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Volumn 27, Issue 3, 2007, Pages 279-316

Modifications of aminoglycoside antibiotics targeting RNA

Author keywords

Aminoglycoside; Drug discovery; Review; Structure activity relationship; Targeting RNA

Indexed keywords

2 DEOXYSTREPTAMINE; 2,5 DIDEOXYSTREPTAMINE DERIVATIVE; AMINOGLYCOSIDE ANTIBIOTIC AGENT; AMINOGLYCOSIDE DERIVATIVE; AZEPANE GLYCOSIDE; CEPHALOSPORIN DERIVATIVE; DEOXYSTRYPTAMINE DERIVATIVE; FRAMYCETIN; GENTAMICIN; GENTAMICIN DERIVATIVE; GLYCOSIDE; GUANIDINOGLYCOSIDE DERIVATIVE; KANAMYCIN A; KANAMYCIN B; KANAMYCIN C; NEAMINE; NEOMYCIN; NEOMYCIN B DERIVATIVE; PAROMAMINE DERIVATIVE; PAROMOMYCIN; PAROMOMYCIN DERIVATIVE; PYRANMYCIN DERIVATIVE; RIBOSOME RNA; TOBRAMYCIN; TOBRAMYCIN DERIVATIVE; UNCLASSIFIED DRUG;

EID: 34247593152     PISSN: 01986325     EISSN: None     Source Type: Journal    
DOI: 10.1002/med.20085     Document Type: Review
Times cited : (56)

References (126)
  • 1
    • 0034595705 scopus 로고    scopus 로고
    • Strategies for the design of drug targeting RNA and RNA-protein complexes
    • Hermann T. Strategies for the design of drug targeting RNA and RNA-protein complexes. Angew Chem Int Ed 2000;39:1890-1905.
    • (2000) Angew Chem Int Ed , vol.39 , pp. 1890-1905
    • Hermann, T.1
  • 3
    • 0036761206 scopus 로고    scopus 로고
    • Rational ligand design for RNA: The role of static structure and conformational flexibility in target recognition
    • Hermann T. Rational ligand design for RNA: The role of static structure and conformational flexibility in target recognition. Biochimie 2002;84:869-875.
    • (2002) Biochimie , vol.84 , pp. 869-875
    • Hermann, T.1
  • 4
    • 0033152070 scopus 로고    scopus 로고
    • and the small molecule world
    • Tor Y. RNA and the small molecule world. Angew Chem Int Ed 1999;38:1579-1582.
    • (1999) Angew Chem Int Ed , vol.38 , pp. 1579-1582
    • Tor, Y.R.1
  • 5
    • 0034783659 scopus 로고    scopus 로고
    • Targeting RNA with small-molecule drugs: Therapeutic promise and chemical challenges
    • Gallego J, Varani G. Targeting RNA with small-molecule drugs: Therapeutic promise and chemical challenges. Acc Chem Res 2001;34:836-843.
    • (2001) Acc Chem Res , vol.34 , pp. 836-843
    • Gallego, J.1    Varani, G.2
  • 6
    • 0032419420 scopus 로고    scopus 로고
    • Saccharide-RNA recognition
    • Hermann T, Westhof E. Saccharide-RNA recognition. Biopoly 1998;48:155-165.
    • (1998) Biopoly , vol.48 , pp. 155-165
    • Hermann, T.1    Westhof, E.2
  • 7
    • 0142106950 scopus 로고    scopus 로고
    • RNA as a drug target: The case of aminoglycosides
    • Vicens Q, Westhof E. RNA as a drug target: The case of aminoglycosides. Chem Bio Chem 2003;4:1018-1023.
    • (2003) Chem Bio Chem , vol.4 , pp. 1018-1023
    • Vicens, Q.1    Westhof, E.2
  • 8
  • 9
    • 14844348264 scopus 로고    scopus 로고
    • Molecular insights into aminoglycoside action and resistance
    • Magnet S, Blanchard JS. 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
  • 10
    • 0035477570 scopus 로고    scopus 로고
    • Carbohydrate-based antibiotics: A new approach to tackling the problem of resistance
    • Ritter TK, Wong C-H. Carbohydrate-based antibiotics: A new approach to tackling the problem of resistance. Angew Chem Int Ed 2001;40:3508-3533.
    • (2001) Angew Chem Int Ed , vol.40 , pp. 3508-3533
    • Ritter, T.K.1    Wong, C.-H.2
  • 11
    • 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
  • 12
    • 0038811889 scopus 로고    scopus 로고
    • Aminoglycoside and its derivatives as ligands to target the ribosome
    • Tok JB-H, Bi L. Aminoglycoside and its derivatives as ligands to target the ribosome. Curr Top Med Chem 2003;3:1001-1019.
    • (2003) Curr Top Med Chem , vol.3 , pp. 1001-1019
    • Tok, J.B.-H.1    Bi, L.2
  • 13
    • 0142011647 scopus 로고    scopus 로고
    • Targeting RNA with small molecules
    • Tor Y. Targeting RNA with small molecules. Chem Bio Chem 2003;4:998-1007.
    • (2003) Chem Bio Chem , vol.4 , pp. 998-1007
    • Tor, Y.1
  • 14
    • 0033591922 scopus 로고    scopus 로고
    • Design and synthesis of new aminoglycoside antibiotics containing neamine as an optimal core structure: Correlation of antibiotic activity with in vitro inhibition of translation
    • Greenberg WA, Priestley ES, Sears PS, Alper PB, Rosenbohm C, Hendrix M, Hung SC, Wong C-H. Design and synthesis of new aminoglycoside antibiotics containing neamine as an optimal core structure: 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    Rosenbohm, C.5    Hendrix, M.6    Hung, S.C.7    Wong, C.-H.8
  • 15
    • 0030985913 scopus 로고    scopus 로고
    • Direct observation of aminoglycoside-RNA interactions by surface plasmon resonance
    • Hendrix M, Priestley ES, Joyce GF, Wong C-H. Direct observation of aminoglycoside-RNA interactions by surface plasmon resonance. J Am Chem Soc 1997;119:3641-3648.
