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

Labdane diterpenes from Juniperus communis L. berries.

Anne Marie Martin1, Emerson Ferreira Queiroz, Andrew Marston

  • 1Laboratory of Pharmacognosy and Phytochemistry, University of Geneva, Geneva, Switzerland.

Phytochemical Analysis : PCA
|February 4, 2006
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

An innovative approach for anti-respiratory syncytial virus compound discovery from plant extracts, combining high-throughput screening and metabolomics.

Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie·2026
Same author

New Marine Actinobacteria Strain, <i>Micromonospora</i> sp. SH-82: Characterization, Specialized Metabolites and Biological Activities.

Microorganisms·2025
Same author

Phenylalkyl Acetophenones and Anacardic Acids from Knema oblongifolia with Synthetic Analogues as Anti-infectives and Antibacterial Agents.

ACS bio & med chem Au·2025
Same author

Genkwanin glycosides are major active compounds in Phaleria nisidai extract mediating improved glucose homeostasis by stimulating glucose uptake into adipose tissues.

Nature communications·2025
Same author

Efficient constitution of a library of rotenoid analogs active against <i>Trypanosoma cruzi</i> from a digitalized plant extract collection.

RSC advances·2025
Same author

New Insights into the French Paradox: Free Radical Scavenging by Resveratrol Yields Cardiovascular Protective Metabolites.

Journal of medicinal chemistry·2025

Researchers identified five diterpenes from Juniperus communis berries, including a novel labdane diterpene. This phytochemical analysis enhances understanding of Juniperus communis chemical constituents.

Area of Science:

  • Phytochemistry
  • Natural Product Chemistry
  • Organic Chemistry

Background:

  • Juniperus communis (common juniper) berries are known for their diverse chemical composition.
  • Phytochemical investigations are crucial for identifying bioactive compounds in medicinal plants.
  • Diterpenes represent a significant class of natural products with various biological activities.

Purpose of the Study:

  • To conduct a phytochemical investigation of the methanol extract of Juniperus communis berries.
  • To isolate and characterize minor compounds present in the extract.
  • To identify any novel chemical entities within the Juniperus communis berry extract.

Main Methods:

  • High-Performance Liquid Chromatography with Ultraviolet detection (HPLC-UV) for initial analysis.

Related Experiment Videos

  • Centrifugal Partition Chromatography (CPC) for the isolation of minor compounds.
  • Spectroscopic methods including Nuclear Magnetic Resonance (NMR), Mass Spectrometry (MS), and High-Resolution Mass Spectrometry (HR-MS) for structure elucidation.
  • Main Results:

    • Five diterpenes were successfully isolated from the methanol extract.
    • One of the isolated compounds was identified as a new labdane diterpene: 15,16-epoxy-12-hydroxy-8(17),13(16),14-labdatrien-19-oic acid.
    • The structures of all isolated diterpenes were confirmed through comprehensive spectroscopic analysis.

    Conclusions:

    • The study successfully identified known and a novel diterpene from Juniperus communis berries.
    • The findings contribute to the detailed phytochemical knowledge of Juniperus communis.
    • This research provides a basis for further investigation into the potential applications of these diterpenes.