메뉴 건너뛰기




Volumn 19, Issue 10, 2013, Pages 1923-1955

Design of combretastatin A-4 analogs as tubulin targeted vascular disrupting agent with special emphasis on their cis-restricted isomers

Author keywords

Anticancer; Antimitotic agents; Antitubulin; Antivascular; CA 4; Combretum caffrum; Cytotoxicity; Structure activity relationship

Indexed keywords

AZETIDINONE DERIVATIVE; BENZOFURAN DERIVATIVE; BENZOTHIOPHENE DERIVATIVE; COLCHICINE; COMBRETASTATIN A4; COUMARIN DERIVATIVE; FURAN DERIVATIVE; IMIDAZOLE DERIVATIVE; INDOLE DERIVATIVE; ISOXAZOLE DERIVATIVE; OXADIAZOLE DERIVATIVE; OXAZOLE DERIVATIVE; PYRAZOLE DERIVATIVE; PYRROLE DERIVATIVE; QUINAZOLINE DERIVATIVE; QUINOLINE DERIVATIVE; TETRAZOLE DERIVATIVE; THIAZOLE DERIVATIVE; THIOPHENE DERIVATIVE; TRIAZOLE DERIVATIVE; TUBULIN; VASCULAR TARGETING AGENT;

EID: 84876727508     PISSN: 13816128     EISSN: 18734286     Source Type: Journal    
DOI: 10.2174/1381612811319100013     Document Type: Review
Times cited : (68)

References (162)
  • 2
    • 24944515311 scopus 로고    scopus 로고
    • A common pharmacophore for a diverse set of colchicine site inhibitors using a structure-based approach
    • Nguyen TL, McGrath C, Hermone AR, et al. A common pharmacophore for a diverse set of colchicine site inhibitors using a structure-based approach. J Med Chem 2005; 48: 6107-16.
    • (2005) J Med Chem , vol.48 , pp. 6107-6116
    • Nguyen, T.L.1    McGrath, C.2    Hermone, A.R.3
  • 4
    • 0021061705 scopus 로고
    • Interactions of combretastatin, a new plantderived antimitotic agent with tubulin
    • Hamel E, Lin CM. Interactions of combretastatin, a new plantderived antimitotic agent with tubulin. Biochem Pharmacol 1983; 32: 3864-7.
    • (1983) Biochem Pharmacol , vol.32 , pp. 3864-3867
    • Hamel, E.1    Lin, C.M.2
  • 5
    • 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, Dempcy RO, Schmidt JM, Pettit GR. Interactions of tubulin with potent natural and synthetic analogs of the antimitotic agent combretastatin: a structure-activity study. Mol Pharmacol 1988; 34: 200-8.
    • (1988) Mol Pharmacol , vol.34 , pp. 200-208
    • Lin, C.M.1    Singh, S.B.2    Chu, P.S.3    Dempcy, R.O.4    Schmidt, J.M.5    Pettit, G.R.6
  • 6
    • 0024427745 scopus 로고
    • Antimitotic natural products Combretastatin A-4 and combretastatin A-2: Studies on the mechanism of their inhibition of the binding of colchicine to tubulin
    • Lin CM, Ho HH, Pettit GR, Hamel E. Antimitotic natural products Combretastatin A-4 and combretastatin A-2: studies on the mechanism of their inhibition of the binding of colchicine to tubulin. Biochemistry 1989; 28: 6984-91.
    • (1989) Biochemistry , vol.28 , pp. 6984-6991
    • Lin, C.M.1    Ho, H.H.2    Pettit, G.R.3    Hamel, E.4
  • 8
    • 0028930050 scopus 로고
    • The interaction with tubulin of a series of stilbenes based on Combretastatin A-4
    • Woods JA, Hadfield JA, Pettit GR, Fox BW, McGown AT. The interaction with tubulin of a series of stilbenes based on Combretastatin A-4. Br J Cancer 1995; 71: 705-11.
    • (1995) Br J Cancer , vol.71 , pp. 705-711
    • Woods, J.A.1    Hadfield, J.A.2    Pettit, G.R.3    Fox, B.W.4    McGown, A.T.5
  • 13
    • 0031980124 scopus 로고    scopus 로고
    • Antineoplastic agents 389. New syntheses of the combretastatin A-4 prodrug
    • Pettit GR, Rhodes MR. Antineoplastic agents 389. New syntheses of the combretastatin A-4 prodrug. Anticancer Drug Des 1998; 13: 183-91.
    • (1998) Anticancer Drug Des , vol.13 , pp. 183-191
    • Pettit, G.R.1    Rhodes, M.R.2
  • 15
    • 0037061622 scopus 로고    scopus 로고
    • Potent orally active heterocyclebased combretastatin A-4 analogs: Synthesis structure-activity relationship, pharmacokinetics and in vivo antitumor activity evaluation
    • Wang L, Woods KW, Li Q, et al. Potent orally active heterocyclebased combretastatin A-4 analogs: synthesis structure-activity relationship, pharmacokinetics and in vivo antitumor activity evaluation. J Med Chem 2002; 45: 1697-711.
    • (2002) J Med Chem , vol.45 , pp. 1697-1711
    • Wang, L.1    Woods, K.W.2    Li, Q.3
  • 16
    • 33846809496 scopus 로고    scopus 로고
    • Synthesis and cytotoxic activities of 4,5-diarylisoxazoles
    • Sun CM, Lin LG, Yu HJ, et al. Synthesis and cytotoxic activities of 4,5-diarylisoxazoles. Bioorg Med Chem Lett 2007; 17: 1078-81.
    • (2007) Bioorg Med Chem Lett , vol.17 , pp. 1078-1081
    • Sun, C.M.1    Lin, L.G.2    Yu, H.J.3
  • 17
    • 0037030605 scopus 로고    scopus 로고
    • A one-pot synthesis of Benzo[b]furan and indole inhibitors of tubulin polymerization
    • Flynn BL, Hamel E, Jung MK. A one-pot synthesis of Benzo[b]furan and indole inhibitors of tubulin polymerization. J Med Chem 2002; 45: 2670-73.
    • (2002) J Med Chem , vol.45 , pp. 2670-2673
    • Flynn, B.L.1    Hamel, E.2    Jung, M.K.3
  • 18
    • 0024195951 scopus 로고
    • Comparative Analysis of Tubulin Sequence. Comparative Biochemistry and Physiology
    • Little M, Seehaus T. Comparative Analysis of Tubulin Sequence. Comparative Biochemistry and Physiology. Comp Biochem Physiol. 1988, 90B: 655-70.
    • (1988) Comp Biochem Physiol. , vol.90 B , pp. 655-670
    • Little, M.1    Seehaus, T.2
  • 19
    • 0032495513 scopus 로고    scopus 로고
    • Structure of the β, α tubulin dimer by electron crystallography
    • Nogales E, Wolf SG, Downing KH. Structure of the β, α tubulin dimer by electron crystallography. Nature 1998; 391: 199-203.
    • (1998) Nature , vol.391 , pp. 199-203
    • Nogales, E.1    Wolf, S.G.2    Downing, K.H.3
  • 20
    • 0032426329 scopus 로고    scopus 로고
    • Tubulin structure: Insights into microtubule properties and functions
    • Downing KH, Nogalest E. Tubulin structure: insights into microtubule properties and functions. Curr Opin Struct Biol 1998; 8: 785-91.
    • (1998) Curr Opin Struct Biol , vol.8 , pp. 785-791
    • Downing, K.H.1    Nogalest, E.2
  • 22
    • 0026812627 scopus 로고
    • Microtubule dynamics
    • Caplow M. Microtubule dynamics. Curr Opin Cell Biol 1992, 4: 58-65
    • (1992) Curr Opin Cell Biol , vol.4 , pp. 58-65
    • Caplow, M.1
  • 23
    • 0036086919 scopus 로고    scopus 로고
    • Drugs that Inhibit Tubulin Polymerization: The Particular Case of Podophyllotoxin and Analogs
    • Desbene S, Renault SG. Drugs that Inhibit Tubulin Polymerization: The Particular Case of Podophyllotoxin and Analogs. Curr Med Chem-Anti-Cancer Agents, 2002; 2: 71-90.
    • (2002) Curr Med Chem-Anti-Cancer Agents , vol.2 , pp. 71-90
    • Desbene, S.1    Renault, S.G.2
  • 24
    • 0033811815 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of aryl azide derivatives of combretastatin A-4 as molecular probes for tubulin
    • Pinney KG, Mejia MP, Villalobos VM, et al. Synthesis and biological evaluation of aryl azide derivatives of combretastatin A-4 as molecular probes for tubulin. Bioorg Med Chem 2000; 8: 2417-25.
    • (2000) Bioorg Med Chem , vol.8 , pp. 2417-2425
    • Pinney, K.G.1    Mejia, M.P.2    Villalobos, V.M.3
  • 25
    • 18744404214 scopus 로고    scopus 로고
    • Review: Postchaperonin tubulin folding cofactors and their role in microtubule dynamics
    • Lopez-Fanarraga M, Avila J, Guasch A, Coll M, Zabala JC. Review: postchaperonin tubulin folding cofactors and their role in microtubule dynamics. J Struct Biol 2001; 135: 219-29.
    • (2001) J Struct Biol , vol.135 , pp. 219-229
    • Lopez-Fanarraga, M.1    Avila, J.2    Guasch, A.3    Coll, M.4    Zabala, J.C.5
  • 26
    • 33646494080 scopus 로고    scopus 로고
    • Structural mechanisms underlying nucleotide dependent self-assembly of tubulin and its relatives
    • Nogales E, Wang HW. Structural mechanisms underlying nucleotide dependent self-assembly of tubulin and its relatives. Curr Opin Struct Biol 2006; 16: 221-229.
