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Volumn 48, Issue 23, 2005, Pages 7096-7098

Identification of novel and improved antimitotic agents derived from noscapine

Author keywords

[No Author keywords available]

Indexed keywords

ANILINE; ANTIMITOTIC AGENT; DNA; NOSCAPINE; PHENOL; TRIFLUOROMETHANESULFONIC ACID; TUBULIN;

EID: 28544446298     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm050674q     Document Type: Article
Times cited : (59)

References (28)
  • 1
    • 1942438028 scopus 로고    scopus 로고
    • Microtubules as a target for anticancer drugs
    • (a) Jordan, M. A.; Wilson L. Microtubules as a Target for Anticancer Drugs. Nat. Rev. Cancer 2004, 4, 253-265.
    • (2004) Nat. Rev. Cancer , vol.4 , pp. 253-265
    • Jordan, M.A.1    Wilson, L.2
  • 2
    • 0029360519 scopus 로고
    • Microtubule dynamics: Taking aim at a moving target
    • (b) Wilson, L.; Jordan, M. A. Microtubule Dynamics: Taking Aim at a Moving Target. Chem. Biol. 1995, 2, 569-573.
    • (1995) Chem. Biol. , vol.2 , pp. 569-573
    • Wilson, L.1    Jordan, M.A.2
  • 3
    • 0036850914 scopus 로고    scopus 로고
    • Discovery and development of antimitotic agents that inhibit tubulin polymerization for the treatment of cancer
    • Li, Q.; Sham, H. L. Discovery and Development of Antimitotic Agents That Inhibit Tubulin Polymerization for the Treatment of Cancer. Expert Opin. Ther. Pat. 2002, 12 (11), 1663-1702.
    • (2002) Expert Opin. Ther. Pat. , vol.12 , Issue.11 , pp. 1663-1702
    • Li, Q.1    Sham, H.L.2
  • 4
    • 0035493789 scopus 로고    scopus 로고
    • A therapeutic area review of oncology products and players
    • Fleming, S.; Lucas, F.; Schofield, M. A Therapeutic Area Review of Oncology Products and Players. Expert Opin. Emerging Drugs 2001, 6 (2), 317-329.
    • (2001) Expert Opin. Emerging Drugs , vol.6 , Issue.2 , pp. 317-329
    • Fleming, S.1    Lucas, F.2    Schofield, M.3
  • 5
    • 0028224534 scopus 로고
    • Cell biological mechanisms of multidrug resistance in tumors
    • Simon, S. M.; Schindler, M. Cell Biological Mechanisms of Multidrug Resistance in Tumors. Proc. Natl. Acad. Sci U.S.A. 1994, 91, 3497-3504.
    • (1994) Proc. Natl. Acad. Sci U.S.A. , vol.91 , pp. 3497-3504
    • Simon, S.M.1    Schindler, M.2
  • 6
    • 0035003021 scopus 로고    scopus 로고
    • Role of formulation vehicles in taxane pharmacology
    • Van Zuylen, L.; Verweij, J.; Sparreboom, A. Role of Formulation Vehicles in Taxane Pharmacology. Invest. New Drugs 2001, 19, 125-141.
    • (2001) Invest. New Drugs , vol.19 , pp. 125-141
    • Van Zuylen, L.1    Verweij, J.2    Sparreboom, A.3
  • 8
    • 17444429486 scopus 로고
    • Synergists and antagonists of mitotic poisons
    • (a) Lettre, H. Synergists and Antagonists of Mitotic Poisons. Ann. N. Y. Acad. Sci. 1954, 58, 1264-1275.
    • (1954) Ann. N. Y. Acad. Sci. , vol.58 , pp. 1264-1275
    • Lettre, H.1
  • 9
    • 0006164865 scopus 로고
    • Narcotin, ein Mitosegift (narcotine, a mitotic poison)
    • (b) Lettre, H.; Albrecht, M. Narcotin, ein Mitosegift (Narcotine, a Mitotic Poison). Naturwissenschaften 1942, 30, 184-185.
    • (1942) Naturwissenschaften , vol.30 , pp. 184-185
    • Lettre, H.1    Albrecht, M.2
  • 10
    • 0032539565 scopus 로고    scopus 로고
