
    • (2003) J. Org. Chem. , vol.68 , pp. 4999-5001
    • Luca, L.D.1    Giacomelli, G.2    Masala, S.3    Porcheddu, A.4
  • 53
    • 0000234498 scopus 로고    scopus 로고
    • A Simple and Advantageous Protocol for the Oxidation of Alcohols with O-iodoxybenzoic Acid (IBX)
    • More, J.D.; Finney, N.S. A Simple and Advantageous Protocol for the Oxidation of Alcohols with O-iodoxybenzoic Acid (IBX). Org. Lett. 2002, 4, 3001-3003.
    • (2002) Org. Lett. , vol.4 , pp. 3001-3003
    • More, J.D.1    Finney, N.S.2
  • 54
    • 33644528891 scopus 로고
    • Readially Accessible12-1-5 Oxidant for the Conversion of Primary and Secondary Alcohols to Aldehydes and Ketones
    • Dess, D.B.; Martin, J.C. Readially Accessible12-1-5 Oxidant for the Conversion of Primary and Secondary Alcohols to Aldehydes and Ketones. J. Org. Chem. 1983, 48, 4155-4156.
    • (1983) J. Org. Chem. , vol.48 , pp. 4155-4156
    • Dess, D.B.1    Martin, J.C.2
  • 55
    • 0037012920 scopus 로고    scopus 로고
    • Peptidotriazoles on Solid Phase: [1,2,3]-triazoles by Regiospecific Copper (I)-catalyzed 1,3-dipolar Cycloadditions of Terminal Alkynes to Azides
    • Tornøe, C.W.; Christensen, C.; Meldal, M. Peptidotriazoles on Solid Phase: [1,2,3]-triazoles by Regiospecific Copper (I)-catalyzed 1,3-dipolar Cycloadditions of Terminal Alkynes to Azides. J. Org. Chem. 2002, 67, 3057-3064.
    • (2002) J. Org. Chem. , vol.67 , pp. 3057-3064
    • Tornøe, C.W.1    Christensen, C.2    Meldal, M.3
  • 56
    • 0037099395 scopus 로고    scopus 로고
    • A Stepwise Huisgen Cycloaddition Process: Copper (I)-catalyzed Regioselective Ligation of Azides and Terminal Alkynes
    • Rostovtsev, V.V.; Green, L.G.; Fokin, V.V.; Sharpless, K.B. A Stepwise Huisgen Cycloaddition Process: Copper (I)-catalyzed Regioselective Ligation of Azides and Terminal Alkynes. Angew. Chem. Int. Ed. 2002, 41, 2596-2599.
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 2596-2599
    • Rostovtsev, V.V.1    Green, L.G.2    Fokin, V.V.3    Sharpless, K.B.4
  • 58
    • 0029766901 scopus 로고    scopus 로고
    • RNA Molecules That Specifically and Stoichiometrically Bind Aminoglycoside Antibiotics with High Affinities
    • Wang, Y.; Killian, J.; Hamasaki, K.; Rando, R.R. RNA Molecules That Specifically and Stoichiometrically Bind Aminoglycoside Antibiotics with High Affinities. Biochemistry 1996, 35, 12338-12346.
    • (1996) Biochemistry , vol.35 , pp. 12338-12346
    • Wang, Y.1    Killian, J.2    Hamasaki, K.3    Rando, R.R.4
  • 59
    • 0031051477 scopus 로고    scopus 로고
    • Specificity of Aminoglycoside Binding to RNA Construct Derived from the 16S rRNA Decoding Region and the HIV-RRE Activator Region
    • Wang, Y.; Hamasaki, K.; Rando, R.R. Specificity of Aminoglycoside Binding to RNA Construct Derived from the 16S rRNA Decoding Region and the HIV-RRE Activator Region. Biochemistry 1997, 36, 768-779.
    • (1997) Biochemistry , vol.36 , pp. 768-779
    • Wang, Y.1    Hamasaki, K.2    Rando, R.R.3
  • 60
    • 0033614825 scopus 로고    scopus 로고
    • Specificity in the Binding of Aminoglycoside to HIV-RRE RNA
    • Wang, Y.; Hamasaki, K.; Rando, R.R. Specificity in the Binding of Aminoglycoside to HIV-RRE RNA. Biochemistry 1999, 38, 8548-8554.
    • (1999) Biochemistry , vol.38 , pp. 8548-8554
    • Wang, Y.1    Hamasaki, K.2    Rando, R.R.3
  • 61
    • 0034852027 scopus 로고    scopus 로고
    • Aminoglycoside Binding to Human and Bacterial A-site rRNA Decoding Region Construct
    • Ryu, D.H.; Rando, R.R. Aminoglycoside Binding to Human and Bacterial A-site rRNA Decoding Region Construct. Bioorg. Med. Chem. 2001, 9, 2601-2608.
