Varicella Zoster Virus gpI Inhibitors, in this context, refer to a class of antiviral chemicals that inhibit the functionality of VZV gpI by targeting various aspects of the viral replication cycle. These inhibitors primarily function by interfering with the viral DNA synthesis or the activity of viral enzymes crucial for replication. The mechanism of action of these inhibitors can be broadly classified into two categories: nucleoside analogues and viral enzyme inhibitors. Nucleoside analogues, such as Acyclovir, Valacyclovir Hydrochloride, Famciclovir, Penciclovir, Cidofovir, Idoxuridine, Vidarabine, Sorivudine, and Trifluridine, mimic the structure of nucleotides, the building blocks of DNA. Once incorporated into the viral DNA during replication, these analogues lead to premature termination of the DNA strand or cause errors in the DNA sequence, thereby inhibiting viral replication. Since gpI is a glycoprotein involved in viral entry and cell-to-cell spread, its functional impact is indirectly diminished due to the reduced replication efficiency of the virus. Acyclovir and Valacyclovir are particularly notable for their high selectivity and low cytotoxicity, making them widely used for VZV infections.
Viral enzyme inhibitors, such as Foscarnet and Tenofovir Disoproxil Fumarate, target specific enzymes required for viral replication. Foscarnet sodium directly inhibits viral DNA polymerase without requiring activation by viral enzymes, which disrupts DNA synthesis. Tenofovir Disoproxil Fumarate is a nucleotide analogue that undergoes conversion to an active form within the host cells and then inhibits the action of viral replication enzymes. By targeting these enzymes, these inhibitors reduce the ability of VZV to replicate, indirectly affecting the role of gpI in the viral lifecycle. Overall, while these inhibitors do not target VZV gpI directly, their impact on viral replication significantly affects the functionality of gpI, thus playing a crucial role in controlling VZV infections.
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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 guanosine analogue that inhibits viral DNA polymerase, thereby impeding VZV replication. | ||||||
Valacyclovir Hydrochloride | 124832-27-5 | sc-204937 sc-204937A | 50 mg 100 mg | $117.00 $150.00 | ||
Enhances bioavailability, following metabolism, inhibits viral replication. | ||||||
Famciclovir | 104227-87-4 | sc-211498 | 100 mg | $123.00 | ||
Inhibits viral DNA synthesis, indirectly affecting VZV gpI. | ||||||
Penciclovir | 39809-25-1 | sc-203183 | 100 mg | $255.00 | ||
Targets viral DNA polymerase, indirectly disrupting VZV replication and gpI functionality. | ||||||
Foscarnet sodium | 63585-09-1 | sc-205330 sc-205330A | 1 g 5 g | $186.00 $663.00 | ||
Inhibits viral DNA polymerase directly, impacting VZV replication and gpI's role in it. | ||||||
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 | |
Inhibits VZV DNA polymerase, indirectly reducing the effectiveness of gpI in viral processes. | ||||||
Cidofovir | 113852-37-2 | sc-482141 | 50 mg | $135.00 | ||
A cytosine analogue, inhibits viral DNA synthesis, indirectly impacting gpI activity. | ||||||
Idoxuridine | 54-42-2 | sc-205720 sc-205720A | 500 mg 1 g | $102.00 $209.00 | ||
Incorporates into viral DNA, disrupting synthesis, indirectly affecting gpI functionality. | ||||||
Vidarabine | 5536-17-4 | sc-205881 sc-205881A | 100 mg 500 mg | $52.00 $137.00 | 1 | |
Inhibits viral DNA polymerase and incorporation into DNA, impacting gpI indirectly. | ||||||
Tenofovir | 147127-20-6 | sc-204335 sc-204335A | 10 mg 50 mg | $154.00 $633.00 | 11 | |
Targets viral replication enzymes, indirectly influencing gpI function in VZV. | ||||||