메뉴 건너뛰기




Volumn 12, Issue 11, 2002, Pages 1663-1702

Discovery and development of antimitotic agents that inhibit tubulin polymerisation for the treatment of cancer

Author keywords

A 289099; A 293620; A 3181315; ABT 751; AC 7700; AC 7739; AM 132; Anhydrovinblastine; Antiangiogenesis; Anticancer; Antimitotic; Antitubulin; Antitumour; AVE8062A; AVE8063A; Cemadotin; CF248; CI 980; COBRA 1; Colchicine; Combretastatin; Cryptophycin; Curacin; D 24851; D 68144; D 82318; Dolastatin; DZ 3358; E7010; E7070; E7820; Eg265; ER 34410; Estramusine; Ethoxyoestradiol; Halichondrin; Halimide; Hemiasterlin; HMN 154; HTI 286; ILX651; Kinesin; KSP; LS 4559; LS 4577; LU223651; MHM 214; Microtubule; Multi drug resistance (MDR); Myoservin; Noscapine; NSC 664171; Oncocidine A1; P glycoprotein; Phenstatin; Phenylahistin; Phosphate prodrug; Ro 31,7453; RPR112378; RPR115781; SB 715992; SPIKET P; Sulfonamide; T138067; T900607; Tubulin; TZT 1027; Vinblastine; Vinca alkaloid; Vincristine; Vindesine; Vinflunine; Vinorelbine; ZD6126; ZD6474

Indexed keywords

A 105972; ALLOCHOLCHINOL PHOSPHATE; ANTIMITOTIC AGENT; CISPLATIN DERIVATIVE; COLCHICINE DERIVATIVE; COMBRETASTATIN A4; DEACETAMIDOCOLCHICINE; DOCETAXEL; DOXORUBICIN; EPOTHILONE DERIVATIVE; GAMMA TUBULIN; IMIDAZOLE; INTRADOSE; N [2 [(4 HYDROXYPHENYL)AMINO] 3 PYRIDINYL] 4 METHOXYBENZENESULFONAMIDE; N ACETYLCOLCHINOL PHOSPHATE; OXADIAZOLE DERIVATIVE; OXAZOLE; OXAZOLONE; PACLITAXEL; PODOPHYLLOTOXIN; PODOPHYLLOTOXIN DERIVATIVE; PROTEIN TYROSINE KINASE INHIBITOR; PYRAZOLE; QUINOLONE DERIVATIVE; SERINE 2 METHOXY 5 [2 (3,4,5 TRIMETHOXYPHENYL)VINYL]ANILIDE; SULFONAMIDE; TAXANE DERIVATIVE; TETRAZOLE DERIVATIVE; THIAZOLE DERIVATIVE; THIOCOLCHICINE; TROPONE DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG; VANDETANIB; VINBLASTINE; VINCA ALKALOID; ZM 445526;

EID: 0036850914     PISSN: 13543776     EISSN: None     Source Type: Journal    
DOI: 10.1517/13543776.12.11.1663     Document Type: Review
Times cited : (156)

References (265)
  • 1
    • 0034743675 scopus 로고    scopus 로고
    • Structural insight into microtubule function
    • NOGALES E: Structural insight into microtubule function. Ann. Rev. Biophys. Biomol. Struct. (2001) 30:397-420.
    • (2001) Ann. Rev. Biophys. Biomol. Struct , vol.30 , pp. 397-420
    • Nogales, E.1
  • 2
    • 0035834521 scopus 로고    scopus 로고
    • Refined structure of αβ-tubulin at 3.5 Å resolution
    • LÖWE J, LI H, DOWNING KH, NOGALES E: Refined structure of αβ-tubulin at 3.5 Å resolution. J. Mol. Biol. (2001) 313:1045-1057.
    • (2001) J. Mol. Biol , vol.313 , pp. 1045-1057
    • Löwe, J.1    Li, H.2    Downing, K.H.3    Nogales, E.4
  • 3
    • 0033256231 scopus 로고    scopus 로고
    • Cancer and cell cycle
    • FORD HJ, PARDEE AB: Cancer and cell cycle. J. Cell. Biochem. (1999) 32/33 (Suppl.):166-172.
    • (1999) J. Cell. Biochem , Issue.32-33 SUPPL. , pp. 166-172
    • Ford, H.J.1    Pardee, A.B.2
  • 4
    • 0031610542 scopus 로고    scopus 로고
    • Use of drugs to study role of microtubule assembly dynamics in living cells
    • Vallee R (Ed.), Academic Press, London
    • JORDAN MA, WILSON L: Use of drugs to study role of microtubule assembly dynamics in living cells. In: Methods in Enzymology. Vallee R (Ed.), Academic Press, London (1998) 298:252-276.
    • (1998) Methods in Enzymology , vol.298 , pp. 252-276
    • Jordan, M.A.1    Wilson, L.2
  • 5
    • 0034518173 scopus 로고    scopus 로고
    • Structural basis for the interaction of tubulin with proteins and drugs that affect microtubule dynamics
    • DOWNING KH: Structural basis for the interaction of tubulin with proteins and drugs that affect microtubule dynamics. Ann. Rev. Cell. Dev. Biology (2000) 16:89-111.
    • (2000) Ann. Rev. Cell. Dev. Biology , vol.16 , pp. 89-111
    • Downing, K.H.1
  • 6
    • 0034788453 scopus 로고    scopus 로고
    • Tyrosine kinase inhibitors: From rational design to clinical trials
    • TRAXLER P, BOLD G, BUCHDUNGER E et al.: Tyrosine kinase inhibitors: from rational design to clinical trials. Med. Res. Rev. (2001) 21:499-512.
    • (2001) Med. Res. Rev , vol.21 , pp. 499-512
    • Traxler, P.1    Bold, G.2    Buchdunger, E.3
  • 7
    • 0033763084 scopus 로고    scopus 로고
    • ZD1839 ('Iressa') as an anticancer agent
    • BASELGA J, AVERBUCH SD: ZD1839 ('Iressa') as an anticancer agent. Drugs (2000) 60(suppl.1):33-40.
    • (2000) Drugs , vol.60 , Issue.SUPPL. 1 , pp. 33-40
    • Baselga, J.1    Averbuch, S.D.2
  • 8
    • 0034121469 scopus 로고    scopus 로고
    • Mechanisms of action and resistance to tubulin-binding agents
    • DUMONTET C: Mechanisms of action and resistance to tubulin-binding agents. Fxp. Opin. Invest. Drugs (2000) 9:779-788.
    • (2000) Fxp. Opin. Invest. Drugs , vol.9 , pp. 779-788
    • Dumontet, C.1
  • 11
    • 0032814671 scopus 로고    scopus 로고
    • New inhibitors of tubulin polymerisation
    • VON ANGERER E: New inhibitors of tubulin polymerisation. Exp. Opin. Ther. Patents (1999) 9:1069-1081.
    • (1999) Exp. Opin. Ther. Patents , vol.9 , pp. 1069-1081
    • Von Angerer, E.1
  • 12
    • 0344994511 scopus 로고    scopus 로고
    • Novel antitumor agents from higher plants
    • LEE KH: Novel antitumor agents from higher plants. Med. Res. Rev. (1999) 19:569-596.
    • (1999) Med. Res. Rev , vol.19 , pp. 569-596
    • Lee, K.H.1
  • 13
    • 0032777463 scopus 로고    scopus 로고
    • Anticancer drug design based on plant-derived natural products
    • LEE KH: Anticancer drug design based on plant-derived natural products. J. Biomed. Sci. (1999) 6:236-250.
    • (1999) J. Biomed. Sci , vol.6 , pp. 236-250
    • Lee, K.H.1
  • 14
    • 0033010658 scopus 로고    scopus 로고
    • Cytoskeletons and and mitotic agents developed in Japan
    • NISHIO K, SAIJO N: Cytoskeletons and and mitotic agents developed in Japan. Anticancer Drug Des. (1999) 14:133-141.
    • (1999) Anticancer Drug Des , vol.14 , pp. 133-141
    • Nishio, K.1    Saijo, N.2
  • 15
    • 0031836174 scopus 로고    scopus 로고
    • Recent progress in the development of tubulin inhibitors as antimitotic antitumor agents
    • SHI Q, CHEN K, MORRISNATSCHKE SL, LEE KH: Recent progress in the development of tubulin inhibitors as antimitotic antitumor agents. Curr. Pharm. Des. (1998) 4:219-248.
    • (1998) Curr. Pharm. Des , vol.4 , pp. 219-248
    • Shi, Q.1    Chen, K.2    Morrisnatschke, S.L.3    Lee, K.H.4
  • 16
    • 0031943558 scopus 로고    scopus 로고
    • Natural organic compounds that affect microtubule functions
    • IWASAKI S: Natural organic compounds that affect microtubule functions. J. Pharm. Soc. Jpn. (1998) 118:111-126.
    • (1998) J. Pharm. Soc. Jpn , vol.118 , pp. 111-126
    • Natural, S.1
  • 17
    • 0031872051 scopus 로고    scopus 로고
    • Tubulin as a target for anticancer drugs - Agents which interact with the mitotic spindle
    • JORDAN A, HADFIELD JA, LAWRENCE NJ, MCGOWN AT: Tubulin as a target for anticancer drugs - agents which interact with the mitotic spindle. Med. Res. Rev. (1998) 18:259-296.
    • (1998) Med. Res. Rev , vol.18 , pp. 259-296
    • Jordan, A.1    Hadfield, J.A.2    Lawrence, N.J.3    Mcgown, A.T.4
  • 18
    • 0001199989 scopus 로고    scopus 로고
    • The colchicine-tubulin interaction - A review
    • GUHA S, BHATTACHARYYA B: The colchicine-tubulin interaction - a review. Curr. Sci. (1997) 73:351-358.
    • (1997) Curr. Sci , vol.73 , pp. 351-358
    • Guha, S.1    Bhattacharyya, B.2
  • 19
    • 0034704077 scopus 로고    scopus 로고
    • Mapping the binding site of colchicinoids on β-tubulin. 2-Chloroacetyl-2- demethylthiocolchicine covalently reacts predominantly with cysteine 239 and secondarily with cysteine 354
    • BAI R. COVELL DG, PEI XF et al.: Mapping the binding site of colchicinoids on β-tubulin. 2-Chloroacetyl-2-demethylthiocolchicine covalently reacts predominantly with cysteine 239 and secondarily with cysteine 354. J. Biol. Chem. (2000) 275:40443-40452.
    • (2000) J. Biol. Chem , vol.275 , pp. 40443-40452
    • Bai, R.1    Covell, D.G.2    Pei, X.F.3
  • 20
    • 0036009887 scopus 로고    scopus 로고
    • Synthesis and antimicrotubule activity of combretatropone derivatives
    • JANIK ME, BANE SL: Synthesis and antimicrotubule activity of combretatropone derivatives. Bioorg. Med. Chem. (2002) 10:1895-1903.
    • (2002) Bioorg. Med. Chem , vol.10 , pp. 1895-1903
    • Janik, M.E.1    Bane, S.L.2
  • 21
    • 0032554863 scopus 로고    scopus 로고
    • Antitumor agents. 185. Synthesis and biological evaluation of tridemethylthiocolchicine analogues as novel topoisomerase II inhibitors
    • GUAN J, ZHU XK, TACHIBANA Y et al.: Antitumor agents. 185. Synthesis and biological evaluation of tridemethylthiocolchicine analogues as novel topoisomerase II inhibitors. J. Med. Chem. (1998) 41:1956-1961.
    • (1998) J. Med. Chem , vol.41 , pp. 1956-1961
    • Guan, J.1    Zhu, X.K.2    Tachibana, Y.3
  • 22
    • 0033576596 scopus 로고    scopus 로고
    • N-deacetyl-N-aminoacylthiocolchicine derivatives: Synthesis and biological evaluation on MDR-positive and MDR-negative human cancer cell lines
    • GELMI MI, MOTTADELLI S, POCAR D et al.: N-deacetyl-N-aminoacylthiocolchicine derivatives: synthesis and biological evaluation on MDR-positive and MDR-negative human cancer cell lines. J. Med. Chem. (1999) 42:5272-5276.
    • (1999) J. Med. Chem , vol.42 , pp. 5272-5276
    • Gelmi, M.I.1    Mottadelli, S.2    Pocar, D.3
  • 24
    • 0033996957 scopus 로고    scopus 로고
    • Novel allocolchicinoids with an eight membered Bring: Design, synthesis and inhibition of tubulin assembly
    • BRECHT R, SEITZ G, GUENARD D, THORET S: Novel allocolchicinoids with an eight membered B ring: design, synthesis and inhibition of tubulin assembly. Bioorg. Med. Chem. (2000) 8:557-562.
    • (2000) Bioorg. Med. Chem , vol.8 , pp. 557-562
    • Brecht, R.1    Seitz, G.2    Guenard, D.3    Thoret, S.4
  • 25
    • 0033241269 scopus 로고    scopus 로고
    • Antitumor agents. 192. Antitubulin effect and cytotoxicity of C(7)-oxygenated allocolchicinoids
    • GUAN J, ZHU XK, BROSSI A et al.: Antitumor agents. 192. Antitubulin effect and cytotoxicity of C(7)-oxygenated allocolchicinoids. Coll. Czech. Chem. Comm. (1999) 64:217-228.
    • (1999) Coll. Czech. Chem. Comm , vol.64 , pp. 217-228
    • Guan, J.1    Zhu, X.K.2    Brossi, A.3
  • 26
    • 0011475585 scopus 로고    scopus 로고
    • ZD6126: A new agent causing selective damage of tumour vasculature
    • 91st Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 2085
    • DAVIS PD, HILL SA, GALBRAITH SM et al.: ZD6126: A new agent causing selective damage of tumour vasculature. 91st Annual Meeting of American Association for Cancer Research. San Francisco, USA (2000). Abstract 2085.
    • (2000)
    • Davis, P.D.1    Hill, S.A.2    Galbraith, S.M.3
  • 27
    • 0011457207 scopus 로고    scopus 로고
    • Comparison of the antitumour activity of ZD6126 administered by different routes
    • 92nd Annual Meeting of American Association for Cancer Research. New Orleanes, USA Abstract 4419
    • DAVIS PD, HILL SA, CHAPLIN DJ, BLAKEY DC: Comparison of the antitumour activity of ZD6126 administered by different routes. 92nd Annual Meeting of American Association for Cancer Research. New Orleanes, USA (2001): Abstract 4419.
    • (2001)
    • Davis, P.D.1    Hill, S.A.2    Chaplin, D.J.3    Blakey, D.C.4
  • 28
    • 0011407550 scopus 로고    scopus 로고
    • ZD6126: A novel vascular targeting agent which causes massive necrosis in a range of human tumour xenograft model
    • 91st Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 2086
    • BLAKEY DC, ASHTON SE, EARDLEY SE et al.: ZD6126: a novel vascular targeting agent which causes massive necrosis in a range of human tumour xenograft model. 91st Annual Meeting of American Association for Cancer Research. San Francisco, USA (2000): Abstract 2086.
    • (2000)
    • Blakey, D.C.1    Ashton, S.E.2    Eardley, S.E.3
  • 29
    • 0011505602 scopus 로고    scopus 로고
    • Activity of a new vascular-targeting agent, CD6126, in pulmonary metastases from human lung adenocarcinoma in nude mice
    • 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 777
    • GOTO H, YANO S, ZHANG H et al.: Activity of a new vascular-targeting agent, CD6126, in pulmonary metastases from human lung adenocarcinoma in nude mice. 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA (2002): Abstract 777.
    • (2002)
    • Goto, H.1    Yano, S.2    Zhang, H.3
  • 30
    • 0011452821 scopus 로고    scopus 로고
    • Vascular targeting activity of ZD6126 in two tumour models growing in athymic rats
    • 92nd Annual Meeting of American Association for Cancer Research. New Orleans, USA Abstract 4421
    • BLAKEY DC, WESTWOOD FR, ASHTON SE: Vascular targeting activity of ZD6126 in two tumour models growing in athymic rats. 92nd Annual Meeting of American Association for Cancer Research. New Orleans, USA (2001): Abstract 4421.
    • (2001)
    • Blakey, D.C.1    Westwood, F.R.2    Ashton, S.E.3
  • 31
    • 0011499746 scopus 로고    scopus 로고
    • MRI evaluation of the effects of ZD6126 on tumor vasculture
    • 92nd Annual Meeting of American Association for Cancer Research. New Orleans, USA Abstract 580
    • EVELHOCH JL, HE Z, POLIN L et al.: MRI evaluation of the effects of ZD6126 on tumor vasculture. 92nd Annual Meeting of American Association for Cancer Research. New Orleans, USA (2001): Abstract 580.
    • (2001)
    • Evelhoch, J.L.1    He, Z.2    Polin, L.3
  • 32
    • 0011498574 scopus 로고    scopus 로고
    • Optimisation of ZD6126 activity in the Galu-6 tumor model
    • 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 778
    • BLAKEY DC, ASHTON SE, WESTWOOD FR, RYAN A: Optimisation of ZD6126 activity in the Galu-6 tumor model. 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA (2002): Abstract 778.
    • (2002)
    • Blakey, D.C.1    Ashton, S.E.2    Westwood, F.R.3    Ryan, A.4
  • 33
    • 0011417718 scopus 로고    scopus 로고
    • The novel vascular-targeting agent ZD6126 enhances the anti-tumor efficacy of cisplatin
    • 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 2594
    • SIEMANN DW, LEPLER S, ROJIANI A: The novel vascular-targeting agent ZD6126 enhances the anti-tumor efficacy of cisplatin. 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA (2002): Abstract 2594.
    • (2002)
    • Siemann, D.W.1    Lepler, S.2    Rojiani, A.3
  • 34
    • 0011417719 scopus 로고    scopus 로고
    • Combination of the VEGF receptor tyrosine kinase inhibitor ZD6474 and vascular-targeting agent ZD6126 produces an enhanced antitumor response
    • 93rd Annual Meeting of American Association for Cancer Raearch. San Francisco, USA Abstract 5351
    • WEDGE SR, KENDREW J, OGILVIE DJ et al.: Combination of the VEGF receptor tyrosine kinase inhibitor ZD6474 and vascular-targeting agent ZD6126 produces an enhanced antitumor response. 93rd Annual Meeting of American Association for Cancer Raearch. San Francisco, USA (2002): Abstract 5351.
