Journal of Medicinal Chemistry · 2007 · 240 citations · 22 references
PharmacyMedicinal ChemistryPharmacologyDrug DesignDrug DiscoveryStructure-activity RelationshipsFatty Acid ChemistryGlucagon-like Peptide-1 Receptor AgonistsPeptide Bond ChemistryPeptide ChemistryPeptide Drug DiscoveryFatty Acid Chain LengthGlucagon-like Peptide 1 Receptor AgonismGlucagon-like PeptidesPeptide Structure - Activity RelationshipsSpacer Systems
We here report a series of derivatives describing the structure-activity relationship around liraglutide, a once-daily human glucagon-like peptide-1 fatty acid derivative, with respect to potency as well as protraction in vivo. The spacer region between the fatty acid and the peptide is mostly important for potency, whereas the fatty acid or fatty acid mimetic is important for both potency and protraction. The length of the fatty acid is the most important parameter for protraction.
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David J. Augeri, Jeffrey A. Robl, David A. Betebenner et al. · Journal of Medicinal Chemistry · 2005 · 621 citations · Full text