    • (2006) Curr Opin Struct Biol , vol.16 , pp. 221-229
    • Nogales, E.1    Wang, H.W.2
  • 27
    • 0024370806 scopus 로고
    • Microtubular structure and tubulin polymerization
    • Mandelkow E, Mandelkow EM. Microtubular structure and tubulin polymerization. Curr Opin Cell Biol 1989; 1: 5-9.
    • (1989) Curr Opin Cell Biol , vol.1 , pp. 5-9
    • Mandelkow, E.1    Mandelkow, E.M.2
  • 29
    • 33846215917 scopus 로고    scopus 로고
    • Protein engineering strategies to improve exposure in solid tumors
    • Beckman RA, Weiner LM, Davis HM. Protein engineering strategies to improve exposure in solid tumors. Cancer 2006; 109: 170-9
    • (2006) Cancer , vol.109 , pp. 170-179
    • Beckman, R.A.1    Weiner, L.M.2    Davis, H.M.3
  • 30
    • 79551570717 scopus 로고    scopus 로고
    • Classification and Toxicities of Vascular Disrupting Agents
    • Hasani A, Leighl N. Classification and Toxicities of Vascular Disrupting Agents. Clinical Lung Cancer 2011; 12: 18-25
    • (2011) Clinical Lung Cancer , vol.12 , pp. 18-25
    • Hasani, A.1    Leighl, N.2
  • 31
    • 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: 82-7.
    • (2001) Lancet Oncol , vol.2 , pp. 82-87
    • Griggs, J.1    Metcalfe, J.C.2    Hesketh, R.3
  • 32
    • 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: 1626-34.
    • (1999) Cancer Res , vol.59 , pp. 1626-1634
    • Tozer, G.M.1    Prise, V.E.2    Wilson, J.3
  • 33
    • 68049108414 scopus 로고    scopus 로고
    • Vascular Disrupting Agents: A Novel Mechanism of Action in the Battle against Non-Small Cell Lung Cancer
    • Gridelli C, Rossi A, Maione P, et al. Vascular Disrupting Agents: A Novel Mechanism of Action in the Battle against Non-Small Cell Lung Cancer. The Oncologist 2009; 14: 612-20.
    • (2009) The Oncologist , vol.14 , pp. 612-620
    • Gridelli, C.1    Rossi, A.2    Maione, P.3
  • 34
    • 33845286942 scopus 로고    scopus 로고
    • Vascular disrupting agents
    • Lippert JW, Vascular disrupting agents. Bioorg Med Chem 2007; 15: 605-15.
    • (2007) Bioorg Med Chem , vol.15 , pp. 605-615
    • Lippert, J.W.1
  • 35
    • 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: 200-8.
    • (1988) Mol Pharmacol , vol.34 , pp. 200-208
    • Lin, C.M.1    Singh, S.B.2    Chu, P.S.3
  • 36
    • 0028930050 scopus 로고
    • The interaction with tubulin of a series of stilbenes based on Combretastatin A-4
    • Woods JA, Hadfield JA, Pettit GR, Fox BW, McGown AT. The interaction with tubulin of a series of stilbenes based on Combretastatin A-4. Br J Cancer 1995; 71: 705-11.
    • (1995) Br J Cancer , vol.71 , pp. 705-711
    • Woods, J.A.1    Hadfield, J.A.2    Pettit, G.R.3    Fox, B.W.4    McGown, A.T.5
  • 38
    • 0037085753 scopus 로고    scopus 로고
    • The tumor vascular targeting agent combretastatin A-4 phosphate induces reorganization of the actin cytoskeleton and early membrane blebbing in human endothelial cells
    • Kanthou C, Tozer GM. The tumor vascular targeting agent combretastatin A-4 phosphate induces reorganization of the actin cytoskeleton and early membrane blebbing in human endothelial cells. Blood 2002; 99: 2060-9.
    • (2002) Blood , vol.99 , pp. 2060-2069
    • Kanthou, C.1    Tozer, G.M.2
  • 39
    • 0036282385 scopus 로고    scopus 로고
    • The biology of the combretastatins as tumour vascular targeting agent
    • Tozer GM, Kanthou C, Parkins CS, Hill SA. The biology of the combretastatins as tumour vascular targeting agent. Int J Exp Pathol 2002; 83: 21-38.
    • (2002) Int J Exp Pathol , vol.83 , pp. 21-38
    • Tozer, G.M.1    Kanthou, C.2    Parkins, C.S.3    Hill, S.A.4
  • 40
    • 0037373826 scopus 로고    scopus 로고
    • The first international conference on vascular targeting: Meeting overview
    • Thorpe PE, Chaplin DJ, Backley DC. The first international conference on vascular targeting: Meeting overview. Cancer Res 2003; 63: 1144-7.
    • (2003) Cancer Res , vol.63 , pp. 1144-1147
    • Thorpe, P.E.1    Chaplin, D.J.2    Backley, D.C.3
  • 41
    • 0035254648 scopus 로고    scopus 로고
    • Angiogenesis: Regulators and clinical applications
    • Liekens S, Clercq ED, Neyts J. Angiogenesis: regulators and clinical applications. Biochem Pharmacol 2001; 61: 253-70.
    • (2001) Biochem Pharmacol , vol.61 , pp. 253-270
    • Liekens, S.1    Clercq, E.D.2    Neyts, J.3
  • 42
    • 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: 6413-22.
    • (2001) Cancer Res , vol.61 , pp. 6413-6422
    • Tozer, G.M.1    Prise, V.E.2    Wilson, J.3
  • 43
    • 27644466314 scopus 로고    scopus 로고
    • Combretastatin A-4 phosphate induces rapid regression of tumor neovessels and growth through interference with vascular endothelial-E-cadherin signaling
    • Vincent L, Kermani P, Young LM, et al. Combretastatin A-4 phosphate induces rapid regression of tumor neovessels and growth through interference with vascular endothelial-E-cadherin signaling. J Clin Invest 2005; 15: 2992-3006.
    • (2005) J Clin Invest , vol.15 , pp. 2992-3006
    • Vincent, L.1    Kermani, P.2    Young, L.M.3
  • 45
    • 37249020371 scopus 로고    scopus 로고
    • Anti-mitotic activity of colchicine and the structural basis for its interaction with tubulin
    • Bhattacharyya B, Panda D, Gupta S, Banerjee M. Anti-mitotic activity of colchicine and the structural basis for its interaction with tubulin. Med Res Rev 2008; 28: 155-83.
    • (2008) Med Res Rev , vol.28 , pp. 155-183
    • Bhattacharyya, B.1    Panda, D.2    Gupta, S.3    Banerjee, M.4
  • 46
    • 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: 259-96.
    • (1998) Med Res Rev , vol.18 , pp. 259-296
    • Jordan, A.1    Hadfield, J.A.2    Lawrence, N.J.3    McGown, A.T.4
  • 47
    • 1942438028 scopus 로고    scopus 로고
    • Microtubules as a target for anticancer drugs
    • Jordan MA, Wilson L. Microtubules as a target for anticancer drugs. Nat Rev Cancer 2004; 4: 253-65.
    • (2004) Nat Rev Cancer , vol.4 , pp. 253-265
    • Jordan, M.A.1    Wilson, L.2
  • 49
    • 0035262598 scopus 로고    scopus 로고
    • Targeting tumour vasculature: The development of combretastatin A-4
    • Griggs J, Metcalfe JC, Hesketh R. Targeting tumour vasculature: the development of combretastatin A-4. The Lancet Oncol 2001; 2: 82-7.
    • (2001) The Lancet Oncol , vol.2 , pp. 82-87
    • Griggs, J.1    Metcalfe, J.C.2    Hesketh, R.3
  • 50
    • 33947717991 scopus 로고    scopus 로고
    • The concise synthesis of chalcone, indanone and indenone analogs of combretastatin A4
    • Kerr DJ, Hamel E, Jung MK, Flynn BL. The concise synthesis of chalcone, indanone and indenone analogs of combretastatin A4. Bioorg Med Chem 2007; 15: 3290-8.
    • (2007) Bioorg Med Chem , vol.15 , pp. 3290-3298
    • Kerr, D.J.1    Hamel, E.2    Jung, M.K.3    Flynn, B.L.4
  • 51
    • 0041421003 scopus 로고    scopus 로고
    • Combretastatin A-4 analogs as antimitotic antitumor agents
    • Nam NH. Combretastatin A-4 analogs as antimitotic antitumor agents. Curr Med Chem 2003; 10: 1697-722.
    • (2003) Curr Med Chem , vol.10 , pp. 1697-1722
    • Nam, N.H.1
  • 52
    • 0036850914 scopus 로고    scopus 로고
    • Discovery and development of antimitotic agents that inhibit tubulin polymerisation for the treatment of cancer
    • Li Q, Sham HL. Discovery and development of antimitotic agents that inhibit tubulin polymerisation for the treatment of cancer. Expert Opin Ther Patents 2002; 12: 1663-702.
    • (2002) Expert Opin Ther Patents , vol.12 , pp. 1663-1702
    • Li, Q.1    Sham, H.L.2
  • 53
    • 0036324971 scopus 로고    scopus 로고
    • Combretastatin anticancer drugs
    • Bibby MC. Combretastatin anticancer drugs. Drug Future 2002; 27: 475-80.
    • (2002) Drug Future , vol.27 , pp. 475-480
    • Bibby, M.C.1
  • 54
    • 0034722897 scopus 로고    scopus 로고
    • New agents in cancer clinical trials
    • Adams J, Elliott PJ. New agents in cancer clinical trials. Oncogene 2000; 19: 6687-92.
    • (2000) Oncogene , vol.19 , pp. 6687-6692
    • Adams, J.1    Elliott, P.J.2
  • 55
    • 0035254648 scopus 로고    scopus 로고
    • Angiogenesis: Regulators and clinical applications
    • Liekens S, De Clercq E, Neyts J. Angiogenesis: regulators and clinical applications. Biochem Pharmacol 2001; 61: 253-70.
