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In contrast, Hep-3, characterized as dextran, is composed exclusively of glucose [46]
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Consequently, we envisage that the model ฮฒGLU inhibitor will be that which is appositely tuned in its lipophilicity and polarity for easy cell penetration, favourable fit into the binding/catalytic pocket of ฮฒGLU for energetically stable binding and strong enzyme inhibition
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