    • Opium alkaloid noscapine is an antitumor agent that arrests metaphase and induces apoptosis in dividing cells
    • (a) Ye, K.; Ke, Y.; Keshava, N.; Shanks, J.; Kapp, J. A.; Tekmal, R. R.; Petros, J.; Joshi, H. C. Opium Alkaloid Noscapine Is an Antitumor Agent That Arrests Metaphase and Induces Apoptosis in Dividing Cells. Proc. Natl. Acad. Sci. U.S.A. 1998, 95, 1601-1606.
    • (1998) Proc. Natl. Acad. Sci. U.S.A. , vol.95 , pp. 1601-1606
    • Ye, K.1    Ke, Y.2    Keshava, N.3    Shanks, J.4    Kapp, J.A.5    Tekmal, R.R.6    Petros, J.7    Joshi, H.C.8
  • 11
    • 0034491250 scopus 로고    scopus 로고
    • Noscapine and analogues as potential chemotherapeutic agents
    • (b) Joshi, H. C.; Zhou, J. Noscapine and Analogues as Potential Chemotherapeutic Agents. Drug News Perspect. 2000, 13 (9), 543-546.
    • (2000) Drug News Perspect. , vol.13 , Issue.9 , pp. 543-546
    • Joshi, H.C.1    Zhou, J.2
  • 12
    • 0033928547 scopus 로고    scopus 로고
    • Noscapine inhibits tumor growth with little toxicity to normal tissues or inhibition of immune responses
    • Ke, Y.; Ye, K.; Grossniklaus, H. E.; Archer, D. R.; Joshi, H. C.; Kapp, J. A. Noscapine Inhibits Tumor Growth with Little Toxicity to Normal Tissues or Inhibition of Immune Responses. Cancer Immunol. Immunother. 2000, 49, 217-225
    • (2000) Cancer Immunol. Immunother. , vol.49 , pp. 217-225
    • Ke, Y.1    Ye, K.2    Grossniklaus, H.E.3    Archer, D.R.4    Joshi, H.C.5    Kapp, J.A.6
  • 16
    • 0000418343 scopus 로고    scopus 로고
    • Palladium-catalyzed amination of aryl triflates
    • Louie, J.; Driver, M. S.; Hamann, B. C. Personal communication
    • (a) Wolfe, J. P.; Buchwald, S. L. Palladium-Catalyzed Amination of Aryl Triflates. J. Org. Chem. 1997, 62, 1264-1267. Louie, J.; Driver, M. S.; Hamann, B. C. Personal communication.
    • (1997) J. Org. Chem. , vol.62 , pp. 1264-1267
    • Wolfe, J.P.1    Buchwald, S.L.2
  • 17
    • 0000777908 scopus 로고    scopus 로고
    • Palladium-catalyzed amination of aryl triflates and importance of triflate addition rate
    • (b) Hartwig, J. F. Palladium-Catalyzed Amination of Aryl Triflates and Importance of Triflate Addition Rate. J. Org. Chem. 1997, 62, 1268-1273.
    • (1997) J. Org. Chem. , vol.62 , pp. 1268-1273
    • Hartwig, J.F.1
  • 18
    • 0032560932 scopus 로고    scopus 로고
    • A highly active catalyst for palladium-catalyzed cross-coupling reactions: Room-temperature suzuki couplings and amination of unactivated aryl chlorides
    • Old, D. W.; Wolfe, J. P.; Buchwald, S. L. A Highly Active Catalyst for Palladium-Catalyzed Cross-Coupling Reactions: Room-Temperature Suzuki Couplings and Amination of Unactivated Aryl Chlorides. J. Am. Chem. Soc. 1998, 120, 9722-9723.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 9722-9723
    • Old, D.W.1    Wolfe, J.P.2    Buchwald, S.L.3
  • 19
    • 0018198927 scopus 로고
    • Neue Reaktionen an Phthalidisochinolinalkaloiden. Alkoxytauschreaktionen und Isomerisierungen an α- Und β-Narcotin
    • Schmidhammer, H.; Klotzer, W. Neue Reaktionen an Phthalidisochinolinalkaloiden. Alkoxytauschreaktionen und Isomerisierungen an α- und β-Narcotin (New Reactions of Phthalidoisoquinoline Alkaloids. Alkoxy Exchange Reactions and Isomerizations of α- and β-Narcotine).Arch. Pharm. (Weinheim, Ger.) 1978, 311, 664-671.
