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

New lanostane-type triterpenoids from Ganoderma applanatum.

Sang Hee Shim1, Jiyoung Ryu, Ju Sun Kim

  • 1Natural Products Research Institute and College of Pharmacy, Seoul National University, 28 Yeungun-dong, Chongno-gu, Seoul 110-460, Korea.

Journal of Natural Products
|July 24, 2004
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

Structually diverse polyketides from an endolicheic fungus Leotiomycetes sp.: discovery of polyene γ-lactone derivatives and antibacterial aspyridone analogues.

Bioorganic chemistry·2026
Same author

Transformation-associated recombination and heterologous expression of noncanonical depsipeptide nonribosomal peptide synthetase derived from marine <i>Streptomyces</i>.

Marine life science & technology·2025
Same author

Anti-Parkinsonian 4-hydroxy-2-pyridones from an endolichenic fungus, Tolypocladium sp. (strain CNC14).

Journal of industrial microbiology & biotechnology·2025
Same author

Novel oxabicyclo[2.2.1]heptane-3-one derivatives with NO inhibitory and cytotoxic activities, and xanthone derivatives from the endolichenic fungus Exophiala sp.

Bioorganic chemistry·2025
Same author

Protopanaxadiol stimulates glucose consumption by modulating the AMP-activated protein kinase pathway in myotubes, hepatoma cells, and adipocytes.

PloS one·2025
Same author

Javanicin inhibits the secretion of hepatitis B virus particles thorough the proteasome-dependent degradation of core protein.

Journal of microbiology, immunology, and infection = Wei mian yu gan ran za zhi·2025
Same journal

Goyangamins A-C, Three Pairs of Enantiomeric 2(1<i>H</i>)-Quinolinone Alkaloid Dimers with Antisenescent Activity from <i>Tetradium daniellii</i>.

Journal of natural products·2026
Same journal

Polycyclic-Fused Cytochalasins with Anti-Liver Fibrosis Activity Produced by the Endophytic Fungus <i>Trichoderma harzianum</i>.

Journal of natural products·2026
Same journal

Oleraciamides A and B: Confirmation and Revision of Structures.

Journal of natural products·2026
Same journal

Synthesis and Stereochemical Revision of Violaceoid E, a Polyoxygenated Cyclohexanoid Natural Product Isolated from <i>Aspergillus violaceofuscus</i> Gasperini.

Journal of natural products·2026
Same journal

Cpumycins A-C, Aminated Benzoic Dimers from <i>Streptomyces</i> sp. CPU-W6, and Their Potential Cardioprotective Activities.

Journal of natural products·2026
Same journal

Editorial Introducing the Collection in Honor of Valerie J. Paul.

Journal of natural products·2026
See all related articles

Four new lanostane triterpenes were identified from Ganoderma applanatum. These compounds, isolated from mushroom extracts, expand our knowledge of fungal metabolites.

Area of Science:

  • Natural Product Chemistry
  • Mycology
  • Organic Chemistry

Background:

  • Ganoderma applanatum is a fungus known for its diverse bioactive compounds.
  • Triterpenes, a class of natural products, often exhibit significant pharmacological properties.
  • Lanostane-type triterpenes are structurally complex and found in various fungi.

Purpose of the Study:

  • To isolate and characterize novel lanostane-type triterpenes from Ganoderma applanatum.
  • To elucidate the chemical structures of these newly discovered compounds.
  • To contribute to the understanding of the chemical diversity within the Ganoderma genus.

Main Methods:

  • Extraction of metabolites from the fruiting bodies of Ganoderma applanatum using methanol.
  • Purification of compounds using chromatographic techniques.

Related Experiment Videos

  • Structure elucidation employing extensive spectroscopic analyses (e.g., NMR, MS).
  • Main Results:

    • Isolation of four new lanostane-type triterpenes.
    • Determination of the chemical structures: 3beta,7beta,20,23xi-tetrahydroxy-11,15-dioxolanosta-8-en-26-oic acid (1), 7beta,20,23xi-trihydroxy-3,11,15-trioxolanosta-8-en-26-oic acid (2), 7beta,23xi-dihydroxy-3,11,15-trioxolanosta-8,20E(22)-dien-26-oic acid (3), and 7beta-hydroxy-3,11,15,23-tetraoxolanosta-8,20E(22)-dien-26-oic acid methyl ester (4).
    • Confirmation of structures through comprehensive spectroscopic data interpretation.

    Conclusions:

    • The study successfully identified four previously unknown lanostane-type triterpenes from Ganoderma applanatum.
    • The findings expand the repertoire of known natural products from this fungal species.
    • This research provides valuable chemical data for future investigations into the biological activities of these triterpenes.