    • (1997) J Am Chem Soc , vol.119 , pp. 3641-3648
    • Hendrix, M.1    Priestley, E.S.2    Joyce, G.F.3    Wong, C.-H.4
  • 16
    • 0030745434 scopus 로고    scopus 로고
    • Hydroxyamines as a new motif for the molecular recognition of phosphodiesters: Implications for aminoglycoside-RNA interactions
    • Hendrix M, Alper PB, Priestley ES, Wong C-H. Hydroxyamines as a new motif for the molecular recognition of phosphodiesters: Implications for aminoglycoside-RNA interactions. Angew Chem Int Ed 1997;36:95-98.
    • (1997) Angew Chem Int Ed , vol.36 , pp. 95-98
    • Hendrix, M.1    Alper, P.B.2    Priestley, E.S.3    Wong, C.-H.4
  • 17
    • 0032569212 scopus 로고    scopus 로고
    • A library approach to the discovery of small molecules that recognize RNA: Use of a 1,3-hydroxyamine motif as core
    • Wong C-H, Hendrix M, Manning DD, Rosenbohm C, Greenberg WA. A library approach to the discovery of small molecules that recognize RNA: Use of a 1,3-hydroxyamine motif as core. J Am Chem Soc 1998;120:8319-8327.
    • (1998) J Am Chem Soc , vol.120 , pp. 8319-8327
    • Wong, C.-H.1    Hendrix, M.2    Manning, D.D.3    Rosenbohm, C.4    Greenberg, W.A.5
  • 18
    • 0035898289 scopus 로고    scopus 로고
    • Parallel synthesis of a small library of novel aminoglycoside analogs based on 2-amino-2-deoxy- D-glucose and D-ribose scaffolds
    • Rosenbohm C, Berghe DV, Vlietinck A, Wengel J. Parallel synthesis of a small library of novel aminoglycoside analogs based on 2-amino-2-deoxy- D-glucose and D-ribose scaffolds. Tetrahedron 2001;57:6277-6287.
    • (2001) Tetrahedron , vol.57 , pp. 6277-6287
    • Rosenbohm, C.1    Berghe, D.V.2    Vlietinck, A.3    Wengel, J.4
  • 19
    • 0022470564 scopus 로고
    • Rapid chemical probing of conformation in 16S ribosomal RNA and 30S ribosomal subunits using primer extension
    • Moazed D, Stern S, Noller HF. Rapid chemical probing of conformation in 16S ribosomal RNA and 30S ribosomal subunits using primer extension. J Mol Biol 1986;187:399-416.
    • (1986) J Mol Biol , vol.187 , pp. 399-416
    • Moazed, D.1    Stern, S.2    Noller, H.F.3
  • 22
    • 22144490214 scopus 로고    scopus 로고
    • Conformational constraint as a means for understanding RNA-aminoglycoside specificity
    • Blount KF, Zhao F, Hermann T, Tor Y. Conformational constraint as a means for understanding RNA-aminoglycoside specificity. J Am Chem Soc 2005;127:9818-9829.
    • (2005) J Am Chem Soc , vol.127 , pp. 9818-9829
    • Blount, K.F.1    Zhao, F.2    Hermann, T.3    Tor, Y.4
  • 23
    • 0030272096 scopus 로고    scopus 로고
    • A structural model for the HIV-1 Rev-RRE complex deduced from altered-specificity rev variants isolated by a rapid genetic strategy
    • Jain C, Belasco J. A structural model for the HIV-1 Rev-RRE complex deduced from altered-specificity rev variants isolated by a rapid genetic strategy. Cell 1996;87:115-125.
    • (1996) Cell , vol.87 , pp. 115-125
    • Jain, C.1    Belasco, J.2
  • 25
    • 0034617166 scopus 로고    scopus 로고
    • Structural rearrangements of HIV-1 Tat-responsive RNA upon binding of neomycin B
    • Faber C, Sticht H, Schweimer K, Rosch P. Structural rearrangements of HIV-1 Tat-responsive RNA upon binding of neomycin B. J Biol Chem 2000;275:20660-20666.
    • (2000) J Biol Chem , vol.275 , pp. 20660-20666
    • Faber, C.1    Sticht, H.2    Schweimer, K.3    Rosch, P.4
  • 26
    • 0034699836 scopus 로고    scopus 로고
    • An aminoglycoside antibiotic, neamine, and its aromatic ring-substituted derivatives as potential inhibitors for HIV-1 RRE-Rev
    • Hamasaki K, Woo M-C, Ueno A. An aminoglycoside antibiotic, neamine, and its aromatic ring-substituted derivatives as potential inhibitors for HIV-1 RRE-Rev. Tetrahedron Lett 2000;41:8327-8332.
    • (2000) Tetrahedron Lett , vol.41 , pp. 8327-8332
    • Hamasaki, K.1    Woo, M.-C.2    Ueno, A.3
  • 27
    • 0034698782 scopus 로고    scopus 로고
    • A high-throughput screening utilizing intramolecular fluorescence resonance energy transfer for the discovery of the molecules that bind HIV-1 TAR RNA specifically
    • Matsumoto C, Hamasaki K, Mihara H, Ueno A. A high-throughput screening utilizing intramolecular fluorescence resonance energy transfer for the discovery of the molecules that bind HIV-1 TAR RNA specifically. Bioorg Med Chem Lett 2000;10:1857-1861.
    • (2000) Bioorg Med Chem Lett , vol.10 , pp. 1857-1861
    • Matsumoto, C.1    Hamasaki, K.2    Mihara, H.3    Ueno, A.4
  • 28
    • 0035951091 scopus 로고    scopus 로고
    • Neomycin B-arginine conjugate, a novel HIV-1 Tat antagonist: Synthesis and anti-HIV activities
    • Litovchick A, Lapidot A, Eisenstein M, Kalinkovich A, Borkow G. Neomycin B-arginine conjugate, a novel HIV-1 Tat antagonist: Synthesis and anti-HIV activities. Biochemistry 2001;40:15612-15623.
