| Weight | 157.104 g/mol |
|---|---|
| Formula | C5H4FN3O2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
Favipiravir (259793-96-9)
Score:
#21 in Virology
,
#605 in Microbiology
,
#4858 in Biology
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- Favipiravir (T-705), a novel viral RNA polymerase inhibitor. (Antiviral Research, 2013)
- T-705 (favipiravir) and related compounds: novel broad-spectrum inhibitors of RNA viral infections. (Antiviral Research, 2009)
- Successful treatment of advanced Ebola virus infection with T-705 (favipiravir) in a small animal model (Antiviral Research, 2014)
- T-705 (favipiravir) activity against lethal H5N1 influenza A viruses (Proceedings of the National Academy of Sciences of the United States of America, 2010)
- Post-exposure efficacy of Oral T-705 (Favipiravir) against inhalational Ebola virus infection in a mouse model (Antiviral Research, 2014)
- Experimental Treatment with Favipiravir for Ebola Virus Disease (the JIKI Trial): A Historically Controlled, Single-Arm Proof-of-Concept Trial in Guinea (PLOS Medicine, 2016)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESC1=C(N=C(C(=O)N1)C(=O)N)F
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- Pubchem - Favipiravir
- Wikipedia - favipiravir
Favipiravir, also known as T-705 or Avigan, is an experimental antiviral drug being developed by Toyama Chemical of Japan with activity against many RNA viruses. Like some other experimental antiviral drugs (T-1105 and T-1106), it is a pyrazinecarboxamide derivative. Favipiravir is active against influenza viruses, West Nile virus, yellow fever virus, foot-and-mouth disease virus as well as other flaviviruses, arenaviruses, bunyaviruses and alphaviruses.
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Favipiravir
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