2'-Fluoro-6'-methylene carbocyclic adenosine and its phosphoramidate prodrug: A novel anti-HBV agent, active against drug-resistant HBV mutants.

Author: ChuChung K, MulamoottilVarughese A, SinghUma S

Paper Details 
Original Abstract of the Article :
Chronic hepatitis B (CHB) is one of the major causes of morbidity and mortality worldwide. Currently, clinically approved nucleos(t)ide analogs (NAs) are very efficient in reducing the load of hepatitis B virus (HBV) with minimum side effects. However, the long-term administration of antiviral drugs...See full text at original site
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引用元:
https://doi.org/10.1002/med.21490

データ提供:米国国立医学図書館(NLM)

Fighting Drug-Resistant Hepatitis B: A New Weapon in the Arsenal

Chronic hepatitis B (CHB) is a major global health problem, with millions of people infected worldwide. While current nucleos(t)ide analogs (NAs) are effective in reducing viral load, the emergence of drug-resistant HBV strains poses a significant challenge. This study introduces two novel carbocyclic NAs, 2'-fluoro-6'-methylene carbocyclic adenosine (FMCA) and its phosphoramidate prodrug (FMCAP), as potential agents against drug-resistant HBV mutants.

A New Oasis in the Fight Against Drug Resistance

Preclinical studies demonstrated that FMCA and FMCAP exhibited potent antiviral activity against adefovir and lamivudine (LMV)-resistant HBV mutants, including triple mutants resistant to both LMV and entecavir (ETV). This suggests that these novel compounds could be valuable additions to combination therapies for treating drug-resistant CHB, providing a new oasis of hope in the battle against this challenging disease.

The Importance of Staying Ahead of the Curve

The emergence of drug resistance is a constant threat in the treatment of viral infections. This study highlights the need for ongoing research and development of novel antiviral agents to stay ahead of evolving viral strains. It's like navigating a desert landscape where the terrain is constantly shifting, requiring adaptability and innovation to overcome new challenges.

Dr.Camel's Conclusion

This study offers a promising new approach to treating drug-resistant CHB. The development of FMCA and FMCAP could significantly enhance our arsenal of antiviral therapies, helping us to navigate the shifting sands of viral resistance and provide effective treatment options for individuals living with CHB.

Date :
  1. Date Completed 2018-11-16
  2. Date Revised 2018-11-16
Further Info :

Pubmed ID

29406612

DOI: Digital Object Identifier

10.1002/med.21490

Related Literature

SNS
PICO Info
in preparation
Languages

English

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