LOC100039794 inhibitors are a class of chemical compounds developed to specifically target and inhibit the function of the protein encoded by the gene LOC100039794. Identified through genomic research, LOC100039794 is characterized by its distinct expression patterns, indicating its potential involvement in certain cellular functions. While the protein encoded by this gene has not been extensively characterized, it is hypothesized to play a role in specific biological pathways based on initial genomic and proteomic analyses. The development of inhibitors targeting the LOC100039794 protein necessitates a comprehensive understanding of its molecular structure and its functional mechanisms within cellular systems. The primary aim of designing LOC100039794 inhibitors is to disrupt the protein's functional interactions, thereby providing insights into its role in cellular processes and potentially influencing these processes. This involves identifying key domains or active sites on the protein crucial for its functionality and creating molecules that can effectively target and inhibit these sites.
The process of developing LOC100039794 inhibitors is an intricate and interdisciplinary undertaking, involving biochemistry, molecular biology, and pharmacology. Researchers engaged in this task focus on elucidating the structural details of the LOC100039794 protein. Employing a range of advanced techniques, they aim to determine the protein's three-dimensional structure, particularly focusing on regions that are significant for its function. This structural understanding is pivotal for the targeted design of inhibitors that are both selective and effective in their inhibitory action. The interaction between these inhibitors and the LOC100039794 protein is a critical aspect of their efficacy. The inhibitors must bind to the protein in a way that disrupts its normal cellular interactions, typically resulting in the formation of a complex that inhibits the protein's typical functions. This interaction demands a precise alignment of the molecular structures of the inhibitor and the protein. In addition to their binding properties, the design of LOC100039794 inhibitors also takes into account factors such as the compound's stability, solubility, and its ability to effectively reach and interact with the target site within biological systems. Researchers also strive to optimize the pharmacokinetic properties of these inhibitors, ensuring they have suitable hydrophobic and hydrophilic characteristics and an appropriate molecular size and shape for efficient interaction. The development of LOC100039794 inhibitors highlights the advanced level of current research in molecular targeting, underscoring the complexity involved in designing specific inhibitors for proteins that are relatively uncharacterized but may hold significant roles in biological processes.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Suberoylanilide Hydroxamic Acid | 149647-78-9 | sc-220139 sc-220139A | 100 mg 500 mg | $130.00 $270.00 | 37 | |
As an HDAC inhibitor, it can alter chromatin accessibility and affect the expression of numerous genes. | ||||||
Nicotinamide | 98-92-0 | sc-208096 sc-208096A sc-208096B sc-208096C | 100 g 250 g 1 kg 5 kg | $43.00 $65.00 $200.00 $815.00 | 6 | |
A form of vitamin B3 that can act as an HDAC inhibitor, potentially altering gene expression patterns. | ||||||
Disulfiram | 97-77-8 | sc-205654 