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249 related items for PubMed ID: 17316580
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. Facile synthesis of sulfonium ion derivatives of 1,5-anhydro-5-thio-L-fucitol as potential alpha-L-fucosidase inhibitors. Gu G, Liu H, Pinto BM. Carbohydr Res; 2006 Nov 06; 341(15):2478-86. PubMed ID: 16930571 [Abstract] [Full Text] [Related]
9. 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]
10. Synthesis of alkylated deoxynojirimycin and 1,5-dideoxy-1,5-iminoxylitol analogues: polar side-chain modification, sulfonium and selenonium heteroatom variants, conformational analysis, and evaluation as glycosidase inhibitors. Szczepina MG, Johnston BD, Yuan Y, Svensson B, Pinto BM. J Am Chem Soc; 2004 Oct 06; 126(39):12458-69. PubMed ID: 15453780 [Abstract] [Full Text] [Related]
11. 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]
12. 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]
13. Probing the intestinal α-glucosidase enzyme specificities of starch-digesting maltase-glucoamylase and sucrase-isomaltase: synthesis and inhibitory properties of 3'- and 5'-maltose-extended de-O-sulfonated ponkoranol. Eskandari R, Jones K, Reddy KR, Jayakanthan K, Chaudet M, Rose DR, Pinto BM. Chemistry; 2011 Dec 23; 17(52):14817-25. PubMed ID: 22127878 [Abstract] [Full Text] [Related]
14. 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]
15. 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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
17. 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 15; 273(12):2673-83. PubMed ID: 16817895 [Abstract] [Full Text] [Related]
18. 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 [Abstract] [Full Text] [Related]
19. 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 [Abstract] [Full Text] [Related]
20. Synthesis of a sulfonium ion analogue of the glycosidase inhibitor swainsonine. Kumar NS, Pinto BM. J Org Chem; 2006 Feb 03; 71(3):1262-4. PubMed ID: 16438551 [Abstract] [Full Text] [Related] Page: [Next] [New Search]