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Journal Abstract Search

177 related items for PubMed ID: 22329423

  • 1. Synthesis and biological evaluation of neopeltolide and analogs.
    Cui Y, Balachandran R, Day BW, Floreancig PE.
    J Org Chem; 2012 Mar 02; 77(5):2225-35. PubMed ID: 22329423
    [Abstract] [Full Text] [Related]

  • 2. Synthesis and biological evaluation of (+)-neopeltolide analogues: importance of the oxazole-containing side chain.
    Fuwa H, Noguchi T, Kawakami M, Sasaki M.
    Bioorg Med Chem Lett; 2014 Jun 01; 24(11):2415-9. PubMed ID: 24792465
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  • 3. Total synthesis of the antiproliferative macrolide (+)-neopeltolide.
    Guinchard X, Roulland E.
    Org Lett; 2009 Oct 15; 11(20):4700-3. PubMed ID: 19775106
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  • 4. Design, Synthesis and Biological Evaluation of Highly Potent Simplified Archazolids.
    Rivière S, Vielmuth C, Ennenbach C, Abdelrahman A, Lemke C, Gütschow M, Müller CE, Menche D.
    ChemMedChem; 2020 Jul 20; 15(14):1348-1363. PubMed ID: 32363789
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  • 5. Total synthesis and structure-activity investigation of the marine natural product neopeltolide.
    Custar DW, Zabawa TP, Hines J, Crews CM, Scheidt KA.
    J Am Chem Soc; 2009 Sep 02; 131(34):12406-14. PubMed ID: 19663512
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  • 6. Discovery and Development of Macrolides as Anticancer Agents.
    Liu R, Hou Y, Gu Y.
    Curr Top Med Chem; 2021 Sep 02; 21(18):1657-1673. PubMed ID: 34315371
    [Abstract] [Full Text] [Related]

  • 7. Antitumor compounds based on a natural product consensus pharmacophore.
    Lagisetti C, Pourpak A, Jiang Q, Cui X, Goronga T, Morris SW, Webb TR.
    J Med Chem; 2008 Oct 09; 51(19):6220-4. PubMed ID: 18788726
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  • 9. Concise synthesis and biological assessment of (+)-neopeltolide and a 16-member stereoisomer library of 8,9-dehydroneopeltolide: identification of pharmacophoric elements.
    Fuwa H, Kawakami M, Noto K, Muto T, Suga Y, Konoki K, Yotsu-Yamashita M, Sasaki M.
    Chemistry; 2013 Jun 17; 19(25):8100-10. PubMed ID: 23606326
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  • 10. Total synthesis and biological evaluation of (+)-neopeltolide and its analogues.
    Fuwa H, Saito A, Naito S, Konoki K, Yotsu-Yamashita M, Sasaki M.
    Chemistry; 2009 Nov 23; 15(46):12807-18. PubMed ID: 19882704
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  • 13. Synthesis of carbamate derivatives of iejimalides. Retention of normal antiproliferative activity and localization of binding in cancer cells.
    Schweitzer D, Zhu J, Jarori G, Tanaka J, Higa T, Davisson VJ, Helquist P.
    Bioorg Med Chem; 2007 May 01; 15(9):3208-16. PubMed ID: 17337191
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  • 14. Synthesis and biological evaluation of 10,11-dihydrodictyostatin, a potent analogue of the marine anticancer agent dictyostatin.
    Paterson I, Gardner NM, Poullennec KG, Wright AE.
    J Nat Prod; 2008 Mar 01; 71(3):364-9. PubMed ID: 18081257
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  • 17. Synthesis and antiproliferative evaluation of new zampanolide mimics.
    Chen G, Patanapongpibul M, Jiang Z, Zhang Q, Zheng S, Wang G, White JD, Chen QH.
    Org Biomol Chem; 2019 Apr 10; 17(15):3830-3844. PubMed ID: 30924817
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  • 19. Insights into the structure-activity relationship of the anticancer compound ZJ-101: A critical role played by the cyclohexene ring.
    Shah AK, Qian S, Zhang D, Head SA, Liu JO, Jin Z.
    Bioorg Med Chem Lett; 2016 Jun 15; 26(12):2890-2892. PubMed ID: 27133592
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  • 20. Synthesis of a ring-expanded bryostatin analogue.
    Trost BM, Yang H, Thiel OR, Frontier AJ, Brindle CS.
    J Am Chem Soc; 2007 Feb 28; 129(8):2206-7. PubMed ID: 17279751
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