Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Lignans from Phyllanthus urinaria.

Chia-Chuan Chang1, Yu-Chin Lien, Karin C S Chen Liu

  • 1School of Pharmacy, College of Medicine, National Taiwan University, Taipei 100, Taiwan, ROC.

Phytochemistry
|July 25, 2003
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Gut microbial resistance and metabolism of selective serotonin reuptake inhibitors drive multidrug resistance and contribute to antidepressant tachyphylaxis.

Drug metabolism and disposition: the biological fate of chemicals·2026
Same author

Exposure to a low dose mixture of endocrine disrupting chemicals alters the brain transcriptome and animal behavior.

bioRxiv : the preprint server for biology·2026
Same author

Altered gene expression and activity of human placental drug-metabolizing cytochrome P450 enzymes across gestation.

Biochemical pharmacology·2026
Same author

Pan-valvular heart disease in a dialysis patient with progressive jaundice: case report.

European heart journal. Case reports·2025
Same author

Oleanane-Type Glycosides with α-Glucosidase Inhibitory Activity from <i>Chenopodium serotinum</i> L., an Everlasting Wild Vegetable.

Journal of agricultural and food chemistry·2025
Same author

Gestational fine particulate matter exposures and spontaneous preterm birth: Elucidating mechanisms using placental transcriptome and metabolome signatures.

Placenta·2025

Phyllanthus urinaria L. yielded four new lignans and nine known ones. Researchers identified their structures and stereochemistry using advanced spectral analysis and chemical methods.

Area of Science:

  • Phytochemistry
  • Natural Product Chemistry
  • Organic Chemistry

Background:

  • Phyllanthus urinaria L. is a plant species known for its diverse phytochemical constituents.
  • Lignans are a class of phenolic compounds with various reported biological activities.
  • Previous research has indicated the presence of bioactive compounds in Phyllanthus species.

Purpose of the Study:

  • To conduct a comprehensive chemical investigation of Phyllanthus urinaria L.
  • To isolate and characterize novel lignan compounds from the plant.
  • To elucidate the structures and absolute stereochemistry of the isolated lignans.

Main Methods:

  • Extraction and isolation of compounds from aerial and root parts of Phyllanthus urinaria L.
  • Structure elucidation using Nuclear Magnetic Resonance (NMR) spectroscopy (1D and 2D NMR).

Related Experiment Videos

  • Determination of absolute stereochemistry through Circular Dichroism (CD) analysis and chemical correlation.
  • Main Results:

    • Isolation of four new lignans: 5-demethoxyniranthin, urinatetralin, dextrobursehernin, and urinaligran.
    • Identification of nine known lignans co-occurring in the plant extracts.
    • Complete structural and stereochemical assignment for all isolated compounds.

    Conclusions:

    • The chemical study of Phyllanthus urinaria L. has expanded the knowledge of its lignan profile.
    • The identified compounds, particularly the new lignans, may possess significant biological properties.
    • This research provides a foundation for further pharmacological investigations of Phyllanthus urinaria L. constituents.