These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
83 related articles for article (PubMed ID: 22472134)
41. An expeditious one-pot synthesis of 1,6-dideoxy-N-alkylated nojirimycin derivatives and their inhibitory effects on the secretion of IFN-gamma and IL-4. Zhou J; Zhang Y; Zhou X; Zhou J; Zhang LH; Ye XS; Zhang XL Bioorg Med Chem; 2008 Feb; 16(4):1605-12. PubMed ID: 18060793 [TBL] [Abstract][Full Text] [Related]
42. A versatile route to L-hexoses: synthesis of L-mannose and L-altrose. Guaragna A; Napolitano C; D'Alonzo D; Pedatella S; Palumbo G Org Lett; 2006 Oct; 8(21):4863-6. PubMed ID: 17020322 [TBL] [Abstract][Full Text] [Related]
43. Preparation of diamino pseudodisaccharide derivatives from 1,6-anhydro-beta-D-hexopyranoses via aziridine-ring cleavage. Kroutil J; Budesínský M Carbohydr Res; 2007 Feb; 342(2):147-53. PubMed ID: 17204257 [TBL] [Abstract][Full Text] [Related]
44. A novel synthesis of beta-D-mannopyranosyl azide by phase transfer catalysis. Abronina PI; Kachala VV; Kononov LO Carbohydr Res; 2009 Jan; 344(2):240-4. PubMed ID: 19013561 [TBL] [Abstract][Full Text] [Related]
45. Improved anomeric selectivity for the aroylation of sugars. Teresa Barros M; Maycock CD; Rodrigues P; Thomassigny C Carbohydr Res; 2004 May; 339(7):1373-6. PubMed ID: 15113677 [TBL] [Abstract][Full Text] [Related]
46. 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]
47. Development of adamantan-1-yl-methoxy-functionalized 1-deoxynojirimycin derivatives as selective inhibitors of glucosylceramide metabolism in man. Wennekes T; van den Berg RJ; Donker W; van der Marel GA; Strijland A; Aerts JM; Overkleeft HS J Org Chem; 2007 Feb; 72(4):1088-97. PubMed ID: 17243712 [TBL] [Abstract][Full Text] [Related]
48. Synthesis of ovalicin starting from D-mannose. Takahashi S; Hishinuma N; Koshino H; Nakata T J Org Chem; 2005 Nov; 70(24):10162-5. PubMed ID: 16292863 [TBL] [Abstract][Full Text] [Related]
54. Asymmetric synthesis of the L-fuco-nojirimycin, a nanomolar alpha-L-fucosidase inhibitor. Dubernet M; Defoin A; Tarnus C Bioorg Med Chem Lett; 2006 Mar; 16(5):1172-4. PubMed ID: 16376079 [TBL] [Abstract][Full Text] [Related]
55. An improved synthesis of a key intermediate for (+)-biotin from D-mannose. Chen FE; Zhao JF; Xiong FJ; Xie B; Zhang P Carbohydr Res; 2007 Nov; 342(16):2461-4. PubMed ID: 17678881 [TBL] [Abstract][Full Text] [Related]
56. 1-Deoxynojirimycin derivatives from the marine sponge Lendenfeldia chondrodes. Sakai R; Kamiya H J Antibiot (Tokyo); 2006 Aug; 59(8):507-11. PubMed ID: 17080688 [TBL] [Abstract][Full Text] [Related]
57. General approach to glycosidase inhibitors. Enantioselective synthesis of deoxymannojirimycin and swainsonine. Martín R; Murruzzu C; Pericàs MA; Riera A J Org Chem; 2005 Mar; 70(6):2325-8. PubMed ID: 15760222 [TBL] [Abstract][Full Text] [Related]
58. Rapid transformation of D-mannose into orthogonally protected D-glucosamine and D-galactosamine thioglycosides. Emmadi M; Kulkarni SS J Org Chem; 2011 Jun; 76(11):4703-9. PubMed ID: 21510706 [TBL] [Abstract][Full Text] [Related]
59. Preparation of 1,6-di-deoxy-d-galacto and 1,6-di-deoxy-l-altro nojirimycin derivatives by aminocyclization of a 1,5-dicarbonyl derivative. Cuffaro D; Landi M; D'Andrea F; Guazzelli L Carbohydr Res; 2019 Aug; 482():107744. PubMed ID: 31306898 [TBL] [Abstract][Full Text] [Related]
60. Comparison of kifunensine and 1-deoxymannojirimycin binding to class I and II alpha-mannosidases demonstrates different saccharide distortions in inverting and retaining catalytic mechanisms. Shah N; Kuntz DA; Rose DR Biochemistry; 2003 Dec; 42(47):13812-6. PubMed ID: 14636047 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]