메뉴 건너뛰기




Volumn 39, Issue 12, 2006, Pages 925-934

Peptide dendrimers as artificial enzymes, receptors, and drug-delivery agents

Author keywords

[No Author keywords available]

Indexed keywords

DENDRIMER; DRUG CARRIER; ESTERASE; PEPTIDE;

EID: 33846222370     PISSN: 00014842     EISSN: None     Source Type: Journal    
DOI: 10.1021/ar050203y     Document Type: Article
Times cited : (227)

References (61)
  • 1
    • 84989581991 scopus 로고
    • Cascade-chain-like and nonskid-chain-like synthesis of molecular cavity topologies
    • Buhler, E.; Wehner, W.; Vögtle, F. Cascade-chain-like and nonskid-chain-like synthesis of molecular cavity topologies. Synthesis 1978, 155-158.
    • (1978) Synthesis , pp. 155-158
    • Buhler, E.1    Wehner, W.2    Vögtle, F.3
  • 2
    • 33845378981 scopus 로고
    • Micelles 1. Cascade molecules - A new approach to micelles - A[27]-Arborol
    • Newkome, G. R.; Yao, Z.-Q.; Baker, G. R.; Gupta, K. Micelles 1. Cascade molecules - A new approach to micelles - A[27]-Arborol. J. Org. Chem. 1985, 50, 2003-2004.
    • (1985) J. Org. Chem , vol.50 , pp. 2003-2004
    • Newkome, G.R.1    Yao, Z.-Q.2    Baker, G.R.3    Gupta, K.4
  • 4
    • 0038817081 scopus 로고
    • Preparation of polymers with controlled molecular architecture. A new convergent approach to dendritic macromolecules
    • Hawker, C. J.; Fréchet, J. M. J. Preparation of polymers with controlled molecular architecture. A new convergent approach to dendritic macromolecules. J. Am. Chem. Soc. 1990, 112, 2566-2568.
    • (1990) J. Am. Chem. Soc , vol.112 , pp. 2566-2568
    • Hawker, C.J.1    Fréchet, J.M.J.2
  • 5
    • 33748225026 scopus 로고
    • Polynitrile- and polyamine-functional poly(trimethylene imine) dendrimers
    • (a) Wörner, C.; Mülhaupt, R. Polynitrile- and polyamine-functional poly(trimethylene imine) dendrimers. Angew. Chem., Int. Ed. Eng. 1993, 32, 1306-1308.
    • (1993) Angew. Chem., Int. Ed. Eng , vol.32 , pp. 1306-1308
    • Wörner, C.1    Mülhaupt, R.2
  • 6
    • 33745374367 scopus 로고
    • Polypropylene imine) dendrimers: Large-scale synthesis by heterogeneously catalyzed hydrogenations
    • (b) de Brabander-van den Berg, E. M. M.; Mejer, E. W. Polypropylene imine) dendrimers: Large-scale synthesis by heterogeneously catalyzed hydrogenations. Angew. Chem., Int. Ed. Eng. 1993, 32, 1308-13011.
    • (1993) Angew. Chem., Int. Ed. Eng , vol.32 , pp. 1308-13011
    • de Brabander-van den Berg, E.M.M.1    Mejer, E.W.2
  • 7
    • 0038674868 scopus 로고    scopus 로고
    • About dendrimers: Structure, physical properties, and applications
    • (a) Bosman, A. W.; Janssen, H. M.; Meijer, E. W. About dendrimers: Structure, physical properties, and applications. Chem. Rev. 1999, 99, 1665-1688.
    • (1999) Chem. Rev , vol.99 , pp. 1665-1688
    • Bosman, A.W.1    Janssen, H.M.2    Meijer, E.W.3
  • 8
    • 0037621395 scopus 로고    scopus 로고
    • Recent developments in dendrimer chemistry
    • (b) Smith, D. K. Recent developments in dendrimer chemistry. Tetrahedron 2003, 59, 3797-3798.
