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Volumn 42, Issue 19, 1999, Pages 3789-3799

Discovery of novel antitumor sulfonamides targeting G1 phase of the cell cycle

Author keywords

[No Author keywords available]

Indexed keywords

INDISULAM; N [2 [(4 HYDROXYPHENYL)AMINO] 3 PYRIDINYL] 4 METHOXYBENZENESULFONAMIDE; SULFONAMIDE; UNCLASSIFIED DRUG;

EID: 0033598320     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm9902638     Document Type: Article
Times cited : (321)

References (40)
  • 1
    • 0030221053 scopus 로고    scopus 로고
    • Understanding and controlling the cell cycle with natural products
    • Hung, D. T.; Jamison, T. F.; Schreiber, S. L. Understanding and controlling the cell cycle with natural products. Chem. Biol. 1996, 3, 623-639.
    • (1996) Chem. Biol. , vol.3 , pp. 623-639
    • Hung, D.T.1    Jamison, T.F.2    Schreiber, S.L.3
  • 3
    • 0030756156 scopus 로고    scopus 로고
    • Mechanism of action of E7010: Inhibition of mitosis by binding to the colchicine site of tubulin
    • Yoshimatsu, K.; Yamaguchi, A.; Yoshino, H.; Koyanagi, N.; Kitoh, K. Mechanism of action of E7010: Inhibition of mitosis by binding to the colchicine site of tubulin. Cancer Res. 1997, 57, 3208-3213.
    • (1997) Cancer Res. , vol.57 , pp. 3208-3213
    • Yoshimatsu, K.1    Yamaguchi, A.2    Yoshino, H.3    Koyanagi, N.4    Kitoh, K.5
  • 10
    • 0029849620 scopus 로고    scopus 로고
    • Cancer cell cycles
    • Sherr, C. J. Cancer cell cycles. Science 1996, 274, 1672-1677.
    • (1996) Science , vol.274 , pp. 1672-1677
    • Sherr, C.J.1
  • 11
    • 0017767153 scopus 로고
    • N-butyrate causes histone modification in HeLa and friend erythroleukaemia cells
    • (a) Riggs, M. G.; Whittaker, R. G.; Neumann, J. R.; Ingram, V. M. n-Butyrate causes histone modification in HeLa and Friend erythroleukaemia cells. Nature 1977, 268, 462-464.
    • (1977) Nature , vol.268 , pp. 462-464
    • Riggs, M.G.1    Whittaker, R.G.2    Neumann, J.R.3    Ingram, V.M.4
  • 12
    • 0028260120 scopus 로고
    • Butyrate as a differentiating agent: Pharmacokinetics, analogues and current status
    • (b) Newmark, H. L.; Lupton, J. R.; Young, C. W. Butyrate as a differentiating agent: pharmacokinetics, analogues and current status. Cancer Lett. 1994, 78, 1-5.
    • (1994) Cancer Lett. , vol.78 , pp. 1-5
    • Newmark, H.L.1    Lupton, J.R.2    Young, C.W.3
  • 13
    • 0344431240 scopus 로고    scopus 로고
    • FR901228, a potent antitumor antibiotic, is a novel histone deacetylase inhibitor
    • Nakajima, H.; Kim, A. B.; Terano, H.; Yoshida, M.; Horinouchi, S. FR901228, a potent antitumor antibiotic, is a novel histone deacetylase inhibitor. Exp. Cell Res. 1998, 241, 126-133.
    • (1998) Exp. Cell Res. , vol.241 , pp. 126-133
    • Nakajima, H.1    Kim, A.B.2    Terano, H.3    Yoshida, M.4    Horinouchi, S.5
  • 14
    • 0029294663 scopus 로고
    • Trichostatin and trapoxin: Novel chemical probes for the role of histone acetylation in chromatin structure and function
    • (a) Yoshida, M.; Horinouchi, S.; Beppu, T. Trichostatin and trapoxin: novel chemical probes for the role of histone acetylation in chromatin structure and function. Bioessays 1995, 17, 423-430.
