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Volumn 47, Issue 17, 2004, Pages 4247-4257

Concise synthesis and structure-activity relationships of combretastatin A-4 analogues, 1-aroylindoles and 3-aroylindoles, as novel classes of potent antitubulin agents

Author keywords

[No Author keywords available]

Indexed keywords

2 METHYL 6 METHOXY 3 (3',4',5' TRIMETHOXYBENZOYL)INDOLE; 6 ETHOXY 3 (3',4',5' TRIMETHOXYBENZOYL)INDOLE; 6 METHOXY 3 (3',4',5' TRIMETHOXYBENZOYL)INDOLE; 6 METHOXY 3 (3',4',5' TRIMETHOXYBENZYL)INDOLE; 6 METHOXY 3 (3',5' DIMETHOXYBENZOYL)INDOLE; ANTINEOPLASTIC AGENT; BENZOPHENONE DERIVATIVE; CARBONYL DERIVATIVE; COMBRETASTATIN A4; COMBRETASTATIN A4 PHOSPHATE; INDOLE DERIVATIVE; METHYL GROUP; PROTEIN INHIBITOR; TUBULIN; UNCLASSIFIED DRUG;

EID: 3843136376     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm049802l     Document Type: Article
Times cited : (182)

References (21)
  • 1
    • 0031872051 scopus 로고    scopus 로고
    • Tubulin as a target for anticancer drugs: Agents which interact with the mitotic spindle
    • Jordan, A.; Hadfield, J. A.; Lawrence, N. J.; McGown, A. T. 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
  • 2
    • 0029965897 scopus 로고    scopus 로고
    • Antimitotic natural products and their interactions with tubulin
    • Hamel, E. Antimitotic Natural Products and Their Interactions with Tubulin. Med. Res. Rev. 1996, 16, 207-231.
    • (1996) Med. Res. Rev. , vol.16 , pp. 207-231
    • Hamel, E.1
  • 3
    • 0037373826 scopus 로고    scopus 로고
    • The first international conference on vascular targeting: Meeting overview
    • Thorpe, P. E.; Chaplin, D. J.; Blakey, D. C. The First International Conference on Vascular Targeting: Meeting Overview. Cancer Res. 2003, 63, 1144-1147.
    • (2003) Cancer Res. , vol.63 , pp. 1144-1147
    • Thorpe, P.E.1    Chaplin, D.J.2    Blakey, D.C.3
  • 4
    • 0023801309 scopus 로고
    • Interactions of tubulin with potent natural and synthetic analogues of the antimitotic agent combretastatin: A structure-activity study
    • Lin, C. M.; Singh, S. B.; Chu, P. S.; Dempcy, R. O.; Schmidt, J. M.; Pettit, G. R.; Hamel, E. Interactions of Tubulin with Potent Natural and Synthetic Analogues 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    Dempcy, R.O.4    Schmidt, J.M.5    Pettit, G.R.6    Hamel, E.7
  • 5
    • 0036282385 scopus 로고    scopus 로고
    • The biology of the combretastatins as tumour vascular targeting agents
    • (a) Tozer, G. M.; Kanthou, C.; Parkins, C. S.; Hill, S. A. The Biology of the Combretastatins as Tumour Vascular Targeting Agents. 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
  • 6
    • 0035262598 scopus 로고    scopus 로고
    • Targeting tumour vasculature: The development of combretastatin A4
    • (b) Griggs, J.; Metcalfe, J. C.; 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
  • 7
    • 0041421003 scopus 로고    scopus 로고
    • Combretastatin A-4 analogues as antimitotic antitumor agents
    • (a) Nam, N. H. Combretastatin A-4 Analogues as Antimitotic Antitumor Agents. Curr. Med. Chem. 2003, 10, 1697-1722.
    • (2003) Curr. Med. Chem. , vol.10 , pp. 1697-1722
    • Nam, N.H.1
  • 8
    • 0036850914 scopus 로고    scopus 로고
    • Discovery and development of antimitotic agents that inhibit tubulin polymerisation for the treatment of cancer
    • (b) Li, Q.; Sham, H. L. Discovery and Development of Antimitotic Agents That Inhibit Tubulin Polymerisation for the Treatment of Cancer. Exp. Opin. Ther. Patents 2002, 12, 1663-1702.
    • (2002) Exp. Opin. Ther. Patents , vol.12 , pp. 1663-1702
    • Li, Q.1    Sham, H.L.2
  • 9
    • 0346433524 scopus 로고    scopus 로고
