1. Anti-infection
  2. SARS-CoV Dengue Virus
  3. Virapinib

Virapinib is a macropinocytosis inhibitor with antiviral activity. Virapinib exhibits broad-spectrum antiviral activity against SARS-CoV-2, monkeypox virus, tick-borne encephalitis virus, and Ebola pseudotyped vesicular stomatitis virus, and it enhances Dengue Virus infection. Virapinib blocks viral entry by inhibiting macropinocytosis, reduces syncytium formation in SARS-CoV-2-infected cells, and impairs cellular entry of SARS-CoV-2 variants. Virapinib upregulates the expression of genes related to sterol biosynthesis. Virapinib can be used in studies related to COVID-19, monkeypox, tick-borne encephalitis, and Ebola virus infection.

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Virapinib

Virapinib Chemical Structure

CAS No. : 1794091-10-3

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Description

Virapinib is a macropinocytosis inhibitor with antiviral activity. Virapinib exhibits broad-spectrum antiviral activity against SARS-CoV-2, monkeypox virus, tick-borne encephalitis virus, and Ebola pseudotyped vesicular stomatitis virus, and it enhances Dengue Virus infection. Virapinib blocks viral entry by inhibiting macropinocytosis, reduces syncytium formation in SARS-CoV-2-infected cells, and impairs cellular entry of SARS-CoV-2 variants. Virapinib upregulates the expression of genes related to sterol biosynthesis. Virapinib can be used in studies related to COVID-19, monkeypox, tick-borne encephalitis, and Ebola virus infection[1][2][3].

In Vitro

Virapinib (0.78-25 μM; 6 h pre-incubation; 72 h total incubation post-virus addition) inhibits SARS-CoV-2 S pseudotyped lentivirus infection in HEK293TACE2 cells in a dose-dependent manner, but has no effect on VSVg pseudotyped lentivirus infection[1].
Virapinib (0.5-10 μM; 6 h pre-incubation; 24 h total incubation post-virus wash-off) dose-dependently inhibits infection by the original SARS-CoV-2 in Vero E6 cells, with no cytotoxicity detected[1].
Virapinib (1-20 μM; 6 h pre-incubation; 24 h total incubation post-virus wash-off) dose-dependently inhibits infection by the original SARS-CoV-2, reduces syncytium formation in A549ACE2 cells, and shows no detectable cytotoxicity[1].
Virapinib (0.5-10 μM; overnight pre-incubation; 24 h total incubation post-virus infection) effectively reduces the infectivity of SARS-CoV-2 in 3D primary human hepatospheres[1].
Virapinib (5-25 μM; 16 h pre-incubation; 2 h dextran incubation) dose-dependently inhibits macropinocytosis in A549 cells and selectively blocks SARS-CoV-2 entry into A549ACE2 cells via the macropinocytosis pathway[1].
Virapinib (5-40 μM for tick-borne encephalitis virus and monkeypox virus; 10-25 μM for Ebola-pseudotyped vesicular stomatitis virus; 6 h pre-incubation) dose-dependently inhibits infections by tick-borne encephalitis virus, monkeypox virus, and Ebola-pseudotyped vesicular stomatitis virus in A549 cells. It shows no activity against Andes virus, only weak activity against adenovirus, and enhances dengue virus infection[1].

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

Real Time qPCR[1]

Cell Line: MCF-7 cells, A549ACE2 cells
Concentration: 10 μM (MCF-7 RNA-seq); 10, 25 μM (A549ACE2 qRT-PCR)
Incubation Time: 6 h incubation (both cell lines)
Result: Showed significant upregulation of genes related to sterol biosynthesis, including HMGCS1, HMGCR, and MVK, in MCF-7 cells via RNA sequencing.
Identified 'steroid biosynthesis' as the most significantly induced pathway via KEGG pathway enrichment analysis.
Increased HMGCR, HMGCS1, and MVK mRNA levels in A549ACE2 cells via qRT-PCR, without altering total cellular cholesterol levels or cholesterol distribution.
Molecular Weight

448.60

Formula

C26H36N6O

CAS No.
SMILES

CC(CC1)CCN1C2=CC=C(C(N3CCC(C4=NC5=C(CCN(C)C5)C(NC)=N4)C3)=O)C=C2

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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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