    • (2003) Tetrahedron , vol.59 , pp. 3797-3798
    • Smith, D.K.1
  • 9
    • 0001857942 scopus 로고    scopus 로고
    • Dendritic encapsulation of function: Applying nature's site isolation principle from biomimetics to materials science
    • (c) Hecht, S.; Fréchet, J. M. J. Dendritic encapsulation of function: Applying nature's site isolation principle from biomimetics to materials science. Angew. Chem. 2001, 113, 76-94;
    • (2001) Angew. Chem , vol.113 , pp. 76-94
    • Hecht, S.1    Fréchet, J.M.J.2
  • 10
  • 12
    • 0028587877 scopus 로고
    • What promise for dendrimers?
    • (e) Tomalia, D. A.; Dvornic, P. R. What promise for dendrimers? Nature 1994, 372, 617-618.
    • (1994) Nature , vol.372 , pp. 617-618
    • Tomalia, D.A.1    Dvornic, P.R.2
  • 14
    • 27744462705 scopus 로고    scopus 로고
    • Dendrimers as artificial enzymes
    • For catalytic dendrimers, see a
    • For catalytic dendrimers, see (a) Kofoed, J.; Reymond, J.-L. Dendrimers as artificial enzymes. Curr. Opin. Chem. Biol. 2005, 9, 656-664.
    • (2005) Curr. Opin. Chem. Biol , vol.9 , pp. 656-664
    • Kofoed, J.1    Reymond, J.-L.2
  • 17
    • 0035470241 scopus 로고    scopus 로고
    • Dendritic catalysts and dendrimers in catalysis
    • (d) Astruc, D.; Chardac, F. Dendritic catalysts and dendrimers in catalysis. Chem. Rev. 2001, 101, 2991-3023.
    • (2001) Chem. Rev , vol.101 , pp. 2991-3023
    • Astruc, D.1    Chardac, F.2
  • 18
    • 15244362815 scopus 로고    scopus 로고
    • Metallodendritic catalysis for redox and carbon-carbon bond forming reactions: A step towards green chemistry
    • (e) Didier, A.; Heuze, K.; Gatard, S.; Mery, D.; Nlate, S.; Plault, L. Metallodendritic catalysis for redox and carbon-carbon bond forming reactions: A step towards green chemistry. Adv. Synth. Catal. 2005, 347, 329-338.
    • (2005) Adv. Synth. Catal , vol.347 , pp. 329-338
    • Didier, A.1    Heuze, K.2    Gatard, S.3    Mery, D.4    Nlate, S.5    Plault, L.6
  • 19
    • 17144405607 scopus 로고    scopus 로고
    • Dendrimer-encapsulated Pd nanoparticles as aqueous, room-temperature catalysts for the Stille reaction
    • (f) Garcia-Martinez, J. C.; Lezutekong, R.; Crooks, R. M. Dendrimer-encapsulated Pd nanoparticles as aqueous, room-temperature catalysts for the Stille reaction. J. Am. Chem. Soc. 2005, 127, 5097-5103.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 5097-5103
    • Garcia-Martinez, J.C.1    Lezutekong, R.2    Crooks, R.M.3
  • 20
    • 27144545752 scopus 로고    scopus 로고
    • Intramolecular carbonylation reactions with recyclable palladium-complexed dendrimers on silica: Synthesis of oxygen, nitrogen, or sulfur-containing medium ring fused heterocycles
    • (g) Lu, S. M.; Alper, H. Intramolecular carbonylation reactions with recyclable palladium-complexed dendrimers on silica: Synthesis of oxygen, nitrogen, or sulfur-containing medium ring fused heterocycles. J. Am. Chem. Soc. 2005, 127, 14776-14784.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 14776-14784
    • Lu, S.M.1    Alper, H.2
  • 21
    • 3142767593 scopus 로고    scopus 로고
    • Phase selectively soluble dendrimer-bound osmium complex: A highly effective and easily recyclable catalyst for olefin dihydroxylation
    • (h) Tang, W.-J.; Yang, N.-F; Yi, B.; Deng, G.-J.; Huang, Y.-Y.; Fan, Q.-H. Phase selectively soluble dendrimer-bound osmium complex: A highly effective and easily recyclable catalyst for olefin dihydroxylation. Chem. Commun. 2004, 1378-1379.
