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

Imino-sugar-based nucleosides.

Vern L Schramm1, Peter C Tyler

  • 1Department of Biochemistry, Albert Einstein College of Medicine, Bronx, NY 10461, USA.

Current Topics in Medicinal Chemistry
|February 7, 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

Isofagomine Derivatives as TcdB Glucosyltransferase Inhibitors.

Journal of medicinal chemistry·2026
Same author

Transition-state analysis of the arginine-specific human ADP-ribosyltransferase 1.

Proceedings of the National Academy of Sciences of the United States of America·2026
Same author

Coupled-enzyme assay for MTAP activity in biological samples.

Analytical biochemistry·2026
Same author

Continuous assay for the dNTP triphosphohydrolase of activated SAMHD1.

Analytical biochemistry·2025
Same author

The anti-cancer transition-state inhibitor MTDIA inhibits human MTAP, inducing autophagy in humanized yeast.

Disease models & mechanisms·2025
Same author

Kinetic Mechanism of the Emergent Anticancer Target, Human ADP-ribosyltransferase 1.

Biochemistry·2025
Same journal

Exploration of a Novel Physicochemical Property Space for the Development of Antimalarial Drugs.

Current topics in medicinal chemistry·2026
Same journal

Computational Drug Design of Natural Product-Based Azole Hybrids for Multifactorial Diseases: Success Stories.

Current topics in medicinal chemistry·2026
Same journal

Simulated Natural Nanoparticles in Bai-Hu-Tang Decoction: Preparation, Characterization, Pharmacokinetics, and Antipyretic Effects.

Current topics in medicinal chemistry·2026
Same journal

Dolabellane Diterpenes from the Marine Brown Alga Dictyota dolabellana and their Potential Antiviral Activity.

Current topics in medicinal chemistry·2026
Same journal

Inhibitory Effects of Flavonoids from the Stems and Leaves of Scutellaria baicalensis Georgi on Oligodendrocyte Pyroptosis Induced by Aβ1-42.

Current topics in medicinal chemistry·2026
Same journal

Mechanism of Huangqishihu Decoction in Treating Liver Fibrosis in Rats Model via Regulation of Oxidative Stress and Nrf2 Signaling Pathway.

Current topics in medicinal chemistry·2026
See all related articles

Imino-sugar nucleosides are potent inhibitors of N-ribosyltransferases, mimicking transition states. This review covers synthetic routes and therapeutic potential for imino- and imino-C-nucleosides in treating disorders.

Area of Science:

  • Medicinal Chemistry
  • Biochemistry
  • Organic Synthesis

Background:

  • N-ribosyltransferases are crucial enzymes in biological pathways.
  • Imino-C-nucleoside analogues show potent inhibitory activity against these enzymes.
  • These analogues mimic the ribooxacarbenium ion transition state of N-ribosyltransferases.

Purpose of the Study:

  • To review synthetic routes for imino- and imino-C-nucleosides.
  • To discuss the N-ribosyltransferases targeted by these analogues.
  • To highlight the therapeutic promise of these compounds for various biological disorders.

Main Methods:

  • Literature review of synthetic methodologies for imino- and imino-C-nucleosides.
  • Analysis of the mechanism of action of imino-C-nucleoside analogues.

Related Experiment Videos

  • Case studies illustrating therapeutic applications.
  • Main Results:

    • Challenging synthetic pathways for imino- and imino-C-nucleosides have been developed.
    • Detailed understanding of enzyme-inhibition mechanisms.
    • Demonstrated potential for treating biological disorders.

    Conclusions:

    • Imino-C-nucleoside analogues represent a promising class of therapeutic agents.
    • Further research into their synthesis and application is warranted.
    • These compounds offer a novel strategy for targeting N-ribosyltransferases.