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Volumn 20, Issue 6, 2009, Pages 1112-1121

Lamellarin D bioconjugates II: Synthesis and cellular internalization of dendrimer and nuclear location signal derivatives

Author keywords

[No Author keywords available]

Indexed keywords

CELL CULTURE; POLYETHYLENE GLYCOLS;

EID: 67649217117     PISSN: 10431802     EISSN: None     Source Type: Journal    
DOI: 10.1021/bc800504t     Document Type: Article
Times cited : (29)

References (30)
  • 1
    • 29544448116 scopus 로고    scopus 로고
    • Polymer conjugates: Nanosized medicines for treating cancer
    • DOI 10.1016/j.tibtech.2005.11.006, PII S0167779905003021
    • Vicent, M. J., and Duncan, R. (2006) Polymer conjugates: nanosized medicines for treating cancer. Trends Biotechnol. 24, 39-47. (Pubitemid 43017749)
    • (2006) Trends in Biotechnology , vol.24 , Issue.1 , pp. 39-47
    • Vicent, M.J.1    Duncan, R.2
  • 2
    • 24644438254 scopus 로고    scopus 로고
    • Lipid-core micelles for targeted drug delivery
    • DOI 10.2174/156720105774370221
    • Torchilin, V. P. (2005) Lipid-core micelles for targeted drug delivery. Curr. Drug Delivery 2, 319-327. (Pubitemid 41282750)
    • (2005) Current Drug Delivery , vol.2 , Issue.4 , pp. 319-327
    • Torchilin, V.P.1
  • 3
    • 1942486331 scopus 로고    scopus 로고
    • Micelles from lipid derivatives of water-soluble polymers as delivery systems for poorly soluble drugs
    • DOI 10.1016/j.addr.2003.12.004, PII S0169409X04000468
    • Lukyanov, A. N., and Torchilin, V. P. (2004) Micelles from lipid derivatives of water-soluble polymers as delivery systems for poorly soluble drugs. Adv. Drug Delivery Rev. 56, 1273-1289. (Pubitemid 38510474)
    • (2004) Advanced Drug Delivery Reviews , vol.56 , Issue.9 , pp. 1273-1289
    • Lukyanov, A.N.1    Torchilin, V.P.2
  • 4
    • 0033539039 scopus 로고    scopus 로고
    • Drug delivery systems employing 1,4- Or 1,6-elimination: Poly(ethylene glycol) prodrugs of amine-containing compounds
    • DOI 10.1021/jm990166e
    • Greenwald, R. B., Pendri, A., Conover, C. D., Zhao, H., Choe, Y. H., Martínez, A., Shum, K., and Guan, S. (1999) Drug delivery systems employing 1,4- or 1,6-elimination: poly(ethylene glycol) prodrugs of amine-containing compounds. J. Med. Chem. 42, 3657-3667. (Pubitemid 29445099)
    • (1999) Journal of Medicinal Chemistry , vol.42 , Issue.18 , pp. 3657-3667
    • Greenwald, R.B.1    Pendri, A.2    Conover, C.D.3    Zhao, H.4    Choe, Y.H.5    Martinez, A.6    Shum, K.7    Guan, S.8
  • 5
    • 13944258970 scopus 로고    scopus 로고
    • Intracellular targeting of polymer-bound drugs for cancer chemotherapy
    • DOI 10.1016/j.addr.2004.10.006, PII S0169409X04002704
    • Nori, A., and Kopecek, J. (2005) Intracellular targeting of polymer-bound drugs for cancer chemotherapy. Adv. Drug Delivery Rev. 57, 609-636. (Pubitemid 40267695)
    • (2005) Advanced Drug Delivery Reviews , vol.57 , Issue.4 SPEC.ISS , pp. 609-636
    • Nori, A.1    Kopecek, J.2
  • 8
    • 27744549237 scopus 로고    scopus 로고
    • Synthesis of acridine-nuclear localization signal (NLS) conjugates and evaluation of their impact on lipoplex and polyplex-based transfection
    • DOI 10.1016/j.ejmech.2005.07.015, PII S0223523405001960
    • Boulanger, C., Di Giorgio, C., and Vierling, P. (2005) Synthesis of acridine-nuclear localization signal (NLS) conjugates and evaluation of their impact on lipoplex and polyplex-based transfection. Eur. J. Med. Chem. 40, 1295-1306. (Pubitemid 41618270)
