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Volumn 40, Issue 19, 1997, Pages 3049-3056

Antitumor agents. 178. Synthesis and biological evaluation of substituted 2-aryl-1,8-naphthyridin-4(1H)-ones as antitumor agents that inhibit tubulin polymerization

Author keywords

[No Author keywords available]

Indexed keywords

1,8 NAPHTHYRIDIN 4 ONE DERIVATIVE; ANTINEOPLASTIC AGENT; COLCHICINE; COMBROSTATIN A4; KETONE DERIVATIVE; PODOPHYLLOTOXIN; TUBULIN; UNCLASSIFIED DRUG;

EID: 0030823308     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm970146h     Document Type: Article
Times cited : (112)

References (16)
  • 1
    • 0031552141 scopus 로고    scopus 로고
    • Antitumor agents 177. Design, synthesis, and biological evaluation of novel etoposide analogs bearing pyrrole-carboxamidino group as DNA topoisomerase II inhibitors
    • Ji, Z.; Wang, K. H.; Bastow, K. F.; Zhu, X. K; Cho, S. J.; Cheng, Y. C.; Lee, K. L. Antitumor agents 177. Design, synthesis, and biological evaluation of novel etoposide analogs bearing pyrrole-carboxamidino group as DNA topoisomerase II inhibitors. Bioorg. Med. Chem. Lett. 1997, 7, 607-612.
    • (1997) Bioorg. Med. Chem. Lett. , vol.7 , pp. 607-612
    • Ji, Z.1    Wang, K.H.2    Bastow, K.F.3    Zhu, X.K.4    Cho, S.J.5    Cheng, Y.C.6    Lee, K.L.7
  • 2
    • 0030738726 scopus 로고    scopus 로고
    • Antitumor agents. 175. 2′,3′,4′,5,6,7-Substituted 2-phenyl-1,8-naphthyridin-4(1H)-ones: Their synthesis, cytotoxicity, and inhibition of tubulin polymerization
    • Chen, K.; Kuo, S. C.; Mauger, A.; Lin, C. M.; Hamel, E.; Lee, K. H. Antitumor agents. 175. 2′,3′,4′,5,6,7-Substituted 2-phenyl-1,8-naphthyridin-4(1H)-ones: Their synthesis, cytotoxicity, and inhibition of tubulin polymerization. J. Med. Chem. 1997, 40, 2266-2275.
    • (1997) J. Med. Chem. , vol.40 , pp. 2266-2275
    • Chen, K.1    Kuo, S.C.2    Mauger, A.3    Lin, C.M.4    Hamel, E.5    Lee, K.H.6
  • 3
    • 0000719887 scopus 로고
    • Status of the NCI preclinical antitumor drug discovery screen
    • De Vita, V. T., Hellman, S., Rosenberg, S. A., Eds; J. B. Lippincoft: Philadelphia
    • Boyd, M. R. Status of the NCI preclinical antitumor drug discovery screen. In Cancer: Principles and Practice of Oncology Updates; De Vita, V. T., Hellman, S., Rosenberg, S. A., Eds; J. B. Lippincoft: Philadelphia, 1989; pp 1-12.
    • (1989) Cancer: Principles and Practice of Oncology Updates , pp. 1-12
    • Boyd, M.R.1
  • 5
    • 0026328348 scopus 로고
    • Interactions of colchicine with tubulín
    • Hastie, S. B. Interactions of colchicine with tubulín. Pharmacol. Ther. 1991, 51, 377-401.
    • (1991) Pharmacol. Ther. , vol.51 , pp. 377-401
    • Hastie, S.B.1
  • 7
    • 0017344821 scopus 로고
    • Podophyllotoxin as a probe for the colchicine binding site of tubulin
    • Cortese, F.; Bhattacharyya, B.; Wolff, J. Podophyllotoxin as a probe for the colchicine binding site of tubulin. J. Bíol. Chem. 1977, 252, 1134-1140.
    • (1977) J. Bíol. Chem. , vol.252 , pp. 1134-1140
    • Cortese, F.1    Bhattacharyya, B.2    Wolff, J.3
  • 8
    • 0020422990 scopus 로고
    • Conformational states of tubulin liganded to colchicine, tropolone methyl ether, and podophyllotoxin
    • Andreu, S. M.; Timasheff, S. Conformational states of tubulin liganded to colchicine, tropolone methyl ether, and podophyllotoxin. Biochemistry 1982, 21, 6465-6476.
    • (1982) Biochemistry , vol.21 , pp. 6465-6476
    • Andreu, S.M.1    Timasheff, S.2
  • 9
    • 0024427745 scopus 로고
    • Antimitotic natural products combretastatin A-4 and combretastatin A-2; studies on the mechanism of their inhibition of binding of colchicine to tubulin