    • (2001) Biochemistry , vol.40 , pp. 15612-15623
    • Litovchick, A.1    Lapidot, A.2    Eisenstein, M.3    Kalinkovich, A.4    Borkow, G.5
  • 29
    • 0035952260 scopus 로고    scopus 로고
    • Aminoglycoside antibiotics, neamine and its derivatives as potent inhibitors for the RNA-protein interactions derived from HIV-1 activators
    • Hamasaki K, Uero A. Aminoglycoside antibiotics, neamine and its derivatives as potent inhibitors for the RNA-protein interactions derived from HIV-1 activators. Bioorg Med Chem Lett 2001;11:591-594.
    • (2001) Bioorg Med Chem Lett , vol.11 , pp. 591-594
    • Hamasaki, K.1    Uero, A.2
  • 30
    • 0033601437 scopus 로고    scopus 로고
    • Synthesis of neamine libraries for RNA recognition using solution phase chemistry
    • Nunns CL, Spence LA, Slater MJ, Berrisford DJ. 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
  • 31
    • 4143107024 scopus 로고    scopus 로고
    • A route for preparing new neamine derivatives targeting HIV-1 TAR RNA
    • Riguet E, Désire J, Baillyb C, Décout J-L. A route for preparing new neamine derivatives targeting HIV-1 TAR RNA. Tetrahedron 2004;60:8053-8064.
    • (2004) Tetrahedron , vol.60 , pp. 8053-8064
    • Riguet, E.1    Désire, J.2    Baillyb, C.3    Décout, J.-L.4
  • 32
    • 0029825658 scopus 로고    scopus 로고
    • Structure of the A site of Escherichia coli 16S ribosomal RNA complexed with an aminoglycoside antibiotic
    • Fourmy D, Recht MI, Blanchard SC, Puglisi JD. Structure of the A site of Escherichia coli 16S ribosomal RNA complexed with an aminoglycoside antibiotic. Science 1996;274:1367-1371.
    • (1996) Science , vol.274 , pp. 1367-1371
    • Fourmy, D.1    Recht, M.I.2    Blanchard, S.C.3    Puglisi, J.D.4
  • 33
    • 0034886697 scopus 로고    scopus 로고
    • Crystal structure of paromomycin docked into the eubacterial ribosomal decoding A Site
    • Vicensl Q, Westhofl E. Crystal structure of paromomycin docked into the eubacterial ribosomal decoding A Site. Structure 2001;9:647-658.
    • (2001) Structure , vol.9 , pp. 647-658
    • Vicensl, Q.1    Westhofl, E.2
  • 34
    • 0037229886 scopus 로고    scopus 로고
    • Comparison of X-ray crystal structure of the 30S subunit-antibiotic complex with NMR structure of decoding site oligonucleotide-paromomycin complex
    • Lynch SR, Jr., Gonzalez RL, Puglisi JD. Comparison of X-ray crystal structure of the 30S subunit-antibiotic complex with NMR structure of decoding site oligonucleotide-paromomycin complex. Structure 2003;11:43-53.
    • (2003) Structure , vol.11 , pp. 43-53
    • Lynch Jr., S.R.1    Gonzalez, R.L.2    Puglisi, J.D.3
  • 37
    • 0033596314 scopus 로고    scopus 로고
    • An antibiotic cloaked by its own resistance enzyme
    • Haddad J, Vakulenko S, Mobashery S. An antibiotic cloaked by its own resistance enzyme. J Am Chem Soc 1999;121:11922-11923.
    • (1999) J Am Chem Soc , vol.121 , pp. 11922-11923
    • Haddad, J.1    Vakulenko, S.2    Mobashery, S.3
  • 38
    • 3342967467 scopus 로고    scopus 로고
    • Deoxystreptamine dimers bind to RNA hairpin loops
    • Liu X, Thomas JR, Hergenrother PJ. Deoxystreptamine dimers bind to RNA hairpin loops. J Am Chem Soc 2004;126:9196-9197.
    • (2004) J Am Chem Soc , vol.126 , pp. 9196-9197
    • Liu, X.1    Thomas, J.R.2    Hergenrother, P.J.3
  • 39
    • 17244378938 scopus 로고    scopus 로고
    • 2-Deoxystreptamine: Central scaffold of aminoglycoside antibiotics
    • Busscher GF, Rutjes FPJT, van Delft FL. 2-Deoxystreptamine: Central scaffold of aminoglycoside antibiotics. Chem Rev 2005;105:775-791.
    • (2005) Chem Rev , vol.105 , pp. 775-791
    • Busscher, G.F.1    Rutjes, F.P.J.T.2    van Delft, F.L.3
  • 40
    • 0034677697 scopus 로고    scopus 로고
    • Design of small molecules that recognize RNA: Development of aminoglycosides as potential antitumor agents that target oncogenic RNA sequences
    • Sucheck SJ, Greenberg WA, Tolbert TJ, Wong C-H. Design of small molecules that recognize RNA: Development of aminoglycosides as potential antitumor agents that target oncogenic RNA sequences. Angew Chem Int Ed 2000;39:1080-1084.
    • (2000) Angew Chem Int Ed , vol.39 , pp. 1080-1084
    • Sucheck, S.J.1    Greenberg, W.A.2    Tolbert, T.J.3    Wong, C.-H.4
  • 42
    • 0037429032 scopus 로고    scopus 로고
    • Probing the functional requirements of the L-haba side-chain of amikacin - Synthesis, 16S A-site rRNA binding, and antibacterial activity
    • Hanessian S, Kornienko A, Swayzeb EE. Probing the functional requirements of the L-haba side-chain of amikacin - Synthesis, 16S A-site rRNA binding, and antibacterial activity. Tetrahedron 2003;59:995-1007.
