Journal of Medicinal Chemistry · 2019 · 20 citations · 36 references
PharmacyMedicinal ChemistryPharmacologyDrug DesignDrug DiscoveryMolecular PharmacologyAllosteric Drug DesignAllosteric Modulator DesignPeptide ChemistryPeptide Drug DiscoveryReceptor PharmacologyReproductive PharmacologyBioactive Peptide MimicsModulator DesignModulator SelectivityPeptide Bond MimicryPreterm Labor PhysiologyProstaglandin ModulationReceptor Ligand MimicrySide Chain Substitution
Peptide mimicry employing a combination of aza-amino acyl proline and indolizidinone residues has been used to develop allosteric modulators of the prostaglandin F2α receptor. The systematic study of the N-terminal phenylacetyl moiety and the conformation and side chain functions of the central turn dipeptide residue has demonstrated the sensitive relationships between modulator activity and topology. Examination of aza-Gly-Pro and aza-Phe-Pro analogs 2a and 2b in a murine preterm labor model featuring treatment with lipopolysaccharide demonstrated their capacity to extend significantly (>20 h) the average time of delivery offering new prototypes for delaying premature birth.
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Anil K. Pandey, Devan Naduthambi, Krista Thomas et al. · Journal of the American Chemical Society · 2013 · 177 citations
Susy Katikana Sebayang, Michael J. Dibley, Patrick J. Kelly et al. · Tropical Medicine & International Health · 2012 · 130 citations