Sie befinden Sich nicht im Netzwerk der Universität Paderborn. Der Zugriff auf elektronische Ressourcen ist gegebenenfalls nur via VPN oder Shibboleth (DFN-AAI) möglich. mehr Informationen...
Ergebnis 9 von 22

Details

Autor(en) / Beteiligte
Titel
3-Substituted coumarins as dual inhibitors of AChE and MAO for the treatment of Alzheimer's disease
Ist Teil von
  • MedChemComm, 2012-02, Vol.3 (2), p.213-218
Erscheinungsjahr
2012
Link zum Volltext
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • The complex etiology of Alzheimer's disease (AD) has encouraged active research in the development of multi-target drugs with two or more complementary biological activities, since they may represent an important advance in the treatment of this disease. A series of 3-substituted coumarins were synthesized and evaluated as monoamino oxidases (MAO) and acetylcholinesterase (AChE) inhibitors. Most of the 3-benzamide coumarin derivatives inhibited both MAO-B and AChE with values in the micromolar range. It might be a promising direction for developing novel drugs as potential agents for the treatment of AD patients. Three series of 3-substituted coumarin derivatives have been synthesized and evaluated as dual hMAO/hAChE inhibitors. The importance of the substituents in that position is determined.
Sprache
Englisch
Identifikatoren
ISSN: 2040-2503
eISSN: 2040-2511
DOI: 10.1039/c1md00221j
Titel-ID: cdi_crossref_primary_10_1039_C1MD00221J
Format

Weiterführende Literatur

Empfehlungen zum selben Thema automatisch vorgeschlagen von bX