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Journal Abstract Search

136 related items for PubMed ID: 20143790

  • 1. 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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  • 2. 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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  • 4. 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
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  • 5. 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. 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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  • 9. The effect of heteroatom substitution of sulfur for selenium in glucosidase inhibitors on intestinal α-glucosidase activities.
    Eskandari R, Jones K, Rose DR, Pinto BM.
    Chem Commun (Camb); 2011 Aug 28; 47(32):9134-6. PubMed ID: 21750824
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  • 10. Potent glucosidase inhibitors: de-O-sulfonated ponkoranol and its stereoisomer.
    Eskandari R, Kuntz DA, Rose DR, Pinto BM.
    Org Lett; 2010 Apr 02; 12(7):1632-5. PubMed ID: 20218632
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  • 11. Role of the side chain stereochemistry in the α-glucosidase inhibitory activity of kotalanol, a potent natural α-glucosidase inhibitor. Part 2.
    Tanabe G, Matsuoka K, Yoshinaga M, Xie W, Tsutsui N, A Amer MF, Nakamura S, Nakanishi I, Wu X, Yoshikawa M, Muraoka O.
    Bioorg Med Chem; 2012 Nov 01; 20(21):6321-34. PubMed ID: 23031648
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  • 12. 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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  • 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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  • 15. 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
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  • 16. Kotalanol, a potent alpha-glucosidase inhibitor with thiosugar sulfonium sulfate structure, from antidiabetic ayurvedic medicine Salacia reticulata.
    Yoshikawa M, Murakami T, Yashiro K, Matsuda H.
    Chem Pharm Bull (Tokyo); 1998 Aug 05; 46(8):1339-40. PubMed ID: 9734318
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  • 18. 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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  • 19. Synthesis and biological evaluation of deoxy salacinols, the role of polar substituents in the side chain on the alpha-glucosidase inhibitory activity.
    Muraoka O, Yoshikai K, Takahashi H, Minematsu T, Lu G, Tanabe G, Wang T, Matsuda H, Yoshikawa M.
    Bioorg Med Chem; 2006 Jan 15; 14(2):500-9. PubMed ID: 16198577
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  • 20. Capillary zone electrophoresis method for the separation of glucosidase inhibitors in extracts of Salacia reticulata, a plant used in ayurvedic treatments of type-2 diabetes.
    Zandberg WF, Mohan S, Kumarasamy J, Pinto BM.
    Anal Chem; 2010 Jun 15; 82(12):5323-30. PubMed ID: 20491445
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