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Volumn 12, Issue 2, 2003, Pages 283-287

Indisulam: An anticancer sulfonamide in clinical development

Author keywords

Anticancer agent; Carbonic anhydrase inhibitor; Cell cycle arrest; G1 phase; Sulfonamide

Indexed keywords

4 METHOXYBENZENESULFONAMIDE; 4 METHYLBENZENESULFONAMIDE; AMIDE; AMYLOID PRECURSOR PROTEIN; ANTIDIABETIC AGENT; ANTIINFECTIVE AGENT; ANTINEOPLASTIC AGENT; ANTITHYROID AGENT; ANTIVIRUS AGENT; BENZENE DERIVATIVE; CARBONATE DEHYDRATASE; CARBONATE DEHYDRATASE INHIBITOR; CYCLIN A; CYCLIN B1; CYCLIN DEPENDENT KINASE 2; CYCLIN E; DIURETIC AGENT; DRUG METABOLITE; FLUOROURACIL; INDISULAM; INDOLE DERIVATIVE; MATRIX METALLOPROTEINASE; N [2 [(4 HYDROXYPHENYL)AMINO] 3 PYRIDINYL] 4 METHOXYBENZENESULFONAMIDE; NITRILE; PLATINUM; PROTEIN P53; RETINOBLASTOMA PROTEIN; SULFONAMIDE; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 0037315480     PISSN: 13543784     EISSN: None     Source Type: Journal    
DOI: 10.1517/13543784.12.2.283     Document Type: Review
Times cited : (188)

References (25)
  • 2
    • 0033765660 scopus 로고    scopus 로고
    • Novel sulphonamide derivatives for the treatment of cancer
    • OWA T, NAGASU T: Novel sulphonamide derivatives for the treatment of cancer. Expert Opin. Ther. Patents (2000) 10:1725-1740.
    • (2000) Expert Opin. Ther. Patents , vol.10 , pp. 1725-1740
    • Owa, T.1    Nagasu, T.2
  • 4
    • 0033598320 scopus 로고    scopus 로고
    • Discovery of novel antitumor sulfonamides targeting G1 phase of the cell cycle
    • OWA T, YOSHINO H, OKAUCHI T et al.: Discovery of novel antitumor sulfonamides targeting G1 phase of the cell cycle. J. Med. Chem. (1999) 42:3789-3799.
    • (1999) J. Med. Chem. , vol.42 , pp. 3789-3799
    • Owa, T.1    Yoshino, H.2    Okauchi, T.3
  • 5
    • 0034608622 scopus 로고    scopus 로고
    • A focused compound library of novel N-(7-indolyl)benzenesulfonamides for the discovery of potent cell cycle inhibitors
    • OWA T, OKAUCHI T, YOSHIMATSU K et al.: A focused compound library of novel N-(7-indolyl)benzenesulfonamides for the discovery of potent cell cycle inhibitors. Bioorg. Med. Chem. Lett. (2000) 10:1223-1226.
    • (2000) Bioorg. Med. Chem. Lett. , vol.10 , pp. 1223-1226
    • Owa, T.1    Okauchi, T.2    Yoshimatsu, K.3
  • 6
    • 0037136031 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of N-(7-Indolyl)-3-pyridinesulfonamide derivatives as potent antitumor agents
    • OWA T, YOSHINO H, OKAUCHI T et al.: Synthesis and biological evaluation of N-(7-Indolyl)-3-pyridinesulfonamide derivatives as potent antitumor agents. Bioorg. Med. Chem. Lett. (2002) 12:2097-2100.
    • (2002) Bioorg. Med. Chem. Lett. , vol.12 , pp. 2097-2100
    • Owa, T.1    Yoshino, H.2    Okauchi, T.3
  • 7
    • 0037168033 scopus 로고    scopus 로고
    • Array-based structure and gene expression relationship study of antitumor sulfonamides including N-[2-[(4-Hydroxyphenyl)amino]-3-pyridinyl]-4-methoxybenzenesulfonamide and N-(3-chloro-7-indolyl)-1,4-benzenedisulfonamide
    • OWA T, YOKOI A, YAMAZAKI Y, YOSHIMATSU K, YAMORI T, NAGASU T: Array-based structure and gene expression relationship study of antitumor sulfonamides including N-[2-[(4-Hydroxyphenyl)amino]-3-pyridinyl]-4-methoxybenzenesulfonamide and N-(3-chloro-7-indolyl)-1,4-benzenedisulfonamide. J. Med. Chem. (2002) 45:4913-4922.