    • (2002)
    • Wedge, S.R.1    Kendrew, J.2    Ogilvie, D.J.3
  • 35
    • 0011410786 scopus 로고    scopus 로고
    • Novel vascular targeting agents: Amino colchicinol derivatives of ZD6126
    • 92nd Annual Meeting of American Association for Cancer Research. New Orleans, USA Abstract 4426
    • ARNOULD JC, BIRD TG, ASHTON SE, BLAKEY DC, DAVIS PD: Novel vascular targeting agents: amino colchicinol derivatives of ZD6126. 92nd Annual Meeting of American Association for Cancer Research. New Orleans, USA (2001): Abstract 4426.
    • (2001)
    • Arnould, J.C.1    Bird, T.G.2    Ashton, S.E.3    Blakey, D.C.4    Davis, P.D.5
  • 36
    • 0032568390 scopus 로고    scopus 로고
    • Antitumor agents - 181 - Synthesis and biological evaluation of 6,7,2′,3′,4m-substituted-1,2, 3,4-tetrahydro-2- phenyl-4- quinolones as a new class of antimitotic antitumor agents
    • XIA Y, YANG ZY, XIA P et al.: Antitumor agents - 181 - synthesis and biological evaluation of 6,7,2′,3′, 4′-substituted-1,2, 3,4-tetrahydro-2- phenyl-4-quinolones as a new class of antimitotic antitumor agents. J. Med. Chem. (1998) 41:1155-1162.
    • (1998) J. Med. Chem , vol.41 , pp. 1155-1162
    • Xia, Y.1    Yang, Z.Y.2    Xia, P.3
  • 37
    • 0035262598 scopus 로고    scopus 로고
    • Targeting tumour vasculature: The development of combretastatin A4
    • GRIGGS J, METCALFE JC, HESKETH R. Targeting tumour vasculature: the development of combretastatin A4. Lancet Oncol. (2001) 2:82-87.
    • (2001) Lancet Oncol , vol.2 , pp. 82-87
    • Griggs, J.1    Metcalfe, J.C.2    Hesketh, R.3
  • 38
    • 15144356733 scopus 로고    scopus 로고
    • Novel combretastatin analogues effective against murine solid tumors - Design and structure-activity relationships
    • OHSUMI K, NAKAGAWA R, FUKUDA Y et al.: Novel combretastatin analogues effective against murine solid tumors - design and structure-activity relationships. J. Med. Chem. (1998) 41:3022-3032.
    • (1998) J. Med. Chem , vol.41 , pp. 3022-3032
    • Ohsumi, K.1    Nakagawa, R.2    Fukuda, Y.3
  • 39
    • 0033119771 scopus 로고    scopus 로고
    • Combretastatin A-4 phosphate as a tumor vascular-targeting agent: Early effects in tumors and normal tissues
    • TOZER GM, PRISE VE, WILSON J et al.: Combretastatin A-4 phosphate as a tumor vascular-targeting agent: early effects in tumors and normal tissues. Cancer Res. (1999) 59:1626-1634.
    • (1999) Cancer Res , vol.59 , pp. 1626-1634
    • Tozer, G.M.1    Prise, V.E.2    Wilson, J.3
  • 40
    • 0035417875 scopus 로고    scopus 로고
    • Mechanisms associated with tumor vascular shut-down induced by combretastatin A-4 phosphate: Intravital microscopy and measurement of vascular permeability
    • TOZER GM, PRISE VE, WILSON J et al.: Mechanisms associated with tumor vascular shut-down induced by combretastatin A-4 phosphate: intravital microscopy and measurement of vascular permeability. Cancer Res. (2001) 61:6413-6422.
    • (2001) Cancer Res , vol.61 , pp. 6413-6422
    • Tozer, G.M.1    Prise, V.E.2    Wilson, J.3
  • 41
    • 0035884395 scopus 로고    scopus 로고
    • The susceptibility of tumors to the antivascular drug combretastatin A4 phosphate correlates with vascular permeability
    • BEAUREGARD DA, HILL SA, CHAPLIN DJ, BRINDLE KM: The susceptibility of tumors to the antivascular drug combretastatin A4 phosphate correlates with vascular permeability. Cancer Res. (2001) 61:6811-6815.
    • (2001) Cancer Res , vol.61 , pp. 6811-6815
    • Beauregard, D.A.1    Hill, S.A.2    Chaplin, D.J.3    Brindle, K.M.4
  • 42
    • 0033793590 scopus 로고    scopus 로고
    • Natural organic compounds that affect microtubule functions: Syntheses and structure-activity relationships of combretastatins, curacin A and their analogs as the colchicine-site ligands on tubulin
    • IWASAKI S, SHIRAI R: Natural organic compounds that affect microtubule functions: syntheses and structure-activity relationships of combretastatins, curacin A and their analogs as the colchicine-site ligands on tubulin. J. Pharm. Soc. Jpn (2000) 120:875-889.
    • (2000) J. Pharm. Soc. Jpn , vol.120 , pp. 875-889
    • Iwasaki, S.1    Shirai, R.2
  • 43
    • 0023801309 scopus 로고
    • Interactions of tubulin with potent natural and synthetic analogs of the antimitotic agent combretastatin: A structure-activity study
    • LIN CM, SINGH SB, CHU PS et al.: Interactions of tubulin with potent natural and synthetic analogs of the antimitotic agent combretastatin: a structure-activity study. Mol. Pharmacol. (1988) 34:200-208.
    • (1988) Mol. Pharmacol , vol.34 , pp. 200-208
    • Lin, C.M.1    Singh, S.B.2    Chu, P.S.3
  • 44
    • 0034694366 scopus 로고    scopus 로고
    • Design, synthesis and cytotoxic activities of naphthyl analogues of combretastatin A-4
    • MAYA AB, DEL REY B, LAMAMIE DE CLAIRAC RP et al.: Design, synthesis and cytotoxic activities of naphthyl analogues of combretastatin A-4. Bioorg. Med. Chem. Lett. (2000) 10:2549-2551.
    • (2000) Bioorg. Med. Chem. Lett , vol.10 , pp. 2549-2551
    • Maya, A.B.1    Del Rey, B.2    Lamamie De Clairac, R.P.3
  • 45
    • 0031798378 scopus 로고    scopus 로고
    • Preparation and evaluation of diarylalkynes as antitumour agents
    • HADFIELD JA, MCGOWN AT: Preparation and evaluation of diarylalkynes as antitumour agents. Synth. Commun. (1998) 28:1421-1431.
    • (1998) Synth. Commun , vol.28 , pp. 1421-1431
    • Hadfield, J.A.1    Mcgown, A.T.2
  • 46
    • 0033814533 scopus 로고    scopus 로고
    • Antineoplastic agents 429. Syntheses of the combretastatin A-1 and combretastatin B-1 prodrugs
    • PETTIT GR, LIPPERT JW III: Antineoplastic agents 429. Syntheses of the combretastatin A-1 and combretastatin B-1 prodrugs. Anti-Cancer Drug Des. (2000) 15:203-216.
    • (2000) Anti-Cancer Drug Des , vol.15 , pp. 203-216
    • Pettit, G.R.1    Lippert J.W. III2
  • 47
    • 0034434231 scopus 로고    scopus 로고
    • Antineoplastic agents 463. Synthesis of combretastatin A-3 diphosphate prodrugs
    • PETTIT GR, MINARDI MD, BOYD MR, PETTIT RK: Antineoplastic agents 463. Synthesis of combretastatin A-3 diphosphate prodrugs. Anti-Cancer Drug Des. (2000) 15:397-403.
    • (2000) Anti-Cancer Drug Des , vol.15 , pp. 397-403
    • Pettit, G.R.1    Minardi, M.D.2    Boyd, M.R.3    Pettit, R.K.4
  • 48
    • 0036253091 scopus 로고    scopus 로고
    • Combretastatin A-1 phosphate a novel tubulin-binding agent with in vivo anti vascular effects in experimental tumours
    • HOLWELL SE, COOPER PA, GROSIOS K et al.: Combretastatin A-1 phosphate a novel tubulin-binding agent with in vivo anti vascular effects in experimental tumours. Anticancer Res. (2002) 22:707-711.
    • (2002) Anticancer Res , vol.22 , pp. 707-711
    • Holwell, S.E.1    Cooper, P.A.2    Grosios, K.3
  • 49
    • 0011514012 scopus 로고    scopus 로고
    • Triarylethylene ligands which incorporate structural motifs reminiscent of combretastatin A-4 and tamoxifan: Synthesis and biological evaluation as tubulin binding compounds
    • 222nd ACS Meeting. Chicago, USA MEDI68
    • PINNEY KG, TANPURE RP: Triarylethylene ligands which incorporate structural motifs reminiscent of combretastatin A-4 and tamoxifan: synthesis and biological evaluation as tubulin binding compounds. 222nd ACS Meeting. Chicago, USA (2001): MEDI68.
    • (2001)
    • Pommey, K.G.1    Tanpure, R.P.2
  • 50
    • 0033504947 scopus 로고    scopus 로고
    • Synthesis and antitumor activities of amino acid prodrugs of amino-combretastatins
    • OHSUMI K, HATANAKA T, NAKAGAWA R et al.: Synthesis and antitumor activities of amino acid prodrugs of amino-combretastatins. Anti-Cancer Drug Des. (1999) 14:539-548.
    • (1999) Anti-Cancer Drug Des , vol.14 , pp. 539-548
    • Ohsumi, K.1    Hatanaka, T.2    Nakagawa, R.3
  • 51
    • 0032734864 scopus 로고    scopus 로고
    • A novel combretastatin A-4 derivative, AC7700, shows marked antitumor activity against advanced solid tumors and orthotopically transplanted tumors
    • NIHEI Y, SUGA Y, MORINAGA Y et al.: A novel combretastatin A-4 derivative, AC7700, shows marked antitumor activity against advanced solid tumors and orthotopically transplanted tumors. Jpn. J. Cancer Res. (1999) 90:1016-1025.
    • (1999) Jpn. J. Cancer Res , vol.90 , pp. 1016-1025
    • Nihei, Y.1    Suga, Y.2    Morinaga, Y.3
  • 52
    • 0033395393 scopus 로고    scopus 로고
    • Evaluation of antivascular and antimitotic effects of tubulin binding agents in solid tumor therapy
    • NIHEI Y, SUZUKI M, OKANO A et al.: Evaluation of antivascular and antimitotic effects of tubulin binding agents in solid tumor therapy. Jpn. J. Cancer Res. (1999) 90:1387-1395.
    • (1999) Jpn. J. Cancer Res , vol.90 , pp. 1387-1395
    • Nihei, Y.1    Suzuki, M.2    Okano, A.3
  • 53
    • 0035146174 scopus 로고    scopus 로고
    • Stoppage of blood flow in 3-methylcholanthrene-induced autochthonous primary tumor due to a novel combretastatin A-4 derivative, AC7700, and its antitumor effect
    • HORI K, SAITO S, SATO Y, KUBOTA K: Stoppage of blood flow in 3-methylcholanthrene-induced autochthonous primary tumor due to a novel combretastatin A-4 derivative, AC7700, and its antitumor effect. Med. Sci. Monitor (2001) 7:26-33.
    • (2001) Med. Sci. Monitor , vol.7 , pp. 26-33
    • Hori, K.1    Saito, S.2    Sato, Y.3    Kubota, K.4
  • 54
    • 0032729686 scopus 로고    scopus 로고
    • Antitumor effects due to irreversible stoppage of tumor tissue blood flow: Evaluation of a novel combretastatin A-4 derivative, AC7700
    • HORI K, SAITO S, NIHEI Y, SUZUKI M, SATO Y. Antitumor effects due to irreversible stoppage of tumor tissue blood flow: evaluation of a novel combretastatin A-4 derivative, AC7700. Jpn. J. Cancer Res. (1999) 90:1026-1038.
    • (1999) Jpn. J. Cancer Res , vol.90 , pp. 1026-1038
    • Hori, K.1    Saito, S.2    Nihei, Y.3    Suzuki, M.4    Sato, Y.5
  • 55
    • 0011453322 scopus 로고    scopus 로고
    • Mouse plasma and tumour pharmacokinetics of AVE8062, a new combretastatin
    • 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 779
    • ARCHIMBAUD Y, FRASCHINI MC et al.: Mouse plasma and tumour pharmacokinetics of AVE8062, a new combretastatin. 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA (2002): Abstract 779.
    • (2002)
    • Archimbaud, Y.1    Fraschini, M.C.2
  • 56
    • 0011410585 scopus 로고    scopus 로고
    • In vivo evaluation of AVE8062A, a compound active on the tumor vasculature
    • 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 780
    • BISSERY MC, LEJEUNE P, VRIGNAUD P: In vivo evaluation of AVE8062A, a compound active on the tumor vasculature. 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA (2002): Abstract 780.
    • (2002)
    • Bissery, M.C.1    Lejeune, P.2    Vrignaud, P.3
  • 57
    • 0011454948 scopus 로고    scopus 로고
    • In vivo antitumor activity and tumor necrosis induced by AVE8062A, a tumor vasculature targeting agent
    • 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 781
    • LEJEUNE P, HODGE TG, VRIGNAUD P, BISSERY MC: In vivo antitumor activity and tumor necrosis induced by AVE8062A, a tumor vasculature targeting agent. 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA (2002): Abstract 781.
    • (2002)
    • Lejeune, P.1    Hodge, T.G.2    Vrignaud, P.3    Bissery, M.C.4
  • 58
    • 0032402626 scopus 로고    scopus 로고
    • Novel B ring modified combretastatin analogues: Syntheses and antineoplastic activity
    • HATANAKA T, FUJITA K, OHSUMI K et al.: Novel B ring modified combretastatin analogues: syntheses and antineoplastic activity. Bioorg. Med. Chem. Lett. (1998) 8:3371-3374.
    • (1998) Bioorg. Med. Chem. Lett , vol.8 , pp. 3371-3374
    • Hatanaka, T.1    Fujita, K.2    Ohsumi, K.3
  • 59
    • 0033594356 scopus 로고    scopus 로고
    • Antineoplastic agents. 410. Asymmetric hydroxylation of transcombretastatin A-4
    • PETTIT GR, TOKI BE, HERALD DL et al.: Antineoplastic agents. 410. Asymmetric hydroxylation of transcombretastatin A-4. J. Med. Chem. (1999) 42:1459-1465.
    • (1999) J. Med. Chem , vol.42 , pp. 1459-1465
    • Pettit, G.R.1    Toki, B.E.2    Herald, D.L.3
  • 60
    • 0033854914 scopus 로고    scopus 로고
    • Antineoplastic agents 440. Asymmetric synthesis and evaluation of the combretastatin A-1 SAR probes (1S,2S)- and (f1R,2R)-1, 2-dihydroxy-1-(2 pm,3′-dihydroxy-4′- methoxyphenyl)-2-(3m′,4′′,5′′- trimethoxyphenyl)-ethane
    • PETTIT GR, LIPPERT JW III, HERALD DL, HAMEL E, PETTIT RK: Antineoplastic agents 440. Asymmetric synthesis and evaluation of the combretastatin A-1 SAR probes (1S,2S)- and (1R,2R)-1, 2-dihydroxy-1-(2m,3′-dihydroxy-4 pm-methoxyphenyl)-2- (3′′,4′′,5′m-trimethoxyphenyl)-ethane. J. Nat. Prod. (2000) 63:969-974.
    • (2000) J. Nat. Prod , vol.63 , pp. 969-974
    • Pettit, G.R.1    Lippert J.W. III2    Herald, D.L.3    Hamel, E.4    Pettit, R.K.5
  • 61
    • 0032483059 scopus 로고    scopus 로고
    • Asymmetric synthesis of antimitotic combretadioxolane with potent antitumor activity against multi-drug resistant cells
    • SHIRAI R, TAKAYAMA H, NISHIKAWA A, KOISO Y, HASHIMOTO Y: Asymmetric synthesis of antimitotic combretadioxolane with potent antitumor activity against multi-drug resistant cells. Bioorg. Med. Chem. Lett. (1998) 8:1997-2000.
    • (1998) Bioorg. Med. Chem. Lett , vol.8 , pp. 1997-2000
    • Shirai, R.1    Takayama, H.2    Nishikawa, A.3    Koiso, Y.4    Hashimoto, Y.5
  • 63
    • 0000732910 scopus 로고    scopus 로고
    • Synthesis of comformationally restricted combretastatins
    • SHIRAI R, OKABE T, IWASAKI S: Synthesis of comformationally restricted combretastatins. Heterocycles (1997) 46:145-148.
    • (1997) Heterocycles , vol.46 , pp. 145-148
    • Shirai, R.1    Okabe, T.2    Iwasaki, S.3
  • 64
    • 0037061622 scopus 로고    scopus 로고
    • Potent, orally active heterocycle-based combretastatin A-4 analogues: Synthesis, structure activity relationship, pharmacokinetics, and in vivo antitumor activity evaluation
    • WANG L, WOODS KW, LI Q et al.: Potent, orally active heterocycle-based combretastatin A-4 analogues: synthesis, structure activity relationship, pharmacokinetics, and in vivo antitumor activity evaluation. J. Med. Chem (2002) 45:1697-1711.
    • (2002) J. Med. Chem , vol.45 , pp. 1697-1711
    • Wang, L.1    Woods, K.W.2    Li, Q.3
  • 65
    • 0032542045 scopus 로고    scopus 로고
    • Syntheses and antitumor activity of cis-restricted combretastatins: 5-membered heterocyclic analogues
    • OHSUMI K, HATANAKA T, FUJITA K et al.: Syntheses and antitumor activity of cis-restricted combretastatins: 5-membered heterocyclic analogues. Bioorg. Med. Chem. Lett. (1998) 8:3153-3158.
    • (1998) Bioorg. Med. Chem. Lett , vol.8 , pp. 3153-3158
    • Ohsumi, K.1    Hatanaka, T.2    Fujita, K.3
  • 67
    • 0037169988 scopus 로고    scopus 로고
    • Synthesis and cytotoxicity of 3,4-diaryl-2(5H)-furanones
    • KIM Y, NAM NH, YOU YJ, AHN BZ: Synthesis and cytotoxicity of 3,4-diaryl-2(5H)-furanones. Bioorg. Med Chem. Lett. (2002) 12:719-722.