    • (2005) European Journal of Medicinal Chemistry , vol.40 , Issue.12 , pp. 1295-1306
    • Boulanger, C.1    Di Giorgio, C.2    Vierling, P.3
  • 9
    • 67649215073 scopus 로고    scopus 로고
    • Lamellarin D bioconjugates I: Synthesis and cellular internalization of PEG-derivatives
    • the previous article in the same issue
    • Pla, D., Francesch, A., Calvo, P., Cuevas, C., Aligué, R., Albericio, F., and Álvarez, M. (2009) Lamellarin D bioconjugates I: synthesis and cellular internalization of PEG-derivatives. Bioconjugate Chem. . the previous article in the same issue.
    • (2009) Bioconjugate Chem.
    • Pla, D.1    Francesch, A.2    Calvo, P.3    Cuevas, C.4    Aligué, R.5    Albericio, F.6    Álvarez, M.7
  • 11
    • 0034000453 scopus 로고    scopus 로고
    • Tumor vascular permeability and the EPR effect in macromolecular therapeutics: A review
    • DOI 10.1016/S0168-3659(99)00248-5, PII S0168365999002485
    • Maeda, H., Wu, J., Sawa, T., Matsumura, Y., and Hori, K. (2000) Tumor vascular permeability and the EPR effect in macromolecular therapeutics: a review. J. Control. Release 65, 271-284. (Pubitemid 30122932)
    • (2000) Journal of Controlled Release , vol.65 , Issue.1-2 , pp. 271-284
    • Maeda, H.1    Wu, J.2    Sawa, T.3    Matsumura, Y.4    Hori, K.5
  • 12
    • 55249122288 scopus 로고    scopus 로고
    • Recent advances in lamellarin alkaloids: Isolation, synthesis and activity
    • Pla, D., Albericio, F., and Álvarez, M. (2008) Recent advances in lamellarin alkaloids: isolation, synthesis and activity. Anti-Cancer Agents Med. Chem. 8, 746-760.
    • (2008) Anti-Cancer Agents Med. Chem. , vol.8 , pp. 746-760
    • Pla, D.1    Albericio, F.2    Álvarez, M.3
  • 14
    • 20144369676 scopus 로고    scopus 로고
    • Molecular determinants of topoisomerase I poisoning by lamellarins: Comparison with camptothecin and structure-activity relationships
    • DOI 10.1021/jm049060w
    • Marco, E., Laine, W., Tardy, C., Lansiaux, A., Iwao, M., Ishibashi, F., Bailly, C., and Gago, F. (2005) Molecular determinants of topoisomerase I poisoning by lamellarins: comparison with camptothecin and structure-activity relationships. J. Med. Chem. 48, 3796-3807. (Pubitemid 40776854)
    • (2005) Journal of Medicinal Chemistry , vol.48 , Issue.11 , pp. 3796-3807
    • Marco, E.1    Laine, W.2    Tardy, C.3    Lansiaux, A.4    Iwao, M.5    Ishibashi, F.6    Bailly, C.7    Gago, F.8
  • 17
    • 0009848001 scopus 로고    scopus 로고
    • DNA topoisomerases as anticancer drug targets: From the laboratory to the clinic
    • Holden, J. A. (2001) DNA topoisomerases as anticancer drug targets: from the laboratory to the clinic. Curr. Med. Chem.: Anti-Cancer Agents 1, 1-25.
    • (2001) Curr. Med. Chem.: Anti-Cancer Agents , vol.1 , pp. 1-25
    • Holden, J.A.1
  • 18
    • 27844519630 scopus 로고    scopus 로고
    • Topoisomerase inhibitors of marine origin and their potential use as anticancer agents
    • DOI 10.1007/b100444, DNA Binders and Related Subjects
    • Dias, N., Vezin, H., Lansiaux, A., and Bailly, C. (2005) Topoisomerase inhibitors of marine origin and their potential use as anticancer agents. Top. Curr. Chem. 253, 89-108. (Pubitemid 44420840)
    • (2005) Topics in Current Chemistry , vol.253 , pp. 89-108
    • Dias, N.1    Vezin, H.2    Lansiaux, A.3    Bailly, C.4
  • 19
    • 33749034730 scopus 로고    scopus 로고
    • Topoisomerase I inhibitors: Camptothecins and beyond
    • DOI 10.1038/nrc1977, PII NRC1977