    • (2002) J. Med. Chem. , vol.45 , pp. 4913-4922
    • Owa, T.1    Yokoi, A.2    Yamazaki, Y.3    Yoshimatsu, K.4    Yamori, T.5    Nagasu, T.6
  • 8
    • 0034773165 scopus 로고    scopus 로고
    • E7070, a novel sulphonamide agent with potent antitumour activity in vitro and in vivo
    • OZAWA Y, SUGI NH, NAGASU T et al.: E7070, a novel sulphonamide agent with potent antitumour activity in vitro and in vivo. Eur. J. Cancer (2001) 37:2275-2282.
    • (2001) Eur. J. Cancer , vol.37 , pp. 2275-2282
    • Ozawa, Y.1    Sugi, N.H.2    Nagasu, T.3
  • 9
    • 0034843846 scopus 로고    scopus 로고
    • Mechanism of action of the novel sulfonamide anticancer agent E7070 on cell cycle progression in human non-small cell lung cancer cells
    • FUKUOKA K, USUDA J, IWAMOTO Y et al.: Mechanism of action of the novel sulfonamide anticancer agent E7070 on cell cycle progression in human non-small cell lung cancer cells. Invest. New Drugs (2001) 19:219-227.
    • (2001) Invest. New Drugs , vol.19 , pp. 219-227
    • Fukuoka, K.1    Usuda, J.2    Iwamoto, Y.3
  • 10
    • 0036463981 scopus 로고    scopus 로고
    • Profiling novel sulfonamide antitumor agents with cell-based phenotypic screens and array-based gene expression analysis
    • YOKOI A, KUROMITSU J, KAWAI T et al.: Profiling novel sulfonamide antitumor agents with cell-based phenotypic screens and array-based gene expression analysis. Mol. Cancer Ther. (2002) 1:275-286.
    • (2002) Mol. Cancer Ther. , vol.1 , pp. 275-286
    • Yokoi, A.1    Kuromitsu, J.2    Kawai, T.3
  • 11
    • 0013163402 scopus 로고    scopus 로고
    • Population pharmacokinetic analysis of the novel anti-cancer agent E7070 in a Phase I study using nonlinear mixed effect modelling (NONMEM)
    • (Abstract 340)
    • VAN KESTEREN C, MATHOT R, RAYMOND E et al.: Population pharmacokinetic analysis of the novel anti-cancer agent E7070 in a Phase I study using nonlinear mixed effect modelling (NONMEM). NCI EORTC Symp. New Drugs Cancer Ther. (2000) 11 (Abstract 340).
    • (2000) NCI EORTC Symp. New Drugs Cancer Ther. , vol.11
    • Van Kesteren, C.1    Mathot, R.2    Raymond, E.3
  • 12
    • 0036789730 scopus 로고    scopus 로고
    • Population pharmacokinetics of the novel anticancer agent E7070 during four Phase I studies: Model building and validation
    • VAN KESTEREN C, MATHOT R, RAYMOND E et al.: Population pharmacokinetics of the novel anticancer agent E7070 during four Phase I studies: Model building and validation. J. Clin. Oncol. (2002) 19:4065-4073.
    • (2002) J. Clin. Oncol. , vol.19 , pp. 4065-4073
    • Van Kesteren, C.1    Mathot, R.2    Raymond, E.3
  • 13
    • 0013122894 scopus 로고    scopus 로고
    • Metabolism and excretion of E7070 after intravenous administration to cancer patients
    • (Abstract 371)
    • VAN DEN BONGARD D H, PLUEM D, ROSING H et al.: Metabolism and excretion of E7070 after intravenous administration to cancer patients. Proc. Am. Soc. Clin. Oncol. (2001) 20 (Abstract 371).
