Off-target toxicity and poor metabolic stability in kinase inhibition lead to high clinical failure rates. These innovations utilize rigid macrocyclic and fused-indole architectures to lock molecular conformations for increased binding selectivity.
Natural source materials often contain trace amounts of therapeutic molecules that are difficult to isolate or utilize effectively. Increasing the yield and purity of these specific chemical constituents addresses the limitation of low natural abundance for pharmacological use.
Natural compounds like forsythiaside are being optimized to address the lack of effective treatments for evolving viral mutations and blood clotting disorders. Overcoming these therapeutic gaps provides a critical advantage in treating complex infectious and cardiovascular pathologies.