    • (2003) Tetrahedron , vol.59 , pp. 995-1007
    • Hanessian, S.1    Kornienko, A.2    Swayzeb, E.E.3
  • 43
    • 0037467430 scopus 로고    scopus 로고
    • The complex of a designer antibiotic with a model aminoacyl site of the 30S ribosomal subunit revealed by X-ray crystallography
    • Russell RJM, Murray JB, Lentzen G, Haddad J, Mobashery S. The complex of a designer antibiotic with a model aminoacyl site of the 30S ribosomal subunit revealed by X-ray crystallography. J Am Chem Soc 2003;125:3410-3411.
    • (2003) J Am Chem Soc , vol.125 , pp. 3410-3411
    • Russell, R.J.M.1    Murray, J.B.2    Lentzen, G.3    Haddad, J.4    Mobashery, S.5
  • 44
    • 0029905917 scopus 로고    scopus 로고
    • Rapid combinatorial synthesis of aminoglycoside antibiotic mimetics: Use of a polyethylene glycol-linked amine and a neamine-derived aldehyde in multiple component condensation as a strategy for the discovery of new inhibitors of the HIV RNA Rev responsive element
    • Park WKC, Auer M, Jaksche H, Wong C-H. Rapid combinatorial synthesis of aminoglycoside antibiotic mimetics: Use of a polyethylene glycol-linked amine and a neamine-derived aldehyde in multiple component condensation as a strategy for the discovery of new inhibitors of the HIV RNA Rev responsive element. J Am Chem Soc 1996;118:10150-10155.
    • (1996) J Am Chem Soc , vol.118 , pp. 10150-10155
    • Park, W.K.C.1    Auer, M.2    Jaksche, H.3    Wong, C.-H.4
  • 45
    • 0034696752 scopus 로고    scopus 로고
    • Aminoglycoside binding in the major groove of duplex RNA: The thermodynamic and electrostatic forces that govern recognition
    • Jin E, Katritch V, Olson WK, Kharatisvili M, Abagyan R, Pilch DS. Aminoglycoside binding in the major groove of duplex RNA: The thermodynamic and electrostatic forces that govern recognition. J Mol Biol 2000;298:95-110.
    • (2000) J Mol Biol , vol.298 , pp. 95-110
    • Jin, E.1    Katritch, V.2    Olson, W.K.3    Kharatisvili, M.4    Abagyan, R.5    Pilch, D.S.6
  • 46
    • 0033117680 scopus 로고    scopus 로고
    • Novel structural templates for estrogen-receptor ligands and prospects for combinatorial synthesis of estrogens
    • Fink BE, Mortensen DS, Stauffer SR, Aron ZD, Katzenellenbogen JA. Novel structural templates for estrogen-receptor ligands and prospects for combinatorial synthesis of estrogens. Chem Biol 1999;6: 205-219.
    • (1999) Chem Biol , vol.6 , pp. 205-219
    • Fink, B.E.1    Mortensen, D.S.2    Stauffer, S.R.3    Aron, Z.D.4    Katzenellenbogen, J.A.5
  • 47
    • 0035979090 scopus 로고    scopus 로고
    • An efficient synthesis of mimetics of neamine for RNA recognition
    • Ding YL, Hofstadler SA, Swayze EE, Griffey RH. An efficient synthesis of mimetics of neamine for RNA recognition. Org Lett 2001;3:1621-1623.
    • (2001) Org Lett , vol.3 , pp. 1621-1623
    • Ding, Y.L.1    Hofstadler, S.A.2    Swayze, E.E.3    Griffey, R.H.4
  • 48
    • 0346250021 scopus 로고    scopus 로고
    • Efficient synthesis of heterocyclic 2-deoxysteptamine derivatives as RNA binding ligands
    • Ding YL, Hofstadler SA, Swayze EE, Griffey RH. Efficient synthesis of heterocyclic 2-deoxysteptamine derivatives as RNA binding ligands. Chem Lett 2003;32:908-909.
    • (2003) Chem Lett , vol.32 , pp. 908-909
    • Ding, Y.L.1    Hofstadler, S.A.2    Swayze, E.E.3    Griffey, R.H.4
  • 49
    • 0042074617 scopus 로고    scopus 로고
    • Design and synthesis of paromomycin-related heterocycle-substituted aminoglycoside mimetics based on a mass spectrometry RNA binding assay
    • Ding YL, Hofstadler SA, Swayze EE, Risen L, Griffey RH. 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.L.1    Hofstadler, S.A.2    Swayze, E.E.3    Risen, L.4    Griffey, R.H.5
  • 51
    • 0034704217 scopus 로고    scopus 로고
    • The structural basis for the action of the antibiotics tetracycline, pactamycin, and hygromycin B on the 30S ribosomal subunit
    • Brodersen DE, Clemons WM, Carter AP, Morgan-Warren RJ, Wimberly BT, Ramakrishnan V. The structural basis for the action of the antibiotics tetracycline, pactamycin, and hygromycin B on the 30S ribosomal subunit. Cell 2000;103:1143-1154.
    • (2000) Cell , vol.103 , pp. 1143-1154
    • Brodersen, D.E.1    Clemons, W.M.2    Carter, A.P.3    Morgan-Warren, R.J.4    Wimberly, B.T.5    Ramakrishnan, V.6
  • 54
    • 0037470560 scopus 로고    scopus 로고
    • Crystal structure of geneticin bound to a bacterial 16S ribosomal RNA A site oligonucleotide
    • Vicens Q, Westhof E. Crystal structure of geneticin bound to a bacterial 16S ribosomal RNA A site oligonucleotide. J Mol Biol 2003;326:1175-1188.
