
Aryltetralone lignans and two 7,8-seco-lignans were isolated from the acetone and hexane extracts of the roots of Holostylis reniformis, together with (-)-galbacin. Their structures were determined by spectroscopic methods.
Holostylis reniformis, lignan, 4' o methylenshicine, drug isolation, Aristolochiaceae, galbacin, Nuclear Magnetic Resonance, acetone, 8,8' epiholostylone, aristoligone, holostylone, Plant Roots, Lignans, 8,8' epiaristoligone, 8' epiaristoligone, aristotetralone, Aryltetralone lignans, controlled study, Nuclear Magnetic Resonance, Biomolecular, Holostylis reniformis extract, Tetralones, nonhuman, Molecular Structure, Plant Extracts, 7,8 seco holostylone a, plant root, Circular Dichroism, Seco-lignans, 7,8 seco holostylone b, ketone derivative, structure analysis, unclassified drug, hexane, drug structure, plant extract, Neolignans, Biomolecular
Holostylis reniformis, lignan, 4' o methylenshicine, drug isolation, Aristolochiaceae, galbacin, Nuclear Magnetic Resonance, acetone, 8,8' epiholostylone, aristoligone, holostylone, Plant Roots, Lignans, 8,8' epiaristoligone, 8' epiaristoligone, aristotetralone, Aryltetralone lignans, controlled study, Nuclear Magnetic Resonance, Biomolecular, Holostylis reniformis extract, Tetralones, nonhuman, Molecular Structure, Plant Extracts, 7,8 seco holostylone a, plant root, Circular Dichroism, Seco-lignans, 7,8 seco holostylone b, ketone derivative, structure analysis, unclassified drug, hexane, drug structure, plant extract, Neolignans, Biomolecular
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