    • (2001) Bioorg. Med. Chem. , vol.9 , pp. 2601-2608
    • Ryu, D.H.1    Rando, R.R.2
  • 62
    • 0037143548 scopus 로고    scopus 로고
    • Stereospecificity of Aminoglycoside-Ribosomal Interactions
    • Ryu, D.H.; Litovchick, A.; Rando, R.R. Stereospecificity of Aminoglycoside-Ribosomal Interactions. Biochemistry 2002, 41, 10499-10509.
    • (2002) Biochemistry , vol.41 , pp. 10499-10509
    • Ryu, D.H.1    Litovchick, A.2    Rando, R.R.3
  • 63
    • 0141483331 scopus 로고    scopus 로고
    • RNA-ligand Interactions: Affinity and Specificity of Aminoglycoside Dimers and Acridine Conjugates to the HIV-1 Rev Response Element
    • Luedtke, N.W.; Liu, Q.; Tor, Y. RNA-ligand Interactions: Affinity and Specificity of Aminoglycoside Dimers and Acridine Conjugates to the HIV-1 Rev Response Element. Biochemistry 2003, 42, 11391-11403.
    • (2003) , vol.42 , pp. 11391-11403
    • Luedtke, N.W.1    Liu, Q.2    Tor, Y.3
  • 65
    • 8544250602 scopus 로고    scopus 로고
    • From Triplex to B-form Duplex Stabalization: Reversal of Target Selectivity by Aminoglycoside Dimers
    • Arya, D.P.; Coffee, R.L.; Xue, L. From Triplex to B-form Duplex Stabalization: Reversal of Target Selectivity by Aminoglycoside Dimers. Bioorg. Med. Chem. Lett. 2004, 14, 4643-4646.
    • (2004) Bioorg. Med. Chem. Lett. , vol.14 , pp. 4643-4646
    • Arya, D.P.1    Coffee, R.L.2    Xue, L.3
  • 66
    • 1642347123 scopus 로고    scopus 로고
    • Fluorescence-based Approach for Detecting and Characterizing Antibiotic-induced Conformational Changes in Ribosomal RNA: Comparing Aminoglycoside Binding to Prokaryotic and Eukaryotic Ribosomal RNA Sequences
    • Kaul, M.; Barbieri, C.M.; Pilch, D.S. Fluorescence-based Approach for Detecting and Characterizing Antibiotic-induced Conformational Changes in Ribosomal RNA: Comparing Aminoglycoside Binding to Prokaryotic and Eukaryotic Ribosomal RNA Sequences. J. Am. Chem. Soc. 2004, 126, 3447-3453.
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 3447-3453
    • Kaul, M.1    Barbieri, C.M.2    Pilch, D.S.3
  • 67
    • 4544240967 scopus 로고    scopus 로고
    • Surface Plasmon Resonance Evaluation of Various Aminoglycoside-RNA Hairpin Interactions Reveal Low Degree of Selectivity
    • Verhelst, S.H.; Michiels, P.J.; van der Marel, G.A.; van Boeckel, C.A.; van Boom, J.H. Surface Plasmon Resonance Evaluation of Various Aminoglycoside-RNA Hairpin Interactions Reveal Low Degree of Selectivity. Chem. Bio. Chem. 2004, 5, 937-942.
    • (2004) Chem. Bio. Chem. , vol.5 , pp. 937-942
    • Verhelst, S.H.1    Michiels, P.J.2    van der Marel, G.A.3    van Boeckel, C.A.4    van Boom, J.H.5
  • 70
    • 31944443056 scopus 로고    scopus 로고
    • Aminoglycoside-induced Reduction in Nucleotide Mobility at the Ribosomal RNA A-site as a Potentially Key Determinant of Antibacterial Activity
    • Kaul, M.; Barbieri, C.M.; Pilch, D.S. Aminoglycoside-induced Reduction in Nucleotide Mobility at the Ribosomal RNA A-site as a Potentially Key Determinant of Antibacterial Activity. J. Am. Chem. Soc. 2006, 128, 1261-1271.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 1261-1271
    • Kaul, M.1    Barbieri, C.M.2    Pilch, D.S.3
  • 72
    • 34548299086 scopus 로고    scopus 로고
    • Tryptophan-to-dye Fluorescence Energy Transfer Applied to Oxygen Sensing by Using Type-3 Copper Proteins
    • Zauner, G.; Strianes, M.; Bubacco, L.; Aartsma, T.J.; Tepper, A.W.J.W.; Canters, G.W. Tryptophan-to-dye Fluorescence Energy Transfer Applied to Oxygen Sensing by Using Type-3 Copper Proteins. Chem. Eur. J. 2007, 13, 7085-7090.
    • (2007) Chem. Eur. J. , vol.13 , pp. 7085-7090
    • Zauner, G.1    Strianes, M.2    Bubacco, L.3    Aartsma, T.J.4    Tepper, A.W.J.W.5    Canters, G.W.6


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