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Journal Abstract Search

116 related items for PubMed ID: 24026016

  • 1. Synthesis and biological evaluation of N-(2-fluorophenyl)-2β-deoxyfuconojirimycin acetamide as a potent inhibitor for α-l-fucosidases.
    Kato A, Okaki T, Ifuku S, Sato K, Hirokami Y, Iwaki R, Kamori A, Nakagawa S, Adachi I, Kiria PG, Onomura O, Minato D, Sugimoto K, Matsuya Y, Toyooka N.
    Bioorg Med Chem; 2013 Nov 01; 21(21):6565-73. PubMed ID: 24026016
    [Abstract] [Full Text] [Related]

  • 2. N-Alkyl-1,5-dideoxy-1,5-imino-l-fucitols as fucosidase inhibitors: Synthesis, molecular modelling and activity against cancer cell lines.
    Zhou J, Negi A, Mirallai SI, Warta R, Herold-Mende C, Carty MP, Ye XS, Murphy PV.
    Bioorg Chem; 2019 Mar 01; 84():418-433. PubMed ID: 30554081
    [Abstract] [Full Text] [Related]

  • 3. Biological properties of D- and L-1-deoxyazasugars.
    Kato A, Kato N, Kano E, Adachi I, Ikeda K, Yu L, Okamoto T, Banba Y, Ouchi H, Takahata H, Asano N.
    J Med Chem; 2005 Mar 24; 48(6):2036-44. PubMed ID: 15771446
    [Abstract] [Full Text] [Related]

  • 4. Roles of mouse sperm-associated alpha-L-fucosidases in fertilization.
    Phopin K, Nimlamool W, Lowe-Krentz LJ, Douglass EW, Taroni JN, Bean BS.
    Mol Reprod Dev; 2013 Apr 24; 80(4):273-85. PubMed ID: 23426913
    [Abstract] [Full Text] [Related]

  • 5. Synthesis of all-cis 2,5-imino-2,5-dideoxy-fucitol and its evaluation as a potent fucosidase and galactosidase inhibitor.
    Ak A, Prudent S, LeNouën D, Defoin A, Tarnus C.
    Bioorg Med Chem Lett; 2010 Dec 15; 20(24):7410-3. PubMed ID: 21050758
    [Abstract] [Full Text] [Related]

  • 6. Development of fucosyltransferase and fucosidase inhibitors.
    Tu Z, Lin YN, Lin CH.
    Chem Soc Rev; 2013 May 21; 42(10):4459-75. PubMed ID: 23588106
    [Abstract] [Full Text] [Related]

  • 7. Asymmetric synthesis of the L-fuco-nojirimycin, a nanomolar alpha-L-fucosidase inhibitor.
    Dubernet M, Defoin A, Tarnus C.
    Bioorg Med Chem Lett; 2006 Mar 01; 16(5):1172-4. PubMed ID: 16376079
    [Abstract] [Full Text] [Related]

  • 8. Novel alpha-L-fucosidase inhibitors from the bark of Angylocalyx pynaertii (Leguminosae).
    Asano N, Yasuda K, Kizu H, Kato A, Fan JQ, Nash RJ, Fleet GW, Molyneux RJ.
    Eur J Biochem; 2001 Jan 01; 268(1):35-41. PubMed ID: 11121099
    [Abstract] [Full Text] [Related]

  • 9. Glycosidase-substrate interactions analysis by STD-NMR spectroscopy: study of alpha-L-fucosidase.
    Berteau O, Sandström C, Bielicki J, Anson DS, Kenne L.
    J Am Chem Soc; 2003 Dec 17; 125(50):15296-7. PubMed ID: 14664566
    [Abstract] [Full Text] [Related]

  • 10. Exploiting the hydrophobic terrain in fucosidases with aryl-substituted pyrrolidine iminosugars.
    Hottin A, Wright DW, Davies GJ, Behr JB.
    Chembiochem; 2015 Jan 19; 16(2):277-83. PubMed ID: 25427942
    [Abstract] [Full Text] [Related]

