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Volumn 70, Issue 3-4, 2011, Pages 345-352

Synthesis and characterisation of novel glycoclusters based on cell penetrating heptakis(6-aminoethylamino-6-deoxy)-β-cyclodextrin

Author keywords

Amino cyclodextrin; Cell penetrating; Glycoclusters; Monosaccharides

Indexed keywords


EID: 80051802239     PISSN: 09230750     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10847-010-9840-2     Document Type: Conference Paper
Times cited : (6)

References (21)
  • 1
    • 33646103431 scopus 로고    scopus 로고
    • Carbohydrates as future anti-adhesion drugs for infectious diseases
    • 1:CAS:528:DC%2BD28Xjsl2msb0%3D
    • N Sharon 2006 Carbohydrates as future anti-adhesion drugs for infectious diseases Biochim. Biophys. Acta 1760 527 537 1:CAS:528:DC%2BD28Xjsl2msb0%3D
    • (2006) Biochim. Biophys. Acta , vol.1760 , pp. 527-537
    • Sharon, N.1
  • 2
    • 33846915674 scopus 로고    scopus 로고
    • Supramolecular chemistry of carbohydrate clusters with cores having guest binding abilities
    • 10.2174/157019307779815875 1:CAS:528:DC%2BD2sXhs1WksLc%3D
    • A Vargas-Berenguel F Ortega-Caballero JM Casas-Solvas 2007 Supramolecular chemistry of carbohydrate clusters with cores having guest binding abilities Mini-Rev. Org. Chem. 4 1 14 10.2174/157019307779815875 1:CAS:528: DC%2BD2sXhs1WksLc%3D
    • (2007) Mini-Rev. Org. Chem. , vol.4 , pp. 1-14
    • Vargas-Berenguel, A.1    Ortega-Caballero, F.2    Casas-Solvas, J.M.3
  • 4
    • 0842328412 scopus 로고    scopus 로고
    • Persubstituted Cyclodextrin-Based Glycoclusters as Inhibitors of Protein-Carbohydrate Recognition Using Purified Plant and Mammalian Lectins and Wild-Type and Lectin-Gene-Transfected Tumor Cells as Targets
    • DOI 10.1021/bc0340666
    • S Andre H Kaltner T Furuike S-I Nishimura HJ Gabius 2004 Persubstituted cyclodextrin-based glycoclusters as inhibitors of protein-carbohydrate recognition using purified plant and mammalian lectins and wild-type and lectin-gene-transfected tumor cells as targets Bioconjug. Chem. 15 87 98 10.1021/bc0340666 1:CAS:528:DC%2BD3sXpt1akurk%3D (Pubitemid 38165984)
    • (2004) Bioconjugate Chemistry , vol.15 , Issue.1 , pp. 87-98
    • Andre, S.1    Kaltner, H.2    Furuike, T.3    Nishimura, S.-I.4    Gabius, H.-J.5
  • 5
    • 0028673204 scopus 로고
    • Recognition ability and cytotoxicity of some oligosaccharidyl substituted β-cyclodextrins
    • 10.1016/S0248-4900(94)80018-9 1:CAS:528:DyaK2MXmsVGksLo%3D
    • F Attioui A Al-Omar E Leray H Parrot-Lopez C Finance R Bonaly 1994 Recognition ability and cytotoxicity of some oligosaccharidyl substituted β-cyclodextrins Biol. Cell 82 161 167 10.1016/S0248-4900(94)80018-9 1:CAS:528:DyaK2MXmsVGksLo%3D
    • (1994) Biol. Cell , vol.82 , pp. 161-167
    • Attioui, F.1    Al-Omar, A.2    Leray, E.3    Parrot-Lopez, H.4    Finance, C.5    Bonaly, R.6
  • 6
    • 1642394970 scopus 로고    scopus 로고
    • A practical synthesis of amphiphilic cyclodextrins fully substituted with sugar residues on the primary face
    • Sallas, F.; Niikura, K.; Nishimura, S.I.: A practical synthesis of amphiphilic cyclodextrins fully substituted with sugar residues on the primary face. Chem. Commun. 596-597 (2004) (Pubitemid 38367143)
    • (2004) Chemical Communications , Issue.5 , pp. 596-597
    • Sallas, F.1    Niikura, K.2    Nishimura, S.-I.3
  • 7
    • 53549132777 scopus 로고    scopus 로고
    • Synthesis, characterisation, and remarkable biological properties of cyclodextrins bearing guanidinoalkylamino and aminoalkylamino groups on their primary side