    • (2004) Chem. Commun , pp. 1378-1379
    • Tang, W.-J.1    Yang, N.-F.2    Yi, B.3    Deng, G.-J.4    Huang, Y.-Y.5    Fan, Q.-H.6
  • 22
    • 0142094062 scopus 로고    scopus 로고
    • Dendronized cyclocopolymers with a radial gradient of polarity and their use to catalyze a difficult esterification
    • (i) Liang, C. O.; Helms, B.; Craig, J.; Frechet, J. M. J. Dendronized cyclocopolymers with a radial gradient of polarity and their use to catalyze a difficult esterification. Chem. Commun. 2003, 2524-2525.
    • (2003) Chem. Commun , pp. 2524-2525
    • Liang, C.O.1    Helms, B.2    Craig, J.3    Frechet, J.M.J.4
  • 23
    • 0032814271 scopus 로고    scopus 로고
    • Catalytic dendrophanes as enzyme mimics: Synthesis, binding properties, micropolarity effect, and catalytic activity of dendritic thiazolio-cyclophanes
    • (a) Habicher, T.; Diederich, F. Catalytic dendrophanes as enzyme mimics: Synthesis, binding properties, micropolarity effect, and catalytic activity of dendritic thiazolio-cyclophanes. Helv. Chim. Acta 1997, 82, 1066-1095.
    • (1997) Helv. Chim. Acta , vol.82 , pp. 1066-1095
    • Habicher, T.1    Diederich, F.2
  • 24
    • 0141888983 scopus 로고    scopus 로고
    • Dendrimeric pyridoxamine enzyme mimics
    • (b) Liu, L.; Breslow, R. Dendrimeric pyridoxamine enzyme mimics. J. Am. Chem. Soc. 2003, 125, 12110-12111.
    • (2003) J. Am. Chem. Soc , vol.125 , pp. 12110-12111
    • Liu, L.1    Breslow, R.2
  • 25
    • 0029157648 scopus 로고
    • A de novo designed protein mimics the native state of natural proteins
    • (a) Raleigh, D. P.; Betz, S. F.; DeGrado, W. F. A de novo designed protein mimics the native state of natural proteins. J. Am. Chem. Soc. 1995, 117, 7558-7559.
    • (1995) J. Am. Chem. Soc , vol.117 , pp. 7558-7559
    • Raleigh, D.P.1    Betz, S.F.2    DeGrado, W.F.3
  • 26
    • 2642670311 scopus 로고    scopus 로고
    • Design of a 20-amino acid, three-stranded β-sheet protein
    • (b) Kortemme, T.; Ramírez-Alvarado, M.; Serrano, L. Design of a 20-amino acid, three-stranded β-sheet protein. Science 1998, 281, 253-256.
    • (1998) Science , vol.281 , pp. 253-256
    • Kortemme, T.1    Ramírez-Alvarado, M.2    Serrano, L.3
  • 27
    • 0034724338 scopus 로고    scopus 로고
    • De novo protein design: Crystallographic characterization of a synthetic peptide containing independent helical and hairpin domains
    • (c) Karle, I. L.; Das, C.; Balaram, P. De novo protein design: Crystallographic characterization of a synthetic peptide containing independent helical and hairpin domains. Proc. Natl. Acad. Sci. U.S.A. 2000, 97, 3034-3037.
    • (2000) Proc. Natl. Acad. Sci. U.S.A , vol.97 , pp. 3034-3037
    • Karle, I.L.1    Das, C.2    Balaram, P.3
  • 28
    • 0035819652 scopus 로고    scopus 로고
    • Discovery and characterization of a discretely folded homotrimeric ββα peptide
    • (d) McDonnell, K. A.; Imperiali, B. Discovery and characterization of a discretely folded homotrimeric ββα peptide. J. Am. Chem. Soc. 2001, 123, 1002-1003.