    • (2002) Bioorg. Med Chem. Lett , vol.12 , pp. 719-722
    • Kim, Y.1    Nam, N.H.2    You, Y.J.3    Ahn, B.Z.4
  • 68
    • 0035801759 scopus 로고    scopus 로고
    • The synthesis and tubulin binding activity of thiophene-based analogues of combretastatin A-4
    • FLYNN BL, FLYNN GP, HAMEL E, JUNG MK: The synthesis and tubulin binding activity of thiophene-based analogues of combretastatin A-4. Bioorg. Med. Chem. Lett. (2001) 11:2341-2343.
    • (2001) Bioorg. Med. Chem. Lett , vol.11 , pp. 2341-2343
    • Flynn, B.L.1    Flynn, G.P.2    Hamel, E..3    Jung, M.K.4
  • 69
    • 0035826341 scopus 로고    scopus 로고
    • A novel palladium-mediated coupling approach to 2,3-disubstituted benzo[b]thiophenes and its application to the synthesis of tubulin binding agents
    • FLYNN BL, VERDIER-PINARD P, HAMEL E: A novel palladium-mediated coupling approach to 2,3-disubstituted benzo[b]thiophenes and its application to the synthesis of tubulin binding agents. Org. Lett. (2001) 3:651-654.
    • (2001) Org. Lett , vol.3 , pp. 651-654
    • Flynn, B.L.1    Verdier-Pinard, P.2    Hamel, E.3
  • 70
    • 4243169514 scopus 로고    scopus 로고
    • Synthesis, X-ray crystal structure and tubulin-binding properties of a benzofuran analogue of the potent cytotoxic agent combretastatin A4
    • BANWELL MG, FLYNN BL, WILLIS AC, HAMEL E: Synthesis, X-ray crystal structure and tubulin-binding properties of a benzofuran analogue of the potent cytotoxic agent combretastatin A4. Aust. J. Chem. (1999) 52:767-774.
    • (1999) Aust. J. Chem , vol.52 , pp. 767-774
    • Banwell, M.G.1    Flynn, B.L.2    Willis, A.C.3    Hamel, E.4
  • 71
    • 0035879010 scopus 로고    scopus 로고
    • A-204197, a new tubulin-binding agent with antimitotic activity in tumor cell lines resistant to known microtubule inhibitors
    • TAHIR SK, HAN EKH, CREDO B et al.: A-204197, a new tubulin-binding agent with antimitotic activity in tumor cell lines resistant to known microtubule inhibitors. Cancer Res. (2001) 61:5480-5485.
    • (2001) Cancer Res , vol.61 , pp. 5480-5485
    • Tahir, S.K.1    Han, E.K.H.2    Credo, B.3
  • 72
    • 0035866356 scopus 로고    scopus 로고
    • Identification and characterization of A-105972, an antineoplastic agent
    • WU-WONG JR, ALDER JD, ALDER L, et al.: Identification and characterization of A-105972, an antineoplastic agent. Cancer Res. (2001) 61:1486-1492.
    • (2001) Cancer Res , vol.61 , pp. 1486-1492
    • Wu-Wong, J.R.1    Alder, J.D.2    Alder, L.3
  • 73
    • 0035818922 scopus 로고    scopus 로고
    • New antimitotic agents with activity in multi-drug-resistant cell lines and in vivo efficacy in murine tumor models
    • SZCZEPANKIEWICZ BG, LIU G, JAE HS et al.: New antimitotic agents with activity in multi-drug-resistant cell lines and in vivo efficacy in murine tumor models. J. Med. Chem. (2001) 44:4416-4430.
    • (2001) J. Med. Chem , vol.44 , pp. 4416-4430
    • Szczepankiewicz, B.G.1    Liu, G.2    Jae, H.S.3
  • 75
    • 0011454162 scopus 로고    scopus 로고
    • Sulfur containing double bond replacement of combretastatin A-4 as antimitotic agents
    • 221st ACS Meeting. San Diego, USA MEDI138
    • WOODS KW, MCCROSKEY RW, STEINER BA et al.: Sulfur containing double bond replacement of combretastatin A-4 as antimitotic agents. 221st ACS Meeting. San Diego, USA (2001): MEDI138.
    • (2001)
    • Woods, K.W.1    Mccroskey, R.W.2    Steiner, B.A.3
  • 76
    • 0032492959 scopus 로고    scopus 로고
    • Antineoplastic agents. 379. Synthesis of phenstatin phosphate
    • PETTIT GR, TOKI B, HERALD DL et al.: Antineoplastic agents. 379. Synthesis of phenstatin phosphate. J. Med. Chem. (1998) 41:1688-1695.
    • (1998) J. Med. Chem , vol.41 , pp. 1688-1695
    • Pettit, G.R.1    Toki, B.2    Herald, D.L.3
  • 77
    • 0034644193 scopus 로고    scopus 로고
    • Antineoplastic agents. 443. Synthesis of the cancer cell growth inhibitor hydroxyphenstatin and its sodium diphosphate prodrug
    • PETTIT GR, GREALISH MP, HERALD DL, BOYD MR, HAMEL E, PETTIT RK: Antineoplastic agents. 443. Synthesis of the cancer cell growth inhibitor hydroxyphenstatin and its sodium diphosphate prodrug. J. Med. Chem. (2000) 43:2731-2737.
    • (2000) J. Med. Chem , vol.43 , pp. 2731-2737
    • Pettit, G.R.1    Grealish, M.P.2    Herald, D.L.3    Boyd, M.R.4    Hamel, E.5    Pettit, R.K.6
  • 78
    • 0031869533 scopus 로고    scopus 로고
    • Antimitotic activity of diaryl compounds with structural features resembling combretastatin A-4
    • ALEKSANDRZAK K, MCGOWN AT, HADFIELD JA: Antimitotic activity of diaryl compounds with structural features resembling combretastatin A-4. Anti-Cancer Drugs (1998) 9:545-550.
    • (1998) Anti-Cancer Drugs , vol.9 , pp. 545-550
    • Aleksandrzak, K.1    Mcgown, A.T.2    Hadfield, J.A.3
  • 79
    • 0011406550 scopus 로고    scopus 로고
    • Studies in anticancer compounds: Synthesis of 6-methsoxy-1-(3m, 4′,5′-trimethoxyphenyl- 3,4-dihydronaphthalene further functionalized at C-5 or C-7
    • 222nd ACS Meeting. Chicago, USA ORGN153
    • GHATAK A, DORSEY J, GARNER CM, MOCHARLA VP, CHEN Z, PINNEY KG: Studies in anticancer compounds: synthesis of 6-methsoxy-1-(3′, 4′, 5′-trimethoxyphenyl-3,4-dihydronaphthalene further functionalized at C-5 or C-7. 222nd ACS Meeting. Chicago, USA (2001): ORGN153.
    • (2001)
    • Ghatak, A.1    Dorsey, J.2    Garner, C.M.3    Mocharla, V.P.4    Chen, Z.5    Pinney, K.G.6
  • 80
    • 0031810637 scopus 로고    scopus 로고
    • Podophyllotoxins: Current status and recent developments
    • DAMAYANTHI Y, LOWN JW: Podophyllotoxins: current status and recent developments. Curr. Med. Chem. (1998) 5:205-252.
    • (1998) Curr. Med. Chem , vol.5 , pp. 205-252
    • Damayanthi, Y.1    Lown, J.W.2
  • 81
    • 0011500374 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of diarylsulfonamides as tubulin polymerisation inhibitors. Discovery of A-318315 and A293620 as orally and intravenously active antitumor agents
    • 93rd Annual Meeting of American Association for Cancer Research 2002. San Francisco, USA Abstract 1313
    • LI Q STEINER BA, WOODS KW et al.: Synthesis and biological evaluation of diarylsulfonamides as tubulin polymerisation inhibitors. Discovery of A-318315 and A293620 as orally and intravenously active antitumor agents. 93rd Annual Meeting of American Association for Cancer Research 2002. San Francisco, USA (2002). Abstract 1313.
    • (2002)
    • Li, Q.1    Steiner, B.A.2    Woods, K.W.3
  • 82
    • 0035833041 scopus 로고    scopus 로고
    • Novel sulfonate derivatives: Potent antimitotic agents
    • GWALTNEY SL, II, IMADE HM, LI Q et al.: Novel sulfonate derivatives: potent antimitotic agents. Bioorg. Med. Chem. Lett. (2001) 11:1671-1673.
    • (2001) Bioorg. Med. Chem. Lett , vol.11 , pp. 1671-1673
    • Gwaltney S.L. II1    Imade, H.M.2    Li, Q.3
  • 83
    • 0035832113 scopus 로고    scopus 로고
    • Novel sulfonate analogues of combretastatin A-4: Potent antimitotic agents
    • GWALTNEY SL, II, IMADE HM, BARR KJ et al.: Novel sulfonate analogues of combretastatin A-4: Potent antimitotic agents. Bioorg. Med. Chem. Lett. (2001) 11:871-874.
    • (2001) Bioorg. Med. Chem. Lett , vol.11 , pp. 871-874
    • Gwaltney S.L. II1    Imade, H.M.2    Barr, K.J.3
  • 84
    • 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. Exp. Opin. Ther. Patents (2000) 10:1725-1740.
    • (2000) Exp. Opin. Ther. Patents , vol.10 , pp. 1725-1740
    • Owa, T.1    Nagasu, T.2
  • 85
    • 0030756156 scopus 로고    scopus 로고
    • Mechanism of action of E7010, an orally active sulfonamide antitumor agent: 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, an orally active sulfonamide antitumor agent: 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
  • 86
    • 0031793404 scopus 로고    scopus 로고
    • Preferential binding of E7010 to murine β3-tubulin and decreased β3-tubulin in E7010-resistant cell lines
    • IWAMOTO Y, NISHIO K, FUKUMOTO H, YOSHIMATSU K, YAMAKIDO M, SAIJO N: Preferential binding of E7010 to murine β3-tubulin and decreased β3-tubulin in E7010-resistant cell lines. Jpn. J. Cancer. Res. (1998) 89:954-962.
    • (1998) Jpn. J. Cancer. Res , vol.89 , pp. 954-962
    • Iwamoto, Y.1    Nishio, K.2    Fukumoto, H.3    Yoshimatsu, K.4    Yamakido, M.5    Saijo, N.6
  • 87
    • 0011454164 scopus 로고    scopus 로고
    • Biological activity of ABT-751: An oral antimitotic agent
    • 93rd Annual Meeting of American Association for Cancer Research San Francisco, USA Abstract 1323
    • ZIELINSKI MOZNY NA, NUKKALA MA, WILSON ST et al.: Biological activity of ABT-751: an oral antimitotic agent. 93rd Annual Meeting of American Association for Cancer Research San Francisco, USA (2002): Abstract 1323.
    • (2002)
    • Zielinski Mozny, N.A.1    Nukkala, M.A.2    Wilson, S.T.3
  • 88
    • 0026719782 scopus 로고
    • Novel sulfonamides as potential, systemically active antitumor agents
    • YOSHINO H, NORIHIRO U, NIIJIMA J et al.: Novel sulfonamides as potential, systemically active antitumor agents. J. Med. Chem. (1994) 35:2496-2497.
    • (1994) J. Med. Chem , vol.35 , pp. 2496-2497
    • Yoshino, H.1    Norihiro, U.2    Niijima, J.3
  • 89
    • 0034916962 scopus 로고    scopus 로고
    • Effect of E7010 on liver metastasis and life span of syngeneic C57BL/6 mice bearing orthotopically transplanted routine Colon 38 tumor
    • FUNAHASHI Y. KOYANAGI N, KITOH K: Effect of E7010 on liver metastasis and life span of syngeneic C57BL/6 mice bearing orthotopically transplanted routine Colon 38 tumor. Cancer Chemother. Pharmacol. (2001) 47:179-184.
    • (2001) Cancer Chemother. Pharmacol , vol.47 , pp. 179-184
    • Funahashi, Y.1    Koyanagi, N.2    Kitoh, K.3
  • 90
    • 0011410381 scopus 로고    scopus 로고
    • Selective effect of the novel antimitotic compound ABT-751 on tumor vasculature: An in vivo rat hemodynamic study
    • 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 783
    • SEGRETI J, POLAKOWSKI J, DIERKS K et al.: Selective effect of the novel antimitotic compound ABT-751 on tumor vasculature: an in vivo rat hemodynamic study. 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA (2002): Abstract 783.
    • (2002)
    • Segreti, J.1    Polakowski, J.2    Dierks, K.3
  • 91
    • 0011468858 scopus 로고    scopus 로고
    • A novel anti-tubulin agent (ABT-751) selectively reduces tumour perfusion in a subcutaneous rat tumour model as measured by MRI
    • 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 784
    • LUO Y, MOHNING KM, NUSS ME et al.: A novel anti-tubulin agent (ABT-751) selectively reduces tumour perfusion in a subcutaneous rat tumour model as measured by MRI. 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA (2002): Abstract 784.
    • (2002)
    • Luo, Y.1    Mohning, K.M.2    Nuss, M.E.3
  • 93
    • 0003350604 scopus 로고
    • ER-34410, a structurally novel sulfonamide as a potential injectable antitumor agent
    • Abstract 2290
    • UEDA N, TSUKAHARA N, WATANABE T et al.: ER-34410, a structurally novel sulfonamide as a potential injectable antitumor agent. Proc. Am. Assoc. Cancer Res. (1995) 36:Abstract 2290.
    • (1995) Proc. Am. Assoc. Cancer Res , vol.36
    • Ueda, N.1    Tsukahara, N.2    Watanabe, T.3
  • 95
    • 85037793353 scopus 로고    scopus 로고
    • Mode of mechanisms of cell death induced by HMN-214, a novel antitumor sulfonamide compound
    • Abstract 225
    • KATOK F, TAKAGI M, KITAZAWA C et al.: Mode of mechanisms of cell death induced by HMN-214, a novel antitumor sulfonamide compound. Proc. Am. Assoc. Cancer Res. (1998) 39:Abstract 225.
    • (1998) Proc. Am. Assoc. Cancer Res , vol.39
    • Katok, F.1    Takagi, M.2    Kitazawa, C.3
  • 96
    • 0011454165 scopus 로고    scopus 로고
    • Apoptosis induction by novel anti-cancer compound, HMN-154 (HMN-176) through suppressing the expression of cell cycle controllers
    • Abstract 319
    • TANAKA H, OHSHIMA N, HIKADA H: Apoptosis induction by novel anti-cancer compound, HMN-154 (HMN-176) through suppressing the expression of cell cycle controllers. Proc. Am. Assoc. Cancer Res. (1998) 39-Abstract 319.
    • (1998) Proc. Am. Assoc. Cancer Res , vol.39
    • Tanaka, H.1    Ohshima, N.2    Hikada, H.3
  • 97
    • 0033052886 scopus 로고    scopus 로고
    • Isolation of cDNAs encoding cellular drug-binding proteins using a novel expression cloning procedure: Drug-western
    • TANAKA H, OHSHIMA N, HIDAKA H: Isolation of cDNAs encoding cellular drug-binding proteins using a novel expression cloning procedure: drug-western. Mol. Pharmacol. (1999) 55:356-363.
    • (1999) Mol. Pharmacol , vol.55 , pp. 356-363
    • Tanaka, H.1    Ohshima, N.2    Hidaka, H.3
  • 98
    • 0011410382 scopus 로고    scopus 로고
    • A Phase I and pharmakokinetic study of HMN-214 administered orally for 21 consecutive days, repeated every 28 days to patients with advanced solid tumours
    • 38th Annual Meeting of American Society of Clinical Oncology. Orlando, USA Abstract 419
    • TAYLOR C, DRAGOVICH T, SIMPSON A, VON HOFF D: A Phase I and pharmakokinetic study of HMN-214 administered orally for 21 consecutive days, repeated every 28 days to patients with advanced solid tumours. 38th Annual Meeting of American Society of Clinical Oncology. Orlando, USA (2002): Abstract 419.
    • (2002)
    • Taylor, C.1    Dragovich, T.2    Simpson, A.3    Von Hoff, D.4
  • 99
    • 0011496318 scopus 로고    scopus 로고
    • A Phase I and pharmacokinetic (PK) study of HMN-214, an oral antimitotubular agent with polo-like and cyclin-dependent kinase inhibitory activities
    • 38th Annual Meeting of American Society of Clinical Oncology. Orlando, USA Abstract 418
    • PATNAIK A, FORERO L, TOLCHERAW et al.: A Phase I and pharmacokinetic (PK) study of HMN-214, an oral antimitotubular agent with polo-like and cyclin-dependent kinase inhibitory activities. 38th Annual Meeting of American Society of Clinical Oncology. Orlando, USA (2002): Abstract 418.
    • (2002)
    • Patnaik, A.1    Forero, L.2    Tolcheraw3
  • 100
    • 0031688155 scopus 로고    scopus 로고
    • Recent advances in the discovery and development of flavonoids and their analogues as antitumor and and-HIV agents
    • WANG HK, XIA Y, YANG ZY, NATSCHKE SL, LEE KH: Recent advances in the discovery and development of flavonoids and their analogues as antitumor and and-HIV agents. Adv. Exper. Med. Biol. (1998) 439:191-225.
    • (1998) Adv. Exper. Med. Biol , vol.439 , pp. 191-225
    • Wang, H.K.1    Xia, Y.2    Yang, Z.Y.3    Natschke, S.L.4    Lee, K.H.5
  • 101
    • 0032543726 scopus 로고    scopus 로고
    • Structure-activity requirements for flavone cytotoxicity and binding to tubulin
    • BEUTLER JA, HAMEL E, VLIETINCK AJ et al.: Structure-activity requirements for flavone cytotoxicity and binding to tubulin. J. Med. Chem. (1998) 41:2333-2338.
    • (1998) J. Med. Chem , vol.41 , pp. 2333-2338
    • Beutler, J.A.1    Hamel, E.2    Vlietinck, A.J.3
  • 102
    • 0011505606 scopus 로고    scopus 로고
    • Aminoflavone (NSC 686288) induction of vytochrome P450 1A1 in sensitive human cell lines is associated with metabolic activation, DNA damage and antiproliferative activity
    • POBST J, KUFFEL MJ, ARNT CR: Aminoflavone (NSC 686288) induction of vytochrome P450 1A1 in sensitive human cell lines is associated with metabolic activation, DNA damage and antiproliferative activity. Clin. Cancer Res. (2001) 7(Suppl.):3797.
