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

Sesterterpenoids.

Yonghong Liu1, Lishu Wang, Jee H Jung

  • 1Key Laboratory of Marine Bio-resources Sustainable Utilization, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou, 510-301, China. yonghongliu@scsio.ac.cn

Natural Product Reports
|November 23, 2007
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

Unraveling the spatial chemical heterogeneity of Lentinula edodes: Integrative metabolomics and machine learning for cultivar and origin classification.

Food chemistry·2026
Same author

Deciphering media-specific differentiation of REY geochemical behavior and health risks regulated by geogenic and anthropogenic factors.

Journal of hazardous materials·2026
Same author

Quantitative source apportionment deciphering hydrogeological and anthropogenic contributions to selenium enrichment in groundwater against deficiency context.

Environmental research·2026
Same author

Hypothermal effects of cold anesthesia on the vitality and muscle quality of live Chinese mitten crab (Eriocheir sinensis).

Food research international (Ottawa, Ont.)·2025
Same author

Development and characterization of CMCS/gelatin based humidity-responsive hydrogel pads with thyme essential oil release for blueberry preservation.

International journal of biological macromolecules·2025
Same author

Stereoselective construction of 5-6-5 aza-tricyclic scaffolds <i>via</i> catalytic asymmetric aza-Piancatelli/Diels-Alder reactions.

Chemical communications (Cambridge, England)·2025
Same journal

SAM-dependent methyltransferases: from chemoenzymatic natural product synthesis to industrial application.

Natural product reports·2026
Same journal

Visual cycle-derived bisretinoids as endogenous natural products: enzyme-free formation, photochemical reactivity, and retinal degeneration.

Natural product reports·2026
Same journal

Non-strigolactone natural products interfering with parasitic weed development.

Natural product reports·2026
Same journal

Biosynthetic crosstalk in bacteria: routes to chimeric natural products.

Natural product reports·2026
Same journal

Genomic scale analysis of assembly-line polyketide synthase diversity and evolution.

Natural product reports·2026
Same journal

Asymmetric synthesis of 3,3-disubstituted oxindoles: methodologies and applications in natural product synthesis.

Natural product reports·2026
See all related articles

This review covers sesterterpenoids, a class of compounds with varied biological activities. These pentaprenyl terpenoids are valuable for biomedical research and chemical synthesis.

Area of Science:

  • Natural Product Chemistry
  • Organic Chemistry
  • Medicinal Chemistry

Background:

  • Sesterterpenoids are a significant class of terpenoids derived from five isoprene units.
  • These compounds are characterized by a C20 skeleton, distinguishing them from other terpenoid classes.
  • Their complex structures often arise from intricate biosynthetic pathways.

Purpose of the Study:

  • To review the existing literature on sesterterpenoids.
  • To highlight the diverse biological properties associated with sesterterpenoids.
  • To underscore their potential as targets for biomedical and synthetic chemistry endeavors.

Main Methods:

  • Comprehensive literature search using scientific databases.
  • Analysis and synthesis of published data on sesterterpenoid structures, properties, and applications.

Related Experiment Videos

  • Classification of sesterterpenoids based on structural and biological characteristics.

    • Main Results:

    • Sesterterpenoids exhibit a wide array of biological activities, including antimicrobial, antifungal, antiviral, cytotoxic, and anti-inflammatory properties.
    • The structural diversity of sesterterpenoids is extensive, encompassing various cyclic and acyclic frameworks.
    • Numerous sesterterpenoids have been isolated from diverse natural sources, particularly fungi and marine organisms.

    Conclusions:

    • Sesterterpenoids represent a rich source of biologically active natural products.
    • Their unique structures and potent activities make them promising leads for drug discovery.
    • Further synthetic and biological investigations are warranted to fully exploit their therapeutic potential.