    • (2001) Biochem Pharmacol , vol.61 , pp. 253-270
    • Liekens, S.1    de Clercq, E.2    Neyts, J.3
  • 57
    • 0034607256 scopus 로고    scopus 로고
    • Antiangiogenesis drugs target specific cancers, mechanisms
    • Randal J. Antiangiogenesis drugs target specific cancers, mechanisms. J Natl Cancer Inst 2000; 92: 520-2.
    • (2000) J Natl Cancer Inst , vol.92 , pp. 520-522
    • Randal, J.1
  • 58
    • 0034470398 scopus 로고    scopus 로고
    • Antiangiogenesis-therapeutic strategies and clinical implications for brain tumors
    • Puduvalli VK, Sawaya R. Antiangiogenesis-therapeutic strategies and clinical implications for brain tumors. J Neurooncol 2000; 50: 189-200.
    • (2000) J Neurooncol , vol.50 , pp. 189-200
    • Puduvalli, V.K.1    Sawaya, R.2
  • 59
    • 18744379774 scopus 로고    scopus 로고
    • Pharmaceutical design of antimitotic agents based on combretastatins
    • Hsieh HP, Liou JP, Mahindroo N. Pharmaceutical design of antimitotic agents based on combretastatins. Curr Pharm Design 2005; 11: 1655-77.
    • (2005) Curr Pharm Design , vol.11 , pp. 1655-1677
    • Hsieh, H.P.1    Liou, J.P.2    Mahindroo, N.3
  • 60
    • 18744409805 scopus 로고    scopus 로고
    • The chemistry and biology of antimitotic chalcones and related enone systems
    • Lawrence NJ, McGown AT. The chemistry and biology of antimitotic chalcones and related enone systems. Curr Pharm Design 2005; 11: 1679-93.
    • (2005) Curr Pharm Design , vol.11 , pp. 1679-1693
    • Lawrence, N.J.1    McGown, A.T.2
  • 61
    • 37349083149 scopus 로고    scopus 로고
    • Combretastatin A-4 analogs as anticancer agents
    • Chaudhary A, Pandeya SN, Kumar P, et al Combretastatin A-4 analogs as anticancer agents. Mini Rev Med Chem 2007; 7: 1186-205
    • (2007) Mini Rev Med Chem , vol.7 , pp. 1186-1205
    • Chaudhary, A.1    Pandeya, S.N.2    Kumar, P.3
  • 62
    • 79851496869 scopus 로고    scopus 로고
    • Developments of combretastatin A-4 derivatives as anticancer agents
    • Shan Y, Zhang J, Liu Z, Wang M, Dong Y. Developments of combretastatin A-4 derivatives as anticancer agents. Curr Med Chem 2011; 18: 523-38.
    • (2011) Curr Med Chem , vol.18 , pp. 523-538
    • Shan, Y.1    Zhang, J.2    Liu, Z.3    Wang, M.4    Dong, Y.5
  • 63
    • 79960006369 scopus 로고    scopus 로고
    • Biological potential and structure-activity relationships of most recently developed vascular disrupting agents: An overview of new derivatives of natural combretastatin A-4
    • Marrelli M, Conforti F, Statti GA, et al. Biological potential and structure-activity relationships of most recently developed vascular disrupting agents: an overview of new derivatives of natural combretastatin A-4. Curr Med Chem 2011; 18: 3035-81.
    • (2011) Curr Med Chem , vol.18 , pp. 3035-3081
    • Marrelli, M.1    Conforti, F.2    Statti, G.A.3
  • 64
    • 1842741030 scopus 로고    scopus 로고
    • Examination of the 1,4-disubstituted azetidinone ring system as a template for combretastatin A-4 conformationally restricted analog design
    • Sun L, Vasilevich NI, Fuselier JA, Hocart SJ, Coy DH. Examination of the 1,4-disubstituted azetidinone ring system as a template for combretastatin A-4 conformationally restricted analog design. Bioorg Med Chem Lett 2004; 14: 2041-6.
    • (2004) Bioorg Med Chem Lett , vol.14 , pp. 2041-2046
    • Sun, L.1    Vasilevich, N.I.2    Fuselier, J.A.3    Hocart, S.J.4    Coy, D.H.5
  • 65
    • 33749649084 scopus 로고    scopus 로고
    • Synthesis and In-vitro biological activity evaluation of the derivatives of combretastatin A-4
    • Yang Z. Synthesis and In-vitro biological activity evaluation of the derivatives of combretastatin A-4. Lett Drug Des Discov 2006; 3: 544-6.
    • (2006) Lett Drug Des Discov , vol.3 , pp. 544-546
    • Yang, Z.1
  • 66
    • 78649326841 scopus 로고    scopus 로고
    • Lead identification of conformationally restricted β-lactam type combretastatin analogs: Synthesis antiproliferative activity and tubulin targeting effects
    • Carr M, Greene LM, Knox AJS, Lloyd DG, Zisterer DM, Meegan MJ. Lead identification of conformationally restricted β-lactam type combretastatin analogs: Synthesis antiproliferative activity and tubulin targeting effects. Eur J Med Chem 2010; 45: 5752-66.
    • (2010) Eur J Med Chem , vol.45 , pp. 5752-5766
    • Carr, M.1    Greene, L.M.2    Knox, A.J.S.3    Lloyd, D.G.4    Zisterer, D.M.5    Meegan, M.J.6
  • 67
    • 84876705485 scopus 로고    scopus 로고
    • 1 2 3-Triazole tethered β-lactam-Chalcone bifunctional hybrids: Synthesis and anticancer evaluation
    • Singh P, Raj R, Kumar V, et al. 1 2 3-Triazole tethered β-lactam-Chalcone bifunctional hybrids: Synthesis and anticancer evaluation. Eur J Med Chem 2011; 46: 1-7.
    • (2011) Eur J Med Chem , vol.46 , pp. 1-7
    • Singh, P.1    Raj, R.2    Kumar, V.3
  • 68
    • 78650312289 scopus 로고    scopus 로고
    • Synthesis and evaluation of azetidinone analogs of combretastatin A-4 as tubulin targeting agents
    • O'Boyle NM, Carr M, Greene LM, et al. Synthesis and evaluation of azetidinone analogs of combretastatin A-4 as tubulin targeting agents. J Med Chem 2010; 53: 8569-84.
    • (2010) J Med Chem , vol.53 , pp. 8569-8584
    • O'Boyle, N.M.1    Carr, M.2    Greene, L.M.3
  • 69
    • 79953166386 scopus 로고    scopus 로고
    • Synthesis evaluation and structural studies of antiproliferative tubulin-targeting azetidin-2-ones
    • O'Boyle NM, Carr M, Greene LM, et al. Synthesis evaluation and structural studies of antiproliferative tubulin-targeting azetidin-2-ones. Bioorg Med Chem 2011; 19: 2306-25.
    • (2011) Bioorg Med Chem , vol.19 , pp. 2306-2325
    • O'Boyle, N.M.1    Carr, M.2    Greene, L.M.3
  • 70
    • 80052949837 scopus 로고    scopus 로고
    • Synthesis biochemical and molecular modelling studies of antiproliferative azetidinones causing microtubule disruption and mitotic catastrophe
    • O'Boyle NM, Carr M, et al. Synthesis biochemical and molecular modelling studies of antiproliferative azetidinones causing microtubule disruption and mitotic catastrophe. Eur J Med Chem 2011; 46: 4595-607.
    • (2011) Eur J Med Chem , vol.46 , pp. 4595-4607
    • O'Boyle, N.M.1    Carr, M.2
  • 71
    • 33646750713 scopus 로고    scopus 로고
    • 4 5-Diaryl 1H-pyrrole-2-carboxylates as Combretastatin A-4/lamellarin T hybrids: Synthesis and evaluation as antimitotic and cytotoxic agents
    • Banwell MG, Hamel E, Hockless DCR, Verdier-Pinard P, Willisa AC, Wong DJ. 4 5-Diaryl 1H-pyrrole-2-carboxylates as Combretastatin A-4/lamellarin T hybrids: Synthesis and evaluation as antimitotic and cytotoxic agents. Bioorg Med Chem 2006; 14: 4627-38.
    • (2006) Bioorg Med Chem , vol.14 , pp. 4627-4638
    • Banwell, M.G.1    Hamel, E.2    Hockless, D.C.R.3    Verdier-Pinard, P.4    Willisa, A.C.5    Wong, D.J.6
  • 72
    • 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: 719-22.
    • (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
  • 73
    • 33747514168 scopus 로고    scopus 로고
    • Synthesis and cytotoxic evaluation of combretafurans potential scaffolds for dual-action antitumoral agents
    • Pirali T, Busacca S, Beltrami L, et al. Synthesis and cytotoxic evaluation of combretafurans potential scaffolds for dual-action antitumoral agents. J Med Chem 2006; 49: 5372-6.
    • (2006) J Med Chem , vol.49 , pp. 5372-5376
    • Pirali, T.1    Busacca, S.2    Beltrami, L.3
  • 74
    • 79960627839 scopus 로고    scopus 로고
    • Regioselective Suzuki coupling of dihaloheteroaromatic compounds as a rapid strategy to synthesize potent rigid combretastatin analogs
    • Theeramunkong S, Caldarelli A, Massarotti A, et al. Regioselective Suzuki coupling of dihaloheteroaromatic compounds as a rapid strategy to synthesize potent rigid combretastatin analogs. J Med Chem 2011; 54: 4977-86.
    • (2011) J Med Chem , vol.54 , pp. 4977-4986
    • Theeramunkong, S.1    Caldarelli, A.2    Massarotti, A.3
  • 75
    • 0035801759 scopus 로고    scopus 로고
    • The synthesis and tubulin binding activity of thiophene-based analogs of combretastatin A-4
    • Flynn BL, Flynn GP, Hamel E, Jung MK. The synthesis and tubulin binding activity of thiophene-based analogs of combretastatin A-4. Bioorg Med Chem Lett 2001; 11: 2341-3.