    • (2001) Clin. Cancer Res , vol.7 , Issue.SUPPL. , pp. 3797
    • Pobst, J.1    Kuffel, M.J.2    Arnt, C.R.3
  • 103
    • 0011514532 scopus 로고    scopus 로고
    • The aryl hydrocarbon receptor mediates sensitivity of MCF-7 breast cancer cells to the antitumor agent NSC 686288
    • LOAIZA PEREZ AI, VISTICA D, KENNEY S et al.: The aryl hydrocarbon receptor mediates sensitivity of MCF-7 breast cancer cells to the antitumor agent NSC 686288. Clin. Cancer Res. (2001) 7(Suppl.):3737.
    • (2001) Clin. Cancer Res , vol.7 , Issue.SUPPL. , pp. 3737
    • Loaiza Perez, A.I.1    Vistica, D.2    Kenney, S.3
  • 104
    • 0011406551 scopus 로고    scopus 로고
    • Intravenous plasma elimination kinetics and toxicity of an aminoflavone in the dog
    • Abstract 390
    • BROWN AP, MORRISEY RL, RODVOLD KA et al.: Intravenous plasma elimination kinetics and toxicity of an aminoflavone in the dog. Proc. Am. Assoc. Cancer Res. (1999) 40-Abstract 390.
    • (1999) Proc. Am. Assoc. Cancer Res , vol.40
    • Brown, A.P.1    Morrisey, R.L.2    Rodvold, K.A.3
  • 105
    • 0003263149 scopus 로고    scopus 로고
    • Pharmacologic evaluations of a novel amino-substituted flavone (NSC 686288) exhibiting unique in vitro and in vivo anticancer activities
    • Abstract 119
    • ALLEY MC, STINSON SF, PACULA COX CM et al.: Pharmacologic evaluations of a novel amino-substituted flavone (NSC 686288) exhibiting unique in vitro and in vivo anticancer activities. Proc. Am. Assoc. Cancer Res. (1999) 40:Abstract 119.
    • (1999) Proc. Am. Assoc. Cancer Res , vol.40
    • Alley, M.C.1    Stinson, S.F.2    Pacula3    Cox, C.M.4
  • 107
    • 0033619997 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of dihydrobenzofuran lignans and related compounds as potential antitumor agents that inhibit tubulin polymerisation
    • PIETERS L, VAN DYCK S, GAO M et al.: Synthesis and biological evaluation of dihydrobenzofuran lignans and related compounds as potential antitumor agents that inhibit tubulin polymerisation. J. Med. Chem. (1999) 42:5475-5481.
    • (1999) J. Med. Chem , vol.42 , pp. 5475-5481
    • Pieters, L.1    Van Dyck, S.2    Gao, M.3
  • 108
    • 0032903696 scopus 로고    scopus 로고
    • Recent advances in the discovery and development of quinolones and analogs as antitumor agents
    • XIA Y, YANG ZY, MORRIS-NATSCHKE SL, LEE KH: Recent advances in the discovery and development of quinolones and analogs as antitumor agents. Curr. Med. Chem. (1999) 6:179-194.
    • (1999) Curr. Med. Chem , vol.6 , pp. 179-194
    • Xia, Y.1    Yang, Z.Y.2    Morris-Natschke, S.L.3    Lee, K.H.4
  • 109
    • 0028036429 scopus 로고
    • Antitumor agents. 155. Synthesis and biological evaluation of 3′,6,7-substituted 2-phenyl -4-quinolones as antimicrorubule agents
    • LI L, WANG HK, KUO SC et al.: Antitumor agents. 155. Synthesis and biological evaluation of 3′,6,7-substituted 2-phenyl-4-quinolones as antimicrorubule agents. J. Med. Chem. (1994) 37:3400-3407.
    • (1994) J. Med. Chem , vol.37 , pp. 3400-3407
    • Li, L.1    Wang, H.K.2    Kuo, S.C.3
  • 110
    • 0035829462 scopus 로고    scopus 로고
    • Antitumor Agents. 211. Fluorinated 2-phenyl-4-quinolone derivatives as antimitotic antitumor agents
    • XIA Y, YANG ZY, XIA P et al.: Antitumor Agents. 211. Fluorinated 2-phenyl-4-quinolone derivatives as antimitotic antitumor agents. J. Med. Chem. (2001) 44:3932-3936.
    • (2001) J. Med. Chem , vol.44 , pp. 3932-3936
    • Xia, Y.1    Yang, Z.Y.2    Xia, P.3
  • 111
    • 0033533865 scopus 로고    scopus 로고
    • Antitumor agents. 196. Substituted 2-thienyl-1, 8-naphthyridin-4-ones: Their synthesis, cytotoxicity, and inhibition of tubulin polymerisation
    • ZHANG SY, BASTOW KF, TACHIBANA Y et al.: Antitumor agents. 196. Substituted 2-thienyl-1,8-naphthyridin-4-ones: their synthesis, cytotoxicity, and inhibition of tubulin polymerisation. J. Med. Chem. (1999) 42:4081-4087.
    • (1999) J. Med. Chem , vol.42 , pp. 4081-4087
    • Zhang, S.Y.1    Bastow, K.F.2    Tachibana, Y.3
  • 112
    • 0035821397 scopus 로고    scopus 로고
    • Antitumor agents. Part 204: Synthesis and biological evaluation of substituted 2-aryl quinazolinones
    • XIA Y. YANG ZY, HOUR MJ et al.: Antitumor agents. Part 204: synthesis and biological evaluation of substituted 2-aryl quinazolinones. Bioarg. Med. Chem. Lett. (2001) 11:1193-1196.
    • (2001) Bioarg. Med. Chem. Lett , vol.11 , pp. 1193-1196
    • Xia, Y.1    Yang, Z.Y.2    Hour, M.J.3
  • 113
    • 0034676319 scopus 로고    scopus 로고
    • 6-Alkylamino- and 2,3-dihydro-3 ′-methoxy- 2-phenyl-4-quinazolinones and related compounds: Their synthesis, cytotoxicity, and inhibition of tubulin polymerisation
    • HOUR MJ, HUANG LJ, KUO SC et al.: 6-Alkylamino- and 2,3-dihydro-3′-methoxy-2- phenyl-4-quinazolinones and related compounds: their synthesis, cytotoxicity, and inhibition of tubulin polymerisation. J. Med. Chem. (2000) 43:4479-4487.
    • (2000) J. Med. Chem , vol.43 , pp. 4479-4487
    • Hour, M.J.1    Huang, L.J.2    Kuo, S.C.3
  • 114
    • 18244398450 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of 2-indolyloxazolines as a new class of tubulin polymerisation inhibitors. Discovery of A-289099 as an orally active antitumor agent
    • LI Q, WOODS KW, CLAIBORNE A et al.: Synthesis and biological evaluation of 2-indolyloxazolines as a new class of tubulin polymerisation inhibitors. Discovery of A-289099 as an orally active antitumor agent. Bioorg. Med. Chem. Lett. (2002) 12:465-469.
    • (2002) Bioorg. Med. Chem. Lett , vol.12 , pp. 465-469
    • Li, Q.1    Woods, K.W.2    Claiborne, A.3
  • 115
    • 0011414058 scopus 로고    scopus 로고
    • Biological activity of A-289099: An indoleoxazoline derivative with antimitotic activity
    • 93d Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 1315
    • TAHIR SK, NUKKALA MA, ZIELENIEWSKI MOZNY NA et al.: Biological activity of A-289099: an indoleoxazoline derivative with antimitotic activity. 93d Annual Meeting of American Association for Cancer Research. San Francisco, USA (2002): Abstract 1315.
    • (2002)
    • Tahir, S.K.1    Nukkala, M.A.2    Zieleniewski3    Mozny, N.A.4
  • 116
    • 0011468859 scopus 로고    scopus 로고
    • Biological efficacy of A-318315: An orally active antimitotic agent
    • 93d Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 1314
    • ZIELENIEWSKI MOZNY NA, CREDO RB, TAHIR SK et al.: Biological efficacy of A-318315: an orally active antimitotic agent. 93d Annual Meeting of American Association for Cancer Research. San Francisco, USA (2002). Abstract 1314.
    • (2002)
    • Zieleniewski1    Mozny, N.A.2    Credo, R.B.3    Tahir, S.K.4
  • 117
    • 0001823765 scopus 로고    scopus 로고
    • Synthesis and antineoplastic activity of combretastatin analogues - Heterocombretastatins
    • MEDARDE M, RAMOS A, CABALLERO E et al.: Synthesis and antineoplastic activity of combretastatin analogues - heterocombretastatins. Eur. J. Med. Chem. (1998) 33:71-77.
    • (1998) Eur. J. Med. Chem , vol.33 , pp. 71-77
    • Medarde, M.1    Ramos, A.2    Caballero, E.3
  • 118
    • 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
  • 119
    • 0034843846 scopus 로고    scopus 로고
    • Mechanisms 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.: Mechanisms 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
  • 120
    • 0034773165 scopus 로고    scopus 로고
    • E7070, a novel sulfonamide agent with potent antitumour activity in vitro and in vivo
    • OZAWA Y, SUGI NH, NAGASU T et al.: E7070, a novel sulfonamide 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
  • 121
    • 0034772246 scopus 로고    scopus 로고
    • Phase I and pharmacokinetic study of E7070, a novel sulfonamide, 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, a novel sulfonamide, 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
  • 122
    • 0000660979 scopus 로고    scopus 로고
    • Population pharmacokinetics and pharmacokinetic-pharmacodynamic relationships of the novel anticancer agent E7070 in four Phase I studies
    • VAN KESTEREN C, MATHOT RA, RAYMOND E et al.: Population pharmacokinetics and pharmacokinetic-pharmacodynamic relationships of the novel anticancer agent E7070 in four Phase I studies. Br. J. Clin. Pharmacol. (2002) 53:553P
    • (2002) Br. J. Clin. Pharmacol , vol.53
    • Van Kesteren, C.1    Mathot, R.A.2    Raymond, E.3
  • 123
    • 0011454559 scopus 로고    scopus 로고
    • Cell and tumor biology 38: Angiogenesis inhibitors IV: Novel inhibitors
    • 91st Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 4093
    • FUNAHASHI Y, SUGI NH, HANEDA T et al.: Cell and tumor biology 38: angiogenesis inhibitors IV: novel inhibitors. 91st Annual Meeting of American Association for Cancer Research. San Francisco, USA (2000). Abstract 4093.
    • (2000)
    • Funahashi, Y.1    Sugi, N.H.2    Haneda, T.3
  • 124
    • 0011475593 scopus 로고    scopus 로고
    • A novel angiogenesis inhibitor, ER-68203-00, II. Anti-angiogenesis potency and therapeutic efficacy in tumor xenograf models
    • 91st Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 4094
    • SEMABA T, FUNAHASHI Y, YAMAMOTO Y et al.: A novel angiogenesis inhibitor, ER-68203-00, II. Anti-angiogenesis potency and therapeutic efficacy in tumor xenograf models. 91st Annual Meeting of American Association for Cancer Research. San Francisco, USA (2000). Abstract 4094.
    • (2000)
    • Semaba, T.1    Funahashi, Y.2    Yamamoto, Y.3
  • 125
    • 0011407199 scopus 로고    scopus 로고
    • Angiogenesis inhibitor, E7820; Enhancement of anti-angiogenic activity through the combination with receptor kinase inhibitors of VEGF or BFGF
    • 91st Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 912
    • ONO N, SEMBA T, HOSHI SS et al.: Angiogenesis inhibitor, E7820; enhancement of anti-angiogenic activity through the combination with receptor kinase inhibitors of VEGF or BFGF. 91st Annual Meeting of American Association for Cancer Research. San Francisco, USA (2002). Abstract 912.
    • (2002)
    • Ono, N.1    Semba, T.2    Hoshi, S.S.3
  • 126
    • 0011453328 scopus 로고    scopus 로고
    • Synthesis and structure-activity relationship of bis-indolylmaleimides as cell cycle inhibitors: Elaboration of the development candidate, Ro 31-7453
    • 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 3655
    • FOTOUHI N, AHMAD M, BANNER B et al.: Synthesis and structure-activity relationship of bis-indolylmaleimides as cell cycle inhibitors: elaboration of the development candidate, Ro 31-7453. 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA (2002) Abstract 3655.
    • (2002)
    • Fotouhi, N.1    Ahmad, M.2    Banner, B.3
  • 127
    • 24844476578 scopus 로고    scopus 로고
    • Design and synthesis of novel orally bioavailable bisindolyl maleimides as cell cycle inhibitors
    • 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 3656
    • KONG N, SPECIAN JR. A, LOVEY A et al.: Design and synthesis of novel orally bioavailable bisindolyl maleimides as cell cycle inhibitors. 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA (2002). Abstract 3656.
    • (2002)
    • Kong, N.1    Specian A., Jr.2    Lovey, A.3
  • 128
    • 0011452831 scopus 로고    scopus 로고
    • Preclinical characterization of Ro 31-7453
    • 92nd Annual Meeting of American Association for Cancer Research; New Orleans, USA Abstract 4893
    • RITLAND S, STEELE T, KEN R et al.: Preclinical characterization of Ro 31-7453. 92nd Annual Meeting of American Association for Cancer Research; New Orleans, USA (2001). Abstract 4893.
    • (2001)
    • Ritland, S.1    Steele, T.2    Ken, R.3
  • 129
    • 0011503182 scopus 로고    scopus 로고
    • A Phase I clinical and pharmacokinetic study of oral Ro 31-7453, a novel cell cycle inhibitor, administered in combination with gemcitabine
    • 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 1369
    • NICOLSON M, BISSET D, CASSIDY J et al.: A Phase I clinical and pharmacokinetic study of oral Ro 31-7453, a novel cell cycle inhibitor, administered in combination with gemcitabine. 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA (2002): Abstract 1369.
    • (2002)
    • Nicolson, M.1    Bisset, D.2    Cassidy, J.3
  • 130
    • 0033575722 scopus 로고    scopus 로고
    • Synthesis and pharmacological activity of diarylindole derivatives. Cytotoxic agents based on combretastatins
    • MEDARDE M, RAMOS AC, CABALLERO E et al.: Synthesis and pharmacological activity of diarylindole derivatives. Cytotoxic agents based on combretastatins. Bioorg. Med. Chem. Lett. (1999) 9:2303-2308.
    • (1999) Bioorg. Med. Chem. Lett , vol.9 , pp. 2303-2308
    • Medarde, M.1    Ramos, A.C.2    Caballero, E.3
  • 132
    • 0032481002 scopus 로고    scopus 로고
    • Methoxy-substituted 3-formyl-2-phenylindoles inhibit tubulin polymerisation
    • GASTPAR R, GOLDBRUNNER M, MARKO D, VON ANGERER E: Methoxy-substituted 3-formyl-2-phenylindoles inhibit tubulin polymerisation. J. Med. Chem. (1998) 41:4965-4972.
    • (1998) J. Med. Chem , vol.41 , pp. 4965-4972
    • Gastpar, R.1    Goldbrunner, M.2    Marko, D.3    Von Angerer, E.4
  • 133
    • 0035924236 scopus 로고    scopus 로고
    • Synthetic 2-aroylindole derivatives as a new class of potent tubulin-inhibitory, antimitotic agents
    • MAHBOOBI S, PONGRATZ H, HUFS KY H et al.: Synthetic 2-aroylindole derivatives as a new class of potent tubulin-inhibitory, antimitotic agents. J. Med. Chem. (2001) 44:4535-4553.
    • (2001) J. Med. Chem , vol.44 , pp. 4535-4553
    • Mahboobi, S.1    Pongratz, H.2    Hufs, K.Y.H.3
  • 134
    • 0024354903 scopus 로고
    • Interaction of the novel agent amphethinile with tubulin
    • MCGOWN AT, FOX BW: Interaction of the novel agent amphethinile with tubulin. Br. J. Cancer (1989) 59:865-868.
    • (1989) Br. J. Cancer , vol.59 , pp. 865-868
    • Mcgown, A.T.1    Fox, B.W.2
  • 135
    • 0035133804 scopus 로고    scopus 로고
    • D-24851, a novel synthetic microtubule inhibitor, exerts curative antitumoral activity in vivo, shows efficacy toward multidrug-resistant tumor cells, and lacks neurotoxicity
    • BACHER G, NICKEL B, EMIG P et al.: D-24851, a novel synthetic microtubule inhibitor, exerts curative antitumoral activity in vivo, shows efficacy toward multidrug-resistant tumor cells, and lacks neurotoxicity, Cancer Res. (2001) 61:392-399.
    • (2001) Cancer Res , vol.61 , pp. 392-399
    • Bacher, G.1    Nickel, B.2    Emig, P.3
  • 136
    • 0011453329 scopus 로고    scopus 로고
    • Potent in vivo antitumor activity of D-24851, a novel tubulin inhibitor, in human xenografts and antimetastatic effect in the renca model
    • 92nd Annual Meeting of American Association for Cancer Research. New Orleanes, USA Abstract 1992
    • NICHEL B, SCHMIDT M, DREVS J et al.: Potent in vivo antitumor activity of D-24851, a novel tubulin inhibitor, in human xenografts and antimetastatic effect in the renca model. 92nd Annual Meeting of American Association for Cancer Research. New Orleanes, USA (2001): Abstract 1992.
    • (2001)
    • Nichel, B.1    Schmidt, M.2    Drevs, J.3
  • 137
    • 0011475594 scopus 로고    scopus 로고
    • Discovery and synthesis of novel N-substituted indolyl-3-glyoxylic acid derivatives with tubulin-binding activity as anticancer agents
    • 91st Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 4888
    • GÜNTHER E, EMIG P, REICHERT D et al.: Discovery and synthesis of novel N-substituted indolyl-3-glyoxylic acid derivatives with tubulin-binding activity as anticancer agents. 91st Annual Meeting of American Association for Cancer Research. San Francisco, USA (2000). Abstract 4888.
