Publication | Open Access
New Aminoimidazoles as β-Secretase (BACE-1) Inhibitors Showing Amyloid-β (Aβ) Lowering in Brain
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Citations
43
References
2012
Year
New AminoimidazolesNeurochemical BiomarkersPharmaceutical ChemistryPre-clinical PharmacologyMolecular PharmacologyMedicinal ChemistryAlzheimer's DiseaseBace-1 InhibitorsProtein MisfoldingNeurologyBrain PathologyMolecular NeuroscienceBiochemistryPharmacological AgentNeuropharmacologyNeuroprotectionDrug DevelopmentPharmacologyNeurodegenerative DiseasesGuinea PigsNatural SciencesNew ClassNeuroscienceMedicineSmall MoleculesDrug Discovery
Amino-2H-imidazoles are described as a new class of BACE-1 inhibitors for the treatment of Alzheimer's disease. Synthetic methods, crystal structures, and structure-activity relationships for target activity, permeability, and hERG activity are reported and discussed. Compound (S)-1m was one of the most promising compounds in this report, with high potency in the cellular assay and a good overall profile. When guinea pigs were treated with compound (S)-1m, a concentration and time dependent decrease in Aβ40 and Aβ42 levels in plasma, brain, and CSF was observed. The maximum reduction of brain Aβ was 40-50%, 1.5 h after oral dosing (100 μmol/kg). The results presented highlight the potential of this new class of BACE-1 inhibitors with good target potency and with low effect on hERG, in combination with a fair CNS exposure in vivo.
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