Author pages are created from data sourced from our academic publisher partnerships and public sources.
Share This Author
Cytotoxic Rocaglate Derivatives from Leaves of Aglaia perviridis
Rocaglates are a series of structurally complex secondary metabolites with considerable cytotoxicity that have been isolated from plants of the Aglaia genus (Meliaceae) and their structures were elucidated based on a joint effort of spectroscopic methods and single-crystal X-ray diffraction.
A novel aporphine alkaloid from Magnolia officinalis.
Rhodomyrtials A and B, Two Meroterpenoids with a Triketone-Sesquiterpene-Triketone Skeleton from Rhodomyrtus tomentosa: Structural Elucidation and Biomimetic Synthesis.
Two unprecedented triketone-sesquiterpene-triketone adducts and five biogenetically related intermediates were isolated from the leaves of Rhodomyrtus tomentosa and exhibited potent metastatic inhibitory activity against DLD-1 cells by suppressing the activation of matrix metalloproteinase (MMP)-2 and MMP-9.
Cytotoxic tirucallane C26 triterpenoids from the stem barks of Aphanamixis grandifolia.
Analysis and pharmacokinetics studies of gastrodin and p-hydroxybenzyl alcohol in dogs using ultra fast liquid chromatography-tandem mass spectrometry method.
Limonoids with diverse frameworks from the stem bark of Entandrophragma angolense and their bioactivities
Entangolensins A–P (1–16), sixteen new limonoids with diverse frameworks, were isolated from the stem bark of Entandrophragma angolense. Their planar structures were elucidated on the basis of…
Identification and analysis of gastrodin and its five metabolites using ultra fast liquid chromatography electrospray ionization tandem mass spectrometry to investigate influence of multiple-dose and…
Antioxidant sordariol dimers from Sordaria macrospora and the absolute configuration determinations of their two simultaneous linear 1,2-diols
Anti-inflammatory lindenane sesquiterpeniods and dimers from Sarcandra glabra and its upregulating AKT/Nrf2/HO-1 signaling mechanism
Polyprenylated Tetraoxygenated Xanthones from the Roots of Hypericum monogynum and Their Neuroprotective Activities.
- Wenjun Xu, Ruijun Li, O. Quasie, Ming-Hua Yang, L. Kong, Jun Luo
- Biology, ChemistryJournal of natural products
- 15 August 2016
The structures of these new polyprenylated xanthones (1-10), a class of compounds rarely found in plants of the genus Hypericum, were elucidated by the interpretation of their HRESIMS, 1D and 2D NMR, and electronic circular dichroism data, and shed new light on the potential on the development of antidepression therapies.