    • (1995) Bioessays , vol.17 , pp. 423-430
    • Yoshida, M.1    Horinouchi, S.2    Beppu, T.3
  • 15
    • 0029932598 scopus 로고    scopus 로고
    • A mammalian histone deacetylase related to the yeast transcriptional regulator Rpd3p
    • (b) Taunton, J.; Hassig, C. A.; Schreiber, S. L. A mammalian histone deacetylase related to the yeast transcriptional regulator Rpd3p. Science 1996, 272, 408-411.
    • (1996) Science , vol.272 , pp. 408-411
    • Taunton, J.1    Hassig, C.A.2    Schreiber, S.L.3
  • 16
    • 0028057513 scopus 로고
    • Effect of UCN-01, a selective inhibitor of protein kinase C, on the cell cycle distribution of human epidermoid carcinoma, A431 cells
    • Akinaga, S.; Nomura, K.; Gomi, K.; Okada, M. Effect of UCN-01, a selective inhibitor of protein kinase C, on the cell cycle distribution of human epidermoid carcinoma, A431 cells. Cancer Chemother. Pharmacol. 1994, 33, 273-280.
    • (1994) Cancer Chemother. Pharmacol. , vol.33 , pp. 273-280
    • Akinaga, S.1    Nomura, K.2    Gomi, K.3    Okada, M.4
  • 20
    • 0029033981 scopus 로고
    • Inhibition of proteasome activities and subunit-specific amino-terminal threonine modification by lactacystin
    • Fenteany, G.; Standaert, R. F.; Lane, W. S.; Choi, S.; Corey, E. J.; Schreiber, S. L. Inhibition of proteasome activities and subunit-specific amino-terminal threonine modification by lactacystin. Science 1995, 268, 726-731.
    • (1995) Science , vol.268 , pp. 726-731
    • Fenteany, G.1    Standaert, R.F.2    Lane, W.S.3    Choi, S.4    Corey, E.J.5    Schreiber, S.L.6
  • 21
    • 0031875042 scopus 로고    scopus 로고
    • The benzoquinone ansamycin 17-allylamino-17-demethoxygeldanamycin binds to HSP90 and shares important biologic activities with geldanamycin
    • Schulte, T. W.; Neckers, L. M. The benzoquinone ansamycin 17-allylamino-17-demethoxygeldanamycin binds to HSP90 and shares important biologic activities with geldanamycin. Cancer Chemother. Pharmacol. 1998, 42, 273-279.
    • (1998) Cancer Chemother. Pharmacol. , vol.42 , pp. 273-279
    • Schulte, T.W.1    Neckers, L.M.2
  • 22
    • 0031005361 scopus 로고    scopus 로고
    • Crystal structure of an HSP90-geldanamycin complex: Targeting of a protein chaperone by an antitumor agent
    • Stebbins, C. E.; Russo, A. A.; Schneider, C.; Rosen, N.; Hartl, F. U.; Pavletich, N. P. Crystal structure of an HSP90-geldanamycin complex: targeting of a protein chaperone by an antitumor agent. Cell 1997, 89, 239-250.
    • (1997) Cell , vol.89 , pp. 239-250
    • Stebbins, C.E.1    Russo, A.A.2    Schneider, C.3    Rosen, N.4    Hartl, F.U.5    Pavletich, N.P.6
  • 23
    • 0025204095 scopus 로고
    • Synthetic analogues of fumagillin that inhibit angiogenesis and suppress tumour growth
    • Ingber, D.; Fujita, T.; Kishimoto, S.; Sudo, K.; Kanamaru, T.; Brem, H.; Folkman, J. Synthetic analogues of fumagillin that inhibit angiogenesis and suppress tumour growth. Nature 1990, 348, 555-557.
    • (1990) Nature , vol.348 , pp. 555-557
    • Ingber, D.1    Fujita, T.2    Kishimoto, S.3    Sudo, K.4    Kanamaru, T.5    Brem, H.6    Folkman, J.7
  • 24
    • 0030924753 scopus 로고    scopus 로고
