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Journal Abstract Search

346 related items for PubMed ID: 20039683

  • 1. 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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  • 2. In silico design, synthesis and evaluation of 3'-O-benzylated analogs of salacinol, a potent α-glucosidase inhibitor isolated from an Ayurvedic traditional medicine "Salacia".
    Tanabe G, Nakamura S, Tsutsui N, Balakishan G, Xie W, Tsuchiya S, Akaki J, Morikawa T, Ninomiya K, Nakanishi I, Yoshikawa M, Muraoka O.
    Chem Commun (Camb); 2012 Sep 07; 48(69):8646-8. PubMed ID: 22820468
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  • 4. Towards the elusive structure of kotalanol, a naturally occurring glucosidase inhibitor.
    Mohan S, Pinto BM.
    Nat Prod Rep; 2010 Apr 07; 27(4):481-8. PubMed ID: 20336233
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  • 6. Naturally occurring sulfonium-ion glucosidase inhibitors and their derivatives: a promising class of potential antidiabetic agents.
    Mohan S, Eskandari R, Pinto BM.
    Acc Chem Res; 2014 Jan 21; 47(1):211-25. PubMed ID: 23964564
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  • 10. 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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  • 12. Isolation, structure identification and SAR studies on thiosugar sulfonium salts, neosalaprinol and neoponkoranol, as potent α-glucosidase inhibitors.
    Xie W, Tanabe G, Akaki J, Morikawa T, Ninomiya K, Minematsu T, Yoshikawa M, Wu X, Muraoka O.
    Bioorg Med Chem; 2011 Mar 15; 19(6):2015-22. PubMed ID: 21345683
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  • 14. Elongation of the side chain by linear alkyl groups increases the potency of salacinol, a potent α-glucosidase inhibitor from the Ayurvedic traditional medicine "Salacia," against human intestinal maltase.
    Takashima K, Sakano M, Kinouchi E, Nakamura S, Marumoto S, Ishikawa F, Ninomiya K, Nakanishi I, Morikawa T, Tanabe G.
    Bioorg Med Chem Lett; 2021 Feb 01; 33():127751. PubMed ID: 33347966
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  • 15. 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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  • 16. 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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  • 17. 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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  • 18. Human intestinal maltase-glucoamylase: crystal structure of the N-terminal catalytic subunit and basis of inhibition and substrate specificity.
    Sim L, Quezada-Calvillo R, Sterchi EE, Nichols BL, Rose DR.
    J Mol Biol; 2008 Jan 18; 375(3):782-92. PubMed ID: 18036614
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  • 19. 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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  • 20. Alpha-glucosidase inhibitor from Kothala-himbutu (Salacia reticulata WIGHT).
    Ozaki S, Oe H, Kitamura S.
    J Nat Prod; 2008 Jun 22; 71(6):981-4. PubMed ID: 18547114
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