메뉴 건너뛰기




Volumn 33, Issue 14, 2003, Pages 2391-2400

Synthesis of doxorubicin conjugates through 14-hydroxy group to melanotransferrin p97

Author keywords

Anticancer drug; Bioconjugate; Blood brain barrier; Brain tumor; Cross linking; Doxorubicin; Drug delivery; Ester bond linkage; Protein carrier

Indexed keywords

9 FLUORENYLMETHYL N SUCCINIMIDYLCARBONATE; AMINO ACID; CARBONIC ACID DERIVATIVE; DOXORUBICIN; GLUTARIC ACID; HYDROXYL GROUP; MELANOTRANSFERRIN P97; SUCCINIC ACID; TRANSFERRIN; UNCLASSIFIED DRUG;

EID: 0042564733     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1081/SCC-120021828     Document Type: Article
Times cited : (8)

References (27)
  • 6
    • 0033106074 scopus 로고    scopus 로고
    • Monoclonal antibody conjugates of doxorubicin prepared with branched linkers: A novel method for increasing the potency of doxorubicin immunoconjugates
    • (b) King, D.H.; Yurgaitis, D.; Willner, D.; Firestone, R.A.; Yang, M.B.; Lasch, S.J.; Hellstron, K.E.; Trail, P.A. Monoclonal antibody conjugates of doxorubicin prepared with branched linkers: a novel method for increasing the potency of doxorubicin immunoconjugates. Bioconjugate Chem. 1999, 10 (2), 279-288.
    • (1999) Bioconjugate Chem , vol.10 , Issue.2 , pp. 279-288
    • King, D.H.1    Yurgaitis, D.2    Willner, D.3    Firestone, R.A.4    Yang, M.B.5    Lasch, S.J.6    Hellstron, K.E.7    Trail, P.A.8
  • 7
    • 0028789361 scopus 로고
    • Conjugation of doxorubicin to monoclonal anticarcinoembryonic antigen antibody via novel thio-directed cross-linking reagents
    • (a) Lau, A.; Berube, G.; Ford, C.H.J. Conjugation of doxorubicin to monoclonal anticarcinoembryonic antigen antibody via novel thio-directed cross-linking reagents. Bioorg. Med. Chem. 1995, 3 (10), 1299-1304;
    • (1995) Bioorg. Med. Chem. , vol.3 , Issue.10 , pp. 1299-1304
    • Lau, A.1    Berube, G.2    Ford, C.H.J.3
  • 8
    • 0030050856 scopus 로고    scopus 로고
    • Preparation and funtional evaluation of new doxorubicin immunoconjugates containing and acid-sensitive linker on small-cell lung cancer cells
    • (b) Froesch, B.A.; Stahel, R.A.; Zangemeister-Wittke, U. Preparation and funtional evaluation of new doxorubicin immunoconjugates containing and acid-sensitive linker on small-cell lung cancer cells. Cancer Immunol. Immunother. 1996, 42 (1), 55-63.
    • (1996) Cancer Immunol. Immunother. , vol.42 , Issue.1 , pp. 55-63
    • Froesch, B.A.1    Stahel, R.A.2    Zangemeister-Wittke, U.3
  • 9
    • 0035793269 scopus 로고    scopus 로고
    • Narrow molecular weight distribution precursors for polymer-drug conjugates
    • (a) Godwin, A.; Hartenstein, M.; Muller, A.H.E.; Brocchini, S. Narrow molecular weight distribution precursors for polymer-drug conjugates. Angew. Chem. Int. Ed. 2001, 40 (3), 594-597;
    • (2001) Angew. Chem. Int. Ed. , vol.40 , Issue.3 , pp. 594-597
    • Godwin, A.1    Hartenstein, M.2    Muller, A.H.E.3    Brocchini, S.4
  • 10
    • 0032472352 scopus 로고    scopus 로고
    • Characterization of physical entrapment and chemical conjugation of adriamycin in polymeric micelles and their design for in vivo delivery to a solid tumor
