The DOI matches its Crossref record; 312 of the 314 references it cites were found in a registry or an index.
Alzheimer's Disease: From Pathology to Therapeutic Approaches
Abstract
Mind how you go: The current strategies for the development of therapies for Alzheimer's disease are very diverse. Particular attention is given to the search for inhibitors (see picture for two examples) of the proteolytic enzyme beta- and gamma-secretase, which inhibits the cleavage of the amyloid precursor proteins into amyloid beta peptides, from which the disease-defining deposits of plaque in the brains of Alzheimer's patients originates.Research on senile dementia and Alzheimer's disease covers an extremely broad range of scientific activities. At the recent international meeting of the Alzheimer's Association (ICAD 2008, Chicago) more than 2200 individual scientific contributions were presented. The aim of this Review is to give an overview of the field and to outline its main areas, starting from behavioral abnormalities and visible pathological findings and then focusing on the molecular details of the pathology. The "amyloid hypothesis" of Alzheimer's disease is given particular attention, since the majority of the ongoing therapeutic approaches are based on its theoretical framework.
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“However, use of non-specific chelators (i.e., CQ) that do not interact selectively with the Aβ–metal species exhibit adverse side effects that will likely limit their long term clinical use.3,28,29,31,44,46–48”
From Bifunctional Compounds for Controlling Metal-Mediated Aggregation of the Aβ42Peptide (2012) · cites this paper as [3]
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“as well as lead to formation of reactive oxygen species (ROS) and oxidative stress.3,26–31,33–36”
From Bifunctional Compounds for Controlling Metal-Mediated Aggregation of the Aβ42Peptide (2012) · cites this paper as [3]
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Items 601–663 of 663
Lin, Y.-W., Fang, C.-H., Liang, Y.-J., Yang, C.-Y., Kuo, W.-T., & Lin, F.-H. (2023) · Figshare · doi:10.6084/m9.figshare.24257424
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Napolitano, L. (2026) · Firenze University Press eBooks · doi:10.36253/979-12-215-0993-9.05
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Napolitano, L. (2026) · Firenze University Press eBooks · doi:10.36253/979-12-215-0993-9.07
Third Section: Design of a dimeric-nanobody specific for Aβ42 oligomers: the Dimeric-DesAb-O
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Napolitano, L. (2026) · Firenze University Press eBooks · doi:10.36253/979-12-215-0993-9.03
Napolitano, L. (2026) · Firenze University Press eBooks · doi:10.36253/979-12-215-0993-9.04
Napolitano, L. (2026) · Firenze University Press eBooks · doi:10.36253/979-12-215-0993-9.02
Conclusion and Future Perspectives
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Synthetic Protein Mimetic Based Therapies for Neurodegeneration
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Artificial Synthetic Protein Mimetics As Pathology-Targeted Therapeutics
Dohoney, R. A. (2026) · Digital Commons - DU (University of Denver) · doi:10.56902/etdcrp.2026.62
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BindingDB Entry 50008097: Novel multi target-directed ligands targeting 5-HT
BindingDB (2021) · UC San Diego · doi:10.7270/q2988bc8
BindingDB Entry 50017954: PROTACs to address the challenges facing small molecule inhibitors.
BindingDB (2023) · UC San Diego · doi:10.7270/q2p55sm1
BindingDB (2010) · UC San Diego · doi:10.7270/q2z89ckn
BindingDB (2020) · UC San Diego · doi:10.7270/q2988b0b
BindingDB Entry 50002507: BACE1 Inhibitory Meroterpenoids from Aspergillus terreus.
BindingDB (2020) · UC San Diego · doi:10.7270/q2r78hv9
BindingDB (2020) · UC San Diego · doi:10.7270/q2vx0kjw
BindingDB (2017) · UC San Diego · doi:10.7270/q2862fbs
BindingDB Entry 50048240: Neuritogenic activity of bi-functional bis-tryptoline triazole.
BindingDB (2018) · UC San Diego · doi:10.7270/q2k07675
BindingDB (2012) · UC San Diego · doi:10.7270/q20p10g5
BindingDB (2022) · UC San Diego · doi:10.7270/q2t72n5b
BindingDB Entry 50007188: Novel multitarget-directed ligands targeting acetylcholinesterase and σ
BindingDB (2021) · UC San Diego · doi:10.7270/q2t72mrj
BindingDB Entry 50034076: Carbazole-containing arylcarboxamides as BACE1 inhibitors.
BindingDB (2012) · UC San Diego · doi:10.7270/q2st7q7h
BindingDB (2020) · UC San Diego · doi:10.7270/q2vm4fxk
Metadata
- Authors
- Jakob‐Roetne, R., & Jacobsen, H.
- Affiliations
- F. Hoffmann-La Roche AG (CH)
- Corresponding author
- Jakob‐Roetne, Roland
- Jacobsen, Helmut
- ORCID
- Jacobsen, Helmut
- Venue
- Angewandte Chemie International Edition
- Publisher
- Wiley
- Published
- 2009-04-07
- Volume
- 48
- Issue
- 17
- Pages
- 3030-3059
- ISSN
- 1433-7851 (ISSN-L)
- 1521-3773
- OpenAlex
- W2065100984
- Cited by
- 626
- References
- 314
- Citations by year
- 2026: 21 · 2025: 19 · 2024: 27 · 2023: 26 · 2022: 39 · 2021: 27 · 2020: 38 · 2019: 37 · 2018: 39 · 2017: 49 · 2016: 40 · 2015: 52 · 2014: 45 · 2013: 45 · 2012: 43
- FWCI
- 4.61
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Angewandte Chemie International Edition (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Pharmacology (medical) › Cholinesterase and Neurodegenerative Diseases
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Keywords
- Alzheimer's disease, amyloid hypothesis, beta-secretase inhibitors, gamma-secretase inhibitors, amyloid precursor protein, amyloid-beta, amyloid plaques, behavioral abnormalities, Alzheimer's disease pathology, Alzheimer's disease therapeutics
- MeSH terms
- Alzheimer Disease, Amyloid, Humans, Protease Inhibitors, Amyloid Precursor Protein Secretases, Drug Discovery
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