    • The anti-angiogenic agent fumagillin covalently binds and inhibits the methionine aminopeptidase, MetAP-2
    • (a) Sin, N.; Meng, L.; Wang, M. Q. W.; Wen, J. J.; Bornmann, W. G.; Crews, C. M. The anti-angiogenic agent fumagillin covalently binds and inhibits the methionine aminopeptidase, MetAP-2. Proc. Natl. Acad. Sci. U.S.A. 1997, 94, 6099-6103.
    • (1997) Proc. Natl. Acad. Sci. U.S.A. , vol.94 , pp. 6099-6103
    • Sin, N.1    Meng, L.2    Wang, M.Q.W.3    Wen, J.J.4    Bornmann, W.G.5    Crews, C.M.6
  • 25
    • 0031171961 scopus 로고    scopus 로고
    • Methionine aminopeptidase (type 2) is the common target for angiogenesis inhibitors AGM-1470 and ovalicin
    • (b) Griffith, E. C.; Su, Z.; Turk, B. E.; Chen, S.; Chang, Y.-H.; Wu, Z.; Biemann, K.; Liu, J. O. Methionine aminopeptidase (type 2) is the common target for angiogenesis inhibitors AGM-1470 and ovalicin. Chem. Biol. 1997, 4, 461-471.
    • (1997) Chem. Biol. , vol.4 , pp. 461-471
    • Griffith, E.C.1    Su, Z.2    Turk, B.E.3    Chen, S.4    Chang, Y.-H.5    Wu, Z.6    Biemann, K.7    Liu, J.O.8
  • 26
    • 0032515029 scopus 로고    scopus 로고
    • Structure of human methionine aminopeptidase-2 complexed with fumagillin
    • (c) Liu, S.; Widom, J.; Kemp, C. W.; Crews, C. M.; Clardy, J. Structure of human methionine aminopeptidase-2 complexed with fumagillin. Science 1998, 282, 1324-1327.
    • (1998) Science , vol.282 , pp. 1324-1327
    • Liu, S.1    Widom, J.2    Kemp, C.W.3    Crews, C.M.4    Clardy, J.5
  • 28
    • 0345219278 scopus 로고
    • Synthesis of 7-nitroindole
    • Singer, H.; Shive, W. Synthesis of 7-nitroindole. J. Org. Chem. 1957, 22, 84-85.
    • (1957) J. Org. Chem. , vol.22 , pp. 84-85
    • Singer, H.1    Shive, W.2
  • 29
    • 0345651101 scopus 로고
    • 7-nitrotryptophan and 7-nitroindole derivatives
    • Hiremath, S. P.; Siddappa, S. 7-Nitrotryptophan and 7-nitroindole derivatives. Chem. Abstr. 1963, 59, 8855-8857.
    • (1963) Chem. Abstr. , vol.59 , pp. 8855-8857
    • Hiremath, S.P.1    Siddappa, S.2
  • 30
    • 84952543103 scopus 로고
    • A one-flask conversion of aldehydes to nitriles using hydroxylamine hydrochloride and selenium dioxide
    • Sosnovsky, G.; Krogh, J. A.; Umhoefer, S. G. A one-flask conversion of aldehydes to nitriles using hydroxylamine hydrochloride and selenium dioxide. Synthesis 1979, 722-724.
    • (1979) Synthesis , pp. 722-724
    • Sosnovsky, G.1    Krogh, J.A.2    Umhoefer, S.G.3
  • 31
    • 0011064328 scopus 로고
    • Preparation and anticonvulsant activity of N-substituted benzenedisulfonamides
    • Holland, G. F.; Funderburk, W. H.; Finger, K. F. Preparation and anticonvulsant activity of N-substituted benzenedisulfonamides. J. Med. Chem. 1963, 6, 307-312.
    • (1963) J. Med. Chem. , vol.6 , pp. 307-312
    • Holland, G.F.1    Funderburk, W.H.2    Finger, K.F.3
  • 32
    • 0021061819 scopus 로고
    • Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
    • Mosmann, T. Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays. J. Immunol. Methods 1983, 65, 55-63.
    • (1983) J. Immunol. Methods , vol.65 , pp. 55-63
    • Mosmann, T.1
  • 33
    • 0003088184 scopus 로고
    • Data display and analysis strategies from NCI disease-oriented in vitro antitumour drug screen
