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227 related items for PubMed ID: 17194097

  • 1. New chain-extended analogues of salacinol and blintol and their glycosidase inhibitory activities. Mapping the active-site requirements of human maltase glucoamylase.
    Nasi R, Sim L, Rose DR, Pinto BM.
    J Org Chem; 2007 Jan 05; 72(1):180-6. PubMed ID: 17194097
    [Abstract] [Full Text] [Related]

  • 2. New synthetic routes to chain-extended selenium, sulfur, and nitrogen analogues of the naturally occurring glucosidase inhibitor salacinol and their inhibitory activities against recombinant human maltase glucoamylase.
    Liu H, Nasi R, Jayakanthan K, Sim L, Heipel H, Rose DR, Pinto BM.
    J Org Chem; 2007 Aug 17; 72(17):6562-72. PubMed ID: 17658854
    [Abstract] [Full Text] [Related]

  • 3. Studies directed toward the stereochemical structure determination of the naturally occurring glucosidase inhibitor, kotalanol: synthesis and inhibitory activities against human maltase glucoamylase of seven-carbon, chain-extended homologues of salacinol.
    Nasi R, Patrick BO, Sim L, Rose DR, Pinto BM.
    J Org Chem; 2008 Aug 15; 73(16):6172-81. PubMed ID: 18651773
    [Abstract] [Full Text] [Related]

  • 4. Synthesis and glycosidase inhibitory activities of chain-modified analogues of the glycosidase inhibitors salacinol and blintol.
    Nasi R, Sim L, Rose DR, Pinto BM.
    Carbohydr Res; 2007 Sep 03; 342(12-13):1888-94. PubMed ID: 17359953
    [Abstract] [Full Text] [Related]

  • 5. Synthesis of analogues of salacinol containing a carboxylate inner salt and their inhibitory activities against human maltase glucoamylase.
    Chen W, Sim L, Rose DR, Pinto BM.
    Carbohydr Res; 2007 Sep 03; 342(12-13):1661-7. PubMed ID: 17597595
    [Abstract] [Full Text] [Related]

  • 6. A new class of glucosidase inhibitor: analogues of the naturally occurring glucosidase inhibitor salacinol with different ring heteroatom substituents and acyclic chain extension.
    Liu H, Sim L, Rose DR, Pinto BM.
    J Org Chem; 2006 Apr 14; 71(8):3007-13. PubMed ID: 16599595
    [Abstract] [Full Text] [Related]

  • 7. Synthesis of 2-deoxy-2-fluoro and 1,2-ene derivatives of the naturally occurring glycosidase inhibitor, salacinol, and their inhibitory activities against recombinant human maltase glucoamylase.
    Choubdar N, Sim L, Rose DR, Pinto BM.
    Carbohydr Res; 2008 Apr 07; 343(5):951-6. PubMed ID: 18295754
    [Abstract] [Full Text] [Related]

  • 8. Efficient synthesis of the glucosidase inhibitor blintol, the selenium analogue of the naturally occurring glycosidase inhibitor salacinol.
    Liu H, Pinto BM.
    J Org Chem; 2005 Jan 21; 70(2):753-5. PubMed ID: 15651838
    [Abstract] [Full Text] [Related]

  • 9. Synthesis of D-lyxitol and D-ribitol analogues of the naturally occurring glycosidase inhibitor salacinol.
    Kumar NS, Pinto BM.
    Carbohydr Res; 2005 Dec 12; 340(17):2612-9. PubMed ID: 16198322
    [Abstract] [Full Text] [Related]

  • 10. Synthesis of phosphate derivatives related to the glycosidase inhibitor salacinol.
    Bhat RG, Kumar NS, Pinto BM.
    Carbohydr Res; 2007 Sep 03; 342(12-13):1934-42. PubMed ID: 17572396
    [Abstract] [Full Text] [Related]

