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Journal Abstract Search

189 related items for PubMed ID: 30781470

  • 1. Position-Selective Synthesis and Biological Evaluation of Four Isomeric A-Ring Amino Derivatives of the Alkaloid Luotonin A.
    Ibric A, Eckerstorfer S, Eder M, Louko I, Tunjic L, Heffeter P, Schueffl HH, Marian B, Haider N.
    Molecules; 2019 Feb 16; 24(4):. PubMed ID: 30781470
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  • 2. Synthesis and topoisomerase poisoning activity of A-ring and E-ring substituted luotonin A derivatives.
    Nacro K, Zha CC, Guzzo PR, Jason Herr R, Peace D, Friedrich TD.
    Bioorg Med Chem; 2007 Jun 15; 15(12):4237-46. PubMed ID: 17418582
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  • 3. A-ring and E-ring modifications of the cytotoxic alkaloid Luotonin A: Synthesis, computational and biological studies.
    Ibric A, Battisti V, Deckardt S, Haller AV, Lee C, Prötsch C, Langer T, Heffeter P, Schueffl HH, Marian B, Haider N.
    Bioorg Med Chem; 2020 May 01; 28(9):115443. PubMed ID: 32201190
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  • 4. A Facile Oxidative Opening of the C-Ring in Luotonin A and Derivatives.
    Ibric A, Dutter K, Marian B, Haider N.
    Molecules; 2017 Sep 12; 22(9):. PubMed ID: 28895937
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  • 5. One-pot synthesis of luotonin A and its analogues.
    Tseng MC, Chu YW, Tsai HP, Lin CM, Hwang J, Chu YH.
    Org Lett; 2011 Mar 04; 13(5):920-3. PubMed ID: 21268635
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  • 6. Design, synthesis and antiproliferative activity of decarbonyl luotonin analogues.
    Almansour AI, Arumugam N, Suresh Kumar R, Mahalingam SM, Sau S, Bianchini G, Menéndez JC, Altaf M, Ghabbour HA.
    Eur J Med Chem; 2017 Sep 29; 138():932-941. PubMed ID: 28753517
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  • 7. D-Ring-Modified Analogues of Luotonin A with Reduced Planarity: Design, Synthesis, and Evaluation of Their Topoisomerase Inhibition-Associated Cytotoxicity.
    Almansour AI, Kumar RS, Arumugam N, Bianchini G, Menéndez JC, Mohammad F, Dupadahalli K, Altaf M.
    Biomed Res Int; 2019 Sep 29; 2019():2514524. PubMed ID: 31815127
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  • 11. Discovery of luotonin A analogues as potent fungicides and insecticides: Design, synthesis and biological evaluation inspired by natural alkaloid.
    Yang GZ, Zhang J, Peng JW, Zhang ZJ, Zhao WB, Wang RX, Ma KY, Li JC, Liu YQ, Zhao ZM, Shang XF.
    Eur J Med Chem; 2020 May 15; 194():112253. PubMed ID: 32222678
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  • 14. Synthesis and topoisomerase I inhibitory properties of luotonin A analogues.
    Cagir A, Eisenhauer BM, Gao R, Thomas SJ, Hecht SM.
    Bioorg Med Chem; 2004 Dec 01; 12(23):6287-99. PubMed ID: 15519171
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  • 15. Topoisomerase I-mediated DNA cleavage as a guide to the development of antitumor agents derived from the marine alkaloid lamellarin D: triester derivatives incorporating amino acid residues.
    Tardy C, Facompré M, Laine W, Baldeyrou B, García-Gravalos D, Francesch A, Mateo C, Pastor A, Jiménez JA, Manzanares I, Cuevas C, Bailly C.
    Bioorg Med Chem; 2004 Apr 01; 12(7):1697-712. PubMed ID: 15028262
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  • 16. Concise synthesis and in vitro anticancer activity of benzo[g][1]benzopyrano[4,3-b]indol-6(13H)-ones (BBPIs), topoisomerase I inhibitors based on the marine alkaloid lamellarin.
    Ishibashi F, Fukuda T, Zha S, Hashirano A, Hirao S, Iwao M.
    Biosci Biotechnol Biochem; 2021 Jan 07; 85(1):181-191. PubMed ID: 33577663
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  • 17. Synthesis and cytotoxic activity of substituted luotonin A derivatives.
    Dallavalle S, Merlini L, Beretta GL, Tinelli S, Zunino F.
    Bioorg Med Chem Lett; 2004 Dec 06; 14(23):5757-61. PubMed ID: 15501036
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  • 20. Synthesis and biochemical properties of E-ring modified luotonin A derivatives.
    Cagir A, Jones SH, Eisenhauer BM, Gao R, Hecht SM.
    Bioorg Med Chem Lett; 2004 May 03; 14(9):2051-4. PubMed ID: 15080977
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