| Cat. No. |
Product Name |
Information |
| PC-70358 |
M2WJ-332
Influenza inhibitor
|
M2WJ-332 is a potent inhibitor of drug-resistant S31N mutant of the M2 ion channel of influenza A virus with IC50 of 153 nM. |
| PC-45139 |
Peramivir
Influenza NA inhibitor
|
Peramivir (RWJ-270201, BCX-1812) is an inhibitor of influenza neuraminidase that prevents new viral particles from being released. |
| PC-45138 |
Peramivir trihydrate
Influenza NA inhibitor
|
Peramivir (RWJ-270201, BCX-1812) is an inhibitor of influenza neuraminidase that prevents new viral particles from being released; an antiviral agent used to treat and prevent influenza A and influenza B. |
| PC-45819 |
Nucleozin
Influenza NP inhibitor
|
Nucleozin is a small-molecule influenza A nucleoprotein (NP) inhibitor that triggers the aggregation of NP and inhibits its nuclear accumulation. |
| PC-45140 |
Oseltamivir phosphate
Influenza NA inhibitor
|
Oseltamivir phosphate (GS-4104, GS4104) is a competitive inhibitor of influenza neuraminidase that prevents new viral particles from being released; an antiviral agent used to treat and prevent influenza A and influenza B. |
| PC-28415 |
HDN2398
IAV NS1 inhibitor
|
HDN2398 is a broad-spectrum influenza inhibitor that blocks multiple functions of viral NS1 protein, exhibits H1N1virusA/ Virginia/ATCC1/2009 inhibition (IC50=3.3 uM) in MDCK cells. |
| PC-27419 |
Deubaloxavir marboxil
Influenza inhibitor
|
Deubaloxavir marboxil is anti-influenza compound that potently and selectively inhibits the cap-dependent endonuclease within the polymerase PA subunit of influenza A and B viruses. |
| PC-27363 |
WXSH0208
Influenza inhibitor, CCHFV endonuclease inhibitor
|
WXSH0208 is a baloxavir marboxil derivative and selective inhibitor of influenza RNA polymerase subunit, inhibits cap-dependent endonuclease (CEN), shows antiviral activity against influenza A and B viruses in vitro, including strains resistant to baloxavir, also inhibits Crimean-Congo haemorrhagic fever virus (CCHFV) endonuclease activity and suppresses viral replication with EC50 of 4.2 uM. |
| PC-27290 |
HEC116094
IAV PB2 inhibitor
|
HEC116094 is a potent, specific inhibitor of influenza A virus polymerase PB2 subunit with IC50 of 0.337 nM. |
| PC-26867 |
Cynaroside
Influenza RdRp inhibitor
|
Cynaroside (Luteolin 7-glucoside) is a flavonoid compound with anti-oxidative capabilities, is also a potent influenza RNA-dependent RNA polymerase (RdRp) inhibitor with IC50 of 32 nM, also inhibits H2O2-induced apoptosis, has cytoprotection against oxidative stress-induced cardiovascular diseases, also disrupts IGF2BP3-RTK interactions as an enhancer of tyrosine kinase inhibitor (TKI) efficacy. |
| PC-26221 |
FNDR-11124
Viral RdRp inhibitor
|
FNDR-11124 is a potent broad-spectrum inhibitor of SARS-CoV-2, influenza, KFDV and representative flaviviruses and alphaviruses, targets viral RNA-dependent RNA polymerases (RdRp) across virus families. |
| PC-25607 |
Licoflavone B
Influenza inhibitor
|
Licoflavone B is an isoprene flavonoid derived from licorice residue and potent anti-influenza agent, selectively targets the viral RNA-dependent RNA polymerase (RdRp) with IC50 of 9.9 uM, effectively suppressing viral replication, also exerts anti-ulcerative colitis (UC) activity through blocking the MAPK pathway. |
