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Description
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Structural modeling, fluorescence polarization displacement, and pull-down assays confirmed that the CPPC16 conjugates retain the ability to compete with an NFAT-derived peptide and bind Cn
The in silico docking analysis revealed encouraging binding energies of Lonafarnib with AChE (11.58 kcal/mol), CRF1 (10.94 kcal/mol), BDNF (5.99 kcal/mol), 5HT1A (10.48 kcal/mol), and 5HT2A (10.77 kcal/mol)

This form is well-absorbed and more stable throughout the digestive tract than other forms on the market
