HSV-2 gE envelope protein inhibitors are a class of chemical compounds that specifically target the glycoprotein E (gE) of herpes simplex virus type 2 (HSV-2). Glycoprotein E is an envelope protein that plays a pivotal role in the virus's ability to spread between cells and evade immune detection. In HSV-2, gE forms a complex with glycoprotein I (gI), and this complex is involved in facilitating cell-to-cell spread of the virus, particularly in polarized cells such as neurons. It also functions in immune evasion by binding to the Fc portion of immunoglobulin G (IgG), which helps the virus avoid antibody-mediated immune responses. By inhibiting the function of the gE protein, these compounds can block key processes in the viral life cycle, especially those related to viral dissemination and immune system interactions.
The mechanism of action of HSV-2 gE inhibitors involves blocking the formation of the gE/gI complex or disrupting the protein's structural integrity, preventing it from functioning effectively in viral spread and immune evasion. These inhibitors may bind to specific regions of the gE protein, interfering with its ability to interact with IgG or with other viral or cellular proteins. By targeting the gE protein, the inhibitors can reduce the virus's ability to propagate through direct cell-to-cell contact, which is a crucial mechanism for HSV-2 in avoiding immune detection. The study of HSV-2 gE inhibitors contributes to understanding the molecular interactions involved in viral spread, immune modulation, and the structural biology of the gE protein itself, offering insights into how viruses exploit host systems to enhance their infectivity and persistence.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Acyclovir | 59277-89-3 | sc-202906 sc-202906A | 50 mg 500 mg | $147.00 $922.00 | 2 | |
A nucleoside analogue that inhibits viral DNA replication. | ||||||
Penciclovir | 39809-25-1 | sc-203183 | 100 mg | $255.00 | ||
Another nucleoside analogue, similar to acyclovir in action. | ||||||
Valacyclovir Hydrochloride | 124832-27-5 | sc-204937 sc-204937A | 50 mg 100 mg | $117.00 $150.00 | ||
A prodrug of acyclovir with better oral bioavailability. | ||||||
Foscarnet sodium | 63585-09-1 | sc-205330 sc-205330A | 1 g 5 g | $186.00 $663.00 | ||
Directly inhibits viral DNA polymerase without requiring activation by viral enzymes. | ||||||
Ganciclovir | 82410-32-0 | sc-203963 sc-203963A | 50 mg 250 mg | $228.00 $413.00 | 1 | |
A nucleoside analogue that inhibits viral replication. | ||||||
Cidofovir | 113852-37-2 | sc-482141 | 50 mg | $135.00 | ||
An acyclic nucleotide analogue that can inhibit HSV-2 replication. | ||||||
Brivudine | 69304-47-8 | sc-205607 sc-205607A sc-205607B sc-205607C | 10 mg 25 mg 100 mg 1 g | $220.00 $460.00 $1000.00 $2100.00 | 4 | |
A thymidine analogue that affects viral replication. | ||||||
Tenofovir | 147127-20-6 | sc-204335 sc-204335A | 10 mg 50 mg | $154.00 $633.00 | 11 | |
An antiretroviral drug that can inhibit HSV-2 replication in high concentrations. | ||||||