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Volumn 52, Issue 6, 1996, Pages 957-962

Intracellularly biorecognizable derivatives of 5-fluorouracil. Implications for site-specific delivery in the human condition

Author keywords

5 fluorouracil; biorecognition; cathepsin B; cathepsin H; polymer carriers; site specific release

Indexed keywords

CATHEPSIN B; CATHEPSIN H; COPOLYMER; DRUG CARRIER; FLUOROURACIL; FLUOROURACIL DERIVATIVE; LYSOSOME ENZYME; N (2 HYDROXYPROPYL)METHACRYLAMIDE; OLIGOPEPTIDE;

EID: 0030603965     PISSN: 00062952     EISSN: None     Source Type: Journal    
DOI: 10.1016/0006-2952(96)00410-8     Document Type: Article
Times cited : (30)

References (20)
  • 1
    • 0346551010 scopus 로고
    • Polymer conjugates with anticancer activity
    • 1. Putnam D and Kopeček J, Polymer conjugates with anticancer activity. Adv Polym Sci 122: 55-123, 1995.
    • (1995) Adv Polym Sci , vol.122 , pp. 55-123
    • Putnam, D.1    Kopeček, J.2
  • 2
    • 0024469053 scopus 로고
    • Anticancer agents coupled to N-(2-hydroxypropyl)methacrylamide copolymers. 3. Evaluation of adriamycin conjugates against mouse leukaemia L1210 in vivo
    • 2. Duncan R, Hume IC, Kopečková P, Ulbrich K, Strohalm J and Kopeček J, Anticancer agents coupled to N-(2-hydroxypropyl)methacrylamide copolymers. 3. Evaluation of adriamycin conjugates against mouse leukaemia L1210 in vivo. J Controlled Release 10: 51-63, 1989.
    • (1989) J Controlled Release , vol.10 , pp. 51-63
    • Duncan, R.1    Hume, I.C.2    Kopečková, P.3    Ulbrich, K.4    Strohalm, J.5    Kopeček, J.6
  • 3
    • 0024928931 scopus 로고
    • Preparation of potentially antitumor-active vinyl polymers having 5-fluorouracil unit as a component
    • 3. Ozaki S, Ohnishi J, Watanabe Y, Nohda T, Nagase T, Akiyama T, Uehara N and Hoshi A, Preparation of potentially antitumor-active vinyl polymers having 5-fluorouracil unit as a component. Polym J 21: 955-958, 1988.
    • (1988) Polym J , vol.21 , pp. 955-958
    • Ozaki, S.1    Ohnishi, J.2    Watanabe, Y.3    Nohda, T.4    Nagase, T.5    Akiyama, T.6    Uehara, N.7    Hoshi, A.8
  • 4
    • 0024243086 scopus 로고
    • Synthesis and anti-tumor activity of vinyl polymers containing 5-fluorouracils attached via carbamoyl bonds to organo-silicon groups
    • 4. Ouchi T, Hagita K, Kwashima M, Inoi T and Tahiro T, Synthesis and anti-tumor activity of vinyl polymers containing 5-fluorouracils attached via carbamoyl bonds to organo-silicon groups. J Controlled Release 8: 141-150, 1988.
    • (1988) J Controlled Release , vol.8 , pp. 141-150
    • Ouchi, T.1    Hagita, K.2    Kwashima, M.3    Inoi, T.4    Tahiro, T.5
  • 5
    • 0026593832 scopus 로고
    • Synthesis and antitumor activity of 6-o-carboxymethyl chitin fixing 5-fluorouracils through pentamethylene, monomethylene spacer groups via amide, ester bonds
    • 5. Ohya Y, Inosaka K and Ouchi T, Synthesis and antitumor activity of 6-O-carboxymethyl chitin fixing 5-fluorouracils through pentamethylene, monomethylene spacer groups via amide, ester bonds. Chem Pharm Bull (Tokyo) 40: 559-561, 1992.
    • (1992) Chem Pharm Bull (Tokyo) , vol.40 , pp. 559-561
    • Ohya, Y.1    Inosaka, K.2    Ouchi, T.3
  • 6
    • 0025984418 scopus 로고
    • Synthesis and antitumor activity of α-1,4-polygalactosamine and N-acetyl-α-1,4-polygalactosamine immobilized 5-fluorouracils through hexamethylene spacer groups via urea, urea bonds
    • 6. Ohya Y, Huang TZ, Ouchi T, Hasegawa K, Tamura J, Kadowaki K, Matumoto T, Suzuki S and Suzuki M, Synthesis and antitumor activity of α-1,4-polygalactosamine and N-acetyl-α-1,4-polygalactosamine immobilized 5-fluorouracils through hexamethylene spacer groups via urea, urea bonds. J Controlled Release 17: 259-266, 1991.
    • (1991) J Controlled Release , vol.17 , pp. 259-266
    • Ohya, Y.1    Huang, T.Z.2    Ouchi, T.3    Hasegawa, K.4    Tamura, J.5    Kadowaki, K.6    Matumoto, T.7    Suzuki, S.8    Suzuki, M.9
  • 7
    • 0029339453 scopus 로고
    • Enantioselective release of 5-fluorouracil from N-(2-hydroxypropyl)methacrylamide-based copolymers via lysosomal enzymes
