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Volumn 23, Issue 5, 2000, Pages 450-454

Synthesis and In Vitro Cytotoxicity of 2-Alkylaminosubstituted Quinoline Derivatives

Author keywords

Antitumor agents; Cytotoxic activity; Doxorubicin; TAS 103

Indexed keywords

ANTINEOPLASTIC AGENT; QUINOLINE DERIVATIVE;

EID: 0034305372     PISSN: 02536269     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF02976570     Document Type: Article
Times cited : (5)

References (7)
  • 1
    • 0031056011 scopus 로고    scopus 로고
    • Synthesis and Antitumor Evaluation of New Thiazolo[5,4-b]quinoline Derivatives
    • and references cited therein
    • Alvarez-Ibarra, C., Fernandez-Cranda, R., Quiroga, M. L., Carbonell, A., Cardenas, F., and Cirait, E. Synthesis and Antitumor Evaluation of New Thiazolo[5,4-b]quinoline Derivatives. J. Med. Chem. 40, 668-676 (1997) and references cited therein.
    • (1997) J. Med. Chem. , vol.40 , pp. 668-676
    • Alvarez-Ibarra, C.1    Fernandez-Cranda, R.2    Quiroga, M.L.3    Carbonell, A.4    Cardenas, F.5    Cirait, E.6
  • 2
    • 0033066292 scopus 로고    scopus 로고
    • In vitro antitumor activity of TAS-103, a novel quinoline derivative that targets topoisomerases I and II
    • and references cited therein
    • Aoyagi, Y., Kobunai, T., Utsugi, T., Oh-hara, T., Yamada, Y., In vitro antitumor activity of TAS-103, a novel quinoline derivative that targets topoisomerases I and II. Jpn. J. Cancer Res. 90, 578-587, (1999) and references cited therein.
    • (1999) Jpn. J. Cancer Res. , vol.90 , pp. 578-587
    • Aoyagi, Y.1    Kobunai, T.2    Utsugi, T.3    Oh-hara, T.4    Yamada, Y.5
  • 4
    • 0033955462 scopus 로고    scopus 로고
    • Mechanism of action of the dual topoisomerase-I and -II inhibitor TAS-103 and activity against (multi)drug resistant cells
    • and references cited therein
    • Minderman, H., Wrzosek, C., Cao, S. S., Utsugi, T., Kobunai, T., Yamada, Y., Rustum, Y. M., Mechanism of action of the dual topoisomerase-I and -II inhibitor TAS-103 and activity against (multi)drug resistant cells. Cancer Chemother. Pharmacol. 45, 78-84 (2000) and references cited therein.
    • (2000) Cancer Chemother. Pharmacol. , vol.45 , pp. 78-84
    • Minderman, H.1    Wrzosek, C.2    Cao, S.S.3    Utsugi, T.4    Kobunai, T.5    Yamada, Y.6    Rustum, Y.M.7
  • 6
    • 0022450027 scopus 로고
    • Cycloaddition Routes to Azaanthraquinone Derivatives. 1. Use of Azadienophiles
    • Potts, K. T., Bhattachaarjee, D., and Walsh E. B., Cycloaddition Routes to Azaanthraquinone Derivatives. 1. Use of Azadienophiles. J. Org. Chem. 51, 2011-2021 (1986).
    • (1986) J. Org. Chem. , vol.51 , pp. 2011-2021
    • Potts, K.T.1    Bhattachaarjee, D.2    Walsh, E.B.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.