    • Combretastatins: From natural products to drug discovery
    • (c) Cirla, A.; Mann, J. Combretastatins: From Natural Products to Drug Discovery. Nat. Prod. Rep. 2003, 20, 558-564.
    • (2003) Nat. Prod. Rep. , vol.20 , pp. 558-564
    • Cirla, A.1    Mann, J.2
  • 15
    • 2442639013 scopus 로고    scopus 로고
    • Synthesis and structure-activity relationships of 3-aminobenzophenones as antimitotic agents
    • Liou, J. P.; Chang, J. Y.; Chang, C. W.; Chang, C. Y.; Mahindroo, N.; Kuo, F. M.; Hsieh, H. P. Synthesis and Structure-Activity Relationships of 3-Aminobenzophenones as Antimitotic Agents. J. Med. Chem. 2004, 47, 2897-2905.
    • (2004) J. Med. Chem. , vol.47 , pp. 2897-2905
    • Liou, J.P.1    Chang, J.Y.2    Chang, C.W.3    Chang, C.Y.4    Mahindroo, N.5    Kuo, F.M.6    Hsieh, H.P.7
  • 16
    • 0030918989 scopus 로고    scopus 로고
    • The use of lewis acid in the reaction of zinc salts of indoles and acyl chloride
    • Yang, C. X.; Patel, H. H.; Ku, Y. Y.; Shah, R.; Sawick, D. The Use of Lewis Acid in the Reaction of Zinc Salts of Indoles and Acyl Chloride. Synth. Commun. 1997, 27, 2125-2132.
    • (1997) Synth. Commun. , vol.27 , pp. 2125-2132
    • Yang, C.X.1    Patel, H.H.2    Ku, Y.Y.3    Shah, R.4    Sawick, D.5
  • 17
    • 0023065565 scopus 로고
    • Isolation, structure, and synthesis of combretastatins A-1 and B-1, potent new inhibitors of microtubule assembly, derived from combretum caffrum
    • Pettit, G. R.; Singh, S. B.; Niven, M. L.; Hamel, E.; Schmidt, J. M. Isolation, Structure, and Synthesis of Combretastatins A-1 and B-1, Potent New Inhibitors of Microtubule Assembly, Derived from Combretum Caffrum. J. Nat. Prod. 1987, 50, 119-131.
    • (1987) J. Nat. Prod. , vol.50 , pp. 119-131
    • Pettit, G.R.1    Singh, S.B.2    Niven, M.L.3    Hamel, E.4    Schmidt, J.M.5
  • 18
    • 0026734208 scopus 로고
    • Synthesis and evaluation of analogues of (z)-1-(4-methoxyphenyl)-2-(3,4, 5-trimethoxyphenyl)ethane as potential cytotoxic and antimitotic agents
    • Cushman, M.; Nagarathnam, D.; Gopal, D.; Lin, C. M.; Hamel, E. Synthesis and Evaluation of Analogues of (Z)-1-(4-Methoxyphenyl)-2-(3,4,5- trimethoxyphenyl)ethane as Potential Cytotoxic and Antimitotic Agents. J. Med. Chem. 1992, 35, 2293-2306.
    • (1992) J. Med. Chem. , vol.35 , pp. 2293-2306
    • Cushman, M.1    Nagarathnam, D.2    Gopal, D.3    Lin, C.M.4    Hamel, E.5
  • 19
    • 3042740981 scopus 로고    scopus 로고
    • BPR0L075, a novel synthetic indole compound with antimitotic activity in human cancer cells, exerts effective antitumoral activity in vivo
    • Kuo, C. C.; Hsieh, H. P.; Pan, W. Y.; Chen, C. P.; Liou, J. P.; Lee, S. J.; Chang, Y. L.; Chen, L. T.; Chen, C. T.; Chang, J. Y. BPR0L075, a Novel Synthetic Indole Compound with Antimitotic Activity in Human Cancer Cells, Exerts Effective Antitumoral Activity in Vivo. Cancer Res. 2004, 64, 4621-4628.
    • (2004) Cancer Res. , vol.64 , pp. 4621-4628
    • Kuo, C.C.1    Hsieh, H.P.2    Pan, W.Y.3    Chen, C.P.4    Liou, J.P.5    Lee, S.J.6    Chang, Y.L.7    Chen, L.T.8    Chen, C.T.9    Chang, J.Y.10
  • 21
    • 0037716242 scopus 로고    scopus 로고
    • Dual inhibition of topoisomerase I tubulin polymerization by BPR0Y007, a novel cytotoxic agent
    • Chang, J. Y.; Hsieh, H. P.; Pan, W. Y.; Liou, J. P.; Bey, S. J.; Chen, L. T.; Song, J. S. Dual Inhibition of Topoisomerase I and Tubulin Polymerization by BPR0Y007, a Novel Cytotoxic Agent. Biochem. Pharmacol. 2003, 65, 2009-2019.
    • (2003) Biochem. Pharmacol. , vol.65 , pp. 2009-2019
    • Chang, J.Y.1    Hsieh, H.P.2    Pan, W.Y.3    Liou, J.P.4    Bey, S.J.5    Chen, L.T.6    Song, J.S.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.