Synthesis of carbon-14 and stable isotope labeled Avagacestat: a novel gamma secretase inhibitor for the treatment of Alzheimer's disease

2014 ◽  
Vol 57 (10) ◽  
pp. 600-605 ◽  
Author(s):  
Richard C. Burrell ◽  
John A. Easter ◽  
Michael P. Cassidy ◽  
Kevin W. Gillman ◽  
Richard E. Olson ◽  
...  
2008 ◽  
Vol 4 ◽  
pp. T461-T461 ◽  
Author(s):  
Steven Jacobsen ◽  
Thomas Comery ◽  
Suzan Aschmies ◽  
Hua Zhou ◽  
Mei Jin ◽  
...  

2009 ◽  
Vol 5 (4S_Part_5) ◽  
pp. P139-P139 ◽  
Author(s):  
Steven Jacobsen ◽  
Thomas Comery ◽  
Anthony Kreft ◽  
Scott Mayer ◽  
Margaret Zaleska ◽  
...  

2013 ◽  
Vol 9 ◽  
pp. P283-P283 ◽  
Author(s):  
Vlad Coric ◽  
Stephen Salloway ◽  
Christopher van Dyck ◽  
Wendy Kerselaers ◽  
Stephen Kaplita ◽  
...  

2002 ◽  
Vol 38 ◽  
pp. 37-49 ◽  
Author(s):  
Janelle Nunan ◽  
David H Small

The proteolytic processing of the amyloid-beta protein precursor plays a key role in the development of Alzheimer's disease. Cleavage of the amyloid-beta protein precursor may occur via two pathways, both of which involve the action of proteases called secretases. One pathway, involving beta- and gamma-secretase, liberates amyloid-beta protein, a protein associated with the neurodegeneration seen in Alzheimer's disease. The alternative pathway, involving alpha-secretase, precludes amyloid-beta protein formation. In this review, we describe the progress that has been made in identifying the secretases and their potential as therapeutic targets in the treatment or prevention of Alzheimer's disease.


Sign in / Sign up

Export Citation Format

Share Document