    • 10.1002/chem.200701650 1:CAS:528:DC%2BD1cXmsVertbY%3D
    • N Mourtzis M Paravatou IM Mavridis ML Roberts K Yannakopoulou 2008 Synthesis, characterisation, and remarkable biological properties of cyclodextrins bearing guanidinoalkylamino and aminoalkylamino groups on their primary side Chem. Eur. J. 14 4188 4200 10.1002/chem.200701650 1:CAS:528:DC%2BD1cXmsVertbY%3D
    • (2008) Chem. Eur. J. , vol.14 , pp. 4188-4200
    • Mourtzis, N.1    Paravatou, M.2    Mavridis, I.M.3    Roberts, M.L.4    Yannakopoulou, K.5
  • 8
    • 66149091850 scopus 로고    scopus 로고
    • Binding of nucleotides and nucleosides to per(6-guanidino-6-deoxy)- cyclodextrins in solution
    • Aggelidou, C.; Mavridis, I.M.; Yannakopoulou, K.: Binding of nucleotides and nucleosides to per(6-guanidino-6-deoxy)-cyclodextrins in solution. Eur. J. Org. Chem. 2299-2305 (2009)
    • (2009) Eur. J. Org. Chem. , pp. 2299-2305
    • Aggelidou, C.1    Mavridis, I.M.2    Yannakopoulou, K.3
  • 9
    • 30744454015 scopus 로고    scopus 로고
    • Diastereoselective synthesis of all eight L-hexoses from L-ascorbic acid
    • DOI 10.1021/jo0521192
    • L Ermolenko NA Sasaki 2006 Diastereoselective synthesis of all eight l-hexoses from l-ascorbic acid J. Org. Chem. 71 693 703 10.1021/jo0521192 1:CAS:528:DC%2BD2MXht1yrs7rI (Pubitemid 43100762)
    • (2006) Journal of Organic Chemistry , vol.71 , Issue.2 , pp. 693-703
    • Ermolenko, L.1    Sasaki, N.A.2
  • 10
    • 0141517571 scopus 로고    scopus 로고
    • One-pot synthesis of multivalent arrays of mannose mono- and disaccharides
    • DOI 10.1016/j.tet.2003.08.011
    • W Hayes HMI Osborn SD Osborne RA Rastall B Romagnoli 2003 One-pot synthesis of multivalent arrays of mannose mono-and disaccharides Tetrahedron 59 7983 7996 10.1016/j.tet.2003.08.011 1:CAS:528:DC%2BD3sXnsVKktrw%3D (Pubitemid 37130323)
    • (2003) Tetrahedron , vol.59 , Issue.40 , pp. 7983-7996
    • Hayes, W.1    Osborn, H.M.I.2    Osborne, S.D.3    Rastall, R.A.4    Romagnoli, B.5
  • 11
    • 0034990954 scopus 로고    scopus 로고
    • Trivalent α-d-mannoside clusters as inhibitors of type-1 fimbriae-mediated adhesion of Escherichia coli: Structural variation and biotinylation
    • 10.1039/b009786l
    • TK Lindhorst S Kötter U Krallmann-Wenzel S Ehlers 2001 Trivalent α-d-mannoside clusters as inhibitors of type-1 fimbriae-mediated adhesion of Escherichia coli: structural variation and biotinylation J. Chem. Soc. Perkin Trans. 1 823 831 10.1039/b009786l
    • (2001) J. Chem. Soc. Perkin Trans. , vol.1 , pp. 823-831
    • Lindhorst, T.K.1    Kötter, S.2    Krallmann-Wenzel, U.3    Ehlers, S.4
  • 12
    • 0037257999 scopus 로고    scopus 로고
    • Synthesis of maleimide-activated carbohydrates as chemoselective tags for site-specific glycosylation of peptides and proteins
    • DOI 10.1021/bc025617f
    • J Ni S Singh L-X Wang 2003 Synthesis of maleimide-activated carbohydrates as chemoselective tags for site-specific glycosylation of peptides and proteins Bioconj. Chem. 14 232 238 10.1021/bc025617f 1:CAS:528:DC%2BD38XpsVSnsr8%3D (Pubitemid 36169037)
    • (2003) Bioconjugate Chemistry , vol.14 , Issue.1 , pp. 232-238
    • Ni, J.1    Singh, S.2    Wang, L.-X.3
  • 13
    • 0037620667 scopus 로고    scopus 로고
    • Cu(II)-Self-assembling bipyridyl-glycoclusters and dendrimers bearing the Tn-antigen cancer marker: Syntheses and lectin binding properties
    • DOI 10.1016/S0040-4020(03)00438-1
    • R Roy JM Kim 2003 Cu(II)-self-assembling bipyridyl-glycoclusters and dendrimers bearing the Tn-antigen cancer marker: syntheses and lectin binding properties Tetrahedron 59 3881 3893 10.1016/S0040-4020(03)00438-1 1:CAS:528:DC%2BD3sXjvVCltrs%3D (Pubitemid 36577608)
