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121 related items for PubMed ID: 20363144

  • 1. 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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  • 3. 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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  • 4. 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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  • 5. 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
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  • 6. 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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  • 8. 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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  • 9. Role of the side chain stereochemistry in the α-glucosidase inhibitory activity of kotalanol, a potent natural α-glucosidase inhibitor.
    Xie W, Tanabe G, Matsuoka K, Amer MF, Minematsu T, Wu X, Yoshikawa M, Muraoka O.
    Bioorg Med Chem; 2011 Apr 01; 19(7):2252-62. PubMed ID: 21420866
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  • 10. Towards the elusive structure of kotalanol, a naturally occurring glucosidase inhibitor.
    Mohan S, Pinto BM.
    Nat Prod Rep; 2010 Apr 01; 27(4):481-8. PubMed ID: 20336233
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  • 13. Probing the active-site requirements of human intestinal N-terminal maltase glucoamylase: the effect of replacing the sulfate moiety by a methyl ether in ponkoranol, a naturally occurring α-glucosidase inhibitor.
    Eskandari R, Jones K, Rose DR, Pinto BM.
    Bioorg Med Chem Lett; 2010 Oct 01; 20(19):5686-9. PubMed ID: 20801033
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  • 14. 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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  • 16. New glucosidase inhibitors from an ayurvedic herbal treatment for type 2 diabetes: structures and inhibition of human intestinal maltase-glucoamylase with compounds from Salacia reticulata.
    Sim L, Jayakanthan K, Mohan S, Nasi R, Johnston BD, Pinto BM, Rose DR.
    Biochemistry; 2010 Jan 26; 49(3):443-51. PubMed ID: 20039683
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  • 17. 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
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  • 19. 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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