Publication | Closed Access
Aetheramides A and B, Potent HIV-Inhibitory Depsipeptides from a Myxobacterium of the New Genus “<i>Aetherobacter</i>”
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Citations
17
References
2012
Year
Peptide EngineeringPeptide SciencePeptide TherapeuticsAntimicrobial ChemotherapyChemical BiologyDrug ResistanceMedicinal ChemistryPotent Hiv-inhibitory DepsipeptidesAntimicrobial ResistanceAntimicrobial CompoundHivPharmacologyFurthermore AetheramidesDistinctive Cyclic PeptidesHuman Colon CarcinomaNatural SciencesPeptide LibraryPeptide TherapeuticPeptide SynthesisMicrobiologyMedicineSmall MoleculesDrug Discovery
Aetheramides are structurally distinctive cyclic peptides isolated from a novel myxobacterial genus proposed to be termed "Aetherobacter". The structures were solved by a combination of NMR analyses, quantum mechanical calculations, and chemical derivatizations. Aetheramides which contain a unique polyketide moiety and two amino acid residues potently inhibited HIV-1 infection with IC(50) values of ~0.015 μM. Furthermore aetheramides showed cytostatic activity against human colon carcinoma (HCT-116) cells with IC(50) values of 0.11 μM.
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