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Planar structural requirement at 4-position of 1-arylsulfonyl-4-phenyl-4,5-dihydro-2-imidazolones for their cytotoxicity

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Abstract

In order to identify the structural requirement at 4-position of 1-arylsulfonyl-4-phenyl-4,5-dihydro-2-limidazolones3 for their cytotoxicity, the corresponding 1-arylsulfonyl-4-cyclohexyl-4,5-dihydro-2-imidazolones4 were synthesized and theirin vitro cytotoxicity against human solid tumor cell lines were measured. Unlike compounds3a-c, cyclohexyl analogues4a-c do not show the cytotoxicity. This dramatic loss of activity of these analogues on the volume change with the bulkier cyclohexyl group indicates that the planar structure at 4-position of 1-arylsulfonyl-4-phenyl-4,5-dihydro-2-limidazolones3 is required for their activity as an important pharmacophoric moiety.

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References Cited

  • Everitt, E. and Wohlfart, C., Spectrophotometric quantitation of anchorage-dependent cell numbers extraction of naphthol blue-black-stained cellular protein.Anal. Biochem., 162(1), 122–9 (1987).

    Article  PubMed  CAS  Google Scholar 

  • Grindey, G. B., Boder, G. B., Grossman, C. S., Howbert, J. J., Poore, G. A., Shaw, W. H., Todd, G. C., and Worzalla, J. F., Further development of diarglsulfonylureas as novel anticancer drugs.Proc. Am. Assoc. Cancer Res., 28, 309 (1987).

    Google Scholar 

  • Grindey, G. B., Identification of diarysulfonylureas as novel anticancer drugs.Proc. Am. Assoc. Cancer Res., 29, 535 (1988).

    Google Scholar 

  • Grindey, G. B., Current status of cancer drug development: Failure or limited success.Cancer Cells, 2, 163–171 (1990).

    PubMed  CAS  Google Scholar 

  • Hainsworth, J. D., Handle, K. R., Satterlee, W. G., Kuttesch, J., Johnson, D. H., Grindey, G. B., Jackson, L. E., and Greco, F. A., Phase I clinical study of N-[(4-chlorophenylamino)]carbonyl-2,3-dihydro-1H-indene-5-sulfonamide (LY186641).Cancer Res., 49, 5217–5220 (1989).

    PubMed  CAS  Google Scholar 

  • Hansch, C., Leo, A.,Exploring QSAR, ACS Professional Reference Book, American Chemical Society, Washington, DC, U. S. A., 1995, pp. 522–528.

    Google Scholar 

  • Houghton, P. J., Bailey, F. C., Germain, G. S., Grindey, G. B., Witt, B. C. and Houghton, J. A., N-(5-indanylsulfonyl)-N′-(4-chlorophenyl)-urea, A novel agent equally cytotoxic to nonproliferlating human colon adenosarcoma cells.Cancer Res., 50, 318–322 (1990).

    PubMed  CAS  Google Scholar 

  • Houghton, P. J., Bailey, F. C., Houghton, J. A., Murti, K. G., Howbert, J. J. and Grindey, G. B., Evidence for mitochondrial localization of N-(4-Methylphenylsulfonyl)-N′-(4-chlorophenyl) urea in human colon adenosarcoma cells.Cancer Res. 50, 664–668 (1990).

    PubMed  CAS  Google Scholar 

  • Howbert, J. J., Grossman, C. S., Crowell, T. A., Rieder, B. J., Harper, R. W., Kramer, K. E., Tao, E. V., Aikins, J., Poore, G. A., Rinzel, S. M., Grindey, G. B., Shaw, W. N., Todd, G. C., Novel Agents Effective against Solid Tumors: The Diarylsulfonylureas. Synthesis, Activities, and Analysis of Quantitative Structure-Activity Relationships.J. Med. Chem., 33, 2393–2407 (1990).

    Article  PubMed  CAS  Google Scholar 

  • Howbert, J. J., Sulofenur.Drugs Future., 16, 517–520 (1991).

    Google Scholar 

  • Jung, S. H., Song, J. S., Lee, H. S., Choi, S. U., and Lee, C. O., Synthesis and evaluation of cytotoxic activity of novel arylsulfonylimidazolidinones.Bioorg. Med. Chem. Lett. 6, 2553–2558 (1996).

    Article  CAS  Google Scholar 

  • Jung, S. H., Song, J. S., Lee, H. S., Choi, S. U., and Lee, C. O., Synthesis and evaluation of cytotoxic activity of novel arylsulfonylimidazolidinones containing sulfonylurea pharmacophore.Arch. Pharm. Res., 19, 570–580 (1996).

    Article  CAS  Google Scholar 

  • Kamthan, A., Scarffe, J. H., Walling, J., Hatty, S., Peters, B., Coleman, R., and Smyth, J. F., A phase II study of solufenur (LY186641) in gastric cancer.Anti-cancer Drugs, 3, 331–335 (1992).

    Article  PubMed  CAS  Google Scholar 

  • Munshi, N. C., Seitz, D. E., Fosella, F., Lippman, S. N., and Einhorn, L. H., Phase II study of sulofenur (LY186641). A novel antineoplastic agent in advanced non-small lung cancer.Proc. Am. Assoc. Cancer Res. 32, 189 (1991).

    Google Scholar 

  • Perrin, D. D., Armarego, W. L. F., and Perrin, D. R.,Purification of laboratory chemicals, 2nd edition. Pergamon Press, Oxford, England, 1982.

    Google Scholar 

  • Schultz, R. M., Merriman, R. L., Toth, J. E., Zimmermann, J. E., Hertel, L. W., Andis, S. L., Dudley, D. E., Rutherford, P. G., Tanzer, L. R., and Grindey, G. B., Evaluation of new anticancer agents against the MIA Paca-2 and PANC-1 human pancreatic carcinoma xenografts.Oncol. Res., 5, 223 (1993).

    PubMed  CAS  Google Scholar 

  • Skehan, P., Storeng, R., Scudiero, D. A., Monks, A., McMahon, J., Vista, D. T., Warren, J. T., Kenny, S., and Boyd, M. R., New Colorimetric cytotoxicity assay for anticancer drug screening,J. Natl. Cancer. Inst., 82, 1107–1112 (1990).

    Article  PubMed  CAS  Google Scholar 

  • Talbot, D. C., Smith, I. E., Nicolson, M. C., Powles, T. J., Button, D., and Walling, J., Phase II trial of the novel sulphonylurea sulofenur in advanced breast cancer.J. Cancer Chemother. Pharmacol., 31, 419–422 (1993).

    Article  CAS  Google Scholar 

  • Taylor, C. W., Alberts, D. S., Ketcham, M. A., Satterlee, W. G., Holdsworth, M. T., Plazia, P. M., Peng, Y. M., Mccloskey, T. M., Roe, D. J., Hamilton, M., and Salmaon, S. E., Clinical pharmacology of a novel diarylsulfonylurea anticancer agent.J. Clin. Oncol., 7, 1733–1740 (1989).

    PubMed  CAS  Google Scholar 

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Jung, SH., Kwak, SJ. Planar structural requirement at 4-position of 1-arylsulfonyl-4-phenyl-4,5-dihydro-2-imidazolones for their cytotoxicity. Arch. Pharm. Res. 20, 283–287 (1997). https://doi.org/10.1007/BF02976159

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