Oral USC-093, a novel homoserinamide analogue of the tyrosinamide (S)-HPMPA prodrug USC-087 has decreased nephrotoxicity while maintaining antiviral efficacy against human adenovirus infection of Syrian hamsters

Author:

Tollefson Ann E.ORCID,Riemann Samantha B.ORCID,Ying Baoling,Spencer Jacqueline F.,Overhulse Justin M.,Kashemirov Boris A.,Wold William S.M.,McKenna Charles E.,Toth KarolyORCID

Funder

National Institutes of Health

Publisher

Elsevier BV

Subject

Virology,Pharmacology

Reference41 articles.

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2. Animal models in human adenovirus research;Bertzbach;Biology,2021

3. Cidofovir diphosphate inhibits adenovirus 5 DNA polymerase via both non-obligate chain termination and direct inhibition, and polymerase mutations confer cidofovir resistance on intact virus;Chamberlain;Antimicrob. Agents Chemother.63,2018

4. Brincidofovir (CMX001) toxicity associated with epithelial apoptosis and crypt drop out in a hematopoietic cell transplant patient: challenges in distinguishing drug toxicity from GVHD;Detweiler;J. Pediatr. Hematol. Oncol.,2018

5. Emerging antiviral therapeutics for human adenovirus infection: recent developments and novel strategies;Dodge;Antivir. Res.,2021

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