HPV18 E6 inhibitors belong to a class of chemical compounds designed to target and modulate the activity of the human papillomavirus type 18 (HPV18) E6 protein. The E6 protein is a viral oncoprotein expressed by certain strains of the human papillomavirus, including HPV18. It plays a pivotal role in the viral life cycle and is implicated in the development and progression of HPV-associated cancers. Specifically, HPV18 E6 is known to interact with various cellular proteins, including tumor suppressor proteins like p53, leading to their degradation and functional inactivation.
Inhibitors within the HPV18 E6 class are developed to disrupt the interactions between the E6 protein and its cellular binding partners. By inhibiting the E6 protein's interactions with key host cell proteins, these compounds aim to prevent the degradation of tumor suppressor proteins and impede the cellular processes that contribute to cancer development. The study of HPV18 E6 inhibitors offers valuable insights into the molecular mechanisms underlying HPV-associated carcinogenesis and provides an avenue for developing strategies to target viral oncoproteins as a means of combating HPV-related cancers.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Retinoic Acid, all trans | 302-79-4 | sc-200898 sc-200898A sc-200898B sc-200898C | 500 mg 5 g 10 g 100 g | $66.00 $325.00 $587.00 $1018.00 | 28 | |
Induces p53 expression, counteracting the degradation caused by HPV18 E6 and potentially inhibiting its oncogenic effects. | ||||||
Curcumin | 458-37-7 | sc-200509 sc-200509A sc-200509B sc-200509C sc-200509D sc-200509F sc-200509E | 1 g 5 g 25 g 100 g 250 g 1 kg 2.5 kg | $37.00 $69.00 $109.00 $218.00 $239.00 $879.00 $1968.00 | 47 | |
Disrupts the E6-p53 interaction, leading to p53 stabilization and restoration of its tumor-suppressive functions. | ||||||
Resveratrol | 501-36-0 | sc-200808 sc-200808A sc-200808B | 100 mg 500 mg 5 g | $80.00 $220.00 $460.00 | 64 | |
Inhibits the E6-mediated degradation of p53, potentially restoring p53's role in cell cycle regulation and apoptosis. | ||||||
MG-132 [Z-Leu- Leu-Leu-CHO] | 133407-82-6 | sc-201270 sc-201270A sc-201270B | 5 mg 25 mg 100 mg | $60.00 $265.00 $1000.00 | 163 | |
A proteasome inhibitor that can block the proteasomal degradation of p53 by interfering with E6's ubiquitin ligase activity. | ||||||