  • 11. Rapid diversity-oriented synthesis in microtiter plates for in situ screening: discovery of potent and selective alpha-fucosidase inhibitors.
    Wu CY, Chang CF, Chen JS, Wong CH, Lin CH.
    Angew Chem Int Ed Engl; 2003 Oct 06; 42(38):4661-4. PubMed ID: 14533157
    [No Abstract] [Full Text] [Related]

  • 12. Homonojirimycin isomers and N-alkylated homonojirimycins: structural and conformational basis of inhibition of glycosidases.
    Asano N, Nishida M, Kato A, Kizu H, Matsui K, Shimada Y, Itoh T, Baba M, Watson AA, Nash RJ, Lilley PM, Watkin DJ, Fleet GW.
    J Med Chem; 1998 Jul 02; 41(14):2565-71. PubMed ID: 9651160
    [Abstract] [Full Text] [Related]

  • 13. Inhibition of alpha-L-fucosidase by derivatives of deoxyfuconojirimycin and deoxymannojirimycin.
    Winchester B, Barker C, Baines S, Jacob GS, Namgoong SK, Fleet G.
    Biochem J; 1990 Jan 01; 265(1):277-82. PubMed ID: 2137330
    [Abstract] [Full Text] [Related]

  • 14. Stereoselective synthesis of (2S,3S,4R,5S)-5-methylpyrrolidine-3,4-diol derivatives that are highly selective alpha-L-fucosidase inhibitors.
    Moreno-Vargas AJ, Carmona AT, Mora F, Vogel P, Robina I.
    Chem Commun (Camb); 2005 Oct 21; (39):4949-51. PubMed ID: 16205810
    [Abstract] [Full Text] [Related]

  • 15. Discovery of different types of inhibition between the human and thermotoga maritima alpha-fucosidases by fuconojirimycin-based derivatives.
    Ho CW, Lin YN, Chang CF, Li ST, Wu YT, Wu CY, Chang CF, Liu SW, Li YK, Lin CH.
    Biochemistry; 2006 May 09; 45(18):5695-702. PubMed ID: 16669613
    [Abstract] [Full Text] [Related]

  • 16. Stereoselective synthesis of 2-acetamido-1,2-dideoxynojirimycin (DNJNAc) and ureido-DNJNAc derivatives as new hexosaminidase inhibitors.
    de la Fuente A, Mena-Barragán T, Farrar-Tobar RA, Verdaguer X, García Fernández JM, Ortiz Mellet C, Riera A.
    Org Biomol Chem; 2015 Jun 21; 13(23):6500-10. PubMed ID: 25975710
    [Abstract] [Full Text] [Related]

  • 17. Three dimensional structure of a bacterial α-l-fucosidase with a 5-membered iminocyclitol inhibitor.
    Wright DW, Moreno-Vargas AJ, Carmona AT, Robina I, Davies GJ.
    Bioorg Med Chem; 2013 Aug 15; 21(16):4751-4. PubMed ID: 23830696
    [Abstract] [Full Text] [Related]

  • 18. Deoxygenative olefination reaction as the key step in the syntheses of deoxy and iminosugars.
    Chang Hsu Y, Hwu JR.
    Chemistry; 2012 Jun 18; 18(25):7686-90. PubMed ID: 22615220
    [Abstract] [Full Text] [Related]

  • 19. Synthesis of 4-amino-4,5-dideoxy-L-lyxofuranose derivatives and their evaluation as fucosidase inhibitors.
    Chevrier C, Le Nouën D, Defoin A, Tarnus C.
    Carbohydr Res; 2011 Jul 15; 346(10):1202-11. PubMed ID: 21550024
    [Abstract] [Full Text] [Related]

  • 20. A second-generation ferrocene-iminosugar hybrid with improved fucosidase binding properties.
    Hottin A, Scandolera A, Duca L, Wright DW, Davies GJ, Behr JB.
    Bioorg Med Chem Lett; 2016 Mar 15; 26(6):1546-1549. PubMed ID: 26897594
    [Abstract] [Full Text] [Related]

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