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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.
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页码:3122 / 3134
页数:13
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