    • (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
  • 76
    • 33745659825 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of 2-amino-3-(3'4'5'-trimethoxybenzoyl)-5-aryl thiophene as a new class of potent antitubulin agents
    • Romagnoli R, Baraldi PG, Pavani MG, et al. Synthesis and biological evaluation of 2-amino-3-(3'4'5'-trimethoxybenzoyl)-5-aryl thiophene as a new class of potent antitubulin agents. J Med Chem 2006; 49: 3906-15.
    • (2006) J Med Chem , vol.49 , pp. 3906-3915
    • Romagnoli, R.1    Baraldi, P.G.2    Pavani, M.G.3
  • 77
    • 33750101726 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of 2-(3'4'5'-trimethoxybenzoyl)-3-amino-5-aryl thiophenes as a new class of tubulin inhibitors
    • Romagnoli R, Baraldi PG, Remusat V, et al. Synthesis and biological evaluation of 2-(3'4'5'-trimethoxybenzoyl)-3-amino-5-aryl thiophenes as a new class of tubulin inhibitors. J Med Chem 2006; 49: 6425-8.
    • (2006) J Med Chem , vol.49 , pp. 6425-6428
    • Romagnoli, R.1    Baraldi, P.G.2    Remusat, V.3
  • 78
    • 43949118077 scopus 로고    scopus 로고
    • Design synthesis and biological evaluation of thiophene analogs of chalcones
    • Romagnoli R, Baraldi PG, Maria DC, et al. Design synthesis and biological evaluation of thiophene analogs of chalcones. Bioorg Med Chem 2008; 16: 5367-76.
    • (2008) Bioorg Med Chem , vol.16 , pp. 5367-5376
    • Romagnoli, R.1    Baraldi, P.G.2    Maria, D.C.3
  • 79
    • 79955473280 scopus 로고    scopus 로고
    • Synthesis of novel antimitotic agents based on 2-amino-3-aroyl-5-(hetero)-arylethynyl thiophene derivatives
    • Romagnoli R, Baraldi PG, Lopez OC, et al. Synthesis of novel antimitotic agents based on 2-amino-3-aroyl-5-(hetero)-arylethynyl thiophene derivatives. Bioorg Med Chem Lett 2011; 21: 2746-51.
    • (2011) Bioorg Med Chem Lett , vol.21 , pp. 2746-2751
    • Romagnoli, R.1    Baraldi, P.G.2    Lopez, O.C.3
  • 80
    • 0032542045 scopus 로고    scopus 로고
    • Synthesis and antitumor activity cis restricted combretastatins: 5-membered heterocyclic analog
    • Ohsumi K, Hatanaka T, Fujita K, et al. Synthesis and antitumor activity cis restricted combretastatins: 5-membered heterocyclic analog. Bioorg Med Chem Lett 1998; 8: 3153-8.
    • (1998) Bioorg Med Chem Lett , vol.8 , pp. 3153-3158
    • Ohsumi, K.1    Hatanaka, T.2    Fujita, K.3
  • 81
    • 17144395159 scopus 로고    scopus 로고
    • Discovery of 2-Arylthiazolidine-4 carboxylic acid amides as a new class of cytotoxic agents for prostate cancer
    • Gududuru V, Hurh E, Dalton JT, Miller DD. Discovery of 2-Arylthiazolidine-4 carboxylic acid amides as a new class of cytotoxic agents for prostate cancer. J Med Chem 2005; 48: 2584-8.
    • (2005) J Med Chem , vol.48 , pp. 2584-2588
    • Gududuru, V.1    Hurh, E.2    Dalton, J.T.3    Miller, D.D.4
  • 82
    • 23644435761 scopus 로고    scopus 로고
    • SAR studies of 2-arylthiazolidine-4-carboxylic acid amides: A novel class of cytotoxic agents for prostate cancer
    • Gududuru V, Hurh E, Sullivan J, Dalton JT, Miller DD. SAR studies of 2-arylthiazolidine-4-carboxylic acid amides: A novel class of cytotoxic agents for prostate cancer. Bioorg Med Chem Lett 2005; 15: 4010-3.
    • (2005) Bioorg Med Chem Lett , vol.15 , pp. 4010-4013
    • Gududuru, V.1    Hurh, E.2    Sullivan, J.3    Dalton, J.T.4    Miller, D.D.5
  • 83
    • 34347373450 scopus 로고    scopus 로고
    • Synthesis and antiproliferative activity of thiazolidine analogs for melanoma
    • Li W, Lu Y, Wang Z, Dalton JT, Miller DD. Synthesis and antiproliferative activity of thiazolidine analogs for melanoma. Bioorg Med Chem Lett 2007; 17: 4113-7.
    • (2007) Bioorg Med Chem Lett , vol.17 , pp. 4113-4117
    • Li, W.1    Lu, Y.2    Wang, Z.3    Dalton, J.T.4    Miller, D.D.5
  • 84
    • 64349111929 scopus 로고    scopus 로고
    • Discovery of 4-substituted methoxybenzoyl-aryl-thiazoles as novel anticancer agents: Synthesis biological evaluation and structure activity relationships
    • Lu Y, Li CM, Wang Z, Ross CR, Chen J, Dalton JT. Li W Miller DD. Discovery of 4-substituted methoxybenzoyl-aryl-thiazoles as novel anticancer agents: synthesis biological evaluation and structure activity relationships. J Med Chem 2009; 52: 1701-11.
    • (2009) J Med Chem , vol.52 , pp. 1701-1711
    • Lu, Y.1    Li, C.M.2    Wang, Z.3    Ross, C.R.4    Chen, J.5    Dalton, J.T.6    Li, W.7    Miller, D.D.8
  • 85
    • 76449093092 scopus 로고    scopus 로고
    • Synthesis in vitro structure activity relationship and in vivo studies of 2-arylthiazolidine-4-carboxylic acid amides as anticancer agents
    • Lu Y, Wang Z, Li CM, et al. Synthesis in vitro structure activity relationship and in vivo studies of 2-arylthiazolidine-4-carboxylic acid amides as anticancer agents. Bioorg Med Chem 2010; 18: 477-95.
    • (2010) Bioorg Med Chem , vol.18 , pp. 477-495
    • Lu, Y.1    Wang, Z.2    Li, C.M.3
  • 86
    • 79960151500 scopus 로고    scopus 로고
    • Design Synthesis and SAR Studies of 4-Substituted methoxybenzoyl-aryl-thiazoles analogs as potent and orally bioavailable anticancer agents
    • Lu Y, Li CM, Wang Z, et al. Design Synthesis and SAR Studies of 4-Substituted methoxybenzoyl-aryl-thiazoles analogs as potent and orally bioavailable anticancer agents. J Med Chem 2011; 54: 4678-93.
    • (2011) J Med Chem , vol.54 , pp. 4678-4693
    • Lu, Y.1    Li, C.M.2    Wang, Z.3
  • 87
    • 78651389459 scopus 로고    scopus 로고
    • Biological activity of 4-substituted methoxybenzoyl-aryl-thiazole: An active microtubule inhibitor
    • Li CM, Wang Z, Lu Y, et al. Biological activity of 4-substituted methoxybenzoyl-aryl-thiazole: an active microtubule inhibitor. Cancer Res 2011; 71: 216-24.
    • (2011) Cancer Res , vol.71 , pp. 216-224
    • Li, C.M.1    Wang, Z.2    Lu, Y.3
  • 88
    • 80955166264 scopus 로고    scopus 로고
    • Balzarini J Brancale A Fu XH Li J Zhang SZ Hamel E. One-pot synthesis and biological evaluation of 2-pyrrolidinyl-4-amino-5-(3'4'5'-trimethoxybenzoyl) thiazole: A unique highly active antimicrotubule agent
    • Romagnoli R, Baraldi PG, Lopez-Cara C, et al. Balzarini J Brancale A Fu XH Li J Zhang SZ Hamel E. One-pot synthesis and biological evaluation of 2-pyrrolidinyl-4-amino-5-(3'4'5'-trimethoxybenzoyl) thiazole: A unique highly active antimicrotubule agent. Eur J Med Chem 2011; 46: 6015-24.
    • (2011) Eur J Med Chem , vol.46 , pp. 6015-6024
    • Romagnoli, R.1    Baraldi, P.G.2    Lopez-Cara, C.3
  • 89
    • 19844363802 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of chalcones and their derived pyrazoles as potential cytotoxic agents
    • Bhat BA, Dhar KL, Puri SC, Saxena AK, Shanmugavel M, Qazi GN. Synthesis and biological evaluation of chalcones and their derived pyrazoles as potential cytotoxic agents. Bioorg Med Chem Lett 2005; 15: 3177-80.
    • (2005) Bioorg Med Chem Lett , vol.15 , pp. 3177-3180
    • Bhat, B.A.1    Dhar, K.L.2    Puri, S.C.3    Saxena, A.K.4    Shanmugavel, M.5    Qazi, G.N.6
  • 90
    • 25844473382 scopus 로고    scopus 로고
    • Synthesis and cytotoxicity of epoxide and pyrazole analogs of the combretastatins
    • LeBlanc R, Dickson J, Brown T, et al. Synthesis and cytotoxicity of epoxide and pyrazole analogs of the combretastatins. Bioorg Med Chem 2005; 13: 6025-34.
    • (2005) Bioorg Med Chem , vol.13 , pp. 6025-6034
    • LeBlanc, R.1    Dickson, J.2    Brown, T.3
  • 91
    • 77950025748 scopus 로고    scopus 로고
    • Pyrazolone-fused combretastatins and their precursors: Synthesis cytotoxicity antitubulin activity and molecular modeling studies
    • Burja B, Cimbora-Zovko T, Tomic S, Jelusic T, Kocevar M, Polanc S, Osmak M. Pyrazolone-fused combretastatins and their precursors: synthesis cytotoxicity antitubulin activity and molecular modeling studies. Bioorg Med Chem 2010; 18: 2375-87.