    • (2001) J. Am. Chem. Soc , vol.123 , pp. 1002-1003
    • McDonnell, K.A.1    Imperiali, B.2
  • 29
    • 0035807809 scopus 로고    scopus 로고
    • Enzyme-like proteins by computational design
    • (e) Bolon, D. L.; Mayo, S. L. Enzyme-like proteins by computational design. Proc. Natl. Acad. Sci. U.S.A. 2001, 98, 14274-14279.
    • (2001) Proc. Natl. Acad. Sci. U.S.A , vol.98 , pp. 14274-14279
    • Bolon, D.L.1    Mayo, S.L.2
  • 30
    • 0035313595 scopus 로고    scopus 로고
    • Designing metal-peptide models for protein structure and function
    • (f) Xing, G.; DeRose, V. J. Designing metal-peptide models for protein structure and function. Curr. Opin. Chem. Biol. 2001, 5, 196-200.
    • (2001) Curr. Opin. Chem. Biol , vol.5 , pp. 196-200
    • Xing, G.1    DeRose, V.J.2
  • 31
    • 0035956544 scopus 로고    scopus 로고
    • Toward the de novo design of a catalytically active helix bundle: A substrate-accessible carboxylate-bridged dinuclear metal center
    • (g) di Constanzo, L.; Wade, H.; Geremia, S.; Randaccio, L.; Pavone, V.; DeGrado, W. F.; Lombardi, A. Toward the de novo design of a catalytically active helix bundle: A substrate-accessible carboxylate-bridged dinuclear metal center. J. Am. Chem. Soc. 2001, 123, 12749-12757.
    • (2001) J. Am. Chem. Soc , vol.123 , pp. 12749-12757
    • di Constanzo, L.1    Wade, H.2    Geremia, S.3    Randaccio, L.4    Pavone, V.5    DeGrado, W.F.6    Lombardi, A.7
  • 32
    • 0037022813 scopus 로고    scopus 로고
    • Converting a maltose receptor into a nascent binuclear copper oxygenase by computational design
    • (h) Benson, D. E.; Haddy, A. E.; Hellinga, H.W. Converting a maltose receptor into a nascent binuclear copper oxygenase by computational design. Biochemistry 2002, 41, 3262-3269.
    • (2002) Biochemistry , vol.41 , pp. 3262-3269
    • Benson, D.E.1    Haddy, A.E.2    Hellinga, H.W.3
  • 33
    • 0842270116 scopus 로고    scopus 로고
    • Enzyme-like proteins from an unselected library of designed amino acid sequences
    • (i) Wey, Y.; Hecht, M. H. Enzyme-like proteins from an unselected library of designed amino acid sequences. Protein Eng. Des. 2004, 17, 67-75.
    • (2004) Protein Eng. Des , vol.17 , pp. 67-75
    • Wey, Y.1    Hecht, M.H.2
  • 34
    • 20044385983 scopus 로고    scopus 로고
    • Peptide and amide bond-containing dendrimers
    • For reviews on synthesis and other applications of peptide dendrimers, see a
    • For reviews on synthesis and other applications of peptide dendrimers, see (a) Crespo, L.; Sanclimens, G.; Pons, M.; Giralt, E.; Royo, M.; Albericio, F. Peptide and amide bond-containing dendrimers. Chem. Rev. 2005, 1663-1681.
    • (2005) Chem. Rev , pp. 1663-1681
    • Crespo, L.1    Sanclimens, G.2    Pons, M.3    Giralt, E.4    Royo, M.5    Albericio, F.6
  • 35
    • 0036177932 scopus 로고    scopus 로고
    • Peptide dendrimers: Applications and synthesis
    • (b) Sadler, K.; Tam, J. P. Peptide dendrimers: Applications and synthesis. Rev. Mol. Biotechnol. 2002, 90, 195-229.
    • (2002) Rev. Mol. Biotechnol , vol.90 , pp. 195-229
    • Sadler, K.1    Tam, J.P.2
  • 39
    • 23944501630 scopus 로고    scopus 로고
    • Gerstman, B. S.; Chapagain, P. P. Self-organization in protein folding and the hydrophobic interaction. J. Chem. Phys. 2005, 123, 054901/1-054901/6.
