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PUBMED FOR HANDHELDS

Journal Abstract Search


241 related items for PubMed ID: 28512026

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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 01; 64():621-8. PubMed ID: 23711769
    [Abstract] [Full Text] [Related]

  • 3. 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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  • 4. Synthesis and evaluation of the apoptosis inducing and CT DNA interaction properties of a series of 4β-carbamoyl 4'-O-demethylepipodophyllotoxins.
    Sang CY, Liu JF, Qin WW, Zhao J, Hui L, Jin YX, Chen SW.
    Eur J Med Chem; 2013 Mar 15; 70():59-67. PubMed ID: 24140948
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  • 5. 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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  • 6. Investigation of podophyllotoxin esters as potential anticancer agents: synthesis, biological studies and tubulin inhibition properties.
    Shareef MA, Duscharla D, Ramasatyaveni G, Dhoke NR, Das A, Ummanni R, Srivastava AK.
    Eur J Med Chem; 2015 Jan 07; 89():128-37. PubMed ID: 25462233
    [Abstract] [Full Text] [Related]

  • 7. Synthesis of a terphenyl substituted 4-aza-2,3-didehydropodophyllotoxin analogues as inhibitors of tubulin polymerization and apoptosis inducers.
    Kamal A, Tamboli JR, Nayak VL, Adil SF, Vishnuvardhan MV, Ramakrishna S.
    Bioorg Med Chem; 2014 May 01; 22(9):2714-23. PubMed ID: 24721832
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. Carbamates of 4'-demethyl-4-deoxypodophyllotoxin: synthesis, cytotoxicity and cell cycle effects.
    Chen SW, Gao YY, Zhou NN, Liu J, Huang WT, Hui L, Jin Y, Jin YX.
    Bioorg Med Chem Lett; 2011 Dec 15; 21(24):7355-8. PubMed ID: 22041063
    [Abstract] [Full Text] [Related]

  • 10. Design, synthesis, biological evaluation, and 3D-QSAR analysis of podophyllotoxin-dioxazole combination as tubulin targeting anticancer agents.
    Wang ZZ, Sun WX, Wang X, Zhang YH, Qiu HY, Qi JL, Pang YJ, Lu GH, Wang XM, Yu FG, Yang YH.
    Chem Biol Drug Des; 2017 Aug 15; 90(2):236-243. PubMed ID: 28079286
    [Abstract] [Full Text] [Related]

  • 11. Cytotoxic activity of a synthetic deoxypodophyllotoxin derivative with an opened D-ring.
    Chen C, Wang CC, Wang Z, Geng WY, Xu H, Song XM, Luo DQ.
    J Asian Nat Prod Res; 2016 May 15; 18(5):486-94. PubMed ID: 27123550
    [Abstract] [Full Text] [Related]

  • 12. 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
    [Abstract] [Full Text] [Related]

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  • 14. 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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  • 19. Synthesis of d-ring modified acid hydrazide derivatives of podophyllotoxin and their anticancer studies as Tubulin inhibiting agents.
    Nerella S, Kankala S, Paidakula S, Gavaji B.
    Bioorg Chem; 2020 Jan 01; 94():103384. PubMed ID: 31776036
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