    • (2010) Bioorg Med Chem , vol.18 , pp. 2375-2387
    • Burja, B.1    Cimbora-Zovko, T.2    Tomic, S.3    Jelusic, T.4    Kocevar, M.5    Polanc, S.6    Osmak, M.7
  • 92
    • 77955981424 scopus 로고    scopus 로고
    • Synthesis and in vitro antitumor activity of new 4 5-dihydropyrazole derivatives
    • Congiu C, Onnis V, Vesci L, Castorina M, Pisano C. Synthesis and in vitro antitumor activity of new 4 5-dihydropyrazole derivatives. Bioorg Med Chem 2010; 18: 6238-48.
    • (2010) Bioorg Med Chem , vol.18 , pp. 6238-6248
    • Congiu, C.1    Onnis, V.2    Vesci, L.3    Castorina, M.4    Pisano, C.5
  • 93
    • 79955390539 scopus 로고    scopus 로고
    • 4,5-Diaryl-3-aminopyrazole derivatives as analogs of combretastatin A-4: Synthesis and biological evaluation
    • Liu T, Cui R, Chen J, Zhang J, He Q, Yang B, Hu Y. 4,5-Diaryl-3-aminopyrazole derivatives as analogs of combretastatin A-4: Synthesis and biological evaluation. Arch Pharm Chem Life Sci 2011; 11: 279-86.
    • (2011) Arch Pharm Chem Life Sci , vol.11 , pp. 279-286
    • Liu, T.1    Cui, R.2    Chen, J.3    Zhang, J.4    He, Q.5    Yang, B.6    Hu, Y.7
  • 94
    • 79957466365 scopus 로고    scopus 로고
    • A novel class of transmethylpyrazoline analogs of combretastatins: Synthesis and invitro biological testing
    • Lee M, Brockway O, Dandavati A, et al. A novel class of transmethylpyrazoline analogs of combretastatins: Synthesis and invitro biological testing. Eur J Med Chem 2011; 46: 3099-104.
    • (2011) Eur J Med Chem , vol.46 , pp. 3099-3104
    • Lee, M.1    Brockway, O.2    Dandavati, A.3
  • 96
    • 13444267332 scopus 로고    scopus 로고
    • Heterocyclic and phenyl double-bond-locked combretastatin analogs possessing potent apoptosis-inducing activity in HL60 and in MDR cell lines
    • Simoni D, Grisolia G, Giannini G, et al. Heterocyclic and phenyl double-bond-locked combretastatin analogs possessing potent apoptosis-inducing activity in HL60 and in MDR cell lines. J Med Chem 2005; 48: 723-36.
    • (2005) J Med Chem , vol.48 , pp. 723-736
    • Simoni, D.1    Grisolia, G.2    Giannini, G.3
  • 98
    • 33646492299 scopus 로고    scopus 로고
    • Isoxazole-type derivatives related to combretastatin A-4 synthesis and biological evaluation
    • Kaffy J, Pontikis R, Carrez D, Croisy A, Monneret C, Florent JC. Isoxazole-type derivatives related to combretastatin A-4 synthesis and biological evaluation. Bioorg Med Chem 2006; 14: 4067-77.
    • (2006) Bioorg Med Chem , vol.14 , pp. 4067-4077
    • Kaffy, J.1    Pontikis, R.2    Carrez, D.3    Croisy, A.4    Monneret, C.5    Florent, J.C.6
  • 99
    • 68649090729 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of 34-diaryl-5-aminoisoxazole derivatives
    • Liu T, Dong X, Xue N, Wub R, He Q, Yang B, Hua Y. Synthesis and biological evaluation of 34-diaryl-5-aminoisoxazole derivatives. Bioorg Med Chem 2009; 17: 6279-85.
    • (2009) Bioorg Med Chem , vol.17 , pp. 6279-6285
    • Liu, T.1    Dong, X.2    Xue, N.3    Wub, R.4    He, Q.5    Yang, B.6    Hua, Y.7
  • 100
    • 77955559364 scopus 로고    scopus 로고
    • Design synthesis and biological evaluation of 3,5-diaryl-isoxazoline/isoxazole pyrrolobenzodiazepine conjugates as potential anticancer agents
    • Kamal A, Reddy JS, Ramaiah MJ, et al. Design synthesis and biological evaluation of 3,5-diaryl-isoxazoline/isoxazole pyrrolobenzodiazepine conjugates as potential anticancer agents. Eur J Med Chem 2010; 45: 3924-37.
    • (2010) Eur J Med Chem , vol.45 , pp. 3924-3937
    • Kamal, A.1    Reddy, J.S.2    Ramaiah, M.J.3
  • 101
    • 79151475531 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of 3,5-diaryl isoxazoline/isoxazole linked 2,3 dihydroquinazolinone hybrids as anticancer agents
    • Kamal A, Bharathi EV, Reddy JS, et al. Synthesis and biological evaluation of 3,5-diaryl isoxazoline/isoxazole linked 2,3 dihydroquinazolinone hybrids as anticancer agents. Eur J Med Chem 2011; 46: 691-703.
    • (2011) Eur J Med Chem , vol.46 , pp. 691-703
    • Kamal, A.1    Bharathi, E.V.2    Reddy, J.S.3
  • 102
    • 33749258555 scopus 로고    scopus 로고
    • Novel imidazolebased combretastatin A-4 analogs: Evaluation of their in vitro antitumor activity and molecular modeling study of their binding to the colchicine site of tubulin
    • Bellina F, Cauteruccio S, Montib S, Rossia R. Novel imidazolebased combretastatin A-4 analogs: evaluation of their in vitro antitumor activity and molecular modeling study of their binding to the colchicine site of tubulin. Bioorg Med Chem Lett 2006; 16: 5757-62.
    • (2006) Bioorg Med Chem Lett , vol.16 , pp. 5757-5762
    • Bellina, F.1    Cauteruccio, S.2    Montib, S.3    Rossia, R.4
  • 104
    • 38749112183 scopus 로고    scopus 로고
    • Design synthesis and in vitro antitumor activity of new 1,4-diarylimidazole-2-ones and their 2-thione analogs
    • Congiu C, Cocco MT, Onnis V. Design synthesis and in vitro antitumor activity of new 1,4-diarylimidazole-2-ones and their 2-thione analogs. Bioorg. Med. Chem. Lett. 2008; 18: 989-93.
    • (2008) Bioorg. Med. Chem. Lett , vol.18 , pp. 989-993
    • Congiu, C.1    Cocco, M.T.2    Onnis, V.3
  • 105
    • 40749119680 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of imidazol-2-one derivatives as potential antitumor agents
    • Xue N, Yang X, Wu R, et al. Synthesis and biological evaluation of imidazol-2-one derivatives as potential antitumor agents. Bioorg Med Chem 2008; 16: 2550-7.
    • (2008) Bioorg Med Chem , vol.16 , pp. 2550-2557
    • Xue, N.1    Yang, X.2    Wu, R.3
  • 106
    • 44149102682 scopus 로고    scopus 로고
    • Synthesis and antiproliferative activity of imidazole and imidazoline analogs for melanoma
    • Chen J, Wang Z, Lu Y, Dalton JT, Miller DD, Li W. Synthesis and antiproliferative activity of imidazole and imidazoline analogs for melanoma. Bioorg Med Chem Lett 2008; 18; 3183-7.
    • (2008) Bioorg Med Chem Lett , vol.18 , pp. 3183-3187
    • Chen, J.1    Wang, Z.2    Lu, Y.3    Dalton, J.T.4    Miller, D.D.5    Li, W.6
  • 107
    • 77958501821 scopus 로고    scopus 로고
    • Discovery of novel 2-aryl-4-benzoyl-imidazoles targeting the colchicines binding site in tubulin as potential anticancer agents
    • Chen J, Wang Z, Li CM, et al. Discovery of novel 2-aryl-4-benzoyl-imidazoles targeting the colchicines binding site in tubulin as potential anticancer agents. J Med Chem 2010; 53: 7414-27.
    • (2010) J Med Chem , vol.53 , pp. 7414-7427
    • Chen, J.1    Wang, Z.2    Li, C.M.3
  • 108
    • 77956765452 scopus 로고    scopus 로고
    • 4-(3-Halo/amino-45-dimethoxyphenyl)-5-aryloxazoles and-N-methylimidazoles that are cytotoxic against Combretastatin A-4 resistant tumor cells and vascular disrupting in a cisplatin resistant germ cell tumor model
    • Schobert R, Biersack B, Dietrich A, Effenberger K, Knauer S, Mueller T. 4-(3-Halo/amino-45-dimethoxyphenyl)-5-aryloxazoles and-N-methylimidazoles that are cytotoxic against Combretastatin A-4 resistant tumor cells and vascular disrupting in a cisplatin resistant germ cell tumor model. J Med Chem 2010; 53: 6595-602.
    • (2010) J Med Chem , vol.53 , pp. 6595-6602
    • Schobert, R.1    Biersack, B.2    Dietrich, A.3    Effenberger, K.4    Knauer, S.5    Mueller, T.6
  • 109
    • 79957517004 scopus 로고    scopus 로고
    • Imidazolone-amide bridges and their effects on tubulin polymerization in cis-locked vinylogous combretastatin A-4 analogs: Synthesis and biological evaluation
    • Li YW, Liu J, Liu N, et al. Imidazolone-amide bridges and their effects on tubulin polymerization in cis-locked vinylogous combretastatin A-4 analogs: Synthesis and biological evaluation. Bioorg Med Chem 2011; 19: 3579-84.
    • (2011) Bioorg Med Chem , vol.19 , pp. 3579-3584
    • Li, Y.W.1    Liu, J.2    Liu, N.3
  • 110
    • 77949492506 scopus 로고    scopus 로고
    • Novel derivatives of 1,3,4-oxadiazoles are potent mitostatic agents featuring strong microtubule depolymerizing activity in the sea urchin embryo and cell culture assays
    • Kiselyov AS, Semenova MN, Chernyshova NB, et al. Novel derivatives of 1,3,4-oxadiazoles are potent mitostatic agents featuring strong microtubule depolymerizing activity in the sea urchin embryo and cell culture assays. Eur J Med Chem 2010; 45: 1683-97.