    • Pommier, Y. (2006) Topoisomerase I inhibitors: camptothecins and beyond. Nat. Rev. Cancer 6, 789-802. (Pubitemid 44450467)
    • (2006) Nature Reviews Cancer , vol.6 , Issue.10 , pp. 789-802
    • Pommier, Y.1
  • 21
    • 36549019051 scopus 로고    scopus 로고
    • Peptide and protein PEGylation III: Advances in chemistry and clinical applications
    • DOI 10.1016/j.addr.2007.08.003, PII S0169409X07001330, Peptide and Protein PEGylation III: Advances in Chemistry and Clinical Applications
    • Veronese, F. M., and Harris, J. M. (2008) Peptide and protein PEGylation III: advances in chemistry and clinical applications. Adv. Drug Delivery Rev. 60, 1-2. (Pubitemid 350181162)
    • (2008) Advanced Drug Delivery Reviews , vol.60 , Issue.1 , pp. 1-2
    • Veronese, F.M.1    Harris, J.M.2
  • 22
    • 67649163255 scopus 로고    scopus 로고
    • note
    • IUPAC nomenclature of Lam-D: 3,11-dihydroxy-2,12-dimethoxy-14-(4-hydroxy- 3-methoxyphenyl)-6H[1]benzopyrano-[4′,3′:4,5]pyrrolo[2,1-a] isoquinoline-6-one.
  • 24
    • 0028906786 scopus 로고
    • Some practical considerations and applications of the National Cancer Institute in vitro anticancer drug discovery screen
    • Boyd, M. R., and Paull, K. D. (1995) Some practical considerations and applications of the National Cancer Institute in vitro anticancer drug discovery screen. Drug Dev. Res. 34, 91-104.
    • (1995) Drug Dev. Res. , vol.34 , pp. 91-104
    • Boyd, M.R.1    Paull, K.D.2
  • 25
    • 35748938434 scopus 로고    scopus 로고
    • Rapid and prolonged stalling of human DNA topoisomerase I in UVA-irradiated genomic areas
    • DOI 10.1016/j.dnarep.2007.06.014, PII S156878640700225X
    • Mielke, C., Kalfalah, F. M., Christensen, M. O., and Boege, F. (2007) Rapid and prolonged stalling of human DNA topoisomerase I in UVA-irradiated genomic areas. DNA Repair 6, 1757-1763. (Pubitemid 350052727)
    • (2007) DNA Repair , vol.6 , Issue.12 , pp. 1757-1763
    • Mielke, C.1    Kalfalah, F.M.2    Christensen, M.O.3    Boege, F.4
  • 26
    • 0141743523 scopus 로고    scopus 로고
    • Solid-phase total synthesis of the pentacyclic system lamellarins U and L
    • DOI 10.1021/ol0351192
    • Cironi, P., Manzanares, I., Albericio, F., and Álvarez, M. (2003) Solid-phase total synthesis of the pentacyclic system lamellarins U and L. Org. Lett. 5, 2959-2962. (Pubitemid 37140812)
    • (2003) Organic Letters , vol.5 , Issue.16 , pp. 2959-2962
    • Cironi, P.1    Manzanares, I.2    Albericio, F.3    Alvarez, M.4
  • 28
    • 0030777451 scopus 로고    scopus 로고
    • Convergent total synthesis of lamellarin K
    • Banwell, M., Flynn, B., and Hockless, D. (1997) Convergent total synthesis of Lamellarin K. Chem. Commun. 2259-2260. (Pubitemid 27510951)
    • (1997) Chemical Communications , Issue.23 , pp. 2259-2260
    • Banwell, M.1    Flynn, B.2    Hockless, D.3
  • 29
    • 67649152418 scopus 로고    scopus 로고
    • note
    • The synthesis of 7 is part of a dendrimer project and will be published in due time.
  • 30
    • 55249114137 scopus 로고    scopus 로고
    • N,N,N′,N′-Tetramethylchloroformamidinium hexafluorophosphate (TCFH), a powerful coupling reagent for bioconjugation
    • Tulla-Puche, J., Torres, A., Calvo, P., Royo, M., and Albericio, F. (2008) N,N,N′,N′-Tetramethylchloroformamidinium hexafluorophosphate (TCFH), a powerful coupling reagent for bioconjugation. Bioconjugate Chem. 19, 1968-1971.
    • (2008) Bioconjugate Chem. , vol.19 , pp. 1968-1971
    • Tulla-Puche, J.1    Torres, A.2    Calvo, P.3    Royo, M.4    Albericio, F.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.