    • (2003) J Mol Biol , vol.326 , pp. 1175-1188
    • Vicens, Q.1    Westhof, E.2
  • 55
    • 0035986708 scopus 로고    scopus 로고
    • Crystal structure of a complex between the aminoglycoside tobramycin and an oligonucleotide containing the ribosomal decoding A site
    • Vicens Q, Westhof E. Crystal structure of a complex between the aminoglycoside tobramycin and an oligonucleotide containing the ribosomal decoding A site. Chem Biol 2002;9:747-755.
    • (2002) Chem Biol , vol.9 , pp. 747-755
    • Vicens, Q.1    Westhof, E.2
  • 59
  • 60
    • 4644305973 scopus 로고    scopus 로고
    • Disaccharide mimetics of the aminoglycoside antibiotic neamine
    • Venot A, Swayze EE, Griffey RH, Boons G-J. Disaccharide mimetics of the aminoglycoside antibiotic neamine. Chem Bio Chem 2004;5:1228-1236.
    • (2004) Chem Bio Chem , vol.5 , pp. 1228-1236
    • Venot, A.1    Swayze, E.E.2    Griffey, R.H.3    Boons, G.-J.4
  • 62
    • 0033673387 scopus 로고    scopus 로고
    • Structures of two RNA domains essential for hepatitis C virus internal ribosome entry site function
    • Lukavsky PJ, Otto GA, Lancaster AM, Sarnow P, Puglisi JD. Structures of two RNA domains essential for hepatitis C virus internal ribosome entry site function. Nat Struct Biol 2000;7:1105-1110.
    • (2000) Nat Struct Biol , vol.7 , pp. 1105-1110
    • Lukavsky, P.J.1    Otto, G.A.2    Lancaster, A.M.3    Sarnow, P.4    Puglisi, J.D.5
  • 65
    • 0021802841 scopus 로고
    • Fused transcript of abl and bcr genes in chronic myelogenous leukaemia
    • Shtivelman E, Lifshitz B, Gale RP, Canaani E. Fused transcript of abl and bcr genes in chronic myelogenous leukaemia. Nature 1985;315:550.
    • (1985) Nature , vol.315 , pp. 550
    • Shtivelman, E.1    Lifshitz, B.2    Gale, R.P.3    Canaani, E.4
  • 66
    • 0041526754 scopus 로고    scopus 로고
    • Surface plasmon resonance study of RNA-aminoglycoside interaction
    • Wong C-H, Liang F-S. Surface plasmon resonance study of RNA-aminoglycoside interaction. Methods Enzymol 2003;362:340-353.
    • (2003) Methods Enzymol , vol.362 , pp. 340-353
    • Wong, C.-H.1    Liang, F.-S.2
  • 68
    • 0026705492 scopus 로고
    • Epidemiology of drug resistance: Implications for a post-antimicrobial era
    • Cohen ML. Epidemiology of drug resistance: Implications for a post-antimicrobial era. Science 1992;257:1050-1055.
    • (1992) Science , vol.257 , pp. 1050-1055
    • Cohen, M.L.1
  • 69
    • 0026760182 scopus 로고
    • The crisis in antibiotic resistance
    • Neu HC. The crisis in antibiotic resistance. Science 1992;257:1064-1072.
    • (1992) Science , vol.257 , pp. 1064-1072
    • Neu, H.C.1
  • 70
    • 34247564829 scopus 로고    scopus 로고
    • Chang C-WT, Hui Y, Elcher B, Wang J, Li J, Rai R. Pyranmycins, a novel class of aminoglycosides with improved acid stability: The SAR of D-pyranoses on ring III of pyranmycin. Org Lett 2002;4:6403-6406.
    • Chang C-WT, Hui Y, Elcher B, Wang J, Li J, Rai R. Pyranmycins, a novel class of aminoglycosides with improved acid stability: The SAR of D-pyranoses on ring III of pyranmycin. Org Lett 2002;4:6403-6406.
  • 71
    • 0037078852 scopus 로고    scopus 로고
    • The synthesis of L-aminosugar and the studies of L-pyranoses on the ring III of pyranmycins
    • Wang J, Li J, Tuttle D, Takemoto JY, Chang C-WT. The synthesis of L-aminosugar and the studies of L-pyranoses on the ring III of pyranmycins. Org Lett 2002;4:3997-4000.
    • (2002) Org Lett , vol.4 , pp. 3997-4000
    • Wang, J.1    Li, J.2    Tuttle, D.3    Takemoto, J.Y.4    Chang, C.-W.T.5
  • 72
    • 0037669300 scopus 로고    scopus 로고
    • Exploring the optimal site for modifications of pyranmycins with the extended arm approach
    • Li J, Wang J, Hui Y, Chang C-WT. Exploring the optimal site for modifications of pyranmycins with the extended arm approach. Org Lett 2003;5:431-434.
    • (2003) Org Lett , vol.5 , pp. 431-434
    • Li, J.1    Wang, J.2    Hui, Y.3    Chang, C.-W.T.4
  • 74
    • 2442556115 scopus 로고    scopus 로고
    • Application of glycodiversification: Expedient synthesis and antibacterial evaluation of a library of kanamycin B analogues
    • Li J, Wang J, Czyryca PJ, Chang H, Orsak TW, Evanson R, Chang C-WT. Application of glycodiversification: Expedient synthesis and antibacterial evaluation of a library of kanamycin B analogues. Org Lett 2004;6:1381-1384.
    • (2004) Org Lett , vol.6 , pp. 1381-1384
    • Li, J.1    Wang, J.2    Czyryca, P.J.3    Chang, H.4    Orsak, T.W.5    Evanson, R.6    Chang, C.-W.T.7
  • 75
    • 0142106443 scopus 로고    scopus 로고
    • A new class of branched aminoglycosides: Pseudopentasaccharide derivatives of neomycin B
    • Fridman M, Belakhov V, Yaron S, Baasov T. A new class of branched aminoglycosides: Pseudopentasaccharide derivatives of neomycin B. Org Lett 2003;5:3575-3578.
