Date published: 2026-5-6

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Clevudine (CAS 163252-36-6)

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Alternate Names:
1-(2-Deoxy-2-fluoro-beta-L-arabinofuranosyl)-5-methyl-2,4(1H,3H)-pyrimidinedione
CAS Number:
163252-36-6
Molecular Weight:
260.22
Molecular Formula:
C10H13FN2O5
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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UBE2A Inhibitors are a class of chemical compounds designed to specifically target and inhibit the function of UBE2A, an E2 ubiquitin-conjugating enzyme. UBE2A is an essential component of the ubiquitin-proteasome system, which is responsible for tagging proteins with ubiquitin molecules, marking them for degradation by the proteasome. UBE2A plays a critical role in the second step of this process, where it facilitates the transfer of ubiquitin from the E1 activating enzyme to the target protein substrate, often in conjunction with a specific E3 ubiquitin ligase. The inhibition of UBE2A provides a valuable tool for scientists to explore the intricacies of protein turnover, regulation, and homeostasis within cells, particularly in understanding how specific proteins are selectively degraded and how this impacts cellular functions. Research utilizing UBE2A Inhibitors allows for a deeper investigation into the ubiquitination process and its broader implications in cellular biology. By inhibiting UBE2A, researchers can study the accumulation of specific proteins that would otherwise be targeted for degradation, thereby revealing their roles in various cellular processes such as DNA repair, signal transduction, and cell cycle regulation. Furthermore, UBE2A is known to interact with a variety of substrates and E3 ligases, and its inhibition can provide insights into the specificity and regulation of these interactions. This inhibition can also be employed to study the effects of dysregulated ubiquitination on cellular pathways, offering a clearer understanding of how ubiquitin-mediated processes contribute to maintaining cellular equilibrium. Overall, UBE2A Inhibitors are essential tools for dissecting the complex dynamics of protein ubiquitination and degradation, aiding in the exploration of fundamental biological mechanisms.


Clevudine (CAS 163252-36-6) References

  1. Effect of a combination of clevudine and emtricitabine with adenovirus-mediated delivery of gamma interferon in the woodchuck model of hepatitis B virus infection.  |  Jacquard, AC., et al. 2004. Antimicrob Agents Chemother. 48: 2683-92. PMID: 15215126
  2. Clevudine inhibits hepatitis delta virus viremia: a pilot study of chronically infected woodchucks.  |  Casey, J., et al. 2005. Antimicrob Agents Chemother. 49: 4396-9. PMID: 16189132
  3. Long-term therapy with clevudine for chronic hepatitis B can be associated with myopathy characterized by depletion of mitochondrial DNA.  |  Seok, JI., et al. 2009. Hepatology. 49: 2080-6. PMID: 19333909
  4. Clevudine for chronic hepatitis B: antiviral response, predictors of response, and development of myopathy.  |  Jang, JH., et al. 2011. J Viral Hepat. 18: 84-90. PMID: 20196804
  5. Efficacy of initial treatment with clevudine in naive patients with chronic hepatitis B.  |  Yang, HW., et al. 2010. Korean J Intern Med. 25: 372-6. PMID: 21179274
  6. Clevudine-induced viral response, associated with continued reduction of HBsAg titer, was durable after the withdrawal of therapy.  |  Lee, HS., et al. 2011. J Gastroenterol. 46: 410-4. PMID: 21181212
  7. Comparison of clevudine and entecavir for treatment-naive patients with chronic hepatitis B virus infection: two-year follow-up data.  |  Yoon, EL., et al. 2011. J Clin Gastroenterol. 45: 893-9. PMID: 21617542
  8. High-dose clevudine impairs mitochondrial function and glucose-stimulated insulin secretion in INS-1E cells.  |  Jang, YO., et al. 2012. BMC Gastroenterol. 12: 4. PMID: 22230186
  9. Long-term treatment outcomes of clevudine in antiviral-naive patients with chronic hepatitis B.  |  Kim, SB., et al. 2012. World J Gastroenterol. 18: 6943-50. PMID: 23322992
  10. Noncompetitive inhibition of hepatitis B virus reverse transcriptase protein priming and DNA synthesis by the nucleoside analog clevudine.  |  Jones, SA., et al. 2013. Antimicrob Agents Chemother. 57: 4181-9. PMID: 23774432
  11. A randomized, open-label study comparing low-dose clevudine plus adefovir combination therapy with clevudine monotherapy in naïve chronic hepatitis B patients.  |  Tak, WY., et al. 2014. Hepatol Int. 8: 375-81. PMID: 25101150
  12. Management of Clevudine-Resistant Chronic Hepatitis B: A Multicenter Cohort Study.  |  Cho, EY., et al. 2017. Gut Liver. 11: 129-135. PMID: 27538443
  13. Clevudine Induced Mitochondrial Myopathy.  |  Park, SH., et al. 2017. J Korean Med Sci. 32: 1857-1860. PMID: 28960041
  14. Clevudine attenuates bleomycin-induced early pulmonary fibrosis via regulating M2 macrophage polarization.  |  Li, S., et al. 2021. Int Immunopharmacol. 101: 108271. PMID: 34700113
  15. Protecting-group-free synthesis of clevudine (L-FMAU), a treatment of the hepatitis B virus.  |  Tremblay, T., et al. 2022. Org Biomol Chem. 20: 8859-8863. PMID: 36331415

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Clevudine, 250 mg

sc-500848
250 mg
$535.00