期刊
BIOORGANIC & MEDICINAL CHEMISTRY
卷 17, 期 17, 页码 6402-6406出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmc.2009.07.020
关键词
Alzheimer's disease; beta-Amyloid plaques; SPECT imaging
资金
- National Institute of Biomedical Innovation (NIBIO)
- Health Labour Sciences Research Grant
This paper describes the synthesis and biological evaluation of a new series of 2,5-diphenyl-1,3,4-oxadiazole (1,3,4-DPOD) derivatives for detecting beta-amyloid plaques in Alzheimer's brains. The affinity for beta-amyloid plaques was assessed by an in vitro binding assay using pre-formed synthetic A beta 42 aggregates. The new series of 1,3,4-DPOD derivatives showed affinity for Ab42 aggregates with K-i values ranging from 20 to 349 nM. The 1,3,4-DPOD derivatives clearly stained beta-amyloid plaques in an animal model of Alzheimer's disease, reflecting the affinity for A beta 42 aggregates in vitro. Compared to 3,5-diphenyl-1,2,4-oxadiazole (1,2,4-DPOD) derivatives, they displayed good penetration of and fast washout from the brain in biodistribution experiments using normal mice. The novel radioiodinated 1,3,4-DPOD derivatives may be useful probes for detecting b-amyloid plaques in the Alzheimer's brain. (C) 2009 Elsevier Ltd. All rights reserved.
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