L. Kong

Publications477
h-index35
Citations6,723
Highly Influential Citations189
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New triterpenoid saponins with strong alpha-glucosidase inhibitory activity from the roots of Gypsophila oldhamiana.
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Studies on the chemical constituents of Psoralea corylifolia L.
A new isoflavone, corylinin (1), along with six known compounds, isopsoralen (2), psoralen (3), sophoracoumestan A (4), neobavaisoflavone (5), daidzin (6) and uracil (7), have been isolated from the…
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Oxidation of ferulic acid by Momordica charantia peroxidase and related anti-inflammation activity changes.
TLDR
Results suggested that MCP as a tool enzyme transformed some complexes such as FA to more active derivatives, and thatFA-2 was a potential inhibitor on inflammation through interference with immune response in the process of inflammation, which maybe was associated with apoptosis of immune related cells induced by FA-2.
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Huang-Lian-Jie-Du-Decotion induced protective autophagy against the injury of cerebral ischemia/reperfusion via MAPK-mTOR signaling pathway.
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Limonoids from the fruits of Aphanamixis polystachya (Meliaceae) and their biological activities.
Seven new prieurianin-type limonoids, aphapolynins C-I (1-7), and a new aphanamolide-type limonoid, aphanamolide B (8), along with seventeen known compounds, were isolated from the fruits of…
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Preparative separation of phenylpropenoid glycerides from the bulbs of Lilium lancifolium by high-speed counter-current chromatography and evaluation of their antioxidant activities
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Potential antidepressant properties of Radix Polygalae (Yuan Zhi).
  • P. Liu, Y. Hu, L. Kong
  • Chemistry
    Phytomedicine : international journal of…
  • 1 August 2010
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Chisopanins A-K, 11 new protolimonoids from Chisocheton paniculatus and their anti-inflammatory activities.
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Cytotoxic Rocaglate Derivatives from Leaves of Aglaia perviridis
TLDR
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.
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[Studies on structure modification of (+)-praeruptorin A].
TLDR
Preliminary bioactivity assay indicated that the new compounds show calcium antagonist activity, but they are not as strong as (+)-praeruptorin A.
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