The following articles (labelled with PubMed ID or TBD) are for your review
PMID | Data | Article Title | Organization |
25461326 |
20 |
Conformationally-locked N-glycosides: exploiting long-range non-glycone interactions in the design of pharmacological chaperones for Gaucher disease. |
Universitat Rovira I Virgili |
25250725 |
295 |
Identification and development of biphenyl substituted iminosugars as improved dual glucosylceramide synthase/neutral glucosylceramidase inhibitors. |
Leiden University |
24803362 |
12 |
Concise synthesis of C-1-cyano-iminosugars via a new Staudinger/aza Wittig/Strecker multicomponent reaction strategy. |
Technical University Graz |
24657053 |
8 |
Docking and SAR studies of calystegines: binding orientation and influence on pharmacological chaperone effects for Gaucher's disease. |
University Of Toyama |
23880081 |
8 |
Rapid modifications of N-substitution in iminosugars: development of newß-glucocerebrosidase inhibitors and pharmacological chaperones for Gaucher disease. |
Genomics Research Center |
19397268 |
21 |
Rational design and synthesis of highly potent pharmacological chaperones for treatment of N370S mutant Gaucher disease. |
Peking University |
23106358 |
96 |
a-1-C-butyl-1,4-dideoxy-1,4-imino-l-arabinitol as a second-generation iminosugar-based orala-glucosidase inhibitor for improving postprandial hyperglycemia. |
University Of Toyama |
22646221 |
11 |
Discovery, structure-activity relationship, and biological evaluation of noninhibitory small molecule chaperones of glucocerebrosidase. |
National Center For Advancing Translation Sciences |
22762530 |
2 |
Conformationally-locked N-glycosides with selectiveß-glucosidase inhibitory activity: identification of a new non-iminosugar-type pharmacological chaperone for Gaucher disease. |
Universitat Rovira I Virgili |
22512696 |
61 |
Potent aminocyclitol glucocerebrosidase inhibitors are subnanomolar pharmacological chaperones for treating gaucher disease. |
Institut De Qu£Mica Avan£Ada De Catalunya (Iqac-Csic) |
22360565 |
20 |
Rapid assembly of a library of lipophilic iminosugars via the thiol-ene reaction yields promising pharmacological chaperones for the treatment of Gaucher disease. |
University Of British Columbia |
24900357 |
16 |
The myo-1,2-Diaminocyclitol Scaffold Defines Potent Glucocerebrosidase Activators and Promising Pharmacological Chaperones for Gaucher Disease. |
TBA |
20557054 |
56 |
Click chemistry approach to new N-substituted aminocyclitols as potential pharmacological chaperones for Gaucher disease. |
Universitat De Barcelona |
18595718 |
51 |
In vitro inhibition of glycogen-degrading enzymes and glycosidases by six-membered sugar mimics and their evaluation in cell cultures. |
Hokuriku University |
10843222 |
17 |
Novel alpha-glucosidase inhibitors with a tetrachlorophthalimide skeleton. |
University Of Tokyo |
10098675 |
6 |
Homoisofagomines: chemical-enzymatic synthesis and evaluation as alpha- and beta-glucosidase inhibitors. |
Technische Universit£T Berlin |
9871687 |
6 |
A new strong inhibitor of beta-mannosidase. |
S.E.S.N.A.B., Pole Sciences Et Technologie, Universit� |
| 63 |
Potent glycosidase inhibitors, N-phenyl cyclic isourea derivatives of 5-amino- and 5-amino-1-C-(hydroxymethyl)-cyclopentane-1,2,3,4-tetraols |
TBA |
| 15 |
The Interaction of Anhydroalditols with Sweet-Almond -glucosidase and Escherichia coli -galactosidase: implications for the design of potent glycosidase inhibitors |
TBA |
21862336 |
9 |
Synthesis and glycosidase inhibitory profiles of functionalised morpholines and oxazepanes. |
University Of Reading |
21546253 |
41 |
Docking and SAR studies of D- and L-isofagomine isomers as humanß-glucocerebrosidase inhibitors. |
University Of Toyama |
21370884 |
80 |
New glucocerebrosidase inhibitors by exploration of chemical diversity of N-substituted aminocyclitols using click chemistry and in situ screening. |
Spanish National Research Council (Consejo Superior De Investigaciones Cienti£?Ficas) |
21292481 |
4 |
Synthesis of N-alkylated noeurostegines and evaluation of their potential as treatment for Gaucher's disease. |
Aarhus University |
24900289 |
155 |
Identification of Potent and Selective Glucosylceramide Synthase Inhibitors from a Library of N-Alkylated Iminosugars |
TBA |
17187079 |
1 |
Structure of acid beta-glucosidase with pharmacological chaperone provides insight into Gaucher disease. |
Harvard Medical School |
20231099 |
9 |
Synthesis of new beta-1-C-alkylated imino-L-iditols: A comparative study of their activity as beta-glucocerebrosidase inhibitors. |
Universit£ |
19931460 |
6 |
Nanomolar affinity, iminosugar-based chemical probes for specific labeling of lysosomal glucocerebrosidase. |
Utrecht University |
| 37 |
Synthesis of a new inhibitor of α-fucosidase |
TBA |
| 5 |
Synthesis of C2-symmetrical polyhydroxyazepanes as inhibitors of glycosidases |
TBA |
| 6 |
β-Glucosidase inhibitors incorporating pyridinium as a glucosyl mimic |
TBA |
| 25 |
Synthesis and biological activity of C-6 modified derivatives of the glucosidase inhibitor 1-deoxynojirimycin. |
TBA |
15165148 |
13 |
Glycosidase-inhibiting pyrrolidines and pyrrolizidines with a long side chain in Scilla peruviana. |
Hokuriku University |
11392550 |
5 |
Powerful probes for glycosidases: novel, fluorescently tagged glycosidase inhibitors. |
Institut FüR Biochemie Der Technischen UniversitäT Graz |
11327590 |
7 |
Novel, lipophilic derivatives of 2,5-dideoxy-2,5-imino-D-mannitol (DMDP) are powerful beta-glucosidase inhibitors. |
Technische UniversitäT Graz |
25359714 |
55 |
Enzymatic Studies of Isoflavonoids as Selective and Potent Inhibitors of Human Leukocyte 5-Lipo-Oxygenase. |
Universidad De Santiago |
14534366 |
25 |
Comparison of [Dmt1]DALDA and DAMGO in binding and G protein activation at mu, delta, and kappa opioid receptors. |
Cornell University |