    • (2010) Eur J Med Chem , vol.45 , pp. 1683-1697
    • Kiselyov, A.S.1    Semenova, M.N.2    Chernyshova, N.B.3
  • 111
    • 79957516149 scopus 로고    scopus 로고
    • Synthesis of novel 1,2,4-oxadiazoles and analogs as potential anticancer agents
    • Kumar D, Patel G, Chavers AK, Chang KH, Shah K. Synthesis of novel 1,2,4-oxadiazoles and analogs as potential anticancer agents. Eur J Med Chem 2011; 46: 3085-92.
    • (2011) Eur J Med Chem , vol.46 , pp. 3085-3092
    • Kumar, D.1    Patel, G.2    Chavers, A.K.3    Chang, K.H.4    Shah, K.5
  • 112
    • 84855777422 scopus 로고    scopus 로고
    • Design, synthesis, biological evaluation and molecular modeling of 1,3,4-oxadiazoline analogs of combretastatin A-4 as novel antitubulin agents
    • Hu Y, Lu X, Luo Y, Yan R, Li QS, Zhu HL. Design, synthesis, biological evaluation and molecular modeling of 1,3,4-oxadiazoline analogs of combretastatin A-4 as novel antitubulin agents. Bioorg Med Chem 2012; 20: 903-9.
    • (2012) Bioorg Med Chem , vol.20 , pp. 903-909
    • Hu, Y.1    Lu, X.2    Luo, Y.3    Yan, R.4    Li, Q.S.5    Zhu, H.L.6
  • 113
    • 74849140125 scopus 로고    scopus 로고
    • Design, synthesis and biological evaluations of 2,5-diaryl,2,3-dihydro-1,3,4-oxadiazoline analogs of combretastatin A-4
    • Lee L, Robb LM, Lee M, et al. Design, synthesis and biological evaluations of 2,5-diaryl,2,3-dihydro-1,3,4-oxadiazoline analogs of combretastatin A-4. J Med Chem 2010; 53: 325-34.
    • (2010) J Med Chem , vol.53 , pp. 325-334
    • Lee, L.1    Robb, L.M.2    Lee, M.3
  • 114
    • 26844456404 scopus 로고    scopus 로고
    • Synthesis and structureactivity relationships of 1,2,4-triazoles as a novel class of potent tubulin polymerization inhibitors
    • Ouyang X, Chen X, Piatnitski EL, et al. Synthesis and structureactivity relationships of 1,2,4-triazoles as a novel class of potent tubulin polymerization inhibitors. Bioorg Med Chem Lett 2005; 15: 5154-9.
    • (2005) Bioorg Med Chem Lett , vol.15 , pp. 5154-5159
    • Ouyang, X.1    Chen, X.2    Piatnitski, E.L.3
  • 117
    • 43049130754 scopus 로고    scopus 로고
    • 1,5-Disubstituted 1,2,3-triazoles as cis-restricted analogs of combretastatin A-4: Synthesis molecular modeling and evaluation as cytotoxic agents and inhibitors of tubulin
    • Odlo K, Hntzen J, Fournier-Dit-Chabert J, et al. 1,5-Disubstituted 1,2,3-triazoles as cis-restricted analogs of combretastatin A-4: synthesis molecular modeling and evaluation as cytotoxic agents and inhibitors of tubulin. Bioorg Med Chem 2008; 16: 4829-38.
    • (2008) Bioorg Med Chem , vol.16 , pp. 4829-4838
    • Odlo, K.1    Hntzen, J.2    Fournier-Dit-Chabert, J.3
  • 118
    • 77952737457 scopus 로고    scopus 로고
    • Synthesis and antitumor activity of 1,5-disubstituted 1,2,4-triazoles as cisrestricted combretastatin analogs
    • Romagnoli R, Baraldi PG, Cruz-Lopez O, et al. Synthesis and antitumor activity of 1,5-disubstituted 1,2,4-triazoles as cisrestricted combretastatin analogs. J Med Chem 2010; 53: 4248-58.
    • (2010) J Med Chem , vol.53 , pp. 4248-4258
    • Romagnoli, R.1    Baraldi, P.G.2    Cruz-Lopez, O.3
  • 119
    • 84862916801 scopus 로고    scopus 로고
    • Synthesis and evaluation of 1,5-Disubstituted tetrazoles as rigid analogs of combretastatin A-4 with potent antiproliferative and antitumor activity
    • Romagnoli R, Baraldi PG, Salvador MK, et al. Synthesis and evaluation of 1,5-Disubstituted tetrazoles as rigid analogs of combretastatin A-4 with potent antiproliferative and antitumor activity. J Med Chem 2012; 55: 475-88.
    • (2012) J Med Chem , vol.55 , pp. 475-488
    • Romagnoli, R.1    Baraldi, P.G.2    Salvador, M.K.3
  • 120
    • 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: 2303-8.
    • (1999) Bioorg Med Chem Lett , vol.9 , pp. 2303-2308
    • Medarde, M.1    Ramos, A.C.2    Caballero, E.3
  • 121
    • 0035924236 scopus 로고    scopus 로고
    • Synthetic 2-aroylindole derivatives as a new class of potent tubulin-inhibitory antimitotic agents
    • Mahboobi S, Pongratz H, Hufsky H, Hockemeyer J, Frieser M, Lyssenko A. Synthetic 2-aroylindole derivatives as a new class of potent tubulin-inhibitory antimitotic agents. J Med Chem 2001; 44: 4535-53.
    • (2001) J Med Chem , vol.44 , pp. 4535-4553
    • Mahboobi, S.1    Pongratz, H.2    Hufsky, H.3    Hockemeyer, J.4    Frieser, M.5    Lyssenko, A.6
  • 122
    • 3843136376 scopus 로고    scopus 로고
    • Concise synthesis and structure-activity relationships of combretastatin A-4 analogs 1-Aroylindoles and 3-Aroylindoles as novel classes of potent antitubulin agents
    • Liou JP, Chang YL, Kuo FM, et al. Concise synthesis and structure-activity relationships of combretastatin A-4 analogs 1-Aroylindoles and 3-Aroylindoles as novel classes of potent antitubulin agents. J Med Chem 2004; 47: 4247-57.
    • (2004) J Med Chem , vol.47 , pp. 4247-4257
    • Liou, J.P.1    Chang, Y.L.2    Kuo, F.M.3
  • 123
    • 33750339847 scopus 로고    scopus 로고
    • Structure-activity relationship studies of 3-Aroylindoles as potent antimitotic agents
    • Liou JP, Mahindroo N, Chang CW, et al. Structure-activity relationship studies of 3-Aroylindoles as potent antimitotic agents. Chem Med Chem 2006; 1: 1106-18.
    • (2006) Chem Med Chem , vol.1 , pp. 1106-1118
    • Liou, J.P.1    Mahindroo, N.2    Chang, C.W.3
  • 124
    • 34548483407 scopus 로고    scopus 로고
    • 4-and 5-Aroylindoles as novel classes of potent antitubulin agents
    • Liou JP, Wu CY, Hsieh HP, et al. 4-and 5-Aroylindoles as novel classes of potent antitubulin agents. J Med Chem 2007; 50: 4548-52.
    • (2007) J Med Chem , vol.50 , pp. 4548-4552
    • Liou, J.P.1    Wu, C.Y.2    Hsieh, H.P.3
  • 125
    • 65549144450 scopus 로고    scopus 로고
    • Synthesis and structure-activity relationships of 1-Benzyl-4,5,6-trimethoxyindoles as a novel class of potent antimitotic agents
    • Lai MJ, Kuo CC, Yeh TK, et al. Synthesis and structure-activity relationships of 1-Benzyl-4,5,6-trimethoxyindoles as a novel class of potent antimitotic agents. Chem Med Chem 2009; 4: 588-93.
    • (2009) Chem Med Chem , vol.4 , pp. 588-593
    • Lai, M.J.1    Kuo, C.C.2    Yeh, T.K.3
  • 126
    • 10044236627 scopus 로고    scopus 로고
    • Arylthioindoles potent inhibitors of tubulin polymerization
    • Martino GD, Regina GL, Coluccia A, et al. Arylthioindoles potent inhibitors of tubulin polymerization. J Med Chem 2004; 47: 6120-3.
    • (2004) J Med Chem , vol.47 , pp. 6120-6123
    • Martino, G.D.1    Regina, G.L.2    Coluccia, A.3
  • 127
    • 32344432249 scopus 로고    scopus 로고
    • Arylthioindoles potent inhibitors of tubulin polymerization. 2. structure activity relationships and molecular modeling studies
    • Martino GD, Edler MC, Regina GL, et al. Arylthioindoles potent inhibitors of tubulin polymerization. 2. structure activity relationships and molecular modeling studies. J Med Chem 2006; 49: 947-54.
    • (2006) J Med Chem , vol.49 , pp. 947-954
    • Martino, G.D.1    Edler, M.C.2    Regina, G.L.3
  • 128
    • 34250869030 scopus 로고    scopus 로고
    • Arylthioindole inhibitors of tubulin polymerization. 3. Biological evaluation structureactivity relationships and molecular modeling studies
    • Regina GL, Edler MC, Brancale A, et al. Arylthioindole inhibitors of tubulin polymerization. 3. Biological evaluation structureactivity relationships and molecular modeling studies. J Med Chem 2007; 50: 2865-74.
