291 related articles for article (PubMed ID: 15453780)
21. Synthesis of nitrogen analogues of salacinol and their evaluation as glycosidase inhibitors.
Ghavami A; Johnston BD; Jensen MT; Svensson B; Pinto BM
J Am Chem Soc; 2001 Jul; 123(26):6268-71. PubMed ID: 11427050
[TBL] [Abstract][Full Text] [Related]
22. Alpha-1-C-alkyl-1-deoxynojirimycin derivatives as potent and selective inhibitors of intestinal isomaltase: remarkable effect of the alkyl chain length on glycosidase inhibitory profile.
Godin G; Compain P; Martin OR; Ikeda K; Yu L; Asano N
Bioorg Med Chem Lett; 2004 Dec; 14(24):5991-5. PubMed ID: 15546715
[TBL] [Abstract][Full Text] [Related]
23. Synthesis and NMR experiments of (4,5,6-13C)-deoxymannojirimycin. A new entry to 13C-labeled glycosidase inhibitors.
Murruzzu C; Alonso M; Canales A; Jiménez-Barbero J; Riera A
Carbohydr Res; 2007 Sep; 342(12-13):1805-12. PubMed ID: 17511974
[TBL] [Abstract][Full Text] [Related]
24. 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; 341(15):2478-86. PubMed ID: 16930571
[TBL] [Abstract][Full Text] [Related]
25. 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; 18(22):7794-8. PubMed ID: 20970346
[TBL] [Abstract][Full Text] [Related]
26. 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; 14(24):8332-40. PubMed ID: 17010621
[TBL] [Abstract][Full Text] [Related]
27. Biological properties of D- and L-1-deoxyazasugars.
Kato A; Kato N; Kano E; Adachi I; Ikeda K; Yu L; Okamoto T; Banba Y; Ouchi H; Takahata H; Asano N
J Med Chem; 2005 Mar; 48(6):2036-44. PubMed ID: 15771446
[TBL] [Abstract][Full Text] [Related]
28. A new class of glycosidase inhibitor: synthesis of salacinol and its stereoisomers.
Ghavami A; Johnston BD; Pinto BM
J Org Chem; 2001 Apr; 66(7):2312-7. PubMed ID: 11281771
[TBL] [Abstract][Full Text] [Related]
29. Efficient synthesis of the glucosidase inhibitor blintol, the selenium analogue of the naturally occurring glycosidase inhibitor salacinol.
Liu H; Pinto BM
J Org Chem; 2005 Jan; 70(2):753-5. PubMed ID: 15651838
[TBL] [Abstract][Full Text] [Related]
30. Synthesis and evaluation of glycosidase inhibitory activity of N-butyl 1-deoxy-D-gluco-homonojirimycin and N-butyl 1-deoxy-L-ido-homonojirimycin.
Markad SD; Karanjule NS; Sharma T; Sabharwal SG; Dhavale DD
Bioorg Med Chem; 2006 Aug; 14(16):5535-9. PubMed ID: 16682208
[TBL] [Abstract][Full Text] [Related]
31. Synthesis of phosphate derivatives related to the glycosidase inhibitor salacinol.
Bhat RG; Kumar NS; Pinto BM
Carbohydr Res; 2007 Sep; 342(12-13):1934-42. PubMed ID: 17572396
[TBL] [Abstract][Full Text] [Related]
32. Zwitterionic glycosidase inhibitors: salacinol and related analogues.
Mohan S; Pinto BM
Carbohydr Res; 2007 Sep; 342(12-13):1551-80. PubMed ID: 17559821
[TBL] [Abstract][Full Text] [Related]
33. Preparation, biochemical characterization and biological properties of radiolabelled N-alkylated deoxynojirimycins.
Mellor HR; Nolan J; Pickering L; Wormald MR; Platt FM; Dwek RA; Fleet GW; Butters TD
Biochem J; 2002 Aug; 366(Pt 1):225-33. PubMed ID: 11982484
[TBL] [Abstract][Full Text] [Related]
34. Synthesis of iminoalditol analogues of galactofuranosides and their activities against glycosidases.
Sandbhor M; Bhasin M; Williams DT; Hsieh M; Wu SH; Zou W
Carbohydr Res; 2008 Nov; 343(17):2878-86. PubMed ID: 18706536
[TBL] [Abstract][Full Text] [Related]
35. Potent and selective inhibition of class II alpha-D-mannosidase activity by a bicyclic sulfonium salt.
Siriwardena A; Strachan H; El-Daher S; Way G; Winchester B; Glushka J; Moremen K; Boons GJ
Chembiochem; 2005 May; 6(5):845-8. PubMed ID: 15800866
[No Abstract] [Full Text] [Related]
36. N-alkylated nitrogen-in-the-ring sugars: conformational basis of inhibition of glycosidases and HIV-1 replication.
Asano N; Kizu H; Oseki K; Tomioka E; Matsui K; Okamoto M; Baba M
J Med Chem; 1995 Jun; 38(13):2349-56. PubMed ID: 7608901
[TBL] [Abstract][Full Text] [Related]
37. Synthesis of a novel class of sulfonium ions as potential inhibitors of UDP-galactopyranose mutase.
Ghavami A; Chen JJ; Mario Pinto B
Carbohydr Res; 2004 Jan; 339(2):401-7. PubMed ID: 14698899
[TBL] [Abstract][Full Text] [Related]
38. Synthesis and biological characterisation of novel N-alkyl-deoxynojirimycin alpha-glucosidase inhibitors.
Rawlings AJ; Lomas H; Pilling AW; Lee MJ; Alonzi DS; Rountree JS; Jenkinson SF; Fleet GW; Dwek RA; Jones JH; Butters TD
Chembiochem; 2009 Apr; 10(6):1101-5. PubMed ID: 19294724
[TBL] [Abstract][Full Text] [Related]
39. Attempted synthesis of 2-acetamido and 2-amino derivatives of salacinol. Ring opening reactions.
Choubdar N; Pinto BM
J Org Chem; 2006 Jun; 71(12):4671-4. PubMed ID: 16749804
[TBL] [Abstract][Full Text] [Related]
40. Glycosidase inhibition by cyclic sulfonium compounds.
Yuasa H; Takada J; Hashimoto H
Bioorg Med Chem Lett; 2001 May; 11(9):1137-9. PubMed ID: 11354361
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