    • Lin, C. M.; Ho, H, H.; Pettit, G. R.; Hamel, E. Antimitotic natural products combretastatin A-4 and combretastatin A-2; studies on the mechanism of their inhibition of binding of colchicine to tubulin. Biochemistry 1989, 28, 6984-6991.
    • (1989) Biochemistry , vol.28 , pp. 6984-6991
    • Lin, C.M.1    Ho, H.H.2    Pettit, G.R.3    Hamel, E.4
  • 10
    • 0029066847 scopus 로고
    • Antineoplastic agents. 291. Isolation and synthesis of combretastatins A-4, A-5, and A-6 (1a)
    • Pettit, G. R.; Singh, S. B.; Boyd, M. R.; Hamel E.; Pettit, R. K.; Schmidt, J. M.; Hogan, F. Antineoplastic agents. 291. Isolation and synthesis of combretastatins A-4, A-5, and A-6 (1a). J. Med. Chem. 1995, 38, 1666-1672.
    • (1995) J. Med. Chem. , vol.38 , pp. 1666-1672
    • Pettit, G.R.1    Singh, S.B.2    Boyd, M.R.3    Hamel, E.4    Pettit, R.K.5    Schmidt, J.M.6    Hogan, F.7
  • 11
    • 84986439459 scopus 로고
    • The synthesis of macrocyclic polyether-diesters incorporating 1,10-phenanthrolino and 1,8-naphthyridino subunits
    • Chandler, C. J.; Deady, L. W.; Reiss, J. A.; Tzimos, V. The synthesis of macrocyclic polyether-diesters incorporating 1,10-phenanthrolino and 1,8-naphthyridino subunits. J. Heterocycl. Chem. 1982, 19, 1017-1019.
    • (1982) J. Heterocycl. Chem. , vol.19 , pp. 1017-1019
    • Chandler, C.J.1    Deady, L.W.2    Reiss, J.A.3    Tzimos, V.4
  • 13
    • 0023760949 scopus 로고
    • The cytotoxic principles of Prunella vulgaris, Psychotria serpens, and Hyptis captitata: Ursolic acid and related derivatives
    • Lee, K. H.; Lin, Y. M.; Wu, T. S.; Zhang, D. C.; Yamagishi, T.; Hayashi, T.; Hall, I. H.; Chang, J. J.; Wu, R. Y.; Yang, T. H. The cytotoxic principles of Prunella vulgaris, Psychotria serpens, and Hyptis captitata: Ursolic acid and related derivatives. Planta Med. 1988, 54, 308-312.
    • (1988) Planta Med. , vol.54 , pp. 308-312
    • Lee, K.H.1    Lin, Y.M.2    Wu, T.S.3    Zhang, D.C.4    Yamagishi, T.5    Hayashi, T.6    Hall, I.H.7    Chang, J.J.8    Wu, R.Y.9    Yang, T.H.10
  • 14
    • 0021163546 scopus 로고
    • Separation of active tubulin and microtubule-associated proteins by ultracentrifugation and isolation of a component causing the formation of microtubule bundles
    • Hamel, E.; Lin. C. M. Separation of active tubulin and microtubule-associated proteins by ultracentrifugation and isolation of a component causing the formation of microtubule bundles. Biochemistry 1984, 23, 4173-4184.
    • (1984) Biochemistry , vol.23 , pp. 4173-4184
    • Hamel, E.1    Lin, C.M.2
  • 15
    • 0028331925 scopus 로고
    • 2-Methoxyestradiol, an endogenous mammalian metabolite, inhibits tubulin polymerization by interacting at the colchicine site
    • D'Amato, R. J.; Lin, C. M.; Flynn, E.; Folkman, J.; Hamel, E. 2-Methoxyestradiol, an endogenous mammalian metabolite, inhibits tubulin polymerization by interacting at the colchicine site. Proc. Natl. Acad. Sci. U.S.A. 1994, 91, 3964-3968.
    • (1994) Proc. Natl. Acad. Sci. U.S.A. , vol.91 , pp. 3964-3968
    • D'Amato, R.J.1    Lin, C.M.2    Flynn, E.3    Folkman, J.4    Hamel, E.5
  • 16
    • 0028036429 scopus 로고
    • Antitumor agents. 155. Synthesis and biological evaluation of 3′, 6,7-substituted 2-phenyl-4-quinolones as antimicrotubule agents
    • Li, L.; Wang, H. K.; Kuo, S. C.; Wu, T. S.; Mauger, A.; Lin, C. M.; Hamel, E.; Lee, K. H. Antitumor agents. 155. Synthesis and biological evaluation of 3′, 6,7-substituted 2-phenyl-4-quinolones as antimicrotubule agents. J. Med. Chem. 1994, 37, 3400-3407.
    • (1994) J. Med. Chem. , vol.37 , pp. 3400-3407
    • Li, L.1    Wang, H.K.2    Kuo, S.C.3    Wu, T.S.4    Mauger, A.5    Lin, C.M.6    Hamel, E.7    Lee, K.H.8


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