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138 related items for PubMed ID: 19331410

  • 1. Structure proof and synthesis of kotalanol and de-O-sulfonated kotalanol, glycosidase inhibitors isolated from an herbal remedy for the treatment of type-2 diabetes.
    Jayakanthan K, Mohan S, Pinto BM.
    J Am Chem Soc; 2009 Apr 22; 131(15):5621-6. PubMed ID: 19331410
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  • 3. 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
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  • 4. Synthesis and biological evaluation of heteroanalogues of kotalanol and de-O-sulfonated kotalanol.
    Mohan S, Jayakanthan K, Nasi R, Kuntz DA, Rose DR, Pinto BM.
    Org Lett; 2010 Mar 05; 12(5):1088-91. PubMed ID: 20143790
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  • 5. Probing the active-site requirements of human intestinal N-terminal maltase-glucoamylase: Synthesis and enzyme inhibitory activities of a six-membered ring nitrogen analogue of kotalanol and its de-O-sulfonated derivative.
    Mohan S, Sim L, Rose DR, Pinto BM.
    Bioorg Med Chem; 2010 Nov 15; 18(22):7794-8. PubMed ID: 20970346
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  • 6. Towards the elusive structure of kotalanol, a naturally occurring glucosidase inhibitor.
    Mohan S, Pinto BM.
    Nat Prod Rep; 2010 Apr 15; 27(4):481-8. PubMed ID: 20336233
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  • 7. 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
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  • 9. 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
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  • 10. 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
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  • 16. 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
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  • 17. 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
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  • 18. 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
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  • 19. Zwitterionic glycosidase inhibitors: salacinol and related analogues.
    Mohan S, Pinto BM.
    Carbohydr Res; 2007 Sep 03; 342(12-13):1551-80. PubMed ID: 17559821
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