    • (2007) J Med Chem , vol.50 , pp. 2865-2874
    • Regina, G.L.1    Edler, M.C.2    Brancale, A.3
  • 129
    • 72249084715 scopus 로고    scopus 로고
    • New arylthioindoles and related bioisosteres at the sulfur bridging group. 4. Synthesis tubulin polymerization cell growth inhibition and molecular modeling studies
    • Regina GL, Sarkar T, Bai R, et al. New arylthioindoles and related bioisosteres at the sulfur bridging group. 4. Synthesis tubulin polymerization cell growth inhibition and molecular modeling studies. J Med Chem 2009; 52: 7512-7.
    • (2009) J Med Chem , vol.52 , pp. 7512-7517
    • Regina, G.L.1    Sarkar, T.2    Bai, R.3
  • 130
    • 84055211830 scopus 로고    scopus 로고
    • Design and synthesis of 2-Heterocyclyl-3-arylthio-1H-indoles as potent tubulin polymerization and cell growth inhibitors with improved metabolic stability
    • Regina GL, Bai R, Rensen W, et al. Design and synthesis of 2-Heterocyclyl-3-arylthio-1H-indoles as potent tubulin polymerization and cell growth inhibitors with improved metabolic stability J Med Chem 2011; 54: 8394-406.
    • (2011) J Med Chem , vol.54 , pp. 8394-8406
    • Regina, G.L.1    Bai, R.2    Rensen, W.3
  • 131
    • 33747199112 scopus 로고    scopus 로고
    • Structure-activity-relationship studies of conformationally restricted analogs of combretastatin A-4 derived from SU5416
    • Pandit B, Sun Y, Chen P, et al. Structure-activity-relationship studies of conformationally restricted analogs of combretastatin A-4 derived from SU5416 Bioorg Med Chem 2006; 14: 6492-501.
    • (2006) Bioorg Med Chem , vol.14 , pp. 6492-6501
    • Pandit, B.1    Sun, Y.2    Chen, P.3
  • 132
    • 33646583529 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of 3,4,5-trimethoxy phenyl indol-3-ylmethane derivatives as potential antivascular agents
    • Dupeyre G, Chabot GG, Thoret S, et al. Synthesis and biological evaluation of 3,4,5-trimethoxy phenyl indol-3-ylmethane derivatives as potential antivascular agents. Bioorg Med Chem 2006; 14: 4410-26.
    • (2006) Bioorg Med Chem , vol.14 , pp. 4410-4426
    • Dupeyre, G.1    Chabot, G.G.2    Thoret, S.3
  • 133
    • 34250170875 scopus 로고    scopus 로고
    • Novel potent antimitotic heterocyclic ketones: Synthesis antiproliferative activity and structure-activity relationships
    • Hu L, Jiang J, Qu J, et al. Novel potent antimitotic heterocyclic ketones: Synthesis antiproliferative activity and structure-activity relationships. Bioorg Med Chem Lett 2007; 17: 3613-7.
    • (2007) Bioorg Med Chem Lett , vol.17 , pp. 3613-3617
    • Hu, L.1    Jiang, J.2    Qu, J.3
  • 134
    • 41649113513 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of 1-Methyl-2-(3-4-5 trimethoxybenzoyl)-3-aminoindoles as a new class of antimitotic agents and tubulin inhibitors
    • Romagnoli R, Baraldi PG, Sarkar T, et al. Synthesis and biological evaluation of 1-Methyl-2-(3-4-5 trimethoxybenzoyl)-3-aminoindoles as a new class of antimitotic agents and tubulin inhibitors. J Med Chem 2008; 51: 1464-8.
    • (2008) J Med Chem , vol.51 , pp. 1464-1468
    • Romagnoli, R.1    Baraldi, P.G.2    Sarkar, T.3
  • 135
    • 44449096594 scopus 로고    scopus 로고
    • Diarylmethyloxime and hydrazone derivatives with 5-indolyl moieties as potent inhibitors of tubulin polymerization
    • Alvarez C, Alvarez R, Corchete P, et al. Diarylmethyloxime and hydrazone derivatives with 5-indolyl moieties as potent inhibitors of tubulin polymerization. Bioorg Med Chem 2008; 16: 5952-61.
    • (2008) Bioorg Med Chem , vol.16 , pp. 5952-5961
    • Alvarez, C.1    Alvarez, R.2    Corchete, P.3
  • 136
    • 48449088613 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of new disubstituted analogs of 6-methoxy-3-(3'4'5'-Trimethoxybenzoyl)-1H-indole (BPR0L075) as potential antivascular agents
    • Ty N, Dupeyre G, Chabot GG, et al. Synthesis and biological evaluation of new disubstituted analogs of 6-methoxy-3-(3'4'5'-Trimethoxybenzoyl)-1H-indole (BPR0L075) as potential antivascular agents. Bioorg Med Chem 2008; 16: 7494-503.
    • (2008) Bioorg Med Chem , vol.16 , pp. 7494-7503
    • Ty, N.1    Dupeyre, G.2    Chabot, G.G.3
  • 137
    • 68549135156 scopus 로고    scopus 로고
    • Synthesis and evaluation of 3-Aroylindoles as anticancer agents: Metabolite approach
    • Wu YS, Coumar MS, Chang JY, et al. Synthesis and evaluation of 3-Aroylindoles as anticancer agents: metabolite approach. J Med Chem 2009; 52: 4941-5.
    • (2009) J Med Chem , vol.52 , pp. 4941-4945
    • Wu, Y.S.1    Coumar, M.S.2    Chang, J.Y.3
  • 139
    • 0033583499 scopus 로고    scopus 로고
    • A new antitubulin agent containing the benzo[b]thiophene ring system
    • Pinney KG, Bounds AD, Dingerman KM, et al. A new antitubulin agent containing the benzo[b]thiophene ring system. Bioorg Med Chem Lett 1999; 9: 1081-6.
    • (1999) Bioorg Med Chem Lett , vol.9 , pp. 1081-1086
    • Pinney, K.G.1    Bounds, A.D.2    Dingerman, K.M.3
  • 140
    • 23644443814 scopus 로고    scopus 로고
    • Synthesis and preliminary biological evaluation of new antitubulin agents containing different benzo heterocycles
    • Romagnoli R, Baraldi PG, Jung MK, et al. Synthesis and preliminary biological evaluation of new antitubulin agents containing different benzo heterocycles. Bioorg Med Chem Lett 2005; 15: 4048-52.
    • (2005) Bioorg Med Chem Lett , vol.15 , pp. 4048-4052
    • Romagnoli, R.1    Baraldi, P.G.2    Jung, M.K.3
  • 141
    • 77955319048 scopus 로고    scopus 로고
    • Substituted 2-(3'4'5'-trimethoxybenzoyl)-benzo[b]thiophene derivatives as potent tubulin polymerization inhibitors
    • Romagnoli R, Baraldi PG, Carrion MD, et al. Substituted 2-(3'4'5'-trimethoxybenzoyl)-benzo[b]thiophene derivatives as potent tubulin polymerization inhibitors. Bioorg Med Chem 2010; 18: 5114-22.
    • (2010) Bioorg Med Chem , vol.18 , pp. 5114-5122
    • Romagnoli, R.1    Baraldi, P.G.2    Carrion, M.D.3
  • 142
    • 78649333056 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of 2-(3'4'5'-trimethoxybenzoyl)-3-aryl/arylaminobenzo[b] thiophene derivatives as a novel class of antiproliferative agents
    • Romagnoli R, Baraldi PG, Cara CL, Hamel E, Basso G, Viola G. Synthesis and biological evaluation of 2-(3'4'5'-trimethoxybenzoyl)-3-aryl/arylaminobenzo[b] thiophene derivatives as a novel class of antiproliferative agents. Eur J Med Chem 2010; 45: 5781-91.
    • (2010) Eur J Med Chem , vol.45 , pp. 5781-5791
    • Romagnoli, R.1    Baraldi, P.G.2    Cara, C.L.3    Hamel, E.4    Basso, G.5    Viola, G.6
  • 143
    • 80052351229 scopus 로고    scopus 로고
    • Discovery of 7-Hydroxy-6-methoxy-2-methyl-3-(3',4',5'-trimethoxybenzoyl)benzo[b]furan (BNC105) a tubulin polymerization inhibitor with potent antiproliferative and tumor vascular disrupting properties
    • Flynn BL, Gill GS, Grobelny DW, et al. Discovery of 7-Hydroxy-6-methoxy-2-methyl-3-(3',4',5'-trimethoxybenzoyl)benzo[b]furan (BNC105) a tubulin polymerization inhibitor with potent antiproliferative and tumor vascular disrupting properties. J Med Chem 2011; 54: 6014-27.
    • (2011) J Med Chem , vol.54 , pp. 6014-6027
    • Flynn, B.L.1    Gill, G.S.2    Grobelny, D.W.3
  • 144
    • 77953423945 scopus 로고    scopus 로고
    • BNC105: A novel tubulin polymerization inhibitor that selectively disrupts tumor vasculature and displays single-agent antitumor efficacy
    • Kremmidiotis G, Leske AF, Lavranos TC, et al. BNC105: A novel tubulin polymerization inhibitor that selectively disrupts tumor vasculature and displays single-agent antitumor efficacy. Mol Cancer Ther 2010; 9: 1562-73.
    • (2010) Mol Cancer Ther , vol.9 , pp. 1562-1573
    • Kremmidiotis, G.1    Leske, A.F.2    Lavranos, T.C.3
  • 145
    • 51649099415 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of 2-(3'4'5'-trimethoxybenzoyl)-3-N, N-dimethylamino benzo[b]furan derivatives as inhibitors of tubulin polymerization
    • Romagnoli R, Baraldi PG, Sarkar T, et al. Synthesis and biological evaluation of 2-(3'4'5'-trimethoxybenzoyl)-3-N, N-dimethylamino benzo[b]furan derivatives as inhibitors of tubulin polymerization. Bioorg Med Chem 2008; 16: 8419-26.
