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Natura

Last updated January 31, 2026
275
Innovation Areas
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Cleavable peptide linker chemistry: NaturaRecent Research Landscape

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.

What technical problems is Natura addressing in Cleavable peptide linker chemistry?

Inadequate inflammatory response control

(18)evidences

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.

Insufficient therapeutic efficacy

(16)evidences

Off-target effects and systemic toxicity limit the efficacy of bioactive compounds. Improving site-specific action reduces collateral damage to healthy tissues.

Insufficient intracellular drug delivery

(13)evidences

Off-target binding and systemic toxicity in pyrazolopyrimidine scaffolds. Enhancing target specificity reduces adverse side effects in therapeutic applications.

Pathogenic crop tissue degradation

(13)evidences

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.