    • (2001) Proc. Am. Soc. Clin. Oncol. , vol.20
    • Van Den Bongard, D.H.1    Pluem, D.2    Rosing, H.3
  • 14
    • 0000287735 scopus 로고    scopus 로고
    • Phase I and pharmacokinetic study of E7070 in patients with solid tumors as single iv infusion, weekly x 4, q 6 weeks
    • (Abstract 3875)
    • DITTRICH C, DUMEZ H, CALVERT H et al.: Phase I and pharmacokinetic study of E7070 in patients with solid tumors as single iv infusion, weekly x 4, q 6 weeks. Proc. Am. Assoc. Cancer Res. (2000) 41 (Abstract 3875).
    • (2000) Proc. Am. Assoc. Cancer Res. , vol.41
    • Dittrich, C.1    Dumez, H.2    Calvert, H.3
  • 15
    • 0000287738 scopus 로고    scopus 로고
    • Phase I trial of five-days continuous infusion E7070 [N-(3-chloro-7-indolyl)-1,4-benzenedisulfonamide] in patients (pts) with solid tumors
    • (Abstract 3876)
    • DROZ JP, ROCHE H, ZANETTA S et al.: Phase I trial of five-days continuous infusion E7070 [N-(3-chloro-7-indolyl)-1,4-benzenedisulfonamide] in patients (pts) with solid tumors. Proc. Am. Assoc. Cancer Res. (2000) 41 (Abstract 3876).
    • (2000) Proc. Am. Assoc. Cancer Res. , vol.41
    • Droz, J.P.1    Roche, H.2    Zanetta, S.3
  • 16
    • 0000287732 scopus 로고    scopus 로고
    • Phase I and pharmacokinetic (PK) study of E7070, a novel sulphonamide, given daily x 5 every 3 weeks as a 1-hour intravenous infusion in patients (pts) with advanced solid tumors
    • (Abstract 3877)
    • PUNT CJA, FUMOLEAU P, WALLE BVD et al.: Phase I and pharmacokinetic (PK) study of E7070, a novel sulphonamide, given daily x 5 every 3 weeks as a 1-hour intravenous infusion in patients (pts) with advanced solid tumors. Proc. Am. Assoc. Cancer Res. (2000) 41 (Abstract 3877).
    • (2000) Proc. Am. Assoc. Cancer Res. , vol.41
    • Punt, C.J.A.1    Fumoleau, P.2    Walle, B.V.D.3
  • 17
    • 0034772246 scopus 로고    scopus 로고
    • Phase I and pharmacokinetic study of E7070, given at a daily times five schedule in patients with solid tumors. A study by the EORTC-early clinical studies group (ECSG)
    • PUNT CJ, FUMOLEAU P, VAN DE WALLE B, FABER MN, RAVIC M, CAMPONE M: Phase I and pharmacokinetic study of E7070, given at a daily times five schedule in patients with solid tumors. A study by the EORTC-early clinical studies group (ECSG). Ann. Oncol. (2001) 12:1289-1293.
    • (2001) Ann. Oncol. , vol.12 , pp. 1289-1293
    • Punt, C.J.1    Fumoleau, P.2    Van De Walle, B.3    Faber, M.N.4    Ravic, M.5    Campone, M.6
  • 18
    • 0036789730 scopus 로고    scopus 로고
    • Population pharmacokinetics of the novel anticancer agent E7070 during four Phase I studies: Model building and validation
    • VAN KESTEREN C, MATHOT RA, RAYMOND E et al.: Population pharmacokinetics of the novel anticancer agent E7070 during four Phase I studies: Model building and validation. J. Clin. Oncol. (2002) 20:4065-4073.
    • (2002) J. Clin. Oncol. , vol.20 , pp. 4065-4073
    • Van Kesteren, C.1    Mathot, R.A.2    Raymond, E.3
  • 19
    • 0037102283 scopus 로고    scopus 로고
    • Phase I and pharmacokinetic study of E7070, a novel chloroindolyl sulfonamide cell-cycle inhibitor as an one hour infusion every three weeks in patients with advanced cancer
    • RAYMOND E, TEN BOKKEL HUINIK WW, TAIEB J et al.: Phase I and pharmacokinetic study of E7070, a novel chloroindolyl sulfonamide cell-cycle inhibitor as an one hour infusion every three weeks in patients with advanced cancer. J. Clin. Oncol. (2002) 20:3508-3521.
