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Synthesis of 1,6-Disubstituted 4,5,6,7-Tetrahydropyrazolo[3,4-c]pyridin-7-one Derivatives and Evaluation of Their Anticancer Activity

  • Devegowda, Vani Nelamane (Life/Health Division, Korea Institute of Science and Technology) ;
  • Seo, Seon-Hee (Life/Health Division, Korea Institute of Science and Technology) ;
  • Pae, Ae Nim (Life/Health Division, Korea Institute of Science and Technology) ;
  • Nam, Ghil-Soo (Life/Health Division, Korea Institute of Science and Technology) ;
  • Choi, Kyung-Il (Life/Health Division, Korea Institute of Science and Technology)
  • Received : 2011.08.23
  • Accepted : 2011.10.24
  • Published : 2012.02.20

Abstract

Promising anticancer compounds of the type 1,6-disubstituted 4,5,6,7-tetrahydropyrazolo[3,4-c]pyridin-7-ones were identified. The target compounds were readily synthesized in a large scale via a sequence of reactions starting from the commercially available primary amines. Their in vitro anti-proliferative activity has been evaluated on prostate (DU-145), colon (HT-29 and HCT-116) and melanoma (A375P) human cancer cell lines. The relationships between the structure and the anticancer activity, covering all tested cancer cell lines, revealed that the compound 5c with 2,4-dimethylphenyl substituent at $R^2$ was the most potent with the $IC_{50}$ values in the range as low as 0.16 to $0.40{\mu}M$.

Keywords

References

  1. Gibbs, J. B. Science 2000, 287, 1969. https://doi.org/10.1126/science.287.5460.1969
  2. Pinto, D. J. P.; Orwat, M. J.; Quan, M. L.; Han, Q.; Galemmo, R. A., Jr.; Amparo, E.; Wells, B.; Ellis, C.; He, M. Y.; Alexander, R. S.; Rossi, K. A.; Smallwood, A.; Wong, P. C.; Luettgen, J. M.; Rendina, A. R.; Knabb, R. M.; Mersinger, L.; Kettner, C.; Bai, S.; He, K.; Wexler, R. R.; Lam, P. Y. S. Bioorg, Med. Chem. Lett. 2006, 16, 4141. https://doi.org/10.1016/j.bmcl.2006.02.069
  3. Fancelli, D.; Berta, D.; Bindi, S.; Cameron, A.; Cappella, P.; Carpinelli, P.; Catana, C.; Forte, B.; Giordano, P.; Giorgini, M. L.; Mantegani, S.; Marsiglio, A.; Meroni, M.; Moll, J.; Pittala, V.; Roletto, F.; Severino, D.; Soncini, C.; Storici, P.; Tonani, R.; Varasi, M.; Vulpetti, A.;Vianello, P. J. Med. Chem. 2005, 48, 3080. https://doi.org/10.1021/jm049076m
  4. Pevarello, P.; Brasca, M. G.; Amici, R.; Orsini, P.; Traquandi, G.; Corti, L.; Piutti, C.; Sansonna, P.; Villa, M.; Pierce, B. S.; Pulici, M.; Giordano, P.; Martina, K.; Fritzen, E. L.; Nugent, R. A.; Casale, E.; Cameron, A.; Ciomei, M.; Roletto, F.; Isacchi, A.; Fogliatto, G.; Pesenti, E.; Pastori, W.; Marsiglio, A.; Leach, K. L.; Clare, P. M.; Fiorentini, F.; Varasi, M.; Vulpetti, A.; Warpehoski, M. A. J. Med. Chem. 2004, 47, 3367. https://doi.org/10.1021/jm031145u
  5. Brasca, M. G.; Albanese, C.; Amici, R.; Ballinari, D.; Corti, L.; Croci, V.; Fancelli, D.; Fiorentini, F.; Nesi, M.; Orsini, P.; Orzi, F.; Pastori, W.; Perrone, E.; Pesenti, E.; Pevarello, P.; Riccardi-Sirtori, F.; Roletto, F.; Roussel, P.; Varasi, M.; Vulpetti, A.; Mercurio, C. Chem. Med. Chem. 2007, 2, 841. https://doi.org/10.1002/cmdc.200600302
  6. Regan, J.; Capolino, A.; Cirillo, P. F.; Gilmore, T.; Graham, A. G.; Hickey, E.; Kroe, R. R.; Madwed, J.; Moriak, M.; Nelson, R.; Pargellis, C. A.; Swinamer, A.; Torcellini, C.; Tsang, M.; Moss, N.J. Med. Chem. 2003, 46, 4676. https://doi.org/10.1021/jm030121k
  7. Blatter, H. M.; Irvington, N. J. US 3423414, 1969.
  8. Gardner, R. A.; Belting, M.; Svensson, K.; Phanstiel Iv, O. J. Med. Chem. 2007, 50, 308. https://doi.org/10.1021/jm0607101
  9. Larsen, S. D.; Dipaolo, B. A. Org. Lett. 2001, 3, 3341. https://doi.org/10.1021/ol016578a
  10. Devegowda, V. N.; Kim, J. H.; Han, K.-C.; Yang, E. G.; Choo, H.; Pae, A. N.; Nam, G.; Choi, K. I. Bioorg. Med. Chem. Lett. 2010, 20, 1630. https://doi.org/10.1016/j.bmcl.2010.01.029

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