    • (2003) Org Lett , vol.5 , pp. 3575-3578
    • Fridman, M.1    Belakhov, V.2    Yaron, S.3    Baasov, T.4
  • 76
    • 0001199519 scopus 로고
    • Oligoamines as simple and efficient catalysts for RNA hydrolysis
    • Yoshinari K, Yamazaki K, Komiyama M. Oligoamines as simple and efficient catalysts for RNA hydrolysis. J Am Chem Soc 1991;113:5899-5901.
    • (1991) J Am Chem Soc , vol.113 , pp. 5899-5901
    • Yoshinari, K.1    Yamazaki, K.2    Komiyama, M.3
  • 77
    • 0001015862 scopus 로고    scopus 로고
    • Kinetic analysis of diamine-catalyzed RNA hydrolysis
    • Komiyama M, Yoshinari K. Kinetic analysis of diamine-catalyzed RNA hydrolysis. J Org Chem 1997;62:2155-2160.
    • (1997) J Org Chem , vol.62 , pp. 2155-2160
    • Komiyama, M.1    Yoshinari, K.2
  • 78
    • 0037025729 scopus 로고    scopus 로고
    • The catalytic activity of ribose-containing polymers for the hydrolysis of phosphodiester and the cleavage of nucleic acid
    • Han MJ, Yoo KS, Kim YH, Chang JY. The catalytic activity of ribose-containing polymers for the hydrolysis of phosphodiester and the cleavage of nucleic acid. Tetrahedron Lett 2002;43:5597-5600.
    • (2002) Tetrahedron Lett , vol.43 , pp. 5597-5600
    • Han, M.J.1    Yoo, K.S.2    Kim, Y.H.3    Chang, J.Y.4
  • 79
    • 34247577803 scopus 로고    scopus 로고
    • Resistant strains included E. coliXL1(pET9d, Pseudomonas aeuriginosa(ATCC 27853, and SalmonellaVirchow (SV49, E. coli XL1-(pET9d) is an antibiotic-sensitive laboratory strain of E. coli that harbors plasmid pET9d with the cloned orf2 gene, which codes for aminoglycoside kinase APH(3′, P. aeuriginosa is a Gram-negative pathogen. The aph(3′)-IIb gene, which codes for APH(3′, is a chromosomal gene that can be found in many clinical isolates of P. aeruginosa, including the ATCC 27853 strain, and likely accounts at least partly for the resistance of Pseudomonas to aminoglycosides. S. Virchow (SV49) is a clinical multidrug-resistant strain obtained from poultry and found to be resistant to streptomycin, tetracycline, ampicillin, sulfa, kanamycin, and neomycin. The mechanism(s) of resistance of this strain is still unknown
    • Resistant strains included E. coliXL1(pET9d), Pseudomonas aeuriginosa(ATCC 27853), and SalmonellaVirchow (SV49). E. coli XL1-(pET9d) is an antibiotic-sensitive laboratory strain of E. coli that harbors plasmid pET9d with the cloned orf2 gene, which codes for aminoglycoside kinase APH(3′). P. aeuriginosa is a Gram-negative pathogen. The aph(3′)-IIb gene, which codes for APH(3′), is a chromosomal gene that can be found in many clinical isolates of P. aeruginosa, including the ATCC 27853 strain, and likely accounts at least partly for the resistance of Pseudomonas to aminoglycosides. S. Virchow (SV49) is a clinical multidrug-resistant strain obtained from poultry and found to be resistant to streptomycin, tetracycline, ampicillin, sulfa, kanamycin, and neomycin. The mechanism(s) of resistance of this strain is still unknown.
  • 83
    • 0034646370 scopus 로고    scopus 로고
    • Combinatorial target-guided ligand assembly: Identification of potent subtype-selective c-Src inhibitors
    • Maly DJ, Choong IC, Ellman JA. Combinatorial target-guided ligand assembly: Identification of potent subtype-selective c-Src inhibitors. Proc Natl Acad Sci USA 2000;97:2419-2424.
    • (2000) Proc Natl Acad Sci USA , vol.97 , pp. 2419-2424
    • Maly, D.J.1    Choong, I.C.2    Ellman, J.A.3
  • 86
    • 12344323881 scopus 로고    scopus 로고
    • Dual effect of synthetic aminoglycosides: Antibacterial activity against bacillus anthracis and inhibition of anthrax lethal factor
    • Fridman M, Belakhov V, Lee LV, 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    Belakhov, V.2    Lee, L.V.3    Liang, F.-S.4    Wong, C.-H.5    Baasov, T.6
  • 88
    • 0034624435 scopus 로고    scopus 로고
    • Neomycin-acridine conjugate: A potent inhibitor of Rev-RRE binding
    • Kirk SR, Luedtke NW, 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
  • 89
    • 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 KH, Jeong S, Hyun S, Shin KJ, 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
  • 90
    • 0038682830 scopus 로고    scopus 로고
    • Combining the best in triplex recognition: Synthesis and nucleic acid binding of a BQQ-neomycin conjugate
    • Arya DP, Xue L, Tennant P. Combining the best in triplex recognition: Synthesis and nucleic acid binding of a BQQ-neomycin conjugate. J Am Chem Soc 2003;125:8070-8071.
    • (2003) J Am Chem Soc , vol.125 , pp. 8070-8071
    • Arya, D.P.1    Xue, L.2    Tennant, P.3
  • 92
    • 0032507263 scopus 로고    scopus 로고
    • Probing the specificity of aminoglycoside-ribosomal RNA interactions with designed synthetic analogs
    • Alper PB, Hendrix M, Sears P, Wong C-H. Probing the specificity of aminoglycoside-ribosomal RNA interactions with designed synthetic analogs. J Am Chem Soc 1998;120:1965-1978.