    • (1978) Arch. Pharm. (Weinheim, Ger.) , vol.311 , pp. 664-671
    • Schmidhammer, H.1    Klotzer, W.2
  • 20
  • 21
    • 28544436984 scopus 로고    scopus 로고
    • note
    • 2O in large-scale reactions.
  • 22
    • 0037031625 scopus 로고    scopus 로고
    • Aqueous hydroxide as a base for palladium-catalyzed animation of aryl chlorides and bromides
    • Kuwano, R.; Utsunomiya, M.; Hartwig, J. F. Aqueous Hydroxide as a Base for Palladium-Catalyzed Animation of Aryl Chlorides and Bromides. J. Org. Chem. 2002, 67, 6479-6486.
    • (2002) J. Org. Chem. , vol.67 , pp. 6479-6486
    • Kuwano, R.1    Utsunomiya, M.2    Hartwig, J.F.3
  • 23
    • 0034712156 scopus 로고    scopus 로고
    • Simple, efficient catalyst system for the palladium-catalyzed amination of aryl chlorides, bromides, and triflates
    • Wolfe, J. P.; Tomori, H.; Sadighi, J. P.; Yin, J.; Buchwald, S. L. Simple, Efficient Catalyst System for the Palladium-Catalyzed Amination of Aryl Chlorides, Bromides, and Triflates. J. Org. Chem. 2000, 65, 1158-1174.
    • (2000) J. Org. Chem. , vol.65 , pp. 1158-1174
    • Wolfe, J.P.1    Tomori, H.2    Sadighi, J.P.3    Yin, J.4    Buchwald, S.L.5
  • 24
    • 0042704188 scopus 로고    scopus 로고
    • Palladium-catalyzed synthesis of arylamines from aryl halides and lithium bis(trimethylsilyl)amide as an ammonia equivalent
    • Lee, S.; Jorgensen, M.; Hartwig, J. F. Palladium-Catalyzed Synthesis of Arylamines from Aryl Halides and Lithium Bis(trimethylsilyl)amide as an Ammonia Equivalent. Org. Lett. 2001, 3, 2729-2732.
    • (2001) Org. Lett. , vol.3 , pp. 2729-2732
    • Lee, S.1    Jorgensen, M.2    Hartwig, J.F.3
  • 25
    • 0033597748 scopus 로고    scopus 로고
    • Room-temperature palladium-catalyzed amination of aryl bromides and chlorides and extended scope of aromatic C-N bond formation with a commercial ligand
    • Hartwig, J. F.; Kawatsura, M.; Hauck, S. I.; Shaughnessy, K. H.; Alcazar-Roman, L. M. Room-Temperature Palladium-Catalyzed Amination of Aryl Bromides and Chlorides and Extended Scope of Aromatic C-N Bond Formation with a Commercial Ligand. J. Org. Chem. 1999, 64, 5575-5580.
    • (1999) J. Org. Chem. , vol.64 , pp. 5575-5580
    • Hartwig, J.F.1    Kawatsura, M.2    Hauck, S.I.3    Shaughnessy, K.H.4    Alcazar-Roman, L.M.5
  • 26
    • 0041996505 scopus 로고    scopus 로고
    • An air and thermally stable one-component catalyst for the amination of aryl chlorides
    • Zim, D.; Buchwald, S. L. An Air and Thermally Stable One-Component Catalyst for the Amination of Aryl Chlorides. Org. Lett. 2003, 5, 2413-2415.
    • (2003) Org. Lett. , vol.5 , pp. 2413-2415
    • Zim, D.1    Buchwald, S.L.2
  • 27
    • 0037379660 scopus 로고    scopus 로고
    • Brominated derivatives of noscapine are potent microtubule-interfering agents that perturb mitosis and inhibit cell proliferation
    • Zhou, J.; Gupta, K; Aggarwal, A. R.; Chandra, R.; Panda, D.; Joshi, H. C. Brominated Derivatives of Noscapine Are Potent Microtubule-Interfering Agents That Perturb Mitosis and Inhibit Cell Proliferation. Mol. Pharmacol. 2003, 63, 799-807.
    • (2003) Mol. Pharmacol. , vol.63 , pp. 799-807
    • Zhou, J.1    Gupta, K.2    Aggarwal, A.R.3    Chandra, R.4    Panda, D.5    Joshi, H.C.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.