187 related articles for article (PubMed ID: 15337448)
1. Synthesis of novel ammonium and selenonium ions and their evaluation as inhibitors of UDP-galactopyranose mutase.
Veerapen N; Yuan Y; Sanders DA; Pinto BM
Carbohydr Res; 2004 Sep; 339(13):2205-17. PubMed ID: 15337448
[TBL] [Abstract][Full Text] [Related]
2. 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; 126(39):12458-69. PubMed ID: 15453780
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Convergent and stereoselective synthesis of iminosugar-containing Galf and UDP-Galf mimicks: evaluation as inhibitors of UDP-Gal mutase.
Liautard V; Desvergnes V; Itoh K; Liu HW; Martin OR
J Org Chem; 2008 Apr; 73(8):3103-15. PubMed ID: 18358048
[TBL] [Abstract][Full Text] [Related]
5. 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; 72(1):180-6. PubMed ID: 17194097
[TBL] [Abstract][Full Text] [Related]
6. 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; 72(17):6562-72. PubMed ID: 17658854
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Inhibitors of UDP-galactopyranose mutase thwart mycobacterial growth.
Dykhuizen EC; May JF; Tongpenyai A; Kiessling LL
J Am Chem Soc; 2008 May; 130(21):6706-7. PubMed ID: 18447352
[TBL] [Abstract][Full Text] [Related]
9. Chemoenzymatic synthesis, inhibition studies, and X-ray crystallographic analysis of the phosphono analog of UDP-Galp as an inhibitor and mechanistic probe for UDP-galactopyranose mutase.
Partha SK; Sadeghi-Khomami A; Slowski K; Kotake T; Thomas NR; Jakeman DL; Sanders DA
J Mol Biol; 2010 Nov; 403(4):578-90. PubMed ID: 20850454
[TBL] [Abstract][Full Text] [Related]
10. Stereoselective synthesis of beta-1-C-substituted 1,4-dideoxy-1,4-imino-D-galactitols and evaluation as UDP-galactopyranose mutase inhibitors.
Desvergnes S; Desvergnes V; Martin OR; Itoh K; Liu HW; Py S
Bioorg Med Chem; 2007 Oct; 15(19):6443-9. PubMed ID: 17662609
[TBL] [Abstract][Full Text] [Related]
11. The UDP-Galp mutase catalyzed isomerization: synthesis and evaluation of 1,4-anhydro-beta-D-galactopyranose and its [2.2.2] methylene homologue.
Sadeghi-Khomami A; Forcada TJ; Wilson C; Sanders DA; Thomas NR
Org Biomol Chem; 2010 Apr; 8(7):1596-602. PubMed ID: 20237670
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Mechanism-based candidate inhibitors of uridine diphosphate galactopyranose mutase (UGM).
Mahdavi-Amiri Y; Mohan S; Borrelli S; Slowski K; Sanders DA; Pinto BM
Carbohydr Res; 2016 Jan; 419():1-7. PubMed ID: 26595659
[TBL] [Abstract][Full Text] [Related]
14. Synthesis and biological evaluation of nonionic substrate mimics of UDP-Galp as candidate inhibitors of UDP galactopyranose mutase (UGM).
Kuppala R; Borrelli S; Slowski K; Sanders DA; Ravindranathan Kartha KP; Pinto BM
Bioorg Med Chem Lett; 2015 May; 25(9):1995-7. PubMed ID: 25819094
[TBL] [Abstract][Full Text] [Related]
15. Synthesis of D-lyxitol and D-ribitol analogues of the naturally occurring glycosidase inhibitor salacinol.
Kumar NS; Pinto BM
Carbohydr Res; 2005 Dec; 340(17):2612-9. PubMed ID: 16198322
[TBL] [Abstract][Full Text] [Related]
16. 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; 71(8):3007-13. PubMed ID: 16599595
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Chemical probes of UDP-galactopyranose mutase.
Carlson EE; May JF; Kiessling LL
Chem Biol; 2006 Aug; 13(8):825-37. PubMed ID: 16931332
[TBL] [Abstract][Full Text] [Related]
19. 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; 73(16):6172-81. PubMed ID: 18651773
[TBL] [Abstract][Full Text] [Related]
20. Diastereoselective synthesis of novel iminosugar-containing UDP-Galf mimics: potential inhibitors of UDP-Gal mutase and UDP-Galf transferases.
Liautard V; Christina AE; Desvergnes V; Martin OR
J Org Chem; 2006 Sep; 71(19):7337-45. PubMed ID: 16958528
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]