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Morphy and Rankovic [32] have suggested a unified term“designed multiple ligands ” (DMLs) i.e., compounds that are rationally designed to exhibit two or more specific pharmacological actions. The advantages of DMLs over the drug combinationsinclude (i) both palliative and disease modifying actions, (ii) addi-tive or synergistic therapeutic responses, (iii) improved drugable characteristics (e.g., blood brain barrier permeability) of the ther-apeutic component, (iv) more predictable PK and PD relationships and (v) prolonged duration of effectiveness [38] . DMLs can be designed as a single molecule either acting on multiple targets or having been capable of exhibiting two or more pharmacological activities in a multifactorial disease. The former types of DMLs can be more appropriately termed as Multitarget compounds (MTCs) while the latter type as Multifunctional compounds (MFCs).
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