PRAMEF21 inhibitors are a class of chemical compounds specifically designed to target and modulate the activity of the PRAMEF21 protein, which is part of the PRAME (Preferentially Expressed Antigen in Melanoma) family. The PRAMEF21 gene encodes a protein that, like other members of the PRAME family, is believed to be involved in the regulation of gene expression and may interact with various transcriptional machinery within the cell. Although the detailed functions of PRAMEF21 are still being elucidated, it is thought to play a role in modulating cellular responses to environmental cues, potentially influencing processes such as cell proliferation, differentiation, and apoptosis. By inhibiting PRAMEF21, researchers can disrupt its normal regulatory functions, allowing them to explore its role in cellular processes and to better understand how it interacts with other proteins and genetic pathways.
The development of PRAMEF21 inhibitors involves a comprehensive approach that includes structural analysis, molecular modeling, and biochemical testing. Initially, structural biology techniques such as X-ray crystallography and cryo-electron microscopy are used to determine the three-dimensional structure of the PRAMEF21 protein. This structural information is critical for identifying key regions of the protein, such as active sites or domains involved in protein-protein interactions, which can be targeted by inhibitors. Computational methods, including molecular docking and virtual screening, are then employed to identify small molecules that can specifically bind to these regions, effectively blocking the protein's activity. Once potential inhibitors are identified, they undergo synthesis and rigorous in vitro testing to evaluate their binding affinity, specificity, and inhibitory potency. These compounds are further optimized through iterative cycles of chemical refinement, enhancing their effectiveness and selectivity. The study of PRAMEF21 inhibitors not only provides valuable tools for dissecting the specific functions of this protein but also contributes to a broader understanding of the molecular mechanisms that regulate gene expression and cellular behavior within the PRAME family.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Trametinib | 871700-17-3 | sc-364639 sc-364639A sc-364639B | 5 mg 10 mg 1 g | $112.00 $163.00 $928.00 | 19 | |
MEK inhibitor, might alter MAPK/ERK pathway, potentially affecting PRAMEF21's regulatory role in cell differentiation. | ||||||
Erlotinib Hydrochloride | 183319-69-9 | sc-202154 sc-202154A | 10 mg 25 mg | $74.00 $119.00 | 33 | |
EGFR inhibitor, could modulate pathways involved in cell proliferation, possibly intersecting with PRAMEF21 activity. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $62.00 $155.00 $320.00 | 233 | |
mTOR inhibitor, might influence signaling pathways relevant to PRAMEF21's function in cell proliferation and survival. | ||||||
Sorafenib | 284461-73-0 | sc-220125 sc-220125A sc-220125B | 5 mg 50 mg 500 mg | $56.00 $260.00 $416.00 | 129 | |
RAF kinase inhibitor, potentially influences cell signaling pathways intersecting with PRAMEF21's function. | ||||||
Palbociclib | 571190-30-2 | sc-507366 | 50 mg | $315.00 | ||
CDK4/6 inhibitor, may impact cell cycle pathways potentially connected to PRAMEF21's activity. | ||||||
AP 24534 | 943319-70-8 | sc-362710 sc-362710A | 10 mg 50 mg | $172.00 $964.00 | 2 | |
BCR-ABL inhibitor, could modulate pathways linked to PRAMEF21's role in cellular proliferation and differentiation. | ||||||
Cobimetinib | 934660-93-2 | sc-507421 | 5 mg | $270.00 | ||
MEK inhibitor, might affect signaling pathways related to PRAMEF21, particularly in cell growth and differentiation. | ||||||
Vandetanib | 443913-73-3 | sc-220364 sc-220364A | 5 mg 50 mg | $167.00 $1353.00 | ||
VEGFR, EGFR, and RET inhibitor, potentially impacts various signaling pathways associated with PRAMEF21's activities. | ||||||