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Pierisketolide A and Pierisketones B and C, Three Diterpenes with an Unusual Carbon Skeleton from the Roots of <i>Pieris formosa</i>
29
Citations
8
References
2017
Year
BiologyMedicinal ChemistryPieris FormosaBiochemistryNatural SciencesX-ray DiffractionOrganic ChemistryThree DiterpenesUnusual Carbon SkeletonPharmacologyDerivative (Chemistry)Pierisketones BNatural Product Synthesis
Pierisketolide A (1) and pierisketones B and C (2 and 3), three diterpenes with an unusual A-homo-B-nor-ent-kaurane carbon skeleton, were isolated from the roots of Pieris formosa. Their structures were characterized by a series of spectroscopic methods, X-ray diffraction, and electronic circular dichroism (ECD). Pierisketolide A (1) exhibited an analgesic effect with a 45% writhe inhibition rate at a dose of 10.0 mg/kg. The plausible biosynthetic pathways of 1-3 are proposed.
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