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Register a new userComputer–Guided Design and Evaluation of Some New Analogues of Glycogen Synthase Kinase-3 Inhibitors for The Treatment Of Alzheimer’s Disease
التصميم المعتمد على الحاسوب و تقييم بعض المضاهئات الجديدة لمثبطات مخلقة الغلوكوجين كيناز-3 لعلاج داء ألزهايمر
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Aِl-Baath University ورقة بحثية
Publication date
2016
fields
Pharmacy
and research's language is
العربية
Created by
Shamra Editor
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أصبح استخدام مثبطات مخلقة الغليكوجين كيناز-3 ( GSK-3) في وقتنا الراهن واحدا من أهم الأهداف الدوائية بغية تطوير مثبطات انتقائية لها تعمل كأدوية واعدة في علاج العديد من الأمراض و خاصة مرض ألزهايمر. يتمتع استهداف إنزيم GSK-3 بأهمية علاجية في العديد من الأمراض كما يعد أحد الحقول المهمة لباحثين سواء في مراكز البحوث الأكاديمية أو الشركات الصيدلانية.
Nowadays, glycogen synthase kinase 3 (GSK-3) inhibitors become one of the most important drug targets for the development of their selective inhibitors serving as promising drugs for the treatment of many diseases, particularly Alzheimer's disease. Targeting GSK-3 enzyme has a therapeutic importance in many diseases and is one of the valuable fields for researchers in both academic research centers and pharmaceutical companies.
References used
Alonso, M. and A. Martinez, 2004, GSK-3 inhibitors: discoveries and developments. Curr Med Chem. 11(6): p. 755-63
De Ferrari, G.V. and N.C. Inestrosa, 2000, Wnt signaling function in Alzheimer's disease. Brain Res Brain Res Rev. 33(1): p. 1-12
Vargas, J.Y., M. Fuenzalida, and N.C. Inestrosa, 2014, In vivo activation of Wnt signaling pathway enhances cognitive function of adult mice and reverses cognitive deficits in an Alzheimer's disease model. J Neurosci. 34(6): p. 2191-202
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