    • 7. Putnam D and Kopeček J, Enantioselective release of 5-fluorouracil from N-(2-hydroxypropyl)methacrylamide-based copolymers via lysosomal enzymes. Bioconjug Chem 6: 483-492, 1995.
    • (1995) Bioconjug Chem , vol.6 , pp. 483-492
    • Putnam, D.1    Kopeček, J.2
  • 8
    • 0028273205 scopus 로고
    • Synthesis of peptide derivatives of 5-fluorouracil
    • 8. Nichifor M and Schacht EH, Synthesis of peptide derivatives of 5-fluorouracil. Tetrahedron 50: 3747-3760, 1994.
    • (1994) Tetrahedron , vol.50 , pp. 3747-3760
    • Nichifor, M.1    Schacht, E.H.2
  • 9
    • 0029089856 scopus 로고
    • Macromolecular prodrugs of 5-fluorouracil. 1: Synthesis and hydrolytic stability
    • 9. Nichifor M, Coessens V and Schacht EH, Macromolecular prodrugs of 5-fluorouracil. 1: Synthesis and hydrolytic stability. J Bioact Comp Polym 10: 199-222, 1995.
    • (1995) J Bioact Comp Polym , vol.10 , pp. 199-222
    • Nichifor, M.1    Coessens, V.2    Schacht, E.H.3
  • 10
    • 0025944975 scopus 로고
    • S-s bridges of cathepsin B and H from bovine spleen: A basis for cathepsin B model building and possible functional implications for discrimination between exo-and endopeptidase activities among cathepsins B, H and L
    • 10. Baudyš M, Meloun B, Gan-Erdene T, Fusek M, Mareš M, Kostka V, Pohl J and Blake CCF, S-S bridges of cathepsin B and H from bovine spleen: A basis for cathepsin B model building and possible functional implications for discrimination between exo-and endopeptidase activities among cathepsins B, H and L. Biomed Biochim Acta 50: 569-577, 1991.
    • (1991) Biomed Biochim Acta , vol.50 , pp. 569-577
    • Baudyš, M.1    Meloun, B.2    Gan-Erdene, T.3    Fusek, M.4    Mareš, M.5    Kostka, V.6    Pohl, J.7    Blake, C.C.F.8
  • 11
    • 0000859980 scopus 로고
    • Polymers containing enzymatically degradable bonds. 8. Degradation of oligopeptide sequences in N-(2-hydroxypropyl)-methacrylamide copolymers by bovine spleen cathepsin B
    • 11. Rejmanová P, Kopeček J, Pohl J, Baudyš M and Kostka V, Polymers containing enzymatically degradable bonds. 8. Degradation of oligopeptide sequences in N-(2-hydroxypropyl)-methacrylamide copolymers by bovine spleen cathepsin B. Makromol Chem 184: 2009-2020, 1983.
    • (1983) Makromol Chem , vol.184 , pp. 2009-2020
    • Rejmanová, P.1    Kopeček, J.2    Pohl, J.3    Baudyš, M.4    Kostka, V.5
  • 14
    • 0023658389 scopus 로고
    • Amino acid sequence of chicken liver cathepsin L
    • 14. Wada K, Takai Y and Tanabe T, Amino acid sequence of chicken liver cathepsin L. Eur J Biochem 167: 13-18, 1987.
    • (1987) Eur J Biochem , vol.167 , pp. 13-18
    • Wada, K.1    Takai, Y.2    Tanabe, T.3
  • 16
    • 0344310530 scopus 로고
    • Identification of cDNA clones encoding a precursor of rat liver cathepsin B
    • 16. San Segundo B, Chan SJ and Steiner DF, Identification of cDNA clones encoding a precursor of rat liver cathepsin B. Proc Natl Acad Sci USA 82: 2320-2324, 1985.
    • (1985) Proc Natl Acad Sci USA , vol.82 , pp. 2320-2324
    • San Segundo, B.1    Chan, S.J.2    Steiner, D.F.3
  • 17
    • 0020770394 scopus 로고
    • Homology of amino acid sequences of rat liver cathepsins B and H with that of papain
    • 17. Takiio K, Towatari T, Katunuma N, Teller DC and Titani K, Homology of amino acid sequences of rat liver cathepsins B and H with that of papain. Proc Natl Acad Sci USA 80: 3666-3670, 1983.
    • (1983) Proc Natl Acad Sci USA , vol.80 , pp. 3666-3670
    • Takiio, K.1    Towatari, T.2    Katunuma, N.3    Teller, D.C.4    Titani, K.5
  • 19
    • 0023946898 scopus 로고
    • Amino acid sequences of the human kidney cathepsins H and L
    • 19. Ritonja A, Popovic T, Kotnik M, Machleidt W and Turk V, Amino acid sequences of the human kidney cathepsins H and L. FEBS Lett 228: 341-345, 1988.
    • (1988) FEBS Lett , vol.228 , pp. 341-345
    • Ritonja, A.1    Popovic, T.2    Kotnik, M.3    Machleidt, W.4    Turk, V.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.