    • (1998) J Am Chem Soc , vol.120 , pp. 1965-1978
    • Alper, P.B.1    Hendrix, M.2    Sears, P.3    Wong, C.-H.4
  • 93
    • 0032212026 scopus 로고    scopus 로고
    • Deciphering RNA recognition: Aminoglycoside binding to the hammerhead ribozyme
    • Tor Y, Hermann T, Westhof E. Deciphering RNA recognition: Aminoglycoside binding to the hammerhead ribozyme. Chem Biol 1998;5:R277-R283.
    • (1998) Chem Biol , vol.5
    • Tor, Y.1    Hermann, T.2    Westhof, E.3
  • 94
    • 0032860283 scopus 로고    scopus 로고
    • tRNA(Phe) binds aminoglycoside antibiotics
    • Kirk SR, Tor Y. tRNA(Phe) binds aminoglycoside antibiotics. Bioorg Med Chem 1999;7:1979-1991.
    • (1999) Bioorg Med Chem , vol.7 , pp. 1979-1991
    • Kirk, S.R.1    Tor, Y.2
  • 95
    • 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
  • 96
    • 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 NW, 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) Biochemistry , vol.42 , pp. 11391-11403
    • Luedtke, N.W.1    Liu, Q.2    Tor, Y.3
  • 97
    • 0035821413 scopus 로고    scopus 로고
    • Binding of dimeric aminoglycosides to the HIV-1 Rev responsive element (RRE) RNA construct
    • Tok JB-H, Dunn LJ, Jean RCD. Binding of dimeric aminoglycosides to the HIV-1 Rev responsive element (RRE) RNA construct. Bioorg Med Chem Lett 2001;11:1127-1131.
    • (2001) Bioorg Med Chem Lett , vol.11 , pp. 1127-1131
    • Tok, J.B.-H.1    Dunn, L.J.2    Jean, R.C.D.3
  • 98
    • 0034679859 scopus 로고    scopus 로고
    • Enhanced binding of aminoglycoside dimers to a "dimerized" A-Site 16S rRNA construct
    • Tok JB-H, Huffman GR. Enhanced binding of aminoglycoside dimers to a "dimerized" A-Site 16S rRNA construct. Bioorg Med Chem Lett 2000;14:1593-1595.
    • (2000) Bioorg Med Chem Lett , vol.14 , pp. 1593-1595
    • Tok, J.B.-H.1    Huffman, G.R.2
  • 99
    • 0035914615 scopus 로고    scopus 로고
    • Novel synthesis and RNA-binding properties of aminoglycoside dimers conjugated via a naphthalene diimide-based intercalator
    • Tok JB-H, Fenke 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    Fenke, J.2
  • 102
    • 3342967467 scopus 로고    scopus 로고
    • Deoxystreptamine dimers bind to RNA hairpin loops
    • Liu X, Thomas JR, Hergenrother PJ. Deoxystreptamine dimers bind to RNA hairpin loops. J Am Chem Soc 2004;126:9196-9197.
    • (2004) J Am Chem Soc , vol.126 , pp. 9196-9197
    • Liu, X.1    Thomas, J.R.2    Hergenrother, P.J.3
  • 103
    • 24744443295 scopus 로고    scopus 로고
    • Size-specific ligands for RNA hairpin loops
    • Thomas JR, Liu X, Hergenrother PJ. Size-specific ligands for RNA hairpin loops. J Am Chem Soc 2005;127:12434-12435.
    • (2005) J Am Chem Soc , vol.127 , pp. 12434-12435
    • Thomas, J.R.1    Liu, X.2    Hergenrother, P.J.3
  • 105
    • 0034614052 scopus 로고    scopus 로고
    • Guanidinoglycosides: A novel family of RNA ligands
    • Luedtke NW, Baker TJ, Goodman M, Tor Y. Guanidinoglycosides: A novel family of RNA ligands. J Am Chem Soc 2000;122:12035-12036.
    • (2000) J Am Chem Soc , vol.122 , pp. 12035-12036
    • Luedtke, N.W.1    Baker, T.J.2    Goodman, M.3    Tor, Y.4
  • 106
    • 0037049170 scopus 로고    scopus 로고
    • Synthesis of novel guanidine incorporated aminoglycosides, guanidinopyranmycins
    • Hui Y, Ptak R, Paulman R, Pallansch M, Chang C-WT. Synthesis of novel guanidine incorporated aminoglycosides, guanidinopyranmycins. Tetrahedron Lett 2002;43:9255-9257.
    • (2002) Tetrahedron Lett , vol.43 , pp. 9255-9257
    • Hui, Y.1    Ptak, R.2    Paulman, R.3    Pallansch, M.4    Chang, C.-W.T.5
  • 107
    • 0034731571 scopus 로고    scopus 로고
    • Synthesis and anti-HIV activity of guanidinoglycosides
    • Baker TJ, Luedtke NW, Tor Y, Goodman M. Synthesis and anti-HIV activity of guanidinoglycosides. J Org Chem 2000;65:9054-9058.
    • (2000) J Org Chem , vol.65 , pp. 9054-9058
    • Baker, T.J.1    Luedtke, N.W.2    Tor, Y.3    Goodman, M.4
  • 108
    • 0141954275 scopus 로고    scopus 로고
    • Cellular uptake of aminoglycosides, guanidinoglycosides, and polyarginine
    • Luedtke NW, Carmichael P, Tor Y. Cellular uptake of aminoglycosides, guanidinoglycosides, and polyarginine. J Am Chem Soc 2003;125:12374-12375.
    • (2003) J Am Chem Soc , vol.125 , pp. 12374-12375
    • Luedtke, N.W.1    Carmichael, P.2    Tor, Y.3
  • 109
    • 0026846684 scopus 로고
    • Activation of HIV transcription by Tat
    • Frankel AD. Activation of HIV transcription by Tat. Curr Opin Genet Dev 1992;2:293-298.
    • (1992) Curr Opin Genet Dev , vol.2 , pp. 293-298
    • Frankel, A.D.1
  • 110
    • 0029741456 scopus 로고    scopus 로고
    • The regulation of human immunodeficiency virus type-1 gene expression
    • Kingsman SM, Kingsman AJ. The regulation of human immunodeficiency virus type-1 gene expression. Eur J Biochem 1996;240:491-507.
