Abstract
Volvalerelactones A and B (1 and 2), two new sesquiterpenoid lactones with an unprecedented 3/7/6 tricyclic ring system, were isolated from the roots of Valeriana officinalis var. latifolia. Their structures and relative configurations were elucidated by spectroscopic data and single-crystal X-ray diffraction crystallography, and the absolute configuration was assigned by computational methods. The possible biosynthetic pathways of 1 and 2 were also proposed.
© 2011 American Chemical Society
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Cholinesterase Inhibitors / chemistry
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Cholinesterase Inhibitors / isolation & purification*
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Cholinesterase Inhibitors / pharmacology
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Crystallography, X-Ray
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Dose-Response Relationship, Drug
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Lactones / chemistry*
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Lactones / isolation & purification*
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Lactones / pharmacology
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Molecular Conformation
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Molecular Structure
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Nerve Growth Factor / drug effects
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Nerve Growth Factor / metabolism
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Neurites / drug effects
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Nuclear Magnetic Resonance, Biomolecular
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PC12 Cells
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Plant Roots / chemistry
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Rats
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Sesquiterpenes / chemistry*
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Sesquiterpenes / isolation & purification*
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Sesquiterpenes / pharmacology
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Valerian / chemistry*
Substances
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Cholinesterase Inhibitors
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Lactones
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Sesquiterpenes
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volvalerelactone A
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volvalerelactone B
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Nerve Growth Factor