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Journal Abstract Search

121 related items for PubMed ID: 30554081

  • 1. 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; 84():418-433. PubMed ID: 30554081
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. 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]

  • 4. 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 15; 268(1):35-41. PubMed ID: 11121099
    [Abstract] [Full Text] [Related]

  • 5. 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 15; 80(4):273-85. PubMed ID: 23426913
    [Abstract] [Full Text] [Related]

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  • 7. 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
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  • 9. 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
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  • 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. 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]

  • 13. 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]

  • 14. 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]

  • 15. Syntheses and biological activities of 1,4-iminoalditol derivatives as alpha-L-fucosidase inhibitors.
    Moreno-Clavijo E, Carmona AT, Moreno-Vargas AJ, Molina L, Robina I.
    Chimia (Aarau); 2011 Jun 18; 65(1-2):40-4. PubMed ID: 21469443
    [Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. Structural basis of alpha-fucosidase inhibition by iminocyclitols with K(i) values in the micro- to picomolar range.
    Wu HJ, Ho CW, Ko TP, Popat SD, Lin CH, Wang AH.
    Angew Chem Int Ed Engl; 2010 May 09; 49(2):337-40. PubMed ID: 19967696
    [No Abstract] [Full Text] [Related]

  • 18. The 'mirror-image' postulate as a guide to the selection and evaluation of pyrrolidines as α-l-fucosidase inhibitors.
    Stocker BL, Jongkees SA, Win-Mason AL, Dangerfield EM, Withers SG, Timmer MS.
    Carbohydr Res; 2013 Feb 15; 367():29-32. PubMed ID: 23295913
    [Abstract] [Full Text] [Related]

  • 19. Convenient synthesis and evaluation of enzyme inhibitory activity of several N-alkyl-, N-phenylalkyl, and cyclic isourea derivatives of 5a-carba-alpha-DL-fucopyranosylamine.
    Ogawa S, Mori M, Takeuchi G, Doi F, Watanabe M, Sakata Y.
    Bioorg Med Chem Lett; 2002 Oct 21; 12(20):2811-4. PubMed ID: 12270152
    [Abstract] [Full Text] [Related]

  • 20. 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]

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