| Title : 6-Hydroxy- and 6-methoxy-beta-carbolines as acetyl- and butyrylcholinesterase inhibitors - Schott_2006_Bioorg.Med.Chem.Lett_16_5840 |
| Author(s) : Schott Y , Decker M , Rommelspacher H , Lehmann J |
| Ref : Bioorganic & Medicinal Chemistry Lett , 16 :5840 , 2006 |
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Abstract :
In the course of studies directed toward the discovery of novel acetyl- and butyrylcholinesterase (AChE and BChE) inhibitors for the treatment of Alzheimer's disease, we focused on beta-carbolines (BCs). 6-Oxygenated beta-carboline and beta-carbolinium derivatives based on the serotonin template were synthesized and tested in vitro for their ability to inhibit AChE and BChE, respectively. Particularly the carbolinium salts, which can be formed by intracerebral methylation out of the tertiary-BC prodrugs, show inhibitory activity levels reaching those of galantamine, physostigmine, and rivastigmine. |
| PubMedSearch : Schott_2006_Bioorg.Med.Chem.Lett_16_5840 |
| PubMedID: 16945529 |
Schott Y, Decker M, Rommelspacher H, Lehmann J (2006)
6-Hydroxy- and 6-methoxy-beta-carbolines as acetyl- and butyrylcholinesterase inhibitors
Bioorganic & Medicinal Chemistry Lett
16 :5840
Schott Y, Decker M, Rommelspacher H, Lehmann J (2006)
Bioorganic & Medicinal Chemistry Lett
16 :5840