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

Furanoflavonoids: an overview.

Rakesh Maurya1, Prem P Yadav

  • 1Medicinal and Process Chemistry Division, Central Drug Research Institute, Chattar Manzil, Lucknow 226 001, India. mauryarakesh@rediffmail.com

Natural Product Reports
|July 13, 2005
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

Phytochemicals Targeting Wnt/β-Catenin in Osteoblasts: Mechanisms, Scaffolds, and Computational Insights for Bone Therapeutics.

Phytotherapy research : PTR·2026
Same author

Learning Through Simulation: Counselor Trainees' Interactions with ChatGPT as a Client.

Behavioral sciences (Basel, Switzerland)·2025
Same author

Intelligent control of integrated on-board charger with improved power quality and reduced charging transients.

ISA transactions·2023
Same author

Tinosporaside from <i>Tinospora cordifolia</i> Encourages Skeletal Muscle Glucose Transport through Both PI-3-Kinase- and AMPK-Dependent Mechanisms.

Molecules (Basel, Switzerland)·2023
Same author

Chlorophyll: the ubiquitous photocatalyst of nature and its potential as an organo-photocatalyst in organic syntheses.

Organic & biomolecular chemistry·2022
Same author

Cladrin alleviates dexamethasone-induced apoptosis of osteoblasts and promotes bone formation through autophagy induction via AMPK/mTOR signaling.

Free radical biology & medicine·2022
Same journal

Inhibitors of nutrient pathways: nature's overlooked antibiotic arsenal.

Natural product reports·2026
Same journal

Challenges in the complexity-to-diversity strategy for natural product-like compound synthesis: two sides of the same coin.

Natural product reports·2026
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
See all related articles

This review details the chemistry and biological effects of furanoflavonoids. It covers 291 compounds, offering a comprehensive overview for researchers in the field.

Area of Science:

  • Phytochemistry
  • Pharmacology
  • Natural Products Chemistry

Background:

  • Furanoflavonoids are a significant class of plant-derived compounds.
  • Understanding their chemical structures and biological activities is crucial.

Purpose of the Study:

  • To comprehensively review the known furanoflavonoids.
  • To summarize their phytochemistry and pharmacological properties.

Main Methods:

  • Literature search and synthesis of existing data.
  • Compilation of information on 291 furanoflavonoid compounds.

Main Results:

  • Detailed description of the phytochemistry of 291 furanoflavonoids.
  • Summary of the pharmacological actions and potential applications of these compounds.

Related Experiment Videos

  • Inclusion of 228 relevant references for further study.

    • Conclusions:

    • Furanoflavonoids represent a diverse group of natural products with varied biological activities.
    • This review serves as a valuable resource for scientists studying furanoflavonoids.