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AD Informer Set: Chemical tools to facilitate Alzheimer's disease drug discovery.
Potjewyd, Frances M; Annor-Gyamfi, Joel K; Aubé, Jeffrey; Chu, Shaoyou; Conlon, Ivie L; Frankowski, Kevin J; Guduru, Shiva K R; Hardy, Brian P; Hopkins, Megan D; Kinoshita, Chizuru; Kireev, Dmitri B; Mason, Emily R; Moerk, Charles T; Nwogbo, Felix; Pearce, Kenneth H; Richardson, Timothy I; Rogers, David A; Soni, Disha M; Stashko, Michael; Wang, Xiaodong; Wells, Carrow; Willson, Timothy M; Frye, Stephen V; Young, Jessica E; Axtman, Alison D.
Afiliação
  • Potjewyd FM; UNC Eshelman School of Pharmacy Division of Chemical Biology and Medicinal Chemistry Structural Genomics Consortium Chapel Hill North Carolina USA.
  • Annor-Gyamfi JK; UNC Eshelman School of Pharmacy Division of Chemical Biology and Medicinal Chemistry Structural Genomics Consortium Chapel Hill North Carolina USA.
  • Aubé J; UNC Eshelman School of Pharmacy Division of Chemical Biology and Medicinal Chemistry Center for Integrative Chemical Biology and Drug Discovery Chapel Hill North Carolina USA.
  • Chu S; Department of Medicine Division of Clinical Pharmacology Indiana University School of Medicine Indianapolis Indiana USA.
  • Conlon IL; UNC Eshelman School of Pharmacy Division of Chemical Biology and Medicinal Chemistry Center for Integrative Chemical Biology and Drug Discovery Chapel Hill North Carolina USA.
  • Frankowski KJ; UNC Eshelman School of Pharmacy Division of Chemical Biology and Medicinal Chemistry Center for Integrative Chemical Biology and Drug Discovery Chapel Hill North Carolina USA.
  • Guduru SKR; UNC Eshelman School of Pharmacy Division of Chemical Biology and Medicinal Chemistry Center for Integrative Chemical Biology and Drug Discovery Chapel Hill North Carolina USA.
  • Hardy BP; UNC Eshelman School of Pharmacy Division of Chemical Biology and Medicinal Chemistry Center for Integrative Chemical Biology and Drug Discovery Chapel Hill North Carolina USA.
  • Hopkins MD; UNC Eshelman School of Pharmacy Division of Chemical Biology and Medicinal Chemistry Center for Integrative Chemical Biology and Drug Discovery Chapel Hill North Carolina USA.
  • Kinoshita C; Department of Laboratory Medicine and Pathology University of Washington Seattle Washington USA.
  • Kireev DB; Institute for Stem Cell and Regenerative Medicine University of Washington Seattle Washington USA.
  • Mason ER; UNC Eshelman School of Pharmacy Division of Chemical Biology and Medicinal Chemistry Center for Integrative Chemical Biology and Drug Discovery Chapel Hill North Carolina USA.
  • Moerk CT; Department of Medicine Division of Clinical Pharmacology Indiana University School of Medicine Indianapolis Indiana USA.
  • Nwogbo F; Department of Laboratory Medicine and Pathology University of Washington Seattle Washington USA.
  • Pearce KH; Institute for Stem Cell and Regenerative Medicine University of Washington Seattle Washington USA.
  • Richardson TI; UNC Eshelman School of Pharmacy Division of Chemical Biology and Medicinal Chemistry Center for Integrative Chemical Biology and Drug Discovery Chapel Hill North Carolina USA.
  • Rogers DA; UNC Eshelman School of Pharmacy Division of Chemical Biology and Medicinal Chemistry Center for Integrative Chemical Biology and Drug Discovery Chapel Hill North Carolina USA.
  • Soni DM; Department of Medicine Division of Clinical Pharmacology Indiana University School of Medicine Indianapolis Indiana USA.
  • Stashko M; UNC Eshelman School of Pharmacy Division of Chemical Biology and Medicinal Chemistry Center for Integrative Chemical Biology and Drug Discovery Chapel Hill North Carolina USA.
  • Wang X; Department of Medicine Division of Clinical Pharmacology Indiana University School of Medicine Indianapolis Indiana USA.
  • Wells C; UNC Eshelman School of Pharmacy Division of Chemical Biology and Medicinal Chemistry Center for Integrative Chemical Biology and Drug Discovery Chapel Hill North Carolina USA.
  • Willson TM; UNC Eshelman School of Pharmacy Division of Chemical Biology and Medicinal Chemistry Center for Integrative Chemical Biology and Drug Discovery Chapel Hill North Carolina USA.
  • Frye SV; UNC Eshelman School of Pharmacy Division of Chemical Biology and Medicinal Chemistry Structural Genomics Consortium Chapel Hill North Carolina USA.
  • Young JE; UNC Eshelman School of Pharmacy Division of Chemical Biology and Medicinal Chemistry Structural Genomics Consortium Chapel Hill North Carolina USA.
  • Axtman AD; UNC Eshelman School of Pharmacy Division of Chemical Biology and Medicinal Chemistry Center for Integrative Chemical Biology and Drug Discovery Chapel Hill North Carolina USA.
Alzheimers Dement (N Y) ; 8(1): e12246, 2022.
Article em En | MEDLINE | ID: mdl-35475262
ABSTRACT

Introduction:

The portfolio of novel targets to treat Alzheimer's disease (AD) has been enriched by the Accelerating Medicines Partnership Program for Alzheimer's Disease (AMP AD) program.

Methods:

Publicly available resources, such as literature and databases, enabled a data-driven effort to identify existing small molecule modulators for many protein products expressed by the genes nominated by AMP AD and suitable positive control compounds to be included in the set. Compounds contained within the set were manually selected and annotated with associated published, predicted, and/or experimental data.

Results:

We built an annotated set of 171 small molecule modulators targeting 98 unique proteins that have been nominated by AMP AD consortium members as novel targets for the treatment of AD. The majority of compounds included in the set are inhibitors. These small molecules vary in their quality and should be considered chemical tools that can be used in efforts to validate therapeutic hypotheses, but which will require further optimization. A physical copy of the AD Informer Set can be requested on the Target Enablement to Accelerate Therapy Development for Alzheimer's Disease (TREAT-AD) website.

Discussion:

Small molecules that enable target validation are important tools for the translation of novel hypotheses into viable therapeutic strategies for AD.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article