Dengue Virus

Dengue virus inhibitors target viral enzymes, replication proteins and host factors of this mosquito-borne flavivirus. Dengue virus (DENV) has a positive-strand RNA genome that is translated into one polyprotein and cleaved into individual proteins. ZINC03129319 and rhodiolin are listed as inhibitors of the protease formed by nonstructural proteins 2B and 3 (NS2B-NS3). NITD008 is an adenosine nucleoside analog that terminates viral RNA synthesis and was reported in 2009 to inhibit all four DENV serotypes. (+)-JNJ-A07 belongs to a compound series that blocks the interaction between NS3 and nonstructural protein 4B (NS4B). U18666A inhibits cholesterol synthesis and transport, host lipid pathways that the virus uses. Compounds with broader activity across related viruses are listed in the neighboring Flavivirus category.

4 Items

  • Prochlorperazine dimaleate
    Cat. No.
    A17405

    Prochlorperazine dimaleate

    Prochlorperazine dimaleate is an orally active dopamine D2 receptor (D2R) antagonist. It demonstrates notable anti-cancer activity in vitro against a range of cancer cell lines, with IC50 values of 6.4 μM for NOX1, 4.5 μM for NOX2, and 2.3 μM for NOX5. Additionally, prochlorperazine dimaleate exhibits antedesmosidic activity against the dengue virus (DENV). This compound is valuable for research aimed at understanding and treating conditions such as nausea, vomiting, migraine, and schizophrenia.

    25 mg
    $25.00
    50 mg
    $35.00
    All 4 sizes
  • (-)-(E)-Guggulsterone
    Cat. No.
    A38882

    (-)-(E)-Guggulsterone

    Synonyms: (E)-Guggulsterone

    (-)-(E)-Guggulsterone is a natural stereoisomer of Guggulsterone that functions as a Farnesoid X Receptor (FXR) antagonist with an IC50 of 24.06 μM. This compound exhibits significant hypolipidemic effects and demonstrates the ability to suppress dengue virus (DENV) replication by enhancing antiviral interferon responses through the activation of Nrf2 and upregulation of HO-1 expression. Additionally, (-)-(E)-Guggulsterone displays antibacterial properties against various strains, including Bacillus subtilis, Staphylococcus aureus, and Pseudomonas aeruginosa, as well as offering cardiac protective and antioxidant benefits in rat models.

    1 mg
    $35.00
    5 mg
    $75.00
    All 6 sizes
  • (Rac)-Modipafant
    Cat. No.
    A50709

    (Rac)-Modipafant

    Synonyms: UK-74505

    (Rac)-Modipafant is a selective, long-acting irreversible antagonist of the platelet activating factor receptor (PAFR). This compound demonstrates significant biological activity by effectively inhibiting PAFR-mediated pathways, which plays a critical role in regulating inflammatory responses. Research applications include the investigation of dengue virus infection mechanisms and the potential therapeutic effects of PAFR blockade in various inflammatory diseases.

    1 mg
    $175.00
    5 mg
    $450.00
    All 6 sizes
  • SDM25N hydrochloride
    Cat. No.
    A50884

    SDM25N hydrochloride

    SDM25N hydrochloride is a potent δ-opioid receptor antagonist that also serves as an effective inhibitor of the dengue virus (DENV). It specifically targets the viral NS4B protein, significantly limiting genomic RNA replication. This compound presents valuable opportunities for research on antiviral strategies and the role of δ-opioid receptors in viral pathogenesis.

    Out of stock

    All 3 sizes

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