    • (2000)
    • Günther, E.1    Emig, P.2    Reichert, D.3
  • 138
    • 18844470366 scopus 로고    scopus 로고
    • Novel Antineoplastic agents with efficacy against multidrug resistant tumour cells
    • MEDINA JC, SHAN B, BECKMANN H et al.: Novel Antineoplastic agents with efficacy against multidrug resistant tumour cells. Bioorg. Med. Chem. Lett. (1998) 8:2653-2656.
    • (1998) Bioorg. Med. Chem. Lett , vol.8 , pp. 2653-2656
    • Medina, J.C.1    Shan, B.2    Beckmann, H.3
  • 139
    • 0011471461 scopus 로고    scopus 로고
    • Identification and detection of T138067 metabolites formed in vitro in the presence of rat hepatic subcellular fractions and in vivo in humans
    • 91st Annual Meeting of American Association for Cancer Research San Francisco, USA Abstract 1380
    • YE Q, FRANKMOELLE W, LE H, WRIGHT R, TIMMERMANS PB: Identification and detection of T138067 metabolites formed in vitro in the presence of rat hepatic subcellular fractions and in vivo in humans. 91st Annual Meeting of American Association for Cancer Research San Francisco, USA (2000): Abstract 1380.
    • (2000)
    • Ye, Q.1    Frankmoelle, W.2    Le, H.3    Wright, R.4    Timmermans, P.B.5
  • 140
    • 13044294012 scopus 로고    scopus 로고
    • Selective, covalent modification of β-tubulin residue Cys-239 by T138067, an antitumor agent with in vivo efficacy against multidrug-resistant tumors
    • SHAN B, MEDINA JC, SANTHA E et al.: Selective, covalent modification of β-tubulin residue Cys-239 by T138067, an antitumor agent with in vivo efficacy against multidrug-resistant tumors. Proc. Natl. Acad. Sci. USA (1999) 96:5686-5691.
    • (1999) Proc. Natl. Acad. Sci. USA , vol.96 , pp. 5686-5691
    • Shan, B.1    Medina, J.C.2    Santha, E.3
  • 141
    • 0033526914 scopus 로고    scopus 로고
    • Novel halogenated sulfonamides inhibit the growth of multidrug resistant MCF-7/ADR cancer cells
    • MEDINA JC, ROCHE D, SHAN B et al.: Novel halogenated sulfonamides inhibit the growth of multidrug resistant MCF-7/ADR cancer cells. Bioorg. Med. Chem. Lett. (1999) 9:1843-1846.
    • (1999) Bioorg. Med. Chem. Lett , vol.9 , pp. 1843-1846
    • Medina, J.C.1    Roche, D.2    Shan, B.3
  • 142
    • 0033860012 scopus 로고    scopus 로고
    • Glurathione S-transferase metabolism of the antineoplastic pentafluorophenylsulfonamide in tissue culture and mice
    • FRANKMOELLE WP, MEDINA JC, SHAN B, NARBUT MR, BECKMANN H: Glurathione S-transferase metabolism of the antineoplastic pentafluorophenylsulfonamide in tissue culture and mice. Drug Metabolism Disposition (2000) 28:951-958.
    • (2000) Drug Metabolism Disposition , vol.28 , pp. 951-958
    • Frankmoelle, W.P.1    Medina, J.C.2    Shan, B.3    Narbut, M.R.4    Beckmann, H.5
  • 143
    • 0011454560 scopus 로고    scopus 로고
    • A Phase I study of anti-microtubule agent T138067-sodium administered daily x 5 every 3 weeks
    • 38th Annual Meeting of American Society of Clinical Oncology. Orlando, USA Abstract 415
    • MOLPUS K, SCHWARTZ G, O'DWYER P et al.: A Phase I study of anti-microtubule agent T138067-sodium administered daily x 5 every 3 weeks. 38th Annual Meeting of American Society of Clinical Oncology. Orlando, USA (2002): Abstract 415.
    • (2002)
    • Molpus, K.1    Schwartz, G.2    O'dwyer, P.3
  • 144
    • 0011451455 scopus 로고    scopus 로고
    • A Phase II study of T138067-sodium in patients (pts) with unresectable hepatocellular carcinoma
    • 38th Annual Meeting of American Society of Clinical Oncology Orlando, USA Abstract 572
    • LEUNG TWT, FEUN L, POSEY J, STAGG RJ, LEVY MD, VENOOK AP: A Phase II study of T138067-sodium in patients (pts) with unresectable hepatocellular carcinoma. 38th Annual Meeting of American Society of Clinical Oncology Orlando, USA (2002): Abstract 572.
    • (2002)
    • Leung, T.W.T.1    Feun, L.2    Posey, J.3    Stagg, R.J.4    Levy, M.D.5    Venook, A.P.6
  • 145
    • 0011498579 scopus 로고    scopus 로고
    • A Phase II study T138067-sodium in prior taxane-treated patients (pts) with locally advanced or metastatic non-small cell lung cancer (NSVLC)
    • 38th Annual Meeting of American Society of Clinical Oncology. Orlando, USA Abstract 1282
    • JAHAN TM, SANDLER A, BURRIS H et al.: A Phase II study T138067-sodium in prior taxane-treated patients (pts) with locally advanced or metastatic non-small cell lung cancer (NSVLC). 38th Annual Meeting of American Society of Clinical Oncology. Orlando, USA (2002): Abstract 1282.
    • (2002)
    • Jahan, T.M.1    Sandler, A.2    Burris, H.3
  • 146
    • 0011505609 scopus 로고    scopus 로고
    • Selective, covalent modification of certain β-tubulin isotypes by T900607, a novel antitumor agent with efficacy against multidrug resistant tumors
    • 91st Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 1920
    • BECKMANN H, SANTHA E, LADD A, PARKA, HOUZE J, BAICHWAL V. Selective, covalent modification of certain β-tubulin isotypes by T900607, a novel antitumor agent with efficacy against multidrug resistant tumors. 91st Annual Meeting of American Association for Cancer Research. San Francisco, USA (2000): Abstract 1920.
    • (2000)
    • Beckmann, H.1    Santha, E.2    Ladd, A.3    Parka, A.4    Houze, J.5    Baichwal, V.6
  • 147
    • 0011414061 scopus 로고    scopus 로고
    • Efficacy of the novel tubulin binding agent, T900607, against human tumor xenografts in mice
    • 91st Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 1919
    • SCHWENDER SW, HOFFMAN LA, THOOLEN MJ, CHOU TC, TIMMERMANS PB: Efficacy of the novel tubulin binding agent, T900607, against human tumor xenografts in mice. 91st Annual Meeting of American Association for Cancer Research. San Francisco, USA (2000): Abstract 1919.
    • (2000)
    • Schwender, S.W.1    Hoffman, L.A.2    Thoolen, M.J.3    Chou, T.C.4    Timmermans, P.B.5
  • 148
    • 0011468861 scopus 로고    scopus 로고
    • Efficacy of combination therapy with the tubulin binding agent, T900607, aaginst MX-1 human mammary tumor xenografts in mice
    • 91st Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 1914
    • SCHWENDER SW, HOFFMAN LA, THOOLEN MJ, TIMMERMANS PB: Efficacy of combination therapy with the tubulin binding agent, T900607, aaginst MX-1 human mammary tumor xenografts in mice. 91st Annual Meeting of American Association for Cancer Research. San Francisco, USA (2000): Abstract 1914.
    • (2000)
    • Schwender, S.W.1    Hoffman, L.A.2    Thoolen, M.J.3    Timmermans, P.B.4
  • 149
    • 0011452832 scopus 로고    scopus 로고
    • Pharmacokinetics of T900607 in preclinical species
    • 91st Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 1921
    • WRIGHT MR, YE Q, THOOLEN MJ, KYNCH HD, STEIN CK, TIMMERMANS PB: Pharmacokinetics of T900607 in preclinical species. 91st Annual Meeting of American Association for Cancer Research. San Francisco, USA (2000): Abstract 1921.
    • (2000)
    • Wright, M.R.1    Ye, Q.2    Thoolen, M.J.3    Kynch, H.D.4    Stein, C.K.5    Timmermans, P.B.6
  • 150
    • 0011499751 scopus 로고    scopus 로고
    • A Phase I study of T900607-sodium administered weekly in patients with refractory cancer
    • 38th Annual Meeting of American Society of Clinical Oncology. Orlando, USA Abstract 416
    • CASSIDY J, KILLHAM P, ASIF-SULEMAN S, GIORDANO H, LEVY M, CARMICHAEL J: A Phase I study of T900607-sodium administered weekly in patients with refractory cancer. 38th Annual Meeting of American Society of Clinical Oncology. Orlando, USA (2002): Abstract 416.
    • (2002)
    • Cassidy, J.1    Killham, P.2    Asif-Suleman, S.3    Giordano, H.4    Levy, M.5    Carmichael, J.6
  • 151
    • 0011454951 scopus 로고    scopus 로고
    • T900607-sodium administered daily x 5 as a 60-minute infusion every 3 weeks: A Phase I studt of T900607-sodium in patients (pts) with refractory cancer
    • 38th Annual Meeting of American Society of Clinical Oncology. Orlando, USA Abstract 417
    • LOCKHART AC, MANI S, OLSEN R et al.: T900607-sodium administered daily x 5 as a 60-minute infusion every 3 weeks: a Phase I studt of T900607-sodium in patients (pts) with refractory cancer. 38th Annual Meeting of American Society of Clinical Oncology. Orlando, USA (2002): Abstract 417.
    • (2002)
    • Lockhart, A.C.1    Mani, S.2    Olsen, R.3
  • 152
    • 0011415565 scopus 로고    scopus 로고
    • Efficacy of T138067 and its analogs against resistant tumor cells that express the MDR1 drug pump, have mutation on β-tubulin, or changes in β-tubulin isotype expression patterns
    • 91st Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 1378
    • MEDINA JC, DEXTER DW, BAICHWAL V et al.: Efficacy of T138067 and its analogs against resistant tumor cells that express the MDR1 drug pump, have mutation on β-tubulin, or changes in β-tubulin isotype expression patterns. 91st Annual Meeting of American Association for Cancer Research. San Francisco, USA (2000): Abstract 1378.
    • (2000)
    • Medina, J.C.1    Dexter, D.W.2    Baichwal, V.3
  • 153
    • 0035950186 scopus 로고    scopus 로고
    • Hydrophilic, prodrug analogues of T138067 are efficacious in controlling tumor growth in vivo and show a decreased ability to cross the blood brain barrier
    • RUBENSTEIN SM, BAICHWAL V, BECKMANN H et al.: Hydrophilic, prodrug analogues of T138067 are efficacious in controlling tumor growth in vivo and show a decreased ability to cross the blood brain barrier. J. Med. Chem. (2001) 44:3599-3605.
    • (2001) J. Med. Chem , vol.44 , pp. 3599-3605
    • Rubenstein, S.M.1    Baichwal, V.2    Beckmann, H.3
  • 154
    • 0034652719 scopus 로고    scopus 로고
    • Microtubule distribution induced in vivo by alkylating of β-tubulin by 1-aryl-3-(2-chloroethyl)ureas, a novel class of soft alkylating agents
    • LEGAULT J, JEAN-FRANCOIS G, MOUNETOU E et al.: Microtubule distribution induced in vivo by alkylating of β-tubulin by 1-aryl-3-(2-chloroethyl)ureas, a novel class of soft alkylating agents. Cancer Res. (2000) 60:985-992.
    • (2000) Cancer Res , vol.60 , pp. 985-992
    • Legault, J.1    Jean-Francois, G.2    Mounetou, E.3
  • 155
    • 0035282634 scopus 로고    scopus 로고
    • Antimitotic antitumor agents: Synthesis, structure-activity relationships, and biological characterization of N-aryl-N-(2-chloroethyl)ureas as new selective alkylating agents
    • MOUNETOU E, LEGAULT J, LACROIX J,: Antimitotic antitumor agents: synthesis, structure-activity relationships, and biological characterization of N-aryl-N-(2-chloroethyl)ureas as new selective alkylating agents. J. Med. Chem. (2001) 44:694-702.
    • (2001) J. Med. Chem , vol.44 , pp. 694-702
    • Mounetou, E.1    Legault, J.2    Lacroix, J.3
  • 156
    • 0032403865 scopus 로고    scopus 로고
    • 3-(Iodoacetamido)-benzoylurea: A novel cancericidal tubulin ligand that inhibits microtubule polymerisation, phosphorylates bcl-2, and induces apoptosis in tumor cells
    • JIANG JD, DAVIS AS, MIDDLETON K et al.: 3-(Iodoacetamido)-benzoylurea: a novel cancericidal tubulin ligand that inhibits microtubule polymerisation, phosphorylates bcl-2, and induces apoptosis in tumor cells. Cancer Res. (1998) 58:5389-5395.
    • (1998) Cancer Res , vol.58 , pp. 5389-5395
    • Jiang, J.D.1    Davis, A.S.2    Middleton, K.3
  • 157
    • 0032523959 scopus 로고    scopus 로고
    • Inhibition of microtubule assembly in tumour cells by 3-bromoacetylamino benzoyurea, a new cancericidal compound
    • JIANG JD, WANG Y, ROBOZ J, STRAUCHEN J, HOLLAND JF, BEKESI JG: Inhibition of microtubule assembly in tumour cells by 3-bromoacetylamino benzoyurea, a new cancericidal compound. Cancer Res. (1998) 58:2126-2133.
    • (1998) Cancer Res , vol.58 , pp. 2126-2133
    • Jiang, J.D.1    Wang, Y.2    Roboz, J.3    Strauchen, J.4    Holland, J.F.5    Bekesi, J.G.6
  • 158
    • 0033583499 scopus 로고    scopus 로고
    • A new antitubulin agent containing the benzo[b]thiophene ring system
    • PINNEY KG, BOUNDS AD, DINGEMAN KM et al.: A new antitubulin agent containing the benzo[b]thiophene ring system. Bioorg. Med. Chem. Lett. (1999) 9:1081-1086.
    • (1999) Bioorg. Med. Chem. Lett , vol.9 , pp. 1081-1086
    • Pinney, K.G.1    Bounds, A.D.2    Dingeman, K.M.3
  • 159
    • 0034670589 scopus 로고    scopus 로고
    • Preparation of new antitubulin ligands through a dual-mode, addition-elimination reaction to a bromosubstituted α,β-unsaturated sulfoxide
    • CHEN Z, MOCHARLA VP, FARMER JM, PETTIT GR, HAMEL E, PINNEY KG: Preparation of new antitubulin ligands through a dual-mode, addition-elimination reaction to a bromosubstituted α,β-unsaturated sulfoxide. J. Org. Chem. (2000) 65:8811-8815.
    • (2000) J. Org. Chem , vol.65 , pp. 8811-8815
    • Chen, Z.1    Mocharla, V.P.2    Farmer, J.M.3    Pettit, G.R.4    Hamel, E.5    Pinney, K.G.6
  • 161
    • 0026485639 scopus 로고
    • Mechanism of binding of the new antimitotic drug MDL 27048 to the colchicine site of tubulin: Equilibrium studies
    • PEYROT V, LEYNADIER D, SARRAZIN M et al.: Mechanism of binding of the new antimitotic drug MDL 27048 to the colchicine site of tubulin: equilibrium studies. Biochem. (1992) 31:11125-11132.
    • (1992) Biochem , vol.31 , pp. 11125-11132
    • Peyrot, V.1    Leynadier, D.2    Sarrazin, M.3
  • 162
    • 0032080796 scopus 로고    scopus 로고
    • Potent antimitotic and cell growth inhibitory properties of substituted chalcones
    • DUCKI S, FORREST R, HADFIELD JA et al.: Potent antimitotic and cell growth inhibitory properties of substituted chalcones. Bioorg. Med. Chem. Lett. (1998) 8:1051-1056.
    • (1998) Bioorg. Med. Chem. Lett , vol.8 , pp. 1051-1056
    • Ducki, S.1    Forrest, R.2    Hadfield, J.A.3
  • 164
    • 0034678788 scopus 로고    scopus 로고
    • Antitumor agents. Part 202: novel 2′-amino chalcones: Design, synthesis and biological evaluation
    • XIA Y, YANG Z, XIA P, BASTOW KF, NAKANISHI Y, LEE KH: Antitumor agents. Part 202: novel 2′-amino chalcones: design, synthesis and biological evaluation. Bioorg. Med Chem. Lett. (2000) 10:699-701.
    • (2000) Bioorg. Med Chem. Lett , vol.10 , pp. 699-701
    • Xia, Y.1    Yang, Z.2    Xia, P.3    Bastow, K.F.4    Nakanishi, Y.5    Lee, K.H.6
  • 165
    • 0034885342 scopus 로고    scopus 로고
    • Enhancement of in vivo antitumor activity of a novel antimitotic 1-phenylpropenone derivative, AM-132, by tumor necrosis factor-alpha or interleukin-6
    • TATSUMI Y, ARIOKA H, IKEDA S et al.: Enhancement of in vivo antitumor activity of a novel antimitotic 1-phenylpropenone derivative, AM-132, by tumor necrosis factor-alpha or interleukin-6. Jpn. J. Cancer Res. (2001) 92:768-777.
    • (2001) Jpn. J. Cancer Res , vol.92 , pp. 768-777
    • Tatsumi, Y.1    Arioka, H.2    Ikeda, S.3
  • 166
    • 0030697347 scopus 로고    scopus 로고
    • (-)- Phenylahistin - A new mammalian cell cycle inhibitor produced by Aspergillus ustus
    • KANOH K, KOHNO S, ASARI T et al.: (-)- Phenylahistin - a new mammalian cell cycle inhibitor produced by Aspergillus ustus. Bioorg. Med. Chem. Lett (1997) 7:2847-2852
    • (1997) Bioorg. Med. Chem. Lett , vol.7 , pp. 2847-2852
    • Kanoh, K.1    Kohno, S.2    Asari, T.3
  • 168
    • 0033031908 scopus 로고    scopus 로고
    • (-)-Phenylahistin arrests cells in mitosis by inhibiting tubulin polymerisation
    • KANOH K, KOHNO S, KATADA J, TAKAHASHI J, UNO I: (-)-Phenylahistin arrests cells in mitosis by inhibiting tubulin polymerisation. J. Antibiot. (1999) 52:134-141.