    • (a) Gerstman, B. S.; Chapagain, P. P. Self-organization in protein folding and the hydrophobic interaction. J. Chem. Phys. 2005, 123, 054901/1-054901/6.
  • 40
    • 4644236471 scopus 로고    scopus 로고
    • Hydrophobic collapse in multidomain protein folding
    • (b) Zhou, R.; Huang, X.; Margulis, C. J.; Berne, B. J. Hydrophobic collapse in multidomain protein folding. Science 2004, 305, 1605-1616.
    • (2004) Science , vol.305 , pp. 1605-1616
    • Zhou, R.1    Huang, X.2    Margulis, C.J.3    Berne, B.J.4
  • 41
    • 0004172764 scopus 로고
    • 2nd ed; Wiley-Interscience: New York
    • (c) Tanford, C. The Hydrophobic Effect, 2nd ed; Wiley-Interscience: New York, 1980.
    • (1980) The Hydrophobic Effect
    • Tanford, C.1
  • 42
    • 0036667305 scopus 로고    scopus 로고
    • Hydrophobic effects and modeling of biophysical aqueous solution interfaces
    • (d) Pratt, L. R.; Pohorille, A. Hydrophobic effects and modeling of biophysical aqueous solution interfaces. Chem. Rev. 2002, 102, 2671-2691.
    • (2002) Chem. Rev , vol.102 , pp. 2671-2691
    • Pratt, L.R.1    Pohorille, A.2
  • 43
    • 0000709062 scopus 로고    scopus 로고
    • Sequence selective binding of peptides by artificial receptors in aqueous solution
    • (e) Breslow, R.; Yang, Z.; Ching, R.; Trojandt, G.; Odobel, F. Sequence selective binding of peptides by artificial receptors in aqueous solution. J. Am. Chem. Soc. 1998, 120, 3536-3537.
    • (1998) J. Am. Chem. Soc , vol.120 , pp. 3536-3537
    • Breslow, R.1    Yang, Z.2    Ching, R.3    Trojandt, G.4    Odobel, F.5
  • 44
    • 5144235335 scopus 로고    scopus 로고
    • Esterolytic peptide dendrimers with a hydrophobic core and catalytic residues on the surface
    • Clouet, A.; Darbre, T.; Reymond, J.-L. Esterolytic peptide dendrimers with a hydrophobic core and catalytic residues on the surface. Adv. Synth. Catal. 2004, 346, 1195-1204.
    • (2004) Adv. Synth. Catal , vol.346 , pp. 1195-1204
    • Clouet, A.1    Darbre, T.2    Reymond, J.-L.3
  • 45
    • 0034715460 scopus 로고    scopus 로고
    • Some other examples: (a) Grayson, S. M.; Fréchet, J. M. J. Synthesis and surface functionalization of aliphatic polyether dendrons. J. Am. Chem. Soc. 2000, 122, 10335-10344.
    • Some other examples: (a) Grayson, S. M.; Fréchet, J. M. J. Synthesis and surface functionalization of aliphatic polyether dendrons. J. Am. Chem. Soc. 2000, 122, 10335-10344.
  • 46
    • 0035913710 scopus 로고    scopus 로고
    • Orthogonal, convergent synthesis of dendrimers based on melamine with one or two unique surface sites for manipulation
    • and references therein
    • (b) Zhang, W.; Nowlan, D. T., III; Thomson, L. M.; Lackowski, W. M.; Simaneck, E. E. Orthogonal, convergent synthesis of dendrimers based on melamine with one or two unique surface sites for manipulation. J. Am. Chem. Soc. 2001, 123, 8914-8922 and references therein.
    • (2001) J. Am. Chem. Soc , vol.123 , pp. 8914-8922
    • Zhang, W.1    Nowlan III, D.T.2    Thomson, L.M.3    Lackowski, W.M.4    Simaneck, E.E.5
  • 47
    • 0037126263 scopus 로고    scopus 로고
    • Functional group diversity in dendrimers
    • (c) Sivanandan, K.; Vutukuri, D.; Thayumanavan, S. Functional group diversity in dendrimers. Org. Lett. 2002, 4, 3751-3753.