    • (2008) Bioorg Med Chem , vol.16 , pp. 8419-8426
    • Romagnoli, R.1    Baraldi, P.G.2    Sarkar, T.3
  • 146
    • 78649331023 scopus 로고    scopus 로고
    • Design synthesis and discovery of 5-hydroxyaurone derivatives as growth inhibitors against HUVEC and some cancer cell lines
    • Cheng H, Zhang L, Liu Y, et al. Design synthesis and discovery of 5-hydroxyaurone derivatives as growth inhibitors against HUVEC and some cancer cell lines. Eur J Med Chem 2010; 45: 5950-7.
    • (2010) Eur J Med Chem , vol.45 , pp. 5950-5957
    • Cheng, H.1    Zhang, L.2    Liu, Y.3
  • 147
    • 0344550356 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of 4-arylcoumarin analogs of combretastatins
    • Bailly C, Bal C, Barbier P, et al. Synthesis and biological evaluation of 4-arylcoumarin analogs of combretastatins. J Med Chem 2003; 46: 5437-44.
    • (2003) J Med Chem , vol.46 , pp. 5437-5444
    • Bailly, C.1    Bal, C.2    Barbier, P.3
  • 148
    • 9744248288 scopus 로고    scopus 로고
    • Discovery of 4-aryl-4Hchromenes as new series of apoptosis inducers using a cell-and caspase-based high-throughput screening assay. 1. Structureactivity relationships of the 4-aryl group
    • Kemnitzer W, Kasibhatla S, Jiang S, et al. Discovery of 4-aryl-4Hchromenes as new series of apoptosis inducers using a cell-and caspase-based high-throughput screening assay. 1. Structureactivity relationships of the 4-aryl group. J Med Chem 2004; 47: 6299-310.
    • (2004) J Med Chem , vol.47 , pp. 6299-6310
    • Kemnitzer, W.1    Kasibhatla, S.2    Jiang, S.3
  • 149
    • 9444265410 scopus 로고    scopus 로고
    • Antivascular and antitumor evaluation of 2-amino-4-(3-bromo-4,5-dimethoxy-phenyl)-3-cyano-4H-chromenes a novel series of anticancer agents
    • Gourdeau H, Leblond L, Hamelin B, et al. Antivascular and antitumor evaluation of 2-amino-4-(3-bromo-4,5-dimethoxy-phenyl)-3-cyano-4H-chromenes a novel series of anticancer agents. Mol Cancer Ther 2004; 3: 1375-83.
    • (2004) Mol Cancer Ther , vol.3 , pp. 1375-1383
    • Gourdeau, H.1    Leblond, L.2    Hamelin, B.3
  • 150
    • 25144441808 scopus 로고    scopus 로고
    • Discovery of 4-aryl-4Hchromenes as new series of apoptosis inducers using a cell-and caspase-based high-throughput screening assay. 2. Structureactivity relationships of the 7-and 5-, 6-, 8-positions
    • Kemnitzer W, Kasibhatla S, Jiang S, et al. Discovery of 4-aryl-4Hchromenes as new series of apoptosis inducers using a cell-and caspase-based high-throughput screening assay. 2. Structureactivity relationships of the 7-and 5-, 6-, 8-positions. Bioorg Med Chem Lett 2005; 15: 4745-51.
    • (2005) Bioorg Med Chem Lett , vol.15 , pp. 4745-4751
    • Kemnitzer, W.1    Kasibhatla, S.2    Jiang, S.3
  • 151
    • 34250904254 scopus 로고    scopus 로고
    • Discovery of 4-aryl-4Hchromenes as new series of apoptosis inducers using a cell-and caspase-based high throughput screening assay. 3. Structureactivity relationships of fused rings at the 7, 8-positions
    • Kemnitzer W, Drewe J, Jiang S, et al. Discovery of 4-aryl-4Hchromenes as new series of apoptosis inducers using a cell-and caspase-based high throughput screening assay. 3. Structureactivity relationships of fused rings at the 7, 8-positions. J Med Chem 2007; 50: 2858-64.
    • (2007) J Med Chem , vol.50 , pp. 2858-2864
    • Kemnitzer, W.1    Drewe, J.2    Jiang, S.3
  • 152
    • 39149095977 scopus 로고    scopus 로고
    • Discovery of 4-Aryl-4Hchromenes as a new series of apoptosis inducers using a cell-and caspase-based high throughput screening assay. 4. Structureactivity relationships of N-alkyl substituted pyrrole fused at the 7, 8-positions
    • Kemnitzer W, Kasibhatla S, Jiang S, et al. Discovery of 4-Aryl-4Hchromenes as a new series of apoptosis inducers using a cell-and caspase-based high throughput screening assay. 4. Structureactivity relationships of N-alkyl substituted pyrrole fused at the 7, 8-positions. J Med Chem 2008; 51: 417-23.
    • (2008) J Med Chem , vol.51 , pp. 417-423
    • Kemnitzer, W.1    Kasibhatla, S.2    Jiang, S.3
  • 153
    • 52949146332 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of polymethoxyl-ated 4-heteroarylcoumarins as tubulin assembly inhibitor
    • Ganina OG, Daras E, Bourgarel-Rey V, et al. Synthesis and biological evaluation of polymethoxyl-ated 4-heteroarylcoumarins as tubulin assembly inhibitor. Bioorg Med Chem 2008; 16: 8806-12.
    • (2008) Bioorg Med Chem , vol.16 , pp. 8806-8812
    • Ganina, O.G.1    Daras, E.2    Bourgarel-Rey, V.3
  • 154
    • 79955830810 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of 4-arylcoumarin analogs of combretastatins Part 2
    • Combes S, Barbier P, Douillard S, et al. Synthesis and biological evaluation of 4-arylcoumarin analogs of combretastatins Part 2. J Med Chem 2011; 54: 3153-62.
    • (2011) J Med Chem , vol.54 , pp. 3153-3162
    • Combes, S.1    Barbier, P.2    Douillard, S.3
  • 155
    • 0034676319 scopus 로고    scopus 로고
    • 6-Alkylamino-and 2,3-dihydro-3β-methoxy-2-phenyl-4-quinazolinones and related compounds: Their synthesis cytotoxicity and inhibition of tubulin polymerization
    • Hour MJ, Huang LJ, Kuo SC, et al. 6-Alkylamino-and 2,3-dihydro-3β-methoxy-2-phenyl-4-quinazolinones and related compounds: their synthesis cytotoxicity and inhibition of tubulin polymerization. J Med Chem 2000; 43: 4479-87.
    • (2000) J Med Chem , vol.43 , pp. 4479-4487
    • Hour, M.J.1    Huang, L.J.2    Kuo, S.C.3
  • 156
    • 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. Bioorg Med Chem 2001; 11: 1193-6.
    • (2001) Bioorg Med Chem , vol.11 , pp. 1193-1196
    • Xia, Y.1    Yang, Z.Y.2    Hour, M.J.3
  • 157
    • 1842557498 scopus 로고    scopus 로고
    • Synthesis cytotoxicity and inhibitory effects on tubulin polymerization of a new 3-heterocyclo substituted 2-styrylquinazolinones
    • Raffa D, Edler MC, Daidone G, et al. Synthesis cytotoxicity and inhibitory effects on tubulin polymerization of a new 3-heterocyclo substituted 2-styrylquinazolinones. Eur J Med Chem 2004; 39: 299-304.
    • (2004) Eur J Med Chem , vol.39 , pp. 299-304
    • Raffa, D.1    Edler, M.C.2    Daidone, G.3
  • 158
    • 34548146803 scopus 로고    scopus 로고
    • Synthesis and bioactivities of 6,7,8-trimethoxy-Naryl-4-aminoquinazoline derivatives
    • Liu G, Hu D, Jin L, et al. Synthesis and bioactivities of 6,7,8-trimethoxy-Naryl-4-aminoquinazoline derivatives. Bioorg Med Chem 2007; 15: 6608-17.
    • (2007) Bioorg Med Chem , vol.15 , pp. 6608-6617
    • Liu, G.1    Hu, D.2    Jin, L.3
  • 159
    • 49449111557 scopus 로고    scopus 로고
    • Asymmetric synthesis of 2, 3-Dihydro-2-arylquinazolin-4-ones: Methodology and application to a potent fluorescent tubulin inhibitor with anticancer activity
    • Chinigo GM, Paige M, Grindrod S, Hamel E, Dakshanamurthy S, Chruszcz M. Minor W, Brown ML. Asymmetric synthesis of 2, 3-Dihydro-2-arylquinazolin-4-ones: Methodology and application to a potent fluorescent tubulin inhibitor with anticancer activity. J Med Chem 2008; 51: 4620-31.
    • (2008) J Med Chem , vol.51 , pp. 4620-4631
    • Chinigo, G.M.1    Paige, M.2    Grindrod, S.3    Hamel, E.4    Dakshanamurthy, S.5    Chruszcz, M.6    Minor, W.7    Brown, M.L.8
  • 160
    • 77949378899 scopus 로고    scopus 로고
    • 5-Amino-2-aroylquinolines as highly potent tubulin polymerization inhibitors
    • Nien CY, Chen YC, Kuo CC, et al. 5-Amino-2-aroylquinolines as highly potent tubulin polymerization inhibitors. J Med Chem 2010; 53; 2309-13.
    • (2010) J Med Chem , vol.53 , pp. 2309-2313
    • Nien, C.Y.1    Chen, Y.C.2    Kuo, C.C.3
  • 162
    • 72049105856 scopus 로고    scopus 로고
    • Combretastatin-like chalcones as inhibitors of microtubule polymerization. Part 2: Structure-based discovery of alpha-aryl chalcones
    • Ducki S, Mackenzie G, Greedy B, et al. Combretastatin-like chalcones as inhibitors of microtubule polymerization. Part 2: Structure-based discovery of alpha-aryl chalcones. Bioorg Med Chem 2009; 17: 7711-22.
    • (2009) Bioorg Med Chem , vol.17 , pp. 7711-7722
    • Ducki, S.1    Mackenzie, G.2    Greedy, B.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.