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Grant: Collaborative Health Research Projects

Dalhousie University

$163,000.00

An interdisciplinary approach towards the development of a disease-stabilizing treatment for Alzheimer's disease

FY 2013-14

Summary
The aim of this research is to develop small drug-like molecules that concomitantly prevent the aberrantmisfolding and aggregation of amyloid beta, tau and alpha-synuclein - three amyloid peptides implicated in thepathogenesis of Alzheimer's disease (AD). With a Canadian-based biotechnology company (TreventisCorporation) identified as a potential industrial partner, the technology will be transferred with the aim ofdeveloping a disease-modifying drug to treat AD. Through a multi-disciplinary collaboration, the followingobjectives will be achieved: 1) A series of recently identified New Chemical Entities (NCEs) will be screenedin vitro through a battery of anti-aggregation and cell toxicity assays (Weaver group -biochemistry/microbiology); 2) 120 NCEs will be synthesized in total by the medicinal chemistry group (Reedgroup - medicinal chemistry) and optimized for drug-like properties and anti-aggregant potency; and 3) Newpalladium-catalyzed technology will be developed and utilized to allow access to the core structure of thetargeted NCEs, thereby allowing access to structural variation within the NCE family that would otherwise notbe feasible by use of conventional synthetic organic methods (Stradiotto group - inorganic chemistry andcatalysis). This novel, multi-component collaboration will be crucial for the success of this project, and willprovide an ideal platform for interdisciplinary training in the translational chemistry of drug design withemphasis on addressing AD - one of the most pressing health-care challenges facing modern society.
Program
Collaborative Health Research Projects
Location
Nova Scotia, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data

As published

Application id
414132-2012
Name nom
Stradiotto, Mark
Department département
Chemistry
Organization id
79
Institution établissement
Dalhousie University
Province en
Nova Scotia
Province fr
Nouvelle-Écosse
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2013
Competition year année de concours
2012
Award amount
163000
Program id
CHRPJ
Program name en
Collaborative Health Research Projects
Program name fr
Projets de recherche concertée sur la santé
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
360
Committee name en
Collaborative Health Research Projects Selection Panel
Committee name fr
Comité de sélection de projets de recherche concertée sur la santé
Area of application code
1211
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Medical and health sciences
Area of application fr
Sciences médicales et de la santé
Research subject code
6400
Research subject group en
Life sciences research related to human health and disease
Research subject group fr
Sciences de la vie liées à la santé publique et aux maladies humaines
Research subject en
Life sciences research related to human health and disease
Research subject fr
Sciences de la vie liées à la santé publique et aux maladies humaines
Partie
2 & 3
Nb partie
3
Application title
An interdisciplinary approach towards the development of a disease-stabilizing treatment for Alzheimer's disease
Keyword
NSERC
Application summary
The aim of this research is to develop small drug-like molecules that concomitantly prevent the aberrantmisfolding and aggregation of amyloid beta, tau and alpha-synuclein - three amyloid peptides implicated in thepathogenesis of Alzheimer's disease (AD). With a Canadian-based biotechnology company (TreventisCorporation) identified as a potential industrial partner, the technology will be transferred with the aim ofdeveloping a disease-modifying drug to treat AD. Through a multi-disciplinary collaboration, the followingobjectives will be achieved: 1) A series of recently identified New Chemical Entities (NCEs) will be screenedin vitro through a battery of anti-aggregation and cell toxicity assays (Weaver group -biochemistry/microbiology); 2) 120 NCEs will be synthesized in total by the medicinal chemistry group (Reedgroup - medicinal chemistry) and optimized for drug-like properties and anti-aggregant potency; and 3) Newpalladium-catalyzed technology will be developed and utilized to allow access to the core structure of thetargeted NCEs, thereby allowing access to structural variation within the NCE family that would otherwise notbe feasible by use of conventional synthetic organic methods (Stradiotto group - inorganic chemistry andcatalysis). This novel, multi-component collaboration will be crucial for the success of this project, and willprovide an ideal platform for interdisciplinary training in the translational chemistry of drug design withemphasis on addressing AD - one of the most pressing health-care challenges facing modern society.