    • (2002) Org. Lett , vol.4 , pp. 3751-3753
    • Sivanandan, K.1    Vutukuri, D.2    Thayumanavan, S.3
  • 48
    • 10044268402 scopus 로고    scopus 로고
    • A strong positive dendritic effect in a peptide dendrimer-catalyzed ester hydrolysis reaction
    • Delort, E.; Darbre, T.; Reymond, J.-L. A strong positive dendritic effect in a peptide dendrimer-catalyzed ester hydrolysis reaction. J. Am. Chem. Soc. 2004, 126, 15642-15643.
    • (2004) J. Am. Chem. Soc , vol.126 , pp. 15642-15643
    • Delort, E.1    Darbre, T.2    Reymond, J.-L.3
  • 49
    • 33744943776 scopus 로고    scopus 로고
    • Synthesis and activity of histidine-containing catalytic peptide dendrimers
    • Delort, E.; Nguyen-Trung, N.-Q.; Darbre T.; Reymond, J.-L. Synthesis and activity of histidine-containing catalytic peptide dendrimers. J. Org. Chem. 2006, 71, 4468-4480.
    • (2006) J. Org. Chem , vol.71 , pp. 4468-4480
    • Delort, E.1    Nguyen-Trung, N.-Q.2    Darbre, T.3    Reymond, J.-L.4
  • 50
    • 0025893762 scopus 로고
    • General method for rapid synthesis of multicomponent peptide mixtures
    • (a) Furka, A.; Sebestyén, F.; Asgedom, M.; Dibó, G. General method for rapid synthesis of multicomponent peptide mixtures. Int. J. Pept. Protein Res. 1991, 37, 487-493.
    • (1991) Int. J. Pept. Protein Res , vol.37 , pp. 487-493
    • Furka, A.1    Sebestyén, F.2    Asgedom, M.3    Dibó, G.4
  • 51
    • 0026419328 scopus 로고
    • A new type of synthetic peptide library for identifying ligand-binding activity
    • (b) Lam, K. S.; Salmon, S. E.; Hersh, E. M.; Hruby, V. J.; Kazmierski, W. M.; Knapp, R. J. A new type of synthetic peptide library for identifying ligand-binding activity. Nature 1991, 354, 82-84.
    • (1991) Nature , vol.354 , pp. 82-84
    • Lam, K.S.1    Salmon, S.E.2    Hersh, E.M.3    Hruby, V.J.4    Kazmierski, W.M.5    Knapp, R.J.6
  • 52
    • 0026419319 scopus 로고
    • Generation and use of synthetic peptide combinatorial libraries for basic research and drug discovery
    • (c) Houghten, R. A.; Pinilla, C.; Blondelle, S. E.; Appel, J. R.; Dooley, C. T.; Cuervo, J. H. Generation and use of synthetic peptide combinatorial libraries for basic research and drug discovery. Nature 1991, 354, 84-86.
    • (1991) Nature , vol.354 , pp. 84-86
    • Houghten, R.A.1    Pinilla, C.2    Blondelle, S.E.3    Appel, J.R.4    Dooley, C.T.5    Cuervo, J.H.6
  • 53
    • 0000577984 scopus 로고    scopus 로고
    • The "one-bead-one- compound" combinatorial library method
    • (d) Lam, K. S.; Lebl, M.; Krchnak, V. The "one-bead-one- compound" combinatorial library method. Chem. Rev. 1997, 97, 411-448.
    • (1997) Chem. Rev , vol.97 , pp. 411-448
    • Lam, K.S.1    Lebl, M.2    Krchnak, V.3
  • 54
    • 0344428136 scopus 로고    scopus 로고
    • Discovery of peptide-zirconium complexes that mediate phosphate hydrolysis by batch screening of a combinatorial undecapeptide library
    • Berkessel, A.; Hérault, D. A. Discovery of peptide-zirconium complexes that mediate phosphate hydrolysis by batch screening of a combinatorial undecapeptide library. Angew. Chem., Int. Ed. 1999, 38, 102-105.