    • (2002) J. Clin. Oncol. , vol.20 , pp. 3508-3521
    • Raymond, E.1    Ten Bokkel Huinik, W.W.2    Taieb, J.3
  • 20
    • 0000902909 scopus 로고    scopus 로고
    • A multicentre randomised Phase II study of E7070 in patients with colorectal cancer who have failed 5-fluorouracil-based chemotherapy
    • (Abstract 611)
    • MAINWARING PN, VAN CUTSEM E, VAN LAETHEM JL et al.: A multicentre randomised Phase II study of E7070 in patients with colorectal cancer who have failed 5-fluorouracil-based chemotherapy. Proc. Am. Soc. Clin. Oncol. (2002) 21 (Abstract 611).
    • (2002) Proc. Am. Soc. Clin. Oncol. , vol.21
    • Mainwaring, P.N.1    Van Cutsem, E.2    Van Laethem, J.L.3
  • 21
    • 0242421438 scopus 로고    scopus 로고
    • Phase II and pharmacodynamic study of E7070 in patients with Non-Small Cell Lung Cancer (NSCLC) who have failed platinum-based chemotherapy
    • (Abstract 1306)
    • TALBOT D, NORBURY C, SLADE M et al.: Phase II and pharmacodynamic study of E7070 in patients with Non-Small Cell Lung Cancer (NSCLC) who have failed platinum-based chemotherapy. Proc. Am. Soc. Clin. Oncol. (2002) 21 (Abstract 1306).
    • (2002) Proc. Am. Soc. Clin. Oncol. , vol.21
    • Talbot, D.1    Norbury, C.2    Slade, M.3
  • 22
    • 0036866878 scopus 로고    scopus 로고
    • E7070: A novel synthetic sulfonamide targeting the cell cycle progression for the treatment of cancer
    • VAN KESTEREN C, BEIJNEN JH, SCHELLENS JH: E7070: a novel synthetic sulfonamide targeting the cell cycle progression for the treatment of cancer. Anti-Cancer Drugs (2002) 13:989-997.
    • (2002) Anti-Cancer Drugs , vol.13 , pp. 989-997
    • Van Kesteren, C.1    Beijnen, J.H.2    Schellens, J.H.3
  • 23
    • 0034018870 scopus 로고    scopus 로고
    • Carbonic anhydrase inhibitors and their therapeutic potential
    • SUPURAN CT, SCOZZAFAVA A: Carbonic anhydrase inhibitors and their therapeutic potential. Expert Opin. Ther. Patents (2000) 10:575-600.
    • (2000) Expert Opin. Ther. Patents , vol.10 , pp. 575-600
    • Supuran, C.T.1    Scozzafava, A.2
  • 24
    • 0036166662 scopus 로고    scopus 로고
    • Applications of carbonic anhydrase inhibitors and activators in therapy
    • SUPURAN CT, SCOZZAFAVA A: Applications of carbonic anhydrase inhibitors and activators in therapy. Expert Opin. Ther. Patents (2002) 12:217-242.
    • (2002) Expert Opin. Ther. Patents , vol.12 , pp. 217-242
    • Supuran, C.T.1    Scozzafava, A.2
  • 25
    • 0002946940 scopus 로고    scopus 로고
    • The roles of carbonic anhydrase isozymes in cancer
    • G Xue, Y Xue, Z Xu, R Holmes, GL Hammond, HA Lim (Eds), World Scientific, Singapore
    • CHEGWIDDEN WR, SPENCER IM, SUPURAN CT: The roles of carbonic anhydrase isozymes in cancer. In: Gene Families: Studies of DNA, RNA, Enzymes and Proteins. G Xue, Y Xue, Z Xu, R Holmes, GL Hammond, HA Lim (Eds), World Scientific, Singapore (2001):157-170.
    • (2001) Gene Families: Studies of DNA, RNA, Enzymes and Proteins , pp. 157-170
    • Chegwidden, W.R.1    Spencer, I.M.2    Supuran, C.T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.