2200336-20-3

Onradivir Chemical Structure
2200336-20-3

Chemical Structure

Onradivir

Synonym(s): ZSP1273

  • CAS No.: 2200336-20-3
  • Formula:C22H22F2N6O2
  • Molecular Weight:440.45

IUPAC Name: L-serine-2,3,3-d3

InChIKey: JCHDJLSIYWBAHI-ZWHBIUKWSA-N

SMILES: FC1=CN=C2C(C(C3=NC(N[C@@H]4[C@H](C5CCC4CC5)C(O)=O)=C(F)C(C6CC6)=N3)=NN2)=C1

Biological Activity: Onradivir (ZSP1273) is an orally active antiviral agent targeting influenza A virus RNA polymerase PB2 subunit with an IC50 of 0.562 nM. Onradivir inhibits cap binding to influenza A virus RNA polymerase PB2 subunit, suppresses viral replication, reduces viral titres and RNA loads, and inhibits influenza A virus infection. Onradivir maintains high survival rates in influenza A virus-infected mice, and reduces influenza A virus titers in a murine model. Onradivir can be used for the research of influenza A virus infection[1][2].

Cat. No. Product Name Purity Description Pricing
HY-145586
Onradivir 99.53% Onradivir (ZSP1273) is an orally active antiviral agent targeting influenza A virus RNA polymerase PB2 subunit with an IC50 of 0.562 nM. Onradivir inhibits cap binding to influenza A virus RNA polymerase PB2 subunit, suppresses viral replication, reduces viral titres and RNA loads, and inhibits influenza A virus infection. Onradivir maintains high survival rates in influenza A virus-infected mice, and reduces influenza A virus titers in a murine model. Onradivir can be used for the research of influenza A virus infection.
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