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Synthesis and study of antitumor activity of 4H-pyrano[3,2-c]pyridines based on N-(2-azidoethyl)- and N-propargyl-3,5-bis(arylidene)piperidin-4-ones

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Abstract

The synthesis of 3,5-bis(arylidene)piperidin-4-ones containing the 2-azidoethyl (azides 1a–d) or propargyl (acetylenes 2a–c) group at the nitrogen atom of the 4-piperidinone ring was described. The in vitro MTT assay for cytotoxicity of these compounds toward the human tumor cell lines PC3, HCT116, and MCF7 and the human embryonic kidney cells HEK293 revealed that N-(2-azidoethyl)-3,5-bis(3-pyridylidene)piperidin-4-one (1c) and N-propargyl-3,5- bis(benzylidene)piperidin-4-one (2a) exhibit high activity (IC50 in the range of 1–5 μmol L–1). The reaction of compounds 1a–d and 2a–c with malononitrile affords the corresponding 4H-pyrano[3,2-c]pyridines 3a–d and 4a–c devoid of cytotoxicity. This is evidence of the importance of preserving the 1,5-diaryl-3-oxo-1,4-pentadiene moiety upon the modification of 3,5-bis(arylidene)piperidin-4-ones in drug design when searching for new antitumor agents based on these compounds.

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Authors and Affiliations

  1. A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 119991, Moscow, Russian Federation

    O. V. Bykhovskaya, I. M. Aladzheva, M. V. Makarov, Z. S. Klemenkova & V. K. Brel

  2. Research Institute of Cancerogenesis, N. N. Blokhin Russian Cancer Research Center, Ministry of Health Care of the Russian Federation, 24 Kashirskoe sh., 115478, Moscow, Russian Federation

    E. Yu. Rybalkina

Authors
  1. O. V. Bykhovskaya
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  2. I. M. Aladzheva
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  3. M. V. Makarov
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  4. E. Yu. Rybalkina
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  5. Z. S. Klemenkova
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  6. V. K. Brel
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Correspondence to M. V. Makarov.

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Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 0104—0110, January, 2017.

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Bykhovskaya, O.V., Aladzheva, I.M., Makarov, M.V. et al. Synthesis and study of antitumor activity of 4H-pyrano[3,2-c]pyridines based on N-(2-azidoethyl)- and N-propargyl-3,5-bis(arylidene)piperidin-4-ones. Russ Chem Bull 66, 104–110 (2017). https://doi.org/10.1007/s11172-017-1707-x

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  • DOI: https://doi.org/10.1007/s11172-017-1707-x

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