    • (2003) Tetrahedron , vol.59 , Issue.22 , pp. 3881-3893
    • Roy, R.1    Kim, J.M.2
  • 14
    • 10644297503 scopus 로고    scopus 로고
    • The use of carbohydrate microarrays to study carbohydrate-cell interactions and to detect pathogens
    • DOI 10.1016/j.chembiol.2004.10.011, PII S1074552104003126
    • MD Disney PH Seeberger 2004 The use of carbohydrate microarrays to study carbohydrate-cell interactions and to detect pathogens Chem. Biol. 11 1701 1707 10.1016/j.chembiol.2004.10.011 1:CAS:528:DC%2BD2cXhtVyqtr%2FI (Pubitemid 39651304)
    • (2004) Chemistry and Biology , vol.11 , Issue.12 , pp. 1701-1707
    • Disney, M.D.1    Seeberger, P.H.2
  • 15
    • 0043072898 scopus 로고    scopus 로고
    • Mannose-BSA conjugates: Comparison between commercially available linkers in reactivity and bioactivity
    • DOI 10.1081/CAR-120023475
    • M Izumi S Okumura H Yuasa H Hashimoto 2003 Mannose-BSA conjugates: comparison between commercially available linkers in reactivity and bioactivity J. Carbohydr. Chem. 22 317 329 10.1081/CAR-120023475 1:CAS:528: DC%2BD3sXltl2lu7Y%3D (Pubitemid 36980865)
    • (2003) Journal of Carbohydrate Chemistry , vol.22 , Issue.5 , pp. 317-329
    • Izumi, M.1    Okumura, S.2    Yuasa, H.3    Hashimoto, H.4
  • 17
    • 0003305648 scopus 로고    scopus 로고
    • The Site-Selective Glycosylation of a Designed Helix-Loop-Helix Polypeptide Motif
    • L Andersson G Stenhagen L Baltzer 1998 The site-selective glycosylation of a designed helix-loop-helix polypeptide motif J. Org. Chem. 63 1366 1367 10.1021/jo971999k 1:CAS:528:DyaK1cXhsFOqtL0%3D (Pubitemid 128496311)
    • (1998) Journal of Organic Chemistry , vol.63 , Issue.5 , pp. 1366-1367
    • Andersson, L.1    Stenhagen, G.2    Baltzer, L.3
  • 19
    • 0026354455 scopus 로고
    • Building blocks for glycopeptides synthesis: Glycosylation of 3-mercaptopropionic acid and Fmoc amino acids with unprotected carboxyl groups
    • 10.1016/0040-4039(91)80548-K 1:CAS:528:DyaK38Xht12msLc%3D
    • M Elofsson B Walse J Kihlberg 1991 Building blocks for glycopeptides synthesis: glycosylation of 3-mercaptopropionic acid and Fmoc amino acids with unprotected carboxyl groups Tetrahedron Lett. 32 7613 7616 10.1016/0040-4039(91) 80548-K 1:CAS:528:DyaK38Xht12msLc%3D
    • (1991) Tetrahedron Lett. , vol.32 , pp. 7613-7616
    • Elofsson, M.1    Walse, B.2    Kihlberg, J.3
  • 20
    • 0027643018 scopus 로고
    • Solid-phase synthesis and conformational studies of glycosylated derivatives of helper-T-cell immunogenic peptides from hen-eg lysozyme
    • DOI 10.1016/0008-6215(93)84026-3
    • M Elofsson S Roy B Walse J Kihlberg 1993 Solid-phase synthesis and conformational studies of glycosylated derivatives of helper-T-cell immunogenic peptides from hen-egg lysozyme Carbohydr. Res. 246 89 103 10.1016/0008-6215(93) 84026-3 1:CAS:528:DyaK2cXnslKhtQ%3D%3D (Pubitemid 23232123)
    • (1993) Carbohydrate Research , vol.246 , pp. 89-103
    • Elofsson, M.1    Roy, S.2    Walse, B.3    Kihlberg, J.4
  • 21
    • 23044440814 scopus 로고    scopus 로고
    • Synthesis of a αMan(1→3)αMan(1→2)αMan glycocluster presented on a β-cyclodextrin scaffold
    • DOI 10.1002/ejoc.200500146
    • Carpenter, C.; Nepogodiev, S.A.: Synthesis of a αMan(1 → 3)αMan(1 → 2)αMan glycocluster presented on a β-cyclodextrin scaffold. Eur. J. Org. Chem. 3286-3296 (2005) (Pubitemid 41059715)
    • (2005) European Journal of Organic Chemistry , Issue.15 , pp. 3286-3296
    • Carpenter, C.1    Nepogodiev, S.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.