Development of Gleevec Analogues for Reducing Production of β-Amyloid Peptides through Shifting β-Cleavage of Amyloid Precursor Proteins

被引:6
|
作者
Sun, Weilin [1 ]
Netzer, William J. [1 ]
Sinha, Anjana [1 ]
Gindinova, Katherina [1 ]
Chang, Emily [1 ]
Sinha, Subhash C. [1 ]
机构
[1] Rockefeller Univ, Lab Mol & Cellular Neurosci, New York, NY 10065 USA
关键词
CANCER RESISTANCE PROTEIN; ALZHEIMERS-DISEASE; IMATINIB MESYLATE; SECRETASE; BRAIN; INHIBITORS; ABCG2; MODEL;
D O I
10.1021/acs.jmedchem.8b02007
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Imatinib mesylate, la, inhibits production of beta-amyloid (A beta) peptides both in cells and in animal models. It reduces both the beta-secretase and gamma-secretase cleavages of the amyloid precursor protein (APP) and mediates a synergistic effect, when combined with a beta-secretase inhibitor, BACE IV. Toward developing more potent brain-permeable leads, we have synthesized and evaluated over 75 la-analogues. Several compounds, including 2a-b and 3a-c, inhibited production of A beta peptides with improved activity in cells. These compounds affected beta-secretase cleavage of APP similarly to la. Compound 2a significantly reduced production of the A beta 42 peptide, when administered (100 mg/kg, twice daily by oral gavage) to 5 months old female mice for 5 days. A combination of compound 2a with BACE IV also reduced A beta levels in cells, more than the additive effect of the two compounds. These results open a new avenue for developing treatments for Alzheimer's disease using la-analogues.
引用
收藏
页码:3122 / 3134
页数:13
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