Pleiotropic Protective Effects of Phytochemicals in Alzheimer's Disease

<table>Chemical structure of (−)-Epigallocatechin-3-gallate. EGCG contains three heterocyclic rings, A, B, and C, and the free radical scavenging property of EGCG is attributed to the presence of trihydroxyl group on the B ring and the gallate moiety at the <svg height="17.9125" id="M1" style="vertical-align:-0.1638pt" version="1.1" viewbox="0 0 16.4125 17.9125" width="16.4125" xmlns="http://www.w3.org/2000/svg" xmlns:xlink="http://www.w3.org/1999/xlink">
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q0 45 -26.5 69.5t-68.5 24.5q-67 0 -120 -79l-20 20l43 63q51 56 127 56h1q66 0 107 -37t41 -95q0 -42 -31 -71q-22 -23 -68 -54z" id="x33"></path></g>
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</svg>position in the C ring.</table>

Oxidative Medicine and Cellular Longevity

fig3

Figure 3

Figure 3: Pleiotropic Protective Effects of Phytochemicals in Alzheimer's Disease 