scholarly journals Fluorous Iminoalditols: A New Family of Glycosidase Inhibitors and Pharmacological Chaperones

ChemBioChem ◽  
2010 ◽  
Vol 11 (14) ◽  
pp. 2026-2033 ◽  
Author(s):  
Georg Schitter ◽  
Andreas J. Steiner ◽  
Gerit Pototschnig ◽  
Elisabeth Scheucher ◽  
Martin Thonhofer ◽  
...  
2001 ◽  
Vol 15 (6) ◽  
pp. 371-375 ◽  
Author(s):  
Ken-Ichiro Kondo ◽  
Hayamitsu Adachi ◽  
Yoshio Nishimura ◽  
Tomio Takeuchi

ChemInform ◽  
2010 ◽  
Vol 22 (18) ◽  
pp. no-no
Author(s):  
R. C. BERNOTAS ◽  
G. PAPANDREOU ◽  
J. URBACH ◽  
B. GANEM

Molecules ◽  
2020 ◽  
Vol 25 (17) ◽  
pp. 4025
Author(s):  
Patrick Weber ◽  
Martin Thonhofer ◽  
Summer Averill ◽  
Gideon J. Davies ◽  
Andres Gonzalez Santana ◽  
...  

Glycosidase inhibitors have shown great potential as pharmacological chaperones for lysosomal storage diseases. In light of this, a series of new cyclopentanoid β-galactosidase inhibitors were prepared and their inhibitory and pharmacological chaperoning activities determined and compared with those of lipophilic analogs of the potent β-d-galactosidase inhibitor 4-epi-isofagomine. Structure-activity relationships were investigated by X-ray crystallography as well as by alterations in the cyclopentane moiety such as deoxygenation and replacement by fluorine of a “strategic” hydroxyl group. New compounds have revealed highly promising activities with a range of β-galactosidase-compromised human cell lines and may serve as leads towards new pharmacological chaperones for GM1-gangliosidosis and Morquio B disease.


2017 ◽  
Vol 15 (41) ◽  
pp. 8709-8712 ◽  
Author(s):  
Emil Lindbäck ◽  
Óscar Lopéz ◽  
Ådne Tobiesen ◽  
José G. Fernández-Bolaños ◽  
Magne O. Sydnes

We present a new type of glycosidase inhibitor including a unique hydrazide imide moiety, which displays inhibition in the low micromolar range.


2000 ◽  
Vol 65 (1) ◽  
pp. 2-11 ◽  
Author(s):  
Yoshio Nishimura ◽  
Eiki Shitara ◽  
Hayamitsu Adachi ◽  
Minako Toyoshima ◽  
Motowo Nakajima ◽  
...  

2016 ◽  
Vol 14 (36) ◽  
pp. 8545-8556 ◽  
Author(s):  
Agnete H. Viuff ◽  
Henrik H. Jensen

Seven novel alkylated or acylated analogues of hexahydropyridazine aza-galacto-fagomine (AGF) was prepared and studied as glycosidase inhibitors with the aim of increasing inhibitory potency and selectivity.


1990 ◽  
Vol 31 (24) ◽  
pp. 3393-3396 ◽  
Author(s):  
Ronald C. Bernotas ◽  
George Papandreou ◽  
Jonathan Urbach ◽  
Bruce Ganem

Author(s):  
Y. P. Lin ◽  
J. S. Xue ◽  
J. E. Greedan

A new family of high temperature superconductors based on Pb2Sr2YCu3O9−δ has recently been reported. One method of improving Tc has been to replace Y partially with Ca. Although the basic structure of this type of superconductors is known, the detailed structure is still unclear, and various space groups has been proposed. In our work, crystals of Pb2Sr2YCu3O9−δ with dimensions up to 1 × 1 × 0.25.mm and with Tc of 84 K have been grown and their superconducting properties described. The defects and crystal symmetry have been investigated using electron microscopy performed on crushed crystals supported on a holey carbon film.Electron diffraction confirmed x-ray diffraction results which showed that the crystals are primitive orthorhombic with a=0.5383, b=0.5423 and c=1.5765 nm. Convergent Beam Electron Diffraction (CBED) patterns for the and axes are shown in Figs. 1 and 2 respectively.


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