  • 11. Synthesis of sulfonium sulfate analogues of disaccharides and their conversion to chain-extended homologues of salacinol: new glycosidase inhibitors.
    Johnston BD, Jensen HH, Pinto BM.
    J Org Chem; 2006 Feb 03; 71(3):1111-8. PubMed ID: 16438529
    [Abstract] [Full Text] [Related]

  • 12. Synthesis, enzymatic activity, and X-ray crystallography of an unusual class of amino acids.
    Chen W, Kuntz DA, Hamlet T, Sim L, Rose DR, Mario Pinto B.
    Bioorg Med Chem; 2006 Dec 15; 14(24):8332-40. PubMed ID: 17010621
    [Abstract] [Full Text] [Related]

  • 13. Synthesis of a biologically active isomer of kotalanol, a naturally occurring glucosidase inhibitor.
    Eskandari R, Jayakanthan K, Kuntz DA, Rose DR, Pinto BM.
    Bioorg Med Chem; 2010 Apr 15; 18(8):2829-35. PubMed ID: 20363144
    [Abstract] [Full Text] [Related]

  • 14. Synthesis of new analogues of salacinol containing a pendant hydroxymethyl group as potential glycosidase inhibitors.
    Nasi R, Pinto BM.
    Carbohydr Res; 2006 Oct 16; 341(14):2305-11. PubMed ID: 16854397
    [Abstract] [Full Text] [Related]

  • 15. Biological evaluation of de-O-sulfonated analogs of salacinol, the role of sulfate anion in the side chain on the alpha-glucosidase inhibitory activity.
    Tanabe G, Yoshikai K, Hatanaka T, Yamamoto M, Shao Y, Minematsu T, Muraoka O, Wang T, Matsuda H, Yoshikawa M.
    Bioorg Med Chem; 2007 Jun 01; 15(11):3926-37. PubMed ID: 17416527
    [Abstract] [Full Text] [Related]

  • 16. Inhibition of recombinant human maltase glucoamylase by salacinol and derivatives.
    Rossi EJ, Sim L, Kuntz DA, Hahn D, Johnston BD, Ghavami A, Szczepina MG, Kumar NS, Sterchi EE, Nichols BL, Pinto BM, Rose DR.
    FEBS J; 2006 Jun 01; 273(12):2673-83. PubMed ID: 16817895
    [Abstract] [Full Text] [Related]

  • 17. Synthesis of 2-amido, 2-amino, and 2-azido derivatives of the nitrogen analogue of the naturally occurring glycosidase inhibitor salacinol and their inhibitory activities against O-GlcNAcase and NagZ enzymes.
    Choubdar N, Bhat RG, Stubbs KA, Yuzwa S, Pinto BM.
    Carbohydr Res; 2008 Jul 21; 343(10-11):1766-77. PubMed ID: 18358456
    [Abstract] [Full Text] [Related]

  • 18. Synthesis of a salacinol analogue and its alpha-glucosidase inhibitory activity.
    Shao Y, Osamu M, Kazuya Y, Yoshiharu M, Eriko Y, Toshie M, Genzoh T, Hisashi M, Masayuki Y, You QD.
    Yao Xue Xue Bao; 2006 Jul 21; 41(7):647-53. PubMed ID: 17007358
    [Abstract] [Full Text] [Related]

  • 19. Synthesis of S-alkylated sulfonium-ions and their glucosidase inhibitory activities against recombinant human maltase glucoamylase.
    Mohan S, Sim L, Rose DR, Pinto BM.
    Carbohydr Res; 2007 May 21; 342(7):901-12. PubMed ID: 17316580
    [Abstract] [Full Text] [Related]

  • 20. Zwitterionic glycosidase inhibitors: salacinol and related analogues.
    Mohan S, Pinto BM.
    Carbohydr Res; 2007 Sep 03; 342(12-13):1551-80. PubMed ID: 17559821
    [Abstract] [Full Text] [Related]

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