    • (1999) Angew. Chem., Int. Ed , vol.38 , pp. 102-105
    • Berkessel, A.1    Hérault, D.A.2
  • 55
    • 0034807976 scopus 로고    scopus 로고
    • Selection of enantioselective acyl transfer catalysts from a pooled peptide library through a fluorescence-based activity assay: An approach to kinetic resolution of secondary alcohols of broad structural scope
    • Copeland, G. T.; Miller, S. J. Selection of enantioselective acyl transfer catalysts from a pooled peptide library through a fluorescence-based activity assay: An approach to kinetic resolution of secondary alcohols of broad structural scope. J. Am. Chem. Soc. 2001, 113, 6496-6502.
    • (2001) J. Am. Chem. Soc , vol.113 , pp. 6496-6502
    • Copeland, G.T.1    Miller, S.J.2
  • 56
    • 5344258255 scopus 로고    scopus 로고
    • A combinatorial approach to catalytic peptide dendrimers
    • (a) Clouet, A.; Darbre, T.; Reymond, J.-L. A combinatorial approach to catalytic peptide dendrimers. Angew. Chem., Int. Ed. 2004, 43, 4612-4615.
    • (2004) Angew. Chem., Int. Ed , vol.43 , pp. 4612-4615
    • Clouet, A.1    Darbre, T.2    Reymond, J.-L.3
  • 57
    • 33644600637 scopus 로고    scopus 로고
    • Combinatorial synthesis, selection, and properties of esterase peptide dendrimers
    • (b) Clouet, A.; Darbre, T.; Reymond, J.-L. Combinatorial synthesis, selection, and properties of esterase peptide dendrimers. Biopolymers 2006, 84, 114-123.
    • (2006) Biopolymers , vol.84 , pp. 114-123
    • Clouet, A.1    Darbre, T.2    Reymond, J.-L.3
  • 58
    • 28644434579 scopus 로고    scopus 로고
    • Designing dendrimers for biological applications
    • Recent reviews: a
    • Recent reviews: (a) Lee, C. C.; MacKay, J. A.; Frechet, J. M. J.; Szoka, F. C. Designing dendrimers for biological applications. Nat. Biotechnol. 2005, 23, 1517-1526.
    • (2005) Nat. Biotechnol , vol.23 , pp. 1517-1526
    • Lee, C.C.1    MacKay, J.A.2    Frechet, J.M.J.3    Szoka, F.C.4
  • 59
    • 12844258906 scopus 로고    scopus 로고
    • Dendrimers and dendritic polymers in drug delivery
    • (b) Gillies, E. R.; Frechet, J. M. J. Dendrimers and dendritic polymers in drug delivery. Drug Discovery Today 2005, 10, 35-43.
    • (2005) Drug Discovery Today , vol.10 , pp. 35-43
    • Gillies, E.R.1    Frechet, J.M.J.2
  • 60
    • 33745703563 scopus 로고    scopus 로고
    • Polymer therapeutics: Concepts and applications
    • (c) Haag, R.; Kratz, F. Polymer therapeutics: Concepts and applications. Angew. Chem., Int. Ed. 2006, 45, 1198-1215.
    • (2006) Angew. Chem., Int. Ed , vol.45 , pp. 1198-1215
    • Haag, R.1    Kratz, F.2
  • 61
    • 21244490025 scopus 로고    scopus 로고
    • Inhibition of mitosis by glycopeptide dendrimer conjugates of colchicine
    • Lagnoux, D.; Darbre, T.; Schmitz, M. L.; Reymond, J.-L. Inhibition of mitosis by glycopeptide dendrimer conjugates of colchicine. Chem.-Eur. J. 2005, 11, 3943-3950.
    • (2005) Chem.-Eur. J , vol.11 , pp. 3943-3950
    • Lagnoux, D.1    Darbre, T.2    Schmitz, M.L.3    Reymond, J.-L.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.