https://www.selleckchem.com/products/tak-981.html
Ser preferentially binds with the aromatic residues in the N-terminal region through π-π stacking interactions, while Mel binds not only with the N-terminal aromatic residues but also with the C-terminal hydrophobic residues via π-π and hydrophobic interactions. This work reveals the disruptive mechanisms of Aβ42 protofibril by Ser and Mel molecules and provides useful information for designing drug candidates against AD.A kind of bimodal polymer end-linked network employing nanoparticles (NPs) as net points has been designed and constr
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