    • (1996) Eur J Biochem , vol.240 , pp. 491-507
    • Kingsman, S.M.1    Kingsman, A.J.2
  • 111
    • 0029911702 scopus 로고    scopus 로고
    • Anti-HIV-1 activity of an oligocationic compound is mediated via gp120 V3 interactions
    • O'Brien WA, Sumner-Smith M, Mao SH, Sadeghi S, Zhao J-Q, Chen ISY. Anti-HIV-1 activity of an oligocationic compound is mediated via gp120 V3 interactions. J Virol 1996;70:2825-2831.
    • (1996) J Virol , vol.70 , pp. 2825-2831
    • O'Brien, W.A.1    Sumner-Smith, M.2    Mao, S.H.3    Sadeghi, S.4    Zhao, J.-Q.5    Chen, I.S.Y.6
  • 112
    • 0031280039 scopus 로고    scopus 로고
    • Specific recognition of HIV-1 TAR RNA by a D-Tat peptide
    • Huq I, Wang X, Rana TM. Specific recognition of HIV-1 TAR RNA by a D-Tat peptide. Nature Struct Biol 1997;4:881-882.
    • (1997) Nature Struct Biol , vol.4 , pp. 881-882
    • Huq, I.1    Wang, X.2    Rana, T.M.3
  • 116
    • 0027476547 scopus 로고
    • Electrostatic interactions modulate the RNA-binding and transactivation specificities of the human immunodeficiency virus and simian immunodeficiency virus Tat proteins
    • Tao J, Frankel AD. Electrostatic interactions modulate the RNA-binding and transactivation specificities of the human immunodeficiency virus and simian immunodeficiency virus Tat proteins. Proc Natl Acad Sci USA 1993;90:1571-1575.
    • (1993) Proc Natl Acad Sci USA , vol.90 , pp. 1571-1575
    • Tao, J.1    Frankel, A.D.2
  • 117
    • 0033028501 scopus 로고    scopus 로고
    • Arginine-aminoglycoside conjugates that bind to HIV transactivation responsive element RNA in vitro
    • Litovchick A, Evdokimov AG, Lapidot A. Arginine-aminoglycoside conjugates that bind to HIV transactivation responsive element RNA in vitro. FEBS Letters 1999;445:73-79.
    • (1999) FEBS Letters , vol.445 , pp. 73-79
    • Litovchick, A.1    Evdokimov, A.G.2    Lapidot, A.3
  • 118
    • 0034696520 scopus 로고    scopus 로고
    • Aminoglycoside-arginine conjugates that bind TAR RNA: Synthesis, characterization, and antiviral activity
    • Litovchick A, Evdokimov AG, Lapidot A. Aminoglycoside-arginine conjugates that bind TAR RNA: Synthesis, characterization, and antiviral activity. Biochemistry 2000;39:2838-2852.
    • (2000) Biochemistry , vol.39 , pp. 2838-2852
    • Litovchick, A.1    Evdokimov, A.G.2    Lapidot, A.3
  • 119
    • 22144490214 scopus 로고    scopus 로고
    • Conformational constraint as a means for understanding RNA-aminoglycoside specificity
    • Blount KF, Zhao F, Hermann T, Tor Y. Conformational constraint as a means for understanding RNA-aminoglycoside specificity. J Am Chem Soc 2005;127:9818-9829.
    • (2005) J Am Chem Soc , vol.127 , pp. 9818-9829
    • Blount, K.F.1    Zhao, F.2    Hermann, T.3    Tor, Y.4
  • 120
    • 24044489584 scopus 로고    scopus 로고
    • Molecular recognition of RNA by neomycin and a restricted neomycin derivative
    • Zhao F, Zhao Q, Blount KF, 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
  • 121
    • 20444433905 scopus 로고    scopus 로고
    • A simple structural-based approach to prevent aminoglycoside inactivation by bacterial defense proteins. Conformational restriction provides effective protection against Neomycin-B nucleotidylation by ANT4
    • Asensio JL, Hidalgo A, Bastida A, Torrado M, Corzana F, Chiara JL, Garcia-Junceda E, Canada J, Jimenez-Barbero J. A simple structural-based approach to prevent aminoglycoside inactivation by bacterial defense proteins. Conformational restriction provides effective protection against Neomycin-B nucleotidylation by ANT4. J Am Chem Soc 2005;127:8278-8279.
    • (2005) J Am Chem Soc , vol.127 , pp. 8278-8279
    • Asensio, J.L.1    Hidalgo, A.2    Bastida, A.3    Torrado, M.4    Corzana, F.5    Chiara, J.L.6    Garcia-Junceda, E.7    Canada, J.8    Jimenez-Barbero, J.9
  • 123
    • 0032547248 scopus 로고    scopus 로고
    • Simple aminols as aminoglycoside surrogates
    • Tok JB-H, Rando RR. Simple aminols as aminoglycoside surrogates. J Am Chem Soc 1998;120:8279-8280.
    • (1998) J Am Chem Soc , vol.120 , pp. 8279-8280
    • Tok, J.B.-H.1    Rando, R.R.2
  • 125
    • 0041654787 scopus 로고    scopus 로고
    • Aminoglycoside-derived cationic lipids for gene transfection: Synthesis of kanamycin A derivatives
    • Sainlos M, Belmont P, Vigneron J-P, Lehn P, Lehn J-M. Aminoglycoside-derived cationic lipids for gene transfection: Synthesis of kanamycin A derivatives. Eur J Org Chem 2003;15:2764-2774.
    • (2003) Eur J Org Chem , vol.15 , pp. 2764-2774
    • Sainlos, M.1    Belmont, P.2    Vigneron, J.-P.3    Lehn, P.4    Lehn, J.-M.5


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