    • Valeriote, F. A., Corbett, T., Baker, L., Eds.; Kluwer Academic Publishers: Amsterdam
    • Boyd, M. R.; Paull, K. D.; Rubinstein, L. R. Data display and analysis strategies from NCI disease-oriented in vitro antitumour drug screen. In Cytotoxic Anticancer Drugs: Models and Concepts for Drug Discovery and Development; Valeriote, F. A., Corbett, T., Baker, L., Eds.; Kluwer Academic Publishers: Amsterdam, 1992; pp 11-34.
    • (1992) Cytotoxic Anticancer Drugs: Models and Concepts for Drug Discovery and Development , pp. 11-34
    • Boyd, M.R.1    Paull, K.D.2    Rubinstein, L.R.3
  • 34
    • 0028906786 scopus 로고
    • Some practical considerations and applications of the NCI in vitro anticancer drug discovery screen
    • Boyd, M. R.; Paull, K. D. Some practical considerations and applications of the NCI in vitro anticancer drug discovery screen. Drug Dev. Res. 1995, 34, 91-109.
    • (1995) Drug Dev. Res. , vol.34 , pp. 91-109
    • Boyd, M.R.1    Paull, K.D.2
  • 35
    • 0019351587 scopus 로고
    • Current result of screening program at the division of cancer treatment, national cancer institute
    • Goldin, A.; Venditti, J. M.; Macdonald, J. S.; Mugia, F. M.; Henney, J. E.; Devita, V. T., Jr. Current result of screening program at the division of cancer treatment, National Cancer Institute. Eur. J. Cancer 1980, 17, 129-142.
    • (1980) Eur. J. Cancer , vol.17 , pp. 129-142
    • Goldin, A.1    Venditti, J.M.2    Macdonald, J.S.3    Mugia, F.M.4    Henney, J.E.5    Devita V.T., Jr.6
  • 36
    • 0345219276 scopus 로고
    • Comparison of tumor response in nude mice to clinical response in donor patient
    • Fiefig, H. H.; Schuchhardt, C.; Henss, H.; Fiedler, L.; Lohr, G. W. Comparison of tumor response in nude mice to clinical response in donor patient. J. Surg. Oncol. 1980, 15, 211-219.
    • (1980) J. Surg. Oncol. , vol.15 , pp. 211-219
    • Fiefig, H.H.1    Schuchhardt, C.2    Henss, H.3    Fiedler, L.4    Lohr, G.W.5
  • 37
    • 0023555793 scopus 로고
    • Human tumor xenografts in the nude mouse and their value as test models in anticancer drug development
    • Winograd, B.; Boven, E.; Lobbezoo, M. W.; Pinedo, H. M. Human tumor xenografts in the nude mouse and their value as test models in anticancer drug development. In Vivo (Athens) 1987, 1, 1-13.
    • (1987) In Vivo (Athens) , vol.1 , pp. 1-13
    • Winograd, B.1    Boven, E.2    Lobbezoo, M.W.3    Pinedo, H.M.4
  • 38
    • 0024117741 scopus 로고
    • Human tumor xenografts as model for drug testing
    • Mattern, J.; Bak, M.; Hahn, E. W.; Volm, M. Human tumor xenografts as model for drug testing. Cancer Metast. Rev. 1988, 7, 263-284.
    • (1988) Cancer Metast. Rev. , vol.7 , pp. 263-284
    • Mattern, J.1    Bak, M.2    Hahn, E.W.3    Volm, M.4
  • 40
    • 0001591496 scopus 로고
    • The preparation of alkyl sulfonyl chlorides from isothioureas. II
    • Sprague, J. M.; Johnson, T. B. The preparation of alkyl sulfonyl chlorides from isothioureas. II. J. Am. Chem. Soc. 1937, 59, 1837-1840.
    • (1937) J. Am. Chem. Soc. , vol.59 , pp. 1837-1840
    • Sprague, J.M.1    Johnson, T.B.2


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