    • (b) Yokoyama, M.; Fukushima, S.; Uehara, R.; Okamoto, K.; Kataoka, K.; Sakurai, Y.; Okano, T. Characterization of physical entrapment and chemical conjugation of adriamycin in polymeric micelles and their design for in vivo delivery to a solid tumor. J. Control. Release 1998, 50 (1), 79-92;
    • (1998) J. Control. Release , vol.50 , Issue.1 , pp. 79-92
    • Yokoyama, M.1    Fukushima, S.2    Uehara, R.3    Okamoto, K.4    Kataoka, K.5    Sakurai, Y.6    Okano, T.7
  • 11
    • 0034614998 scopus 로고    scopus 로고
    • Structure-activity relationships of carboxymethylpullulan-peptide-doxorubicin conjugates - Systematic modification of peptide spacer
    • (c) Nogusa, H.; Yano, T.; Kashima, N.; Yamamoto, K.; Okuno, S.; Hamana, H. Structure-activity relationships of carboxymethylpullulan-peptide-doxorubicin conjugates - systematic modification of peptide spacer. Bioorg. Med. Chem. Lett. 2000, 10 (3), 227-230;
    • (2000) Bioorg. Med. Chem. Lett. , vol.10 , Issue.3 , pp. 227-230
    • Nogusa, H.1    Yano, T.2    Kashima, N.3    Yamamoto, K.4    Okuno, S.5    Hamana, H.6
  • 12
    • 0041461026 scopus 로고    scopus 로고
    • High-molecular weight HMPA copolymer-adriamycin conjugates
    • (d) Dvorak, M.; Kopeckova, P.; Kopecek, J. High-molecular weight HMPA copolymer-adriamycin conjugates. J. Control. Release 1999, 60 (3), 321-332;
    • (1999) J. Control. Release , vol.60 , Issue.3 , pp. 321-332
    • Dvorak, M.1    Kopeckova, P.2    Kopecek, J.3
  • 14
    • 0032402354 scopus 로고    scopus 로고
    • Capthepsin B-sensitive dipeptide prodrugs. 1. A model study of structural requirements for efficient release of doxorubicin
    • (a) Dubowchik, G.M.; Firestone, R.A. Capthepsin B-sensitive dipeptide prodrugs. 1. A model study of structural requirements for efficient release of doxorubicin. Bioorg. Med. Chem. Lett. 1998, 8 (23), 3341-3346;
    • (1998) Bioorg. Med. Chem. Lett. , vol.8 , Issue.23 , pp. 3341-3346
    • Dubowchik, G.M.1    Firestone, R.A.2
  • 15
    • 0032402572 scopus 로고    scopus 로고
    • Capthepsin B-sensitive dipeptide prodrugs. 2. Models of anticancer drugs pacitaxel (Taxol), mitomycin C and doxorubicin
    • (b) Dubowchik, G.M.; Mosure, K.; Knipe, J.O.; Firestone, R.A. Capthepsin B-sensitive dipeptide prodrugs. 2. Models of anticancer drugs pacitaxel (Taxol), mitomycin C and doxorubicin. Bioorg. Med. Chem. Lett. 1998, 8 (23), 3347-3352.
    • (1998) Bioorg. Med. Chem. Lett. , vol.8 , Issue.23 , pp. 3347-3352
    • Dubowchik, G.M.1    Mosure, K.2    Knipe, J.O.3    Firestone, R.A.4
  • 16
    • 0035904966 scopus 로고    scopus 로고
    • Targeted drug conjugates: Principles and progress
    • Garnett, M.C. Targeted drug conjugates: principles and progress. Adv. Drug Delivery Rev. 2001, 53 (2), 171-216.
    • (2001) Adv. Drug Delivery Rev. , vol.53 , Issue.2 , pp. 171-216
    • Garnett, M.C.1
  • 17
    • 0034126420 scopus 로고    scopus 로고
    • New advances in the transport of doxorubicin through the blood-brain barrier by a peptide vector-mediated strategy
    • (a) Rousselle, C.; Clair, P.; Lefauconnier, J.-M.; Kaczorek, M.; Scherrmann, J.-M. Temsamani, J. New advances in the transport of doxorubicin through the blood-brain barrier by a peptide vector-mediated strategy. Mol. Pharmacol. 2000, 57 (4), 679-686;
