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426 related items for PubMed ID: 29886322

  • 1. Synthesis and biological evaluation of podophyllotoxin derivatives as selective antitumor agents.
    Wu GR, Xu B, Yang YQ, Zhang XY, Fang K, Ma T, Wang H, Xue NN, Chen M, Guo WB, Jia XH, Wang PL, Lei HM.
    Eur J Med Chem; 2018 Jul 15; 155():183-196. PubMed ID: 29886322
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  • 5. 4β-[(4-Alkyl)-1,2,3-triazol-1-yl] podophyllotoxins as anticancer compounds: design, synthesis and biological evaluation.
    Reddy DM, Srinivas J, Chashoo G, Saxena AK, Sampath Kumar HM.
    Eur J Med Chem; 2011 Jun 15; 46(6):1983-91. PubMed ID: 21477899
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  • 7. A rational design strategy of the novel topoisomerase II inhibitors for the synthesis of the 4-O-(2-pyrazinecarboxylic)-4'-demethylepipodophyllotoxin with antitumor activity by diminishing the relaxation reaction of topoisomerase II-DNA decatenation.
    Zhao W, Chen L, Li HM, Wang DJ, Li DS, Chen T, Yuan ZP, Tang YJ.
    Bioorg Med Chem; 2014 Jun 01; 22(11):2998-3007. PubMed ID: 24775914
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  • 8. 4β-amidotriazole linked podophyllotoxin congeners: DNA topoisomerase-IIα inhibition and potential anticancer agents for prostate cancer.
    Reddy VG, Bonam SR, Reddy TS, Akunuri R, Naidu VGM, Nayak VL, Bhargava SK, Kumar HMS, Srihari P, Kamal A.
    Eur J Med Chem; 2018 Jan 20; 144():595-611. PubMed ID: 29289884
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  • 9. Design, synthesis and anti-cancer activity evaluation of podophyllotoxin-norcantharidin hybrid drugs.
    Han HW, Qiu HY, Hu C, Sun WX, Yang RW, Qi JL, Wang XM, Lu GH, Yang YH.
    Bioorg Med Chem Lett; 2016 Jul 15; 26(14):3237-3242. PubMed ID: 27262599
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  • 10. Synthesis and cytotoxic activity on human cancer cells of carbamate derivatives of 4β-(1,2,3-triazol-1-yl)podophyllotoxin.
    Liu JF, Sang CY, Xu XH, Zhang LL, Yang X, Hui L, Zhang JB, Chen SW.
    Eur J Med Chem; 2013 Jun 15; 64():621-8. PubMed ID: 23711769
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  • 11. One-pot synthesis of podophyllotoxin-thiourea congeners by employing NH₂SO₃H/NaI: Anticancer activity, DNA topoisomerase-II inhibition, and apoptosis inducing agents.
    Shankaraiah N, Kumar NP, Amula SB, Nekkanti S, Jeengar MK, Naidu VG, Reddy TS, Kamal A.
    Bioorg Med Chem Lett; 2015 Oct 01; 25(19):4239-44. PubMed ID: 26292628
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  • 12. One-pot synthesis and biological evaluation of N-(aminosulfonyl)-4-podophyllotoxin carbamates as potential anticancer agents.
    Xu XH, Guan XW, Feng SL, Ma YZ, Chen SW, Hui L.
    Bioorg Med Chem Lett; 2017 Jul 01; 27(13):2890-2894. PubMed ID: 28512026
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  • 13. Synthesis and anticancer activity of dimeric podophyllotoxin derivatives.
    Zi CT, Yang L, Xu FQ, Dong FW, Yang D, Li Y, Ding ZT, Zhou J, Jiang ZH, Hu JM.
    Drug Des Devel Ther; 2018 Jul 01; 12():3393-3406. PubMed ID: 30349193
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  • 14. Synthesis and biological evaluation of a series of podophyllotoxins derivatives as a class of potent antitubulin agents.
    Liu Y, Wei D, Zhao Y, Cheng W, Lu Y, Ma Y, Li X, Han C, Wei Y, Cao H, Zhao C.
    Bioorg Med Chem; 2012 Nov 01; 20(21):6285-95. PubMed ID: 23022053
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  • 15. Synthesis and biological evaluation of a novel artesunate-podophyllotoxin conjugate as anticancer agent.
    Zhang L, Chen F, Zhang Z, Chen Y, Wang J.
    Bioorg Med Chem Lett; 2016 Jan 01; 26(1):38-42. PubMed ID: 26615886
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  • 16. Synthesis and cytotoxicity evaluation of novel podophyllotoxin derivatives.
    Chengniu W, Zhonghua W, Yu Z, Chunyan N, Xiaodong Z, Li Z.
    Arch Pharm (Weinheim); 2011 Nov 01; 344(11):735-40. PubMed ID: 21887802
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  • 17. Synthesis of hybrid 4-deoxypodophyllotoxin-5-fluorouracil compounds that inhibit cellular migration and induce cell cycle arrest.
    Guan XW, Xu XH, Feng SL, Tang ZB, Chen SW, Hui L.
    Bioorg Med Chem Lett; 2016 Mar 15; 26(6):1561-1566. PubMed ID: 26873416
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  • 18. Design and synthesis of piperazine acetate podophyllotoxin ester derivatives targeting tubulin depolymerization as new anticancer agents.
    Sun WX, Ji YJ, Wan Y, Han HW, Lin HY, Lu GH, Qi JL, Wang XM, Yang YH.
    Bioorg Med Chem Lett; 2017 Sep 01; 27(17):4066-4074. PubMed ID: 28757065
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  • 19. Synthesis and biological evaluation of podophyllotoxin congeners as tubulin polymerization inhibitors.
    Kamal A, Srinivasa Reddy T, Polepalli S, Shalini N, Reddy VG, Subba Rao AV, Jain N, Shankaraiah N.
    Bioorg Med Chem; 2014 Oct 01; 22(19):5466-75. PubMed ID: 25131956
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  • 20. Synthesis and bioevaluation and doking study of 1H-pyrrolo[2,3-b]pyridine derivatives bearing aromatic hydrazone moiety as c-Met inhibitors.
    Wang W, Xu S, Duan Y, Liu X, Li X, Wang C, Zhao B, Zheng P, Zhu W.
    Eur J Med Chem; 2018 Feb 10; 145():315-327. PubMed ID: 29331754
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