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Setrobuvir

Cat. No. M27748
Setrobuvir Structure
Synonym:

ANA598

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Quality Control & Documentation
Biological Activity

Setrobuvir (ANA598) is an orally active non-nucleosidic HCV NS5B polymerase inhibitor. ANA-598 inhibits both de novo RNA synthesis and primer extension, with IC50s between 4 and 5 nM. Setrobuvir also shows excellent binding affinity to SARS-CoV-2 RdRp and induces RdRp inhibition.

Chemical Information
Molecular Weight 560.62
Formula C25H25FN4O6S2
CAS Number 1071517-39-9
Storage Please store the product under the recommended conditions in the Certificate of Analysis.
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Abdo A Elfiky. Future Microbiol. Dual targeting of RdRps of SARS-CoV-2 and the mucormycosis-causing fungus: an in silico perspective

[2] Vrish Dhwaj Ashwlayan, et al. Saudi J Biol Sci. Insight into the biological impact of COVID-19 and its vaccines on human health

[3] Rashed Noor. Tzu Chi Med J. Antiviral drυgs against severe acute respiratory syndrome coronavirus 2 infection triggering the coronavirus disease-19 pandemic

[4] Donald M Jensen, et al. Liver Int. Interferon-free regimens containing setrobuvir for patients with genotype 1 chronic hepatitis C: a randomized, multicenter study

[5] Navita L Mallalieu, et al. Clin Ther. Pharmacokinetics and pharmacodynamics of setrobuvir, an orally administered hepatitis C virus non-nucleoside analogue inhibitor

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