    • (2000) Mol. Pharmacol. , vol.57 , Issue.4 , pp. 679-686
    • Rousselle, C.1    Clair, P.2    Lefauconnier, J.-M.3    Kaczorek, M.4    Scherrmann, J.-M.5    Temsamani, J.6
  • 18
    • 0034059501 scopus 로고    scopus 로고
    • Enhanced delivery improves the efficacy of a tumor-specific doxorubicin immunoconjugate in a human brain tumor xenograft model
    • (b) Remsen, L.G.; Trail, P.A.; Hellstrom, I.; Hellstrom, K.E.; Neuwelt, E.A. Enhanced delivery improves the efficacy of a tumor-specific doxorubicin immunoconjugate in a human brain tumor xenograft model. Neurosurgery 2000, 46 (3), 704-709.
    • (2000) Neurosurgery , vol.46 , Issue.3 , pp. 704-709
    • Remsen, L.G.1    Trail, P.A.2    Hellstrom, I.3    Hellstrom, K.E.4    Neuwelt, E.A.5
  • 21
    • 0041562653 scopus 로고    scopus 로고
    • Efficient one-pot synthesis of doxorubicin conjugates through its amino group to melanotransferrin p97
    • Chen, Q.; Sowa, D.; Cai, L.J. Gabathuler, R. Efficient one-pot synthesis of doxorubicin conjugates through its amino group to melanotransferrin p97. Synth. Commun. 2003, 33 (14), 2399-2419.
    • (2003) Synth. Commun. , vol.33 , Issue.14 , pp. 2399-2419
    • Chen, Q.1    Sowa, D.2    Cai, L.J.3    Gabathuler, R.4
  • 22
    • 0043065558 scopus 로고    scopus 로고
    • Synthesis of doxorubicin conjugates through hydrazone bonds to melanotransferrin p97
    • Chen, Q.; Sowa, D.; Gabathuler, R. Synthesis of doxorubicin conjugates through hydrazone bonds to melanotransferrin p97. Synth. Commun. 2003, 33 (14), 2375-2388.
    • (2003) Synth. Commun. , vol.33 , Issue.14 , pp. 2375-2388
    • Chen, Q.1    Sowa, D.2    Gabathuler, R.3
  • 24
    • 0032539609 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of cytoxic analogs of somatostatin containing doxorubicin or its intensely potent derivative, 2-pyrrolino-doxorubicin
    • (a) Nagy, A.; Schally, A.V.; Halmos, G.; Armatis, P.; Cai, R.Z.; Csernus, V.; Kovacs, M.; Koppan, M.; Szepeshazi, K. Synthesis and biological evaluation of cytoxic analogs of somatostatin containing doxorubicin or its intensely potent derivative, 2-pyrrolino-doxorubicin. Proc. Natl. Acad. Sci. USA 1998, 95 (4), 1794-1799;
    • (1998) Proc. Natl. Acad. Sci. USA , vol.95 , Issue.4 , pp. 794-1799
    • Nagy, A.1    Schally, A.V.2    Halmos, G.3    Armatis, P.4    Cai, R.Z.5    Csernus, V.6    Kovacs, M.7    Koppan, M.8    Szepeshazi, K.9
  • 26
    • 0031030324 scopus 로고    scopus 로고
    • Design, synthesis, and in vitro evaluation of cytotoxic analogs of bombesin-like, peptides containing doxorubicin or its intensely potent derivative, 2-pyrrolino-doxorubicin
    • (c) Nagy, A.; Armatis, P.; Cai, R.Z.; Szepeshazi, K.; Halmos, G.; Schally, A.V. Design, synthesis, and in vitro evaluation of cytotoxic analogs of bombesin-like, peptides containing doxorubicin or its intensely potent derivative, 2-pyrrolino-doxorubicin. Proc. Natl. Acad. Sci. USA 1997, 94 (2), 625-656.
    • (1997) Proc. Natl. Acad. Sci. USA , vol.94 , Issue.2 , pp. 625-656
    • Nagy, A.1    Armatis, P.2    Cai, R.Z.3    Szepeshazi, K.4    Halmos, G.5    Schally, A.V.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.