1. Anti-infection Others
  2. Influenza Virus Drug Derivative
  3. Antiviral agent 80

Antiviral agent 80 is a conjugate of Zanamivir (HY-13210) and Amantadine (HY-13317), acting as a dual inhibitor of influenza virus M2 ion channel/neuraminidase (NA). Antiviral agent 80 exhibits potent inhibitory activity against both wild-type and drug-resistant influenza neuraminidase mutants, with an IC50 value range of 1.50 nM to 120.4 nM. Antiviral agent 80 can be used in influenza-related research.

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Antiviral agent 80

Antiviral agent 80 Chemical Structure

CAS No. : 3110745-57-5

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Description

Antiviral agent 80 is a conjugate of Zanamivir (HY-13210) and Amantadine (HY-13317), acting as a dual inhibitor of influenza virus M2 ion channel/neuraminidase (NA). Antiviral agent 80 exhibits potent inhibitory activity against both wild-type and drug-resistant influenza neuraminidase mutants, with an IC50 value range of 1.50 nM to 120.4 nM. Antiviral agent 80 can be used in influenza-related research[1].

In Vitro

Antiviral agent 80 (Compound 7j) exhibits potent inhibitory activity against both wild-type and drug-resistant influenza neuraminidase (NA) mutants, with IC50 values ranging from 1.50 nM to 120.4 nM. Specifically, its IC50 values against N9, N1, and N1 (H275Y) are 1.5 nM, 1.69 nM, and 2.05 nM, respectively[1].
Antiviral agent 80 protects MDCK cells from influenza A virus-induced cytopathic effects, with an EC50 value ranging from 11.13 nM to 12.55 nM and a CC50 greater than 200 μM, indicating high selectivity[1].
Antiviral agent 80 (5 μM; 24 h) induces proteasome-dependent NA degradation in HEK293T cells transfected with NA plasmid, with a degradation rate of approximately 95%; it does not upregulate autophagy markers in BEAS-2B, HEK293T or A549 cells[1].
Antiviral agent 80 can efficiently cross cell membranes and accumulate in MDCK cells, with intracellular retention rates of 88.8% and 19.1% at pretreatment concentrations of 100 μM and 25 μM, respectively; after removing extracellular compounds by washing, its EC50 against A/WSN/1933 only slightly increases from 11.13 nM to 48.0 nM, indicating that this compound possesses strong intracellular antiviral activity[1].
Antiviral agent 80 inhibits multiple stages of the influenza A virus life cycle in MDCK cells, which is evidenced by the reduction in M1 protein levels[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Western Blot Analysis[1]

Cell Line: HEK293T cells transfected with NA plasmids; BEAS-2B, HEK293T, A549 cells
Concentration: 5 μM (NA degradation); 5 μM (MG-132, proteasome inhibitor); 100 μM (chloroquine, lysosomal inhibitor)
Incubation Time: 24 h (NA degradation)
Result: Reduced NA protein levels in a dose- and time-dependent manner in HEK293T cells transfected with NA plasmids, with ~95% degradation observed after 24 h treatment with 5 μM.
Blocked NA degradation in the presence of 5 μM proteasome inhibitor MG-132 but not 100 μM lysosomal inhibitor chloroquine.
Did not upregulate autophagy markers (LC3-II, ATG5, ATG7) in BEAS-2B, HEK293T, or A549 cells, unlike Amantadine.
Molecular Weight

580.63

Formula

C26H40N6O9

CAS No.
SMILES

CC(N[C@H]1[C@H]([C@H](OC(NCCNC(C23CC4CC(C3)CC(C4)C2)=O)=O)[C@H](O)CO)OC(C(O)=O)=C[C@@H]1NC(N)=N)=O

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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Product Name:
Antiviral agent 80
Cat. No.:
HY-181885
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