Structure-activity Relationship Studies


Peptide drugs are becoming increasingly popular due to their high affinity and specificity for their biological target, plus their low toxicity. Lead optimisation can further enhance their pharmacological properties. Lipidation/PEGylation, side-chain substitution, macrocyclisation, truncation, N-methylation and alanine scanning are techniques often used to achieve this outcome. Modpep can perform a comprehensive SAR study for your lead compound in a timely manner.

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