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Synthesis and antitumor activity of fluorinated derivatives of [i,j]-annelated quinolones

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Pharmaceutical Chemistry Journal Aims and scope

Tri- and pentacyclic fluoroquinolones were synthesized by intramolecular cyclization of the corresponding 3-hydrazinopolyfluorobenzoylacrylates followed by substitution of fluorine atoms by amine residues. The antitumor activity of the resulting compounds was studied at the National Cancer Institute using cultures of 60 cell lines of nine groups, including leukemia, lung tumor, large intestine tumor, CNS tumor, melanoma, ovary tumor, renal tumor, prostate tumor, and breast tumor. Relationships between structure and antitumor activity were analyzed. In vivo experimental data from hollow fiber tests are presented for two derivatives.

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This study was supported by State Contract GK-02.740.11.0260 and Scientific Schools grant No. NSh-65261.2010.3.

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Correspondence to É. V. Nosova.

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Translated from Khimiko-Farmatsevticheskii Zhurnal, Vol. 45, No. 4, pp. 12 – 14, April, 2011.

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Lipunova, G.N., Nosova, É.V., Sidorova, L.P. et al. Synthesis and antitumor activity of fluorinated derivatives of [i,j]-annelated quinolones. Pharm Chem J 45, 208–210 (2011). https://doi.org/10.1007/s11094-011-0595-x

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  • DOI: https://doi.org/10.1007/s11094-011-0595-x

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