Abstract |
1. As an extension of our previous study of quinacrine and its derivatives, chelating chemicals were screened to obtain more effective, better brain-permeable antiprion compounds using either prion-infected neuroblastoma cells or brain capillary endothelial cells.2. Eleven chemicals were found to have antiprion activity. Most of them shared a common structure consisting of benzene or naphthalene at either end of an azo bond. Structure-activity data suggest that chelating activity is not necessary but might contribute to the antiprion action.3. Chrysoidine, a representative compound found here, was about 27 times more effective in the antiprion activity and five times more efficiently permeable through the brain capillary endothelial cells than quinacrine was.4. These chemicals might be useful as compounds for development of therapeutics for prion diseases.
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Authors | Katsumi Doh-ura, Kazuhiko Tamura, Yoshiharu Karube, Mikihiko Naito, Takashi Tsuruo, Yasufumi Kataoka |
Journal | Cellular and molecular neurobiology
(Cell Mol Neurobiol)
Vol. 27
Issue 3
Pg. 303-16
(May 2007)
ISSN: 0272-4340 [Print] United States |
PMID | 17235694
(Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Chelating Agents
- PrPSc Proteins
- Prions
- Recombinant Proteins
- chrysoidine
- p-Aminoazobenzene
- Quinacrine
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Topics |
- Animals
- Brain
(drug effects, metabolism)
- Cell Membrane Permeability
(drug effects)
- Chelating Agents
(pharmacology)
- Drug Evaluation, Preclinical
- Endothelial Cells
(drug effects, metabolism)
- Mice
- Models, Biological
- PrPSc Proteins
(metabolism)
- Prion Diseases
(prevention & control)
- Prions
(antagonists & inhibitors, drug effects, metabolism)
- Protein Binding
- Quinacrine
(pharmacology, therapeutic use)
- Recombinant Proteins
(metabolism)
- Tumor Cells, Cultured
- p-Aminoazobenzene
(analogs & derivatives, pharmacology, therapeutic use)
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