Abstract
Alzheimer's disease drug discovery regarding exploration into the molecules and processes has focused on the intrinsic causes of the brain disorder correlated with the accumulation of amyloid-β. An anti-amyloidogenic bis-styrylbenzene derivative, KMS80013, showed excellent oral bioavailability (F=46.2%), facilitated brain penetration (26%, iv) in mouse and target specific in vivo efficacy in acute AD mouse model attenuating the cognitive deficiency in Y-maze test. Acute toxicity (LD50 >2000 mg/kg) and hERG channel inhibition (14% at 10 μM) results indicated safety of KMS80013.
Copyright © 2013. Published by Elsevier Ltd.
MeSH terms
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Administration, Oral
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Alzheimer Disease / drug therapy
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Aniline Compounds / chemistry*
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Aniline Compounds / pharmacokinetics
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Aniline Compounds / therapeutic use
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Animals
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Benzene Derivatives / chemistry*
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Benzene Derivatives / pharmacokinetics
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Benzene Derivatives / therapeutic use
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Brain / metabolism
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Disease Models, Animal
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Ether-A-Go-Go Potassium Channels / antagonists & inhibitors
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Ether-A-Go-Go Potassium Channels / metabolism
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Half-Life
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Male
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Mice
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Mice, Inbred ICR
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Stilbenes / chemistry*
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Stilbenes / pharmacokinetics
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Stilbenes / therapeutic use
Substances
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Aniline Compounds
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Benzene Derivatives
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Ether-A-Go-Go Potassium Channels
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KMS80013
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Stilbenes