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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

104 related articles for article (PubMed ID: 16481162)

  • 41. A facile synthesis of D-glucose-type gem-diamine 1-N-iminosugars: a new family of glucosidase inhibitors.
    Shitara E; Nishimura Y; Kojima F; Takeuchi T
    Bioorg Med Chem; 1999 Jun; 7(6):1241-6. PubMed ID: 10428397
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Iminosugar glycosidase inhibitors: structural and thermodynamic dissection of the binding of isofagomine and 1-deoxynojirimycin to beta-glucosidases.
    Zechel DL; Boraston AB; Gloster T; Boraston CM; Macdonald JM; Tilbrook DM; Stick RV; Davies GJ
    J Am Chem Soc; 2003 Nov; 125(47):14313-23. PubMed ID: 14624580
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Nucleophilic opening of epoxyazepanes: expanding the family of polyhydroxyazepane-based glycosidase inhibitors.
    Li H; Schütz C; Favre S; Zhang Y; Vogel P; Sinaÿ P; Blériot Y
    Org Biomol Chem; 2006 May; 4(9):1653-62. PubMed ID: 16633556
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Synthesis of new analogues of salacinol containing a pendant hydroxymethyl group as potential glycosidase inhibitors.
    Nasi R; Pinto BM
    Carbohydr Res; 2006 Oct; 341(14):2305-11. PubMed ID: 16854397
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Synthesis of pyrrolidine homoazasugars and 3,4-dihydroxy-5-hydroxymethylprolines using aldol additions of metalated bislactim ethers to 2,4-O-ethylidene-D-erythroses.
    Blanco O; Pato C; Ruiz M; Ojea V
    Org Biomol Chem; 2009 Jun; 7(11):2310-21. PubMed ID: 19462040
    [TBL] [Abstract][Full Text] [Related]  

  • 46. A concise synthesis of N-substituted fagomine derivatives and the systematic exploration of their α-glycosidase inhibition.
    Jiang FX; Liu QZ; Zhao D; Luo CT; Guo CP; Ye WC; Luo C; Chen H
    Eur J Med Chem; 2014 Apr; 77():211-22. PubMed ID: 24642564
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Powerful probes for glycosidases: novel, fluorescently tagged glycosidase inhibitors.
    Hermetter A; Scholze H; Stütz AE; Withers SG; Wrodnigg TM
    Bioorg Med Chem Lett; 2001 May; 11(10):1339-42. PubMed ID: 11392550
    [TBL] [Abstract][Full Text] [Related]  

  • 48. 1-Deoxy-D-galactonojirimycins with dansyl capped N-substituents as β-galactosidase inhibitors and potential probes for GM1 gangliosidosis affected cell lines.
    Fröhlich RF; Furneaux RH; Mahuran DJ; Saf R; Stütz AE; Tropak MB; Wicki J; Withers SG; Wrodnigg TM
    Carbohydr Res; 2011 Sep; 346(12):1592-8. PubMed ID: 21645885
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Fluorescent-tagged sp2-iminosugars with potent β-glucosidase inhibitory activity.
    Aguilar-Moncayo M; García-Moreno MI; Stütz AE; García Fernández JM; Wrodnigg TM; Ortiz Mellet C
    Bioorg Med Chem; 2010 Nov; 18(21):7439-45. PubMed ID: 20889348
    [TBL] [Abstract][Full Text] [Related]  

  • 50. The first synthesis of substituted azepanes mimicking monosaccharides: a new class of potent glycosidase inhibitors.
    Li H; Blériot Y; Chantereau C; Mallet JM; Sollogoub M; Zhang Y; Rodríguez-García E; Vogel P; Jiménez-Barbero J; Sinaÿ P
    Org Biomol Chem; 2004 May; 2(10):1492-9. PubMed ID: 15136805
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Fine tuning of beta-glucosidase inhibitory activity in the 2,5-dideoxy-2,5-imino-D-mannitol (DMDP) system.
    Wrodnigg TM; Stütz AE; Tarling CA; Withers SG
    Carbohydr Res; 2006 Jul; 341(10):1717-22. PubMed ID: 16616905
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Synthesis and inhibitory activity of glycosidase inhibitors, glycosylamino-oxazolines.
    Uchida C; Ogawa S
    Bioorg Med Chem; 1996 Feb; 4(2):275-81. PubMed ID: 8814885
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Synthesis and inhibitory activities of novel C-3 substituted azafagomines: a new type of selective inhibitors of α-L-fucosidases.
    Moreno-Clavijo E; Carmona AT; Moreno-Vargas AJ; Rodríguez-Carvajal MA; Robina I
    Bioorg Med Chem; 2010 Jul; 18(13):4648-60. PubMed ID: 20570156
    [TBL] [Abstract][Full Text] [Related]  

  • 54. N- and C-alkylation of seven-membered iminosugars generates potent glucocerebrosidase inhibitors and F508del-CFTR correctors.
    Désiré J; Mondon M; Fontelle N; Nakagawa S; Hirokami Y; Adachi I; Iwaki R; Fleet GW; Alonzi DS; Twigg G; Butters TD; Bertrand J; Cendret V; Becq F; Norez C; Marrot J; Kato A; Blériot Y
    Org Biomol Chem; 2014 Nov; 12(44):8977-96. PubMed ID: 25277226
    [TBL] [Abstract][Full Text] [Related]  

  • 55. 1-Deoxynojirimycins with dansyl capped N-substituents as probes for Morbus Gaucher affected cell lines.
    Fröhlich RF; Furneaux RH; Mahuran DJ; Rigat BA; Stütz AE; Tropak MB; Wicki J; Withers SG; Wrodnigg TM
    Carbohydr Res; 2010 Jul; 345(10):1371-6. PubMed ID: 20471633
    [TBL] [Abstract][Full Text] [Related]  

  • 56. 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]  

  • 57. The synthesis of hybrids of D-galactose with 1-deoxynojirimycin analogues as glycosidase inhibitors.
    Reddy BG; Vankar YD
    Angew Chem Int Ed Engl; 2005 Mar; 44(13):2001-4. PubMed ID: 15724263
    [No Abstract]   [Full Text] [Related]  

  • 58. Biological evaluation of de-O-sulfonated analogs of salacinol, the role of sulfate anion in the side chain on the alpha-glucosidase inhibitory activity.
    Tanabe G; Yoshikai K; Hatanaka T; Yamamoto M; Shao Y; Minematsu T; Muraoka O; Wang T; Matsuda H; Yoshikawa M
    Bioorg Med Chem; 2007 Jun; 15(11):3926-37. PubMed ID: 17416527
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Difluoromethylenated polyhydroxylated pyrrolidines: facile synthesis, crystal structure and biological evaluation.
    Wang RW; Xu J; Lopez O; Bols M; Qing FL
    Future Med Chem; 2009 Aug; 1(5):991-7. PubMed ID: 21426093
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Glucocerebrosidase enhancers for selected Gaucher disease genotypes by modification of α-1-C-substituted imino-D-xylitols (DIXs) by click chemistry.
    Serra-Vinardell J; Díaz L; Casas J; Grinberg D; Vilageliu L; Michelakakis H; Mavridou I; Aerts JM; Decroocq C; Compain P; Delgado A
    ChemMedChem; 2014 Aug; 9(8):1744-54. PubMed ID: 24976039
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.