181 related articles for article (PubMed ID: 11931107)
1. Enantiospecific synthesis of 1-azafagomine.
Ernholt BV; Thomsen Ib B; Lohse A; Plesner IW; Jensen KB; Hazell RG; Liang X; Jakobsen A; Bols M
Chemistry; 2000 Jan; 6(2):278-87. PubMed ID: 11931107
[TBL] [Abstract][Full Text] [Related]
2. Advances in the synthesis of homochiral (-)-1-azafagomine and (+)-5-epi-1-azafagomine. 1-N-phenyl carboxamide derivatives of both enantiomers of 1-azafagomine: Leads for the synthesis of active α-glycosidase inhibitors.
Alves MJ; Costa FT; Duarte VC; Fortes AG; Martins JA; Micaelo NM
J Org Chem; 2011 Dec; 76(23):9584-92. PubMed ID: 22017265
[TBL] [Abstract][Full Text] [Related]
3. Synthesis of 5-azacastanospermine, a conformationally restricted azafagomine analogue.
Søndergaard K; Liang X; Bols M
Chemistry; 2001 Jun; 7(11):2324-31. PubMed ID: 11446635
[TBL] [Abstract][Full Text] [Related]
4. Anomer-selective glycosidase inhibition by 2-N-alkylated 1-azafagomines.
Lopez Lopez O; Bols M
Chembiochem; 2007 Apr; 8(6):657-61. PubMed ID: 17352429
[TBL] [Abstract][Full Text] [Related]
5. Homonojirimycin isomers and N-alkylated homonojirimycins: structural and conformational basis of inhibition of glycosidases.
Asano N; Nishida M; Kato A; Kizu H; Matsui K; Shimada Y; Itoh T; Baba M; Watson AA; Nash RJ; Lilley PM; Watkin DJ; Fleet GW
J Med Chem; 1998 Jul; 41(14):2565-71. PubMed ID: 9651160
[TBL] [Abstract][Full Text] [Related]
6. Diels-Alder cycloaddition in the synthesis of 1-azafagomine, analogs, and derivatives as glycosidase inhibitors.
Salgueiro DA; Sousa CE; Fortes AG; Alves MJ
Mini Rev Med Chem; 2012 Dec; 12(14):1465-76. PubMed ID: 22827178
[TBL] [Abstract][Full Text] [Related]
7. Synthesis and evaluation of isourea-type glycomimetics related to the indolizidine and trehazolin glycosidase inhibitor families.
García-Moreno MI; Díaz-Pérez P; Ortiz Mellet C; García Fernández JM
J Org Chem; 2003 Nov; 68(23):8890-901. PubMed ID: 14604359
[TBL] [Abstract][Full Text] [Related]
8. Glycosidase inhibition by ring-modified castanospermine analogues: tackling enzyme selectivity by inhibitor tailoring.
Aguilar-Moncayo M; Gloster TM; Turkenburg JP; García-Moreno MI; Ortiz Mellet C; Davies GJ; García Fernández JM
Org Biomol Chem; 2009 Jul; 7(13):2738-47. PubMed ID: 19532990
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Versatile approach for the synthesis of novel seven-membered iminocyclitols via ring-closing metathesis dihydroxylation reaction.
Lin CC; Pan YS; Patkar LN; Lin HM; Tzou DL; Subramanian T; Lin CC
Bioorg Med Chem; 2004 Jun; 12(12):3259-67. PubMed ID: 15158794
[TBL] [Abstract][Full Text] [Related]
11. Convergent approach toward the synthesis of the stereoisomers of C-6 homologues of 1-deoxynojirimycin and their analogues: evaluation as specific glycosidase inhibitors.
Pandey G; Dumbre SG; Khan MI; Shabab M
J Org Chem; 2006 Oct; 71(22):8481-8. PubMed ID: 17064023
[TBL] [Abstract][Full Text] [Related]
12. Iminoalditol-amino acid hybrids: synthesis and evaluation as glycosidase inhibitors.
Steiner AJ; Stütz AE; Tarling CA; Withers SG; Wrodnigg TM
Carbohydr Res; 2007 Sep; 342(12-13):1850-8. PubMed ID: 17442281
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Synthesis and evaluation of sulfamide-type indolizidines as glycosidase inhibitors.
Benltifa M; García Moreno MI; Ortiz Mellet C; García Fernández JM; Wadouachi A
Bioorg Med Chem Lett; 2008 May; 18(9):2805-8. PubMed ID: 18420407
[TBL] [Abstract][Full Text] [Related]
15. Facile, efficient, and enantiospecific syntheses of 1,1'-N-linked pseudodisaccharides as a new class of glycosidase inhibitors.
Shing TK; Kwong CS; Cheung AW; Kok SH; Yu Z; Li J; Cheng CH
J Am Chem Soc; 2004 Dec; 126(49):15990-2. PubMed ID: 15584732
[TBL] [Abstract][Full Text] [Related]
16. Processing glucosidase inhibition by 1-azafagomine.
Muroi M; Ando O; Bols M; Takatsuki A
Biosci Biotechnol Biochem; 2000 May; 64(5):1103-5. PubMed ID: 10879494
[TBL] [Abstract][Full Text] [Related]
17. Flexible synthesis and biological evaluation of novel 5-deoxyadenophorine analogues.
Pearson MS; Saad RO; Dintinger T; Amri H; Mathé-Allainmat M; Lebreton J
Bioorg Med Chem Lett; 2006 Jun; 16(12):3262-7. PubMed ID: 16603357
[TBL] [Abstract][Full Text] [Related]
18. Structure-activity relationships in aminocyclopentitol glycosidase inhibitors.
Dickson LG; Leroy E; Reymond JL
Org Biomol Chem; 2004 Apr; 2(8):1217-26. PubMed ID: 15064801
[TBL] [Abstract][Full Text] [Related]
19. Synthesis and deconvolution of the first combinatorial library of glycosidase inhibitors.
Lohse A; Jensen KB; Lundgren K; Bols M
Bioorg Med Chem; 1999 Sep; 7(9):1965-71. PubMed ID: 10530945
[TBL] [Abstract][Full Text] [Related]
20. Synthesis and glycosidase inhibitory activity of noeurostegine-a new and potent inhibitor of beta-glucoside hydrolases.
Rasmussen TS; Jensen HH
Org Biomol Chem; 2010 Jan; 8(2):433-41. PubMed ID: 20066281
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