    • (1999) J. Antibiot , vol.52 , pp. 134-141
    • Kanoh, K.1    Kohno, S.2    Katada, J.3    Takahashi, J.4    Uno, I.5
  • 170
    • 0034549484 scopus 로고    scopus 로고
    • Total synthesis of anti-microtubule diketopiperazine derivatives: Phenylahistin and aurantiamine
    • HAYASHI Y, ORIKASA S, TANAKA K, KANOH K, KISO Y: Total synthesis of anti-microtubule diketopiperazine derivatives: phenylahistin and aurantiamine. J. Org. Chem. (2000) 65:8402-8405.
    • (2000) J. Org. Chem , vol.65 , pp. 8402-8405
    • Hayashi, Y.1    Orikasa, S.2    Tanaka, K.3    Kanoh, K.4    Kiso, Y.5
  • 171
    • 0032143275 scopus 로고    scopus 로고
    • Tryprostatin A, a specific and novel inhibitor of microtubule assembly
    • USUI T, KONFOH M, CUI C, MAYUMI T, OSADA H: Tryprostatin A, a specific and novel inhibitor of microtubule assembly. Biochem. J. (1998) 333:543-548.
    • (1998) Biochem. J , vol.333 , pp. 543-548
    • Usui, T.1    Konfoh, M.2    Cui, C.3    Mayumi, T.4    Osada, H.5
  • 172
    • 0033811071 scopus 로고    scopus 로고
    • Synthesis and evaluation of microtubule assembly inhibition and cytotoxicity of prenylated derivatives of cyclo-L-Trp-L-Pro
    • SANZ-CERVERA JF, STOCKING EM, USUI T, OSADA H, WILLIAMS RM: Synthesis and evaluation of microtubule assembly inhibition and cytotoxicity of prenylated derivatives of cyclo-L-Trp-L-Pro. Bioorg. Med. Chem. (2000) 8:2407-2415.
    • (2000) Bioorg. Med. Chem , vol.8 , pp. 2407-2415
    • Sanz-Cervera, J.F.1    Stocking, E.M.2    Usui, T.3    Osada, H.4    Williams, R.M.5
  • 173
    • 0037061593 scopus 로고    scopus 로고
    • Biological activity of the tryprostatins and their diastereomers on human carcinoma cell lines
    • ZHAO S, SMITH KS, DEVEAU AM et al.: Biological activity of the tryprostatins and their diastereomers on human carcinoma cell lines. J. Med. Chem. (2002) 45:1559-1562.
    • (2002) J. Med. Chem , vol.45 , pp. 1559-1562
    • Zhao, S.1    Smith, K.S.2    Deveau, A.M.3
  • 174
    • 0034774026 scopus 로고    scopus 로고
    • Exisulind, a selective apoptotic antineoplastic drug
    • GOLUBOFF ET: Exisulind, a selective apoptotic antineoplastic drug. Exp. Opin. Invest. Drugs (2001) 10:1875-1882.
    • (2001) Exp. Opin. Invest. Drugs , vol.10 , pp. 1875-1882
    • Goluboff, E.T.1
  • 175
    • 0036118264 scopus 로고    scopus 로고
    • Preclinical and clinical studies of docetaxel and exisulind in the treatment of human lung cancer
    • BUNN PA Jr, CHAN DC, EARLE K et al.: Preclinical and clinical studies of docetaxel and exisulind in the treatment of human lung cancer. Semin. Oncol. (2002) 29:87-94.
    • (2002) Semin. Oncol , vol.29 , pp. 87-94
    • Bunn P.A., Jr.1    Chan, D.C.2    Earle, K.3
  • 176
    • 0034234978 scopus 로고    scopus 로고
    • Exisulind induction of apoptosis involves guanosine 3′,5′-cyclic monophosphate phosphodiesterase inhibition, protein kinase G activation, and attenuated beta-catenin
    • THOMPSON WJ, PIAZZA GA, LI H et al.: Exisulind induction of apoptosis involves guanosine 3′,5′-cyclic monophosphate phosphodiesterase inhibition, protein kinase G activation, and attenuated beta-catenin. Cancer Res. (2000) 60:3338-3342.
    • (2000) Cancer Res , vol.60 , pp. 3338-3342
    • Thompson, W.J.1    Piazza, G.A.2    Li, H.3
  • 177
    • 0033755261 scopus 로고    scopus 로고
    • Cyclic GMP mediates apoptosis induced by sulindac derivatives via activation of c-Jun NH2-terminal kinase 1
    • SOH JW, MAO Y, KIM MG et al.: Cyclic GMP mediates apoptosis induced by sulindac derivatives via activation of c-Jun NH2-terminal kinase 1. Clin. Cancer Res. (2000) 6:4136-4141.
    • (2000) Clin. Cancer Res , vol.6 , pp. 4136-4141
    • Soh, J.W.1    Mao, Y.2    Kim, M.G.3
  • 178
    • 0011511498 scopus 로고    scopus 로고
    • G2/M cell cycle arrest by the pro-apoptotic cGMP phosphodiesterase inhibitor, CP248, in SW480 colon cancer cells involves inhibition of tubulin polymerisation via the colchicine binding site
    • 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 1319
    • FETTER JR. WHITEHEAD C, YOON J-T et al.: G2/M cell cycle arrest by the pro-apoptotic cGMP phosphodiesterase inhibitor, CP248, in SW480 colon cancer cells involves inhibition of tubulin polymerisation via the colchicine binding site. 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA (2002). Abstract 1319.
    • (2002)
    • Fetter, J.R.1    Whitehead, C.2    Yoon, J.-T.3
  • 179
    • 0033213814 scopus 로고    scopus 로고
    • Sulindac derivatives inhibit growth and induce apoptosis in human prostate cancer cell lines
    • LIM JT, PIAZZA GA, HAN EK et al.: Sulindac derivatives inhibit growth and induce apoptosis in human prostate cancer cell lines. Biochem. Pharmacol. (1999) 58:1097-1107.
    • (1999) Biochem. Pharmacol , vol.58 , pp. 1097-1107
    • Lim, J.T.1    Piazza, G.A.2    Han, E.K.3
  • 180
    • 17944366045 scopus 로고    scopus 로고
    • Design, synthesis and antiproliferative activity of tripentones: A new series of antitubulin agents
    • LISOWSKI V, ENGUEHARD C, LANCELOT J et al.: Design, synthesis and antiproliferative activity of tripentones: a new series of antitubulin agents. Bioorg. Med. Chem. Lett. (2001) 11:2205-2208.
    • (2001) Bioorg. Med. Chem. Lett , vol.11 , pp. 2205-2208
    • Lisowski, V.1    Enguehard, C.2    Lancelot, J.3
  • 181
    • 0032169560 scopus 로고    scopus 로고
    • Oncocidin A1: A novel tubulin-binding drug with antitumor activity against human breast and ovarian carcinoma xenografts in nude mice
    • CHEN X, PINE P, KNAPP AM, TUSE D, LADEROUTE KR: Oncocidin A1: a novel tubulin-binding drug with antitumor activity against human breast and ovarian carcinoma xenografts in nude mice. Biochem. Pharmacol. (1998) 56:623-633.
    • (1998) Biochem. Pharmacol , vol.56 , pp. 623-633
    • Chen, X.1    Pine, P.2    Knapp, A.M.3    Tuse, D.4    Laderoute, K.R.5
  • 182
    • 4244129619 scopus 로고    scopus 로고
    • Molecular pharmacology of methyl-3,5-diiodo-4 (4′-methoxyphenoxy) benzoate (DIME) and its non-hydrolyzible ethanone analog (DIPE) (Review)
    • KUN E, MENDELEYEV J: Molecular pharmacology of methyl-3,5-diiodo-4 (4′-methoxyphenoxy) benzoate (DIME) and its non-hydrolyzible ethanone analog (DIPE) (Review). Int. J. Mol. Med. (1998) 2:585-590.
    • (1998) Int. J. Mol. Med , vol.2 , pp. 585-590
    • Kun, E.1    Mendeleyev, J.2
  • 183
    • 0034892665 scopus 로고    scopus 로고
    • The novel tubulin-binding drug BTO-956 inhibits R3230Ac mammary carcinoma growth and angiogenesis in Fischer 344 rats
    • SHAN SQ, LOCKHART AC, SAITO WY, KNAPP AM, LADEROUTE KR, DEWHIRST MW: The novel tubulin-binding drug BTO-956 inhibits R3230Ac mammary carcinoma growth and angiogenesis in Fischer 344 rats. Clin. Cancer Res. (2001) 7:2590-2596.
    • (2001) Clin. Cancer Res , vol.7 , pp. 2590-2596
    • Shan, S.Q.1    Lockhart, A.C.2    Saito, W.Y.3    Knapp, A.M.4    Laderoute, K.R.5    Dewhirst, M.W.6
  • 184
    • 0033401285 scopus 로고    scopus 로고
    • Synthesis and antitumor activity of novel pyrimidinyl pyrazole derivatives
    • NAITO H, SUGIMORI M, MITSUI I et al.: Synthesis and antitumor activity of novel pyrimidinyl pyrazole derivatives. Chem. Pharm. Bull. (Tokyo) (1999) 47:1679-1684.
    • (1999) Chem. Pharm. Bull. (Tokyo) , vol.47 , pp. 1679-1684
    • Naito, H.1    Sugimori, M.2    Mitsui, I.3
  • 185
    • 0034093594 scopus 로고    scopus 로고
    • Antiproliferative activity and mechanism of action of DZ-33 58, a novel pyrimidinyl pyrazole derivative
    • IWAHANA M, OCHI Y, EJIMA A. Antiproliferative activity and mechanism of action of DZ-33 58, a novel pyrimidinyl pyrazole derivative. Anticancer Res. (2000) 20:785-792.
    • (2000) Anticancer Res , vol.20 , pp. 785-792
    • Iwahana, M.1    Ochi, Y.2    Ejima, A.3
  • 186
    • 0011723947 scopus 로고    scopus 로고
    • Synthesis and antitumor activity of novel pyrimidinyl pyrazole derivatives. II. optimisation of the phenylpiperazine moiety of 1-[5- mediyl-1-(2 -pyrimidinyl)-4 -pyrazolyl]-3 -phenylpiperainyl-1 -transpropenes
    • NAITO H, OHSUKI S, SUGIMORI M et al.: Synthesis and antitumor activity of novel pyrimidinyl pyrazole derivatives. II. optimisation of the phenylpiperazine moiety of 1-[5-mediyl-1 -(2-pyrimidinyl) -4-pyrazolyl]- 3-phenylpiperainyl -1-transpropenes. Chem. Pharm. Bull. (Tokyo) (2002) 50:453-462.
    • (2002) Chem. Pharm. Bull. (Tokyo) , vol.50 , pp. 453-462
    • Naito, H.1    Ohsuki, S.2    Sugimori, M.3
  • 187
    • 0011475596 scopus 로고    scopus 로고
    • 1-Phenyl-4 -piperazinyl-carbonyl -substituted heterocyclic derivatives-a new class of highly potent compounds with inhibitory effects on the tubulin polymerisation
    • 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 3654
    • GÜNTHER EG, EMIG P, BAASNER S, SCHMIDT P, AUE B, POLYMEROPOULOS E: 1-Phenyl-4 -piperazinyl-carbonyl -substituted heterocyclic derivatives-a new class of highly potent compounds with inhibitory effects on the tubulin polymerisation. 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA (2002). Abstract 3654.
    • (2002)
    • Günther, E.G.1    Emig, P.2    Baasner, S.3    Schmidt, P.4    Aue, B.5    Polymeropoulos, E.6
  • 188
    • 0028044792 scopus 로고
    • Inhibition of microtubules and cell cycle arrest by a new 1-deaza-7,8-dihydropteridine antitumor drug, CI 980, and by its chiral isomer, NSC 613863
    • DE INES C, LEYNADIER D, BARASOAIN I et al.: Inhibition of microtubules and cell cycle arrest by a new 1-deaza-7,8-dihydropteridine antitumor drug, CI 980, and by its chiral isomer, NSC 613863. Cancer Res. (1994) 54:75-84.
    • (1994) Cancer Res , vol.54 , pp. 75-84
    • De Ines, C.1    Leynadier, D.2    Barasoain, I.3
  • 189
    • 0030887268 scopus 로고    scopus 로고
    • Phase I and pharmacological study of CI-980, a novel synthetic antimicrorubule agent
    • ROWINSKY EK, LONG GS, NOE DA et al.: Phase I and pharmacological study of CI-980, a novel synthetic antimicrorubule agent. Clin. Cancer Res. (1997) 3:401-407.
    • (1997) Clin. Cancer Res , vol.3 , pp. 401-407
    • Rowinsky, E.K.1    Long, G.S.2    Noe, D.A.3
  • 190
    • 0033503146 scopus 로고    scopus 로고
    • Phase I and pharmacokinetic study of CI-980 in recurrent pediatric solid tumor cases: A Pediatric Oncology Group study
    • BERNSTEIN ML, BARUCHEL S, DEVINE S et al.: Phase I and pharmacokinetic study of CI-980 in recurrent pediatric solid tumor cases: a Pediatric Oncology Group study. J. Pediatr Hematol. Oncol. (1999) 21:494-500.
    • (1999) J. Pediatr Hematol. Oncol , vol.21 , pp. 494-500
    • Bernstein, M.L.1    Baruchel, S.2    Devine, S.3
  • 191
    • 0030679692 scopus 로고    scopus 로고
    • A phase I trial and pharmacokinetic evaluation of CI-980 in patients with advanced solid tumors
    • SKLARIN NT, LATHIA CD, BENSON L et al.: A phase I trial and pharmacokinetic evaluation of CI-980 in patients with advanced solid tumors. Invest. New Drugs (1997) 15:235-246.
    • (1997) Invest. New Drugs , vol.15 , pp. 235-246
    • Sklarin, N.T.1    Lathia, C.D.2    Benson, L.3
  • 192
    • 0036199652 scopus 로고    scopus 로고
    • A phase II study of CI-980 in previously untreated extensive small cell lung cancer: An Ohio State University phase II research consortium study
    • THOMAS JP, MOORE T, KRAUT EH, BALCERZAK SP, GALLOWAY S, VANDRE DD: A phase II study of CI-980 in previously untreated extensive small cell lung cancer: an Ohio State University phase II research consortium study. Cancer Invest. (2002) 20:192-198.
    • (2002) Cancer Invest , vol.20 , pp. 192-198
    • Thomas, J.P.1    Moore, T.2    Kraut, E.H.3    Balcerzak, S.P.4    Galloway, S.5    Vandre, D.D.6
  • 193
    • 0034857890 scopus 로고    scopus 로고
    • Phase II trial of CI-980 in patients with disseminated malignant melanoma and no prior chemotherapy
    • A Southwest Oncology Group study
    • WHITEHEAD RP, UNGER JM, FLAHERTY LE et al.: Phase II trial of CI-980 in patients with disseminated malignant melanoma and no prior chemotherapy. A Southwest Oncology Group study. Invest. New Drugs (2001) 19:239-243.
    • (2001) Invest. New Drugs , vol.19 , pp. 239-243
    • Whitehead, R.P.1    Unger, J.M.2    Flaherty, L.E.3
  • 194
    • 0031871874 scopus 로고    scopus 로고
    • Phase II study of CI-980 (NSC 635370) in patients with previously treated advanced soft-tissue sarcomas
    • PATEL SR, BURGESS MA, PAPADOPOLOUS NE et al.: Phase II study of CI-980 (NSC 635370) in patients with previously treated advanced soft-tissue sarcomas. Invest. New Drugs (1998) 16:87-92.
    • (1998) Invest. New Drugs , vol.16 , pp. 87-92
    • Patel, S.R.1    Burgess, M.A.2    Papadopolous, N.E.3
  • 195
    • 15444354410 scopus 로고    scopus 로고
    • Phase II study of i.v. CI-980 in patients with advanced platinum refractory epithelial ovarian carcinoma
    • KUDELKA AP, HASENBURG A, VERSCHRAEGEN CF et al.: Phase II study of i.v. CI-980 in patients with advanced platinum refractory epithelial ovarian carcinoma. Anticancer Drugs (1998) 9:405-409.
    • (1998) Anticancer Drugs , vol.9 , pp. 405-409
    • Kudelka, A.P.1    Hasenburg, A.2    Verschraegen, C.F.3
  • 196
    • 0030725152 scopus 로고    scopus 로고
    • Phase II trial of intravenous CI-980 (NSC 370147) in patients with metastatic coloreccal carcinoma. Model for prospective evaluation of neurotoxicity
    • PAZDUR R, MEYERS C, DIAZ-CANTON E et al.: Phase II trial of intravenous CI-980 (NSC 370147) in patients with metastatic coloreccal carcinoma. Model for prospective evaluation of neurotoxicity. Am. J. Clin. Oncol. (1997) 20:573-576.
    • (1997) Am. J. Clin. Oncol , vol.20 , pp. 573-576
    • Pazdur, R.1    Meyers, C.2    Diaz-Canton, E.3
  • 197
    • 0032033637 scopus 로고    scopus 로고
    • Discovery of podophyllotoxins
    • IMBERT TF: Discovery of podophyllotoxins. Biochim. (1998) 80:207-222.
    • (1998) Biochim , vol.80 , pp. 207-222
    • Imbert, T.F.1
  • 198
    • 0031913357 scopus 로고    scopus 로고
    • Structure-activity analysis of the interaction of curacin A, the potent colchicine site antimitotic agent, with tubulin and effects of analogs on the growth of MCF-7 breast cancer cells
    • VERDIER-PINARD P, LAI JY, YOO HD et al.: Structure-activity analysis of the interaction of curacin A, the potent colchicine site antimitotic agent, with tubulin and effects of analogs on the growth of MCF-7 breast cancer cells. Mol. Pharmacol. (1998) 53:62-76.
    • (1998) Mol. Pharmacol , vol.53 , pp. 62-76
    • Verdier-Pinard, P.1    Lai, J.Y.2    Yoo, H.D.3
  • 199
    • 0033214211 scopus 로고    scopus 로고
    • Biosynthesis of radiolabeled curacin A and its rapid and apparently irreversible binding to the colchicine site of tubulin
    • VERDIER-PINARD P, SITACHITTA N, ROSSI JV, SACKETT DL, GERWICK WH, HAMEL E: Biosynthesis of radiolabeled curacin A and its rapid and apparently irreversible binding to the colchicine site of tubulin. Arch. Biochem. Biophy. (1999) 370:51-58.
    • (1999) Arch. Biochem. Biophy , vol.370 , pp. 51-58
    • Verdier-Pinard, P.1    Sitachitta, N.2    Rossi, J.V.3    Sackett, D.L.4    Gerwick, W.H.5    Hamel, E.6
  • 200
    • 0037171849 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of structurally highly modified analogues of the antimitotic natural product curacin A
    • WIPF P, REEVES JT, BALACHANDRAN R, DAY BW: Synthesis and biological evaluation of structurally highly modified analogues of the antimitotic natural product curacin A. J. Med. Chem. (2002) 45:1901-1917.
    • (2002) J. Med. Chem , vol.45 , pp. 1901-1917
    • Wipf, P.1    Reeves, J.T.2    Balachandran, R.3    Day, B.W.4
  • 201
    • 0034048658 scopus 로고    scopus 로고
    • RPR112378 and RPR115781: Two representatives of a new family of microtubule assembly inhibitors
    • COMBEAU C, PROVOST J, LANCELIN F et al.: RPR112378 and RPR115781: two representatives of a new family of microtubule assembly inhibitors. Mol. Pharmacol. (2000) 57:553-563.
    • (2000) Mol. Pharmacol , vol.57 , pp. 553-563
    • Combeau, C.1    Provost, J.2    Lancelin, F.3
  • 202
    • 0029008622 scopus 로고
    • Synthesis, antitubulin and antimitotic activity, and cytotoxicity of analogs of 2-methoxyestradiol, an endogenous mammalian metabolite of estradiol that inhibits tubulin polymerisation by binding to the colchicine binding site
    • CUSHMAN M, HE HM, KATZENELLENBOGEN JA, LIN CM, HAMEL E: Synthesis, antitubulin and antimitotic activity, and cytotoxicity of analogs of 2-methoxyestradiol, an endogenous mammalian metabolite of estradiol that inhibits tubulin polymerisation by binding to the colchicine binding site. J. Med. Chem. (1995) 38:2041-2049.
    • (1995) J. Med. Chem , vol.38 , pp. 2041-2049
    • Cushman, M.1    He, H.M.2    Katzenellenbogen, J.A.3    Lin, C.M.4    Hamel, E.5
  • 204
    • 0030767873 scopus 로고    scopus 로고
    • Synthesis of analogs of 2-mcthoxyestradiol with enhanced inhibitory effects on tubulin polymerisation and cancer cell growth
    • CUSHMAN M, HE HM, KATZENELLENBOGEN JA et al.: Synthesis of analogs of 2-mcthoxyestradiol with enhanced inhibitory effects on tubulin polymerisation and cancer cell growth. J. Med. Chem. (1997) 40:2323-2334.
    • (1997) J. Med. Chem , vol.40 , pp. 2323-2334
    • Cushman, M.1    He, H.M.2    Katzenellenbogen, J.A.3
  • 205
    • 0033918981 scopus 로고    scopus 로고
    • Synthesis of B ring homologated estradiol analogues that modulate tubulin polymerisation and microtubule stability
    • WANG Z, YANG D, MOHANAKRISHNAN AK et al.: Synthesis of B ring homologated estradiol analogues that modulate tubulin polymerisation and microtubule stability. J. Med. Chem. (2000) 43:2419-2429.
    • (2000) J. Med. Chem , vol.43 , pp. 2419-2429
    • Wang, Z.1    Yang, D.2    Mohanakrishnan, A.K.3
  • 206
    • 0036139263 scopus 로고    scopus 로고
    • In vitro and in vivo activity of LS 4477 and LS 4559, novel analogues of the tubulin binder estramustine
    • NICHOLSON KM, PHILLIPS RM, SHNYDER SD, BIBBY MC: In vitro and in vivo activity of LS 4477 and LS 4559, novel analogues of the tubulin binder estramustine. Eur. J. Cancer (2002) 38:194-204.
    • (2002) Eur. J. Cancer , vol.38 , pp. 194-204
    • Nicholson, K.M.1    Phillips, R.M.2    Shnyder, S.D.3    Bibby, M.C.4
  • 207
    • 0034858240 scopus 로고    scopus 로고
    • Vinflunine, a second generation novel Vinca alkaloid with a distinctive pharmacological profile, now in clinical development and prospects for future mitotic blockcrs
    • HILL BT: Vinflunine, a second generation novel Vinca alkaloid with a distinctive pharmacological profile, now in clinical development and prospects for future mitotic blockcrs. Curr. Pharm. Des. (2001) 7:1199-1212.
    • (2001) Curr. Pharm. Des , vol.7 , pp. 1199-1212
    • Hill, B.T.1
  • 208
    • 0034581185 scopus 로고    scopus 로고
    • Energetics of Vinca alkaloid interactions with tubulin
    • LOBERT S, CORREIA JJ: Energetics of Vinca alkaloid interactions with tubulin. Methods Enzymol. (2000) 323:77-103.
    • (2000) Methods Enzymol , vol.323 , pp. 77-103
    • Lobert, S.1    Correia, J.J.2
  • 209
    • 0034856849 scopus 로고    scopus 로고
    • Cryptophycins: A novel class of potent antimitotic antitumor depsipeptides
    • SHIH C, TEICHER BA: Cryptophycins: a novel class of potent antimitotic antitumor depsipeptides. Curr. Pharm. Des. (2001) 7:1259-1276.
    • (2001) Curr. Pharm. Des , vol.7 , pp. 1259-1276
    • Shih, C.1    Teicher, B.A.2
  • 210
    • 0001466422 scopus 로고    scopus 로고
    • Antimitotic agents
    • DeVita VT, Hellman S, Rosenberg SA (Eds), Lippincott-Raven, Philadelphia
    • ROWINSKY EK, DONEHOWER RC: Antimitotic agents. In: Cancer: Principles and Practice of Oncology DeVita VT, Hellman S, Rosenberg SA (Eds), Lippincott-Raven, Philadelphia (1997):468-472.
    • (1997) Cancer: Principles and Practice of Oncology , pp. 468-472
    • Rowinsky, E.K.1    Donehower, R.C.2
  • 211
    • 0034741810 scopus 로고    scopus 로고
    • Modifications in the "upper" velbenamine part of the Vinca alkaloids have major implications for tubulin interacting activities
    • FAHY J: Modifications in the "upper" velbenamine part of the Vinca alkaloids have major implications for tubulin interacting activities. Curr. Pharm. Des. (2001) 7:1181-1197.
    • (2001) Curr. Pharm. Des , vol.7 , pp. 1181-1197
    • Fahy, J.1
  • 212
    • 0034074996 scopus 로고    scopus 로고
    • Vinorelbine-a clinical review
    • GREGORY RK, SMITH I: Vinorelbine-a clinical review. Br. J. Cancer (2000) 82:1907-1913.
    • (2000) Br. J. Cancer , vol.82 , pp. 1907-1913
    • Gregory, R.K.1    Smith, I.2
  • 213
    • 0011407555 scopus 로고    scopus 로고
    • Phase I evaluation of anhydrovinblastine in patients with advanced malignancies
    • 91st Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 3895
    • SCHWARTZ GN, BONG D, LEICHMAN CG, LEICHMAN LL: Phase I evaluation of anhydrovinblastine in patients with advanced malignancies. 91st Annual Meeting of American Association for Cancer Research. San Francisco, USA (2000): Abstract 3895.
    • (2000)
    • Schwartz, G.N.1    Bong, D.2    Leichman, C.G.3    Leichman, L.L.4
  • 214
    • 0011498580 scopus 로고    scopus 로고
    • A Phase I and pharmacokinetic study of anhydrovinblastine
    • 38th Annual Meeting of American Society of Clinical Ontology Orlando, USA Abstract 421
    • RAMNATH N, SCHWARTZ GN, BOOKER B et al.: A Phase I and pharmacokinetic study of anhydrovinblastine. 38th Annual Meeting of American Society of Clinical Ontology Orlando, USA (2002): Abstract 421.
    • (2002)
    • Ramnath, N.1    Schwartz, G.N.2    Booker, B.3
  • 215
    • 0034773326 scopus 로고    scopus 로고
    • Vinflunine, the latest Vinca alkaloid in clinical development. A review of its preclinical anticancer properties
    • KRUCZYNSKI A, HILL BT: Vinflunine, the latest Vinca alkaloid in clinical development. A review of its preclinical anticancer properties. Critical Rev. Oncology-Hematology (2001) 40:159-173.
    • (2001) Critical Rev. Oncology-Hematology , vol.40 , pp. 159-173
    • Kruczynski, A.1    Hill, B.T.2
  • 216
    • 0031780236 scopus 로고    scopus 로고
    • A comparison of thermodynamic parameters for vinorelbine-and vinflunine-induced tubulin self-association by sedimentation velocity
    • LOBERT S, INGRAM JW, HILL BT, CORREIA JJ: A comparison of thermodynamic parameters for vinorelbine-and vinflunine-induced tubulin self-association by sedimentation velocity. Mol. Pharmacol. (1998) 53:908-915.
    • (1998) Mol. Pharmacol , vol.53 , pp. 908-915
    • Lobert, S.1    Ingram, J.W.2    Hill, B.T.3    Correia, J.J.4
  • 217
    • 0011505764 scopus 로고    scopus 로고
    • Phase I trial of vinflunine (L0070) a novel fluorinated Vinca alkaloid in patients (pts) with advanced solid malignancies: Final results
    • 92nd Annual Meeting of American Association for Cancer Research. Orlando, USA Abstract 4478
    • FUMOLEAU P, RAYMOND E, BENNOUNA J et al.: Phase I trial of vinflunine (L0070) a novel fluorinated Vinca alkaloid in patients (pts) with advanced solid malignancies: final results. 92nd Annual Meeting of American Association for Cancer Research. Orlando, USA (2001): Abstract 4478.
    • (2001)
    • Fumoleau, P.1    Raymond, E.2    Bennouna, J.3
  • 218
    • 0011417727 scopus 로고    scopus 로고
    • Significant antiangiogenic activity and marked inhibition of growth of an orthotopic colon cancer model and colon liver metastases by vinflunine, the most recent Vinca alkaloid in clinical development
    • 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 1332
    • KRUCZYNSKI A, RICOME C, ASTRUC J et al.: Significant antiangiogenic activity and marked inhibition of growth of an orthotopic colon cancer model and colon liver metastases by vinflunine, the most recent Vinca alkaloid in clinical development. 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA (2002): Abstract 1332.
    • (2002)
    • Kruczynski, A.1    Ricome, C.2    Astruc, J.3
  • 219
    • 0035214366 scopus 로고    scopus 로고
    • A new bis-indole, KARs, induces selective M arrest with specific spindle aberration in neuroblastoma cell line SH-SY5Y
    • COMIN-ANDUIX B, AGELL N, BACHS O, OVADI J, CASCANTE M: A new bis-indole, KARs, induces selective M arrest with specific spindle aberration in neuroblastoma cell line SH-SY5Y. Mol. Pharmacol. (2001) 60:1235-1242.
    • (2001) Mol. Pharmacol , vol.60 , pp. 1235-1242
    • Comin-Anduix, B.1    Agell, N.2    Bachs, O.3    Ovadi, J.4    Cascante, M.5
  • 220
    • 9844224483 scopus 로고    scopus 로고
    • Discovery of cryptophycin-1 and BCN-183577: Examples of strategies and problems in the detection of antitumor activity in mice
    • CORBETT TH, VALERIOTE FA, DEMCHIK L et al.: Discovery of cryptophycin-1 and BCN-183577: examples of strategies and problems in the detection of antitumor activity in mice. Invest. New Drugs (1997) 15:207-218.
    • (1997) Invest. New Drugs , vol.15 , pp. 207-218
    • Corbett, T.H.1    Valeriote, F.A.2    Demchik, L.3
  • 221
    • 0032482920 scopus 로고    scopus 로고
    • Antiproliferative mechanism of action of cryptophycin-52: Kinetic stabilization of microtubule dynamics by high-affinity binding to microrubule ends
    • PANDA D, DELUCA K, WILLLAMS D, JORDAN MA, WILSON L: Antiproliferative mechanism of action of cryptophycin-52: kinetic stabilization of microtubule dynamics by high-affinity binding to microrubule ends. Proc. Natl. Acad. Sci. USA (1998) 95:9313-9318.
    • (1998) Proc. Natl. Acad. Sci. USA , vol.95 , pp. 9313-9318
    • Panda, D.1    Deluca, K.2    Willlams, D.3    Jordan, M.A.4    Wilson, L.5
  • 223
    • 0034913052 scopus 로고    scopus 로고
    • Cryptophycin-induced hyperphosphorylation of Bcl-2, cell cycle arrest and growth inhibition in human H460 NSCLC cells
    • LU K, DEMPSEY J, SCHULTZ RM, SHIH C, TEICHER BA: Cryptophycin-induced hyperphosphorylation of Bcl-2, cell cycle arrest and growth inhibition in human H460 NSCLC cells. Cancer Chemother. Pharmacol. (2001) 47:170-178.
    • (2001) Cancer Chemother. Pharmacol , vol.47 , pp. 170-178
    • Lu, K.1    Dempsey, J.2    Schultz, R.M.3    Shih, C.4    Teicher, B.A.5
  • 224
    • 0036181751 scopus 로고    scopus 로고
    • The cryptophycins: Their synthesis and anticancer activity
    • EGGEN M, GEORG GI: The cryptophycins: their synthesis and anticancer activity. Med. Res. Rev. (2002) 22:85-101.
    • (2002) Med. Res. Rev , vol.22 , pp. 85-101
    • Eggen, M.1    Georg, G.I.2
  • 225
    • 0003373485 scopus 로고    scopus 로고
    • A Phase II study of LY355703 (cryptophycin) as first-line therapy for stage IIIb or IV NCSLC subjects: Preliminary analysis
    • GOTH G, SCHOTT K, OHNMACHT U, MANEGOLD C, GATZEMEIER U: A Phase II study of LY355703 (cryptophycin) as first-line therapy for stage IIIb or IV NCSLC subjects: preliminary analysis. Eur. J. Cancer (2001) 37:S48.
    • (2001) Eur. J. Cancer , vol.37
    • Goth, G.1    Schott, K.2    Ohnmacht, U.3    Manegold, C.4    Gatzemeier, U.5
  • 226
    • 0011511501 scopus 로고    scopus 로고
    • Salvage therapy with cryptophycin-52 (C52) in platinum-treated non-small cell lung cancer (NSCLC)
    • 38th Annud Meeting of American Society of Clinical Oncology. Orlando, USA Abstract 2688
    • HAUSNER PF, EDELMAN MJ, DESANTO J, DOYLE LA, GRANDARA DR, ISRAEL V: Salvage therapy with cryptophycin-52 (C52) in platinum-treated non-small cell lung cancer (NSCLC). 38th Annud Meeting of American Society of Clinical Oncology. Orlando, USA (2002): Abstract 2688.
    • (2002)
    • Hausner, P.F.1    Edelman, M.J.2    Desanto, J.3    Doyle, L.A.4    Grandara, D.R.5    Israel, V.6
  • 227
    • 0032993329 scopus 로고    scopus 로고
    • The discovery and development of marine compounds with pharmaceutical potential
    • MUNRO MH, BLUNT JW. DUMDEI EJ et al.: The discovery and development of marine compounds with pharmaceutical potential. J. Biotechnol. (1999) 70:15-25.
    • (1999) J. Biotechnol , vol.70 , pp. 15-25
    • Munro, M.H.1    Blunt, J.W.2    Dumdei, E.J.3
  • 228
    • 0035110756 scopus 로고    scopus 로고
    • In vitro and in vivo anticancer activities of synthetic macrocyclic ketone analogues of halichondrin B
    • TOWLE MJ, SALVATO KA, BUDROW J et al.: In vitro and in vivo anticancer activities of synthetic macrocyclic ketone analogues of halichondrin B. Cancer Res. (2001) 61:1013-1021.
    • (2001) Cancer Res , vol.61 , pp. 1013-1021
    • Towle, M.J.1    Salvato, K.A.2    Budrow, J.3
  • 229
    • 0011413737 scopus 로고    scopus 로고
    • In vivo anticancer activity of synthetic halichondrin B macrocyclic ketone analogs ER-076349 and ER-086526 correlates with ability to induce irreversible mitotic blocks
    • 92nd Annual Meeting of American Association for Cancer Research. New Orleans, USA Abstract 1976
    • TOWLE MJ, SALVATO KA, BUDROW J et al.: In vivo anticancer activity of synthetic halichondrin B macrocyclic ketone analogs ER-076349 and ER-086526 correlates with ability to induce irreversible mitotic blocks. 92nd Annual Meeting of American Association for Cancer Research. New Orleans, USA (2001). Abstract 1976.
    • (2001)
    • Towle, M.J.1    Salvato, K.A.2    Budrow, J.3
  • 230
    • 0035798205 scopus 로고    scopus 로고
    • A total synthesis of (-)-hemiasterlin using N-Bts methodology
    • VEDEJS E, KONGKITTINGAM C: A total synthesis of (-)-hemiasterlin using N-Bts methodology. J. Org. Chem. (2001) 66:7355-7364.
    • (2001) J. Org. Chem , vol.66 , pp. 7355-7364
    • Vedejs, E.1    Kongkittingam, C.2
  • 231
    • 0032769659 scopus 로고    scopus 로고
    • Cytotoxic and tubulin-interactive hemiasterlins from Auletta sp. and Siphonochalina spp. sponges
    • GAMBLE WR, DURSO NA, FULLER RW et al.: Cytotoxic and tubulin-interactive hemiasterlins from Auletta sp. and Siphonochalina spp. sponges. Bioorg. Med. Chem. (1999) 7:1611-1615.
    • (1999) Bioorg. Med. Chem , vol.7 , pp. 1611-1615
    • Gamble, W.R.1    Durso, N.A.2    Fuller, R.W.3
  • 232
    • 0033607202 scopus 로고    scopus 로고
    • Interactions of the sponge-derived antimitotic tripeptide hemiasterlin with tubulin: Comparison with dolastatin 10 and cryptophycin 1
    • BAI R, DURSO NA, SACKETT DL, HAMEL E: Interactions of the sponge-derived antimitotic tripeptide hemiasterlin with tubulin: comparison with dolastatin 10 and cryptophycin 1. Biochem. (1999) 38:14302-14310.
    • (1999) Biochem , vol.38 , pp. 14302-14310
    • Bai, R.1    Durso, N.A.2    Sackett, D.L.3    Hamel, E.4
  • 233
    • 0011414063 scopus 로고    scopus 로고
    • Synthesis and biogical activity of analogs of the and microtubule agent HTI-286
    • 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 3653
    • ZASK A, BIRNBURG G, CHEUNG K et al.: Synthesis and biogical activity of analogs of the and microtubule agent HTI-286. 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA (2002):Abstract 3653.
    • (2002)
    • Zask, A.1    Birnburg, G.2    Cheung, K.3
  • 234
    • 0011505612 scopus 로고    scopus 로고
    • HTI-286, a synthetic analog of the antimicrotubule tripeptide hemiasterlin, potently inhibits growth of cultured tumor cells, overcomes resistance to paclitaxel mediated by various mechanisms, and demonstrates intravenous and oral in vivo efficacy
    • 93rd Annual Meeting of American Association for Cancer Research San Francisco, USA Abstract 1316
    • LOGANZO F, DISCAFANI C, ANNABLE T et al.: HTI-286, a synthetic analog of the antimicrotubule tripeptide hemiasterlin, potently inhibits growth of cultured tumor cells, overcomes resistance to paclitaxel mediated by various mechanisms, and demonstrates intravenous and oral in vivo efficacy. 93rd Annual Meeting of American Association for Cancer Research San Francisco, USA (2002)-Abstract 1316.
    • (2002)
    • Loganzo, F.1    Discafani, C.2    Annable, T.3
  • 235
    • 0032925417 scopus 로고    scopus 로고
    • The dolastatins, a family of promising antineoplastic agents
    • PONCET J: The dolastatins, a family of promising antineoplastic agents. Curr. Pharm. Des. (1999) 5:139-162.
    • (1999) Curr. Pharm. Des , vol.5 , pp. 139-162
    • Poncet, J.1
  • 236
    • 0032950658 scopus 로고    scopus 로고
    • Accivity of dolastatin 10 against small-cell lung cancer in vitro and in vivo: Induction of apoptosis and bcl-2 modification
    • KALEMKERIAN GP, OU X, ADIL MR et al.: Accivity of dolastatin 10 against small-cell lung cancer in vitro and in vivo: induction of apoptosis and bcl-2 modification. Cancer Chemother: Pharmacol. (1999) 43:507-515.
    • (1999) Cancer Chemother: Pharmacol , vol.43 , pp. 507-515
    • Kalemkerian, G.P.1    Ou, X.2    Adil, M.R.3
  • 237
    • 0033760668 scopus 로고    scopus 로고
    • Induction of apoptosis in human cancer cells by TZT-1027, an antimicrotubule agent
    • WATANABE J, NATSUME T, FUJIO N, MIYASAKA K, KOBAYASHI M: Induction of apoptosis in human cancer cells by TZT-1027, an antimicrotubule agent. Apoptosis (2000) 5:345-353.
    • (2000) Apoptosis , vol.5 , pp. 345-353
    • Watanabe, J.1    Natsume, T.2    Fujio, N.3    Miyasaka, K.4    Kobayashi, M.5
  • 238
    • 0029953141 scopus 로고    scopus 로고
    • Antitumour evaluation of dolastatins 10 and 15 and their measurement in plasma by radioimmunoassay
    • AHERNE GW, HARDCASTLE A, VALENTI M et al.: Antitumour evaluation of dolastatins 10 and 15 and their measurement in plasma by radioimmunoassay. Cancer Chemother. Pharmacol. (1996) 38:225-232.
    • (1996) Cancer Chemother. Pharmacol , vol.38 , pp. 225-232
    • Aherne, G.W.1    Hardcastle, A.2    Valenti M. et, al.3
  • 240
    • 0036192228 scopus 로고    scopus 로고
    • Preclinical study of dolastatin-10 in dogs with spontaneous neoplasia
    • THAMM DH, MACEWEN EG, PHILLIPS BS et al.: Preclinical study of dolastatin-10 in dogs with spontaneous neoplasia. Cancer Chemother. Pharmacol. (2002) 49:251-255.
    • (2002) Cancer Chemother. Pharmacol , vol.49 , pp. 251-255
    • Thamm, D.H.1    Macewen, E.G.2    Phillips, B.S.3
  • 241
    • 0032611152 scopus 로고    scopus 로고
    • Clinical trials referral resource. Clinical trials of dolastatin-10
    • WRIGHT JJ, BLATNER G, CHESON BD: Clinical trials referral resource. Clinical trials of dolastatin-10. Oncol (Huntington) (1999) 13:68-70.
    • (1999) Oncol. (Huntington) , vol.13 , pp. 68-70
    • Wright, J.J.1    Blatner, G.2    Cheson, B.D.3
  • 242
    • 0034093431 scopus 로고    scopus 로고
    • Phase II study of dolastatin-10 in patients with advanced non-small-cell lung cancer
    • KRUG LM, MILLER VA, KALEMKERIAN GP et al.: Phase II study of dolastatin-10 in patients with advanced non-small-cell lung cancer. Annals Oncol. (2000) 11:227-228.
    • (2000) Annals Oncol , vol.11 , pp. 227-228
    • Krug, L.M.1    Miller, V.A.2    Kalemkerian, G.P.3
  • 243
    • 0011511503 scopus 로고    scopus 로고
    • Phase I study of TZT-1027, an inhibitor of tubulin polymerisation, given weekly x 3 as a 1-hour intravenous infusion in patients (PTS) with solid tumors
    • 38th Annual Meeting of American Society of Clinical Oncology. Onlardo, USA Abstract 420
    • YAMAMOTO N, ANDOH M, KAWAHARA M, FUKUOKA M, NIITANI H: Phase I study of TZT-1027, an inhibitor of tubulin polymerisation, given weekly x 3 as a 1-hour intravenous infusion in patients (PTS) with solid tumors. 38th Annual Meeting of American Society of Clinical Oncology. Onlardo, USA (2002)-Abstract 420.
    • (2002)
    • Yamamoto, N.1    Andoh, M.2    Kawahara, M.3    Fukuoka, M.4    Niitani, H.5
  • 244
    • 0011409191 scopus 로고    scopus 로고
    • Preliminary result of a Phase I trial of TZT-1027, an inhibitor of tubulin polymerisation, in patients with advanced non-small cell lung cancer
    • 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 2744
    • HORTI J: Preliminary result of a Phase I trial of TZT-1027, an inhibitor of tubulin polymerisation, in patients with advanced non-small cell lung cancer. 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA (2002):Abstract 2744.
    • (2002)
    • Horti, J.1
  • 245
    • 0033041116 scopus 로고    scopus 로고
    • NO AUTHORS LISTED: TZT-1027
    • NO AUTHORS LISTED: TZT-1027. Drugs Fut. (1999) 24:404-409.
    • (1999) Drugs Fut , vol.24 , pp. 404-409
  • 246
    • 0032759955 scopus 로고    scopus 로고
    • Synthesis and cytostatic properties of structure-simplified analogs of dolastatin 15
    • HU MK, HUANG WS: Synthesis and cytostatic properties of structure-simplified analogs of dolastatin 15. J. Peptide Res. (1999) 54:460-467.
    • (1999) J. Peptide Res , vol.54 , pp. 460-467
    • Hu, M.K.1    Huang, W.S.2
  • 247
    • 0029013101 scopus 로고
    • LU103793 (NSC D669356): A synthetic peptide that interacts with microtubules and inhibits mitosis
    • DE ARRUDA M, COCCHIARO CA, NELSON CM et al.: LU103793 (NSC D669356): a synthetic peptide that interacts with microtubules and inhibits mitosis. Cancer Res. (1995) 55:3085-3092.
    • (1995) Cancer Res , vol.55 , pp. 3085-3092
    • De Arruda, M.1    Cocchiaro, C.A.2    Nelson, C.M.3
  • 248
    • 0035008045 scopus 로고    scopus 로고
    • Activity of the dolastatin analogue, LU103793, in malignant melanoma
    • SMYTH J, BONETERRE ME, SCHELLENS J et al.: Activity of the dolastatin analogue, LU103793, in malignant melanoma. Ann. Oncol, (2001) 12:509-511.
    • (2001) Ann. Oncol , vol.12 , pp. 509-511
    • Smyth, J.1    Boneterre, M.E.2    Schellens, J.3
  • 249
    • 0011405615 scopus 로고    scopus 로고
    • Preclinical pharmacology of LU223651, orally available analog of cemadotin HCl
    • 90st Annual Meeting of American Association for Cancer Research. Philadelphia, USA Abstract 1908
    • NELSON CM, CONLON D, SMITH PA et al.: Preclinical pharmacology of LU223651, orally available analog of cemadotin HCl. 90st Annual Meeting of American Association for Cancer Research. Philadelphia, USA (1999):Abstract 1908.
    • (1999)
    • Nelson, C.M.1    Conlon, D.2    Smith, P.A.3
  • 250
    • 0011505613 scopus 로고    scopus 로고
    • Oral antitumor activity of dalastatin 15 analog, LU223651, against human ovarian carcinoma xenografts
    • 91st Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 1927
    • NICOLETTI MI, TURATTO M, MARTINELLI M, RARLOZZARI T, GIAVAZZI R. Oral antitumor activity of dalastatin 15 analog, LU223651, against human ovarian carcinoma xenografts. 91st Annual Meeting of American Association for Cancer Research. San Francisco, USA (2000):Abstract 1927.
    • (2000)
    • Nicoletti, M.I.1    Turatto, M.2    Martinelli, M.3    Rarlozzari, T.4    Giavazzi, R.5
  • 251
    • 0011415567 scopus 로고    scopus 로고
    • A Phase I clinical trial of ILX651, a dolastatin-15 analog, administered as a 30-minute intravenous infusion every other day x 3 doses every 21 days in patients with advanced solid tumors
    • 38th Annual Meeting of American Association of Clinical Research. Orlando, USA Abstract 414
    • MICHAELSON MD, RYAN DP, FRAM R et al.: A Phase I clinical trial of ILX651, a dolastatin-15 analog, administered as a 30-minute intravenous infusion every other day x 3 doses every 21 days in patients with advanced solid tumors. 38th Annual Meeting of American Association of Clinical Research. Orlando, USA (2002):Abstract 414.
    • (2002)
    • Michaelson, M.D.1    Ryan, D.P.2    Fram, R.3
  • 252
    • 0011406557 scopus 로고    scopus 로고
    • A Phase I and pharmacokinetic study of the dolastatin 15 analog ILX651
    • 38th Annual Meeting of American Association of Clinical Research Orlando, USA Abstract 1743
    • EBBINGHAUS SW, DUNN H, JENNINGS L, DIJK SV, FRAM R:A Phase I and pharmacokinetic study of the dolastatin 15 analog ILX651. 38th Annual Meeting of American Association of Clinical Research Orlando, USA (2002):Abstract 1743.
    • (2002)
    • Ebbinghaus, S.W.1    Dunn, H.2    Jennings, L.3    Dijk, S.V.4    Fram, R.5
  • 253
    • 0032539565 scopus 로고    scopus 로고
    • Opium alkaloid noscapine is an antitumor agent that arrests metaphase and induces apoptosis in dividing cells
    • YE K, KE Y, KESHAVA N et al.: Opium alkaloid noscapine is an antitumor agent that arrests metaphase and induces apoptosis in dividing cells. Proc. Natl. Acad Sci. USA (1998) 95:1601-1606.
    • (1998) Proc. Natl. Acad Sci. USA , vol.95 , pp. 1601-1606
    • Ye, K.1    Ke, Y.2    Keshava, N.3
  • 254
    • 0035861653 scopus 로고    scopus 로고
    • Sustained activation of p34(cdc2) is required for noscapine-induced apoptosis
    • YE K, ZHOU J, LANDEN JW, BRADBURY EM, JOSHI HC: Sustained activation of p34(cdc2) is required for noscapine-induced apoptosis. J. Biol. Chem. (2001) 276:46697-46700.
    • (2001) J. Biol. Chem , vol.276 , pp. 46697-46700
    • Ye, K.1    Zhou, J.2    Landen, J.W.3    Bradbury, E.M.4    Joshi, H.C.5
  • 255
    • 0344959399 scopus 로고    scopus 로고
    • Noscapine hydrochloride disrupts the mitotic spindle in mammalian cells and induces aneuploidy as well as polyploidy in cultured human lymphocytes
    • SCHULER M, MUEHLBAUER P, GUZZIE P, EASTMOND DA: Noscapine hydrochloride disrupts the mitotic spindle in mammalian cells and induces aneuploidy as well as polyploidy in cultured human lymphocytes. Mutagenesis (1999) 14:51-56.
    • (1999) Mutagenesis , vol.14 , pp. 51-56
    • Schuler, M.1    Muehlbauer, P.2    Guzzie, P.3    Eastmond, D.A.4
  • 256
    • 4243989145 scopus 로고    scopus 로고
    • The microtubule inhibitor noscapine for the treatment of glioblastoma in immunodefficient mice
    • 92nd Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 1361
    • LANDEN JW ARCHER DR, DAVIS TP, WAINER BH, JOSHI HC: The microtubule inhibitor noscapine for the treatment of glioblastoma in immunodefficient mice. 92nd Annual Meeting of American Association for Cancer Research. San Francisco, USA (2000):Abstract 1361.
    • (2000)
    • Landen, J.W.1    Archer, D.R.2    Davis, T.P.3    Wainer, B.H.4    Joshi, H.C.5
  • 257
    • 0035924176 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of myoseverin derivatives: Microtubule assembly inhibitors
    • CHANG Y-T, WIGNALL SM, ROSANIA GR et al.: Synthesis and biological evaluation of myoseverin derivatives: microtubule assembly inhibitors. J. Med. Chem. (2001) 44:4497-4500.
    • (2001) J. Med. Chem , vol.44 , pp. 4497-4500
    • Chang, Y.-T.1    Wignall, S.M.2    Rosania, G.R.3
  • 258
    • 0034016816 scopus 로고    scopus 로고
    • Myoseverin, a microtubule-binding molecule with novel cellular effects
    • ROSANIA GR, CHANG Y-T, PEREZ O et al.: Myoseverin, a microtubule-binding molecule with novel cellular effects. Nat. Biotechnol. (2000) 18:304-308.
    • (2000) Nat. Biotechnol , vol.18 , pp. 304-308
    • Rosania, G.R.1    Chang, Y.-T.2    Perez, O.3
  • 259
    • 0034778207 scopus 로고    scopus 로고
    • Rationally designed antimitotic agents with pro-apoptotic activity
    • UCKUN FM: Rationally designed antimitotic agents with pro-apoptotic activity. Curr. Pharm. Des. (2001) 7:1627-1639.
    • (2001) Curr. Pharm. Des , vol.7 , pp. 1627-1639
    • Uckun, F.M.1
  • 260
    • 0034844713 scopus 로고    scopus 로고
    • Spongistatins as tubulin targeting agents
    • UCKUN FM, MAO C, JAN ST et al.: Spongistatins as tubulin targeting agents. Curr. Pharm. Des. (2001) 7:1291-1296.
    • (2001) Curr. Pharm. Des , vol.7 , pp. 1291-1296
    • Uckun, F.M.1    Mao, C.2    Jan, S.T.3
  • 261
    • 0034608324 scopus 로고    scopus 로고
    • COBRA-1, a rationally-designed epoxy-THF containing compound with potent tubulin depolymerising activity as a novel anticancer agent
    • JAN ST, MAO C, VASSILEV AO, NAVARA CS, UCKUN FM: COBRA-1, a rationally-designed epoxy-THF containing compound with potent tubulin depolymerising activity as a novel anticancer agent. Bioorg. Med. Chem. Lett. (2000) 10:1193-1197.
    • (2000) Bioorg. Med. Chem. Lett , vol.10 , pp. 1193-1197
    • Jan, S.T.1    Mao, C.2    Vassilev, A.O.3    Navara, C.S.4    Uckun, F.M.5
  • 262
    • 0034970301 scopus 로고    scopus 로고
    • Epothilones and their analogues - A new class of promising microtubule inhibitors
    • FLORSHEIMER A, ALTMANN KH: Epothilones and their analogues - a new class of promising microtubule inhibitors. Exp. Opin. Ther. Patents (2001) 11:951-968.
    • (2001) Exp. Opin. Ther. Patents , vol.11 , pp. 951-968
    • Florsheimer, A.1    Altmann, K.H.2
  • 263
    • 0027360552 scopus 로고
    • Mechanism of mitotic block and inhibition of cell proliferation by taxol at low concentrations
    • JORDAN MA, TOSO RJ, THROWER D, WILSON L: Mechanism of mitotic block and inhibition of cell proliferation by taxol at low concentrations. Proc. Natl. Acad. Sci. USA (1993) 90:9552-9556.
    • (1993) Proc. Natl. Acad. Sci. USA , vol.90 , pp. 9552-9556
    • Jordan, M.A.1    Toso, R.J.2    Thrower, D.3    Wilson, L.4
  • 264
    • 0011500378 scopus 로고    scopus 로고
    • Mitotic kinesin-targeted antitumour agents: Discovery, lead optimisation and anti-tumor activity of a series of novel quinazolinones as inhibitors of kinesin spindle protein (KSP)
    • 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 3648
    • BERGNES G, HA ED, FENG B et al.: Mitotic kinesin-targeted antitumour agents: discovery, lead optimisation and anti-tumor activity of a series of novel quinazolinones as inhibitors of kinesin spindle protein (KSP). 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA (2002):Abstract 3648.
    • (2002)
    • Bergnes, G.1    Ha, E.D.2    Feng, B.3
  • 265
    • 0011503188 scopus 로고    scopus 로고
    • SB-715992, a potent and selective inhibitor of KSP mitotic kinesin, demonstrates broad-spectrum activity in advanced murine tumors and human tumor xenografts
    • 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA Abstract 1335
    • JOHNSON RK, MCCABE FL, CAUDER E et al.: SB-715992, a potent and selective inhibitor of KSP mitotic kinesin, demonstrates broad-spectrum activity in advanced murine tumors and human tumor xenografts. 93rd Annual Meeting of American Association for Cancer Research. San Francisco, USA (2002):Abstract 1335.
    • (2002)
    • Johnson, R.K.1    Mccabe, F.L.2    Cauder, E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.