PRAME (preferentially expressed antigen in melanoma) inhibitors represent a class of chemical compounds that have garnered considerable interest in the field of oncology due to their potential for targeting cancer-specific antigens. The PRAME protein, encoded by the PRAME gene, is a tumor-associated antigen that is selectively expressed in a variety of malignancies, including melanoma, lung cancer, and leukemia, while showing minimal expression in normal healthy tissues. PRAME inhibitors are meticulously designed molecules with the primary aim of blocking or modulating the activity of the PRAME protein. These inhibitors can act through various mechanisms, such as binding to specific regions on the PRAME protein's surface, disrupting protein-protein interactions, or interfering with critical post-translational modifications that are essential for its proper function. The design process of these inhibitors involves utilizing cutting-edge computational tools, molecular docking, and structural biology approaches to predict and optimize their interactions with the PRAME protein.
By inhibiting the PRAME protein, these compounds hold the potential to exert profound effects on cancer cells. This may include interfering with tumor cell growth, survival pathways, cell cycle progression, or even triggering programmed cell death (apoptosis). The precise mechanisms through which PRAME inhibitors exert their effects are the subject of intense scientific investigation.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | $132.00 $1064.00 | 115 | |
A proteasome inhibitor for multiple myeloma and mantle cell lymphoma. | ||||||
Ixazomib | 1072833-77-2 | sc-489103 sc-489103A | 10 mg 50 mg | $311.00 $719.00 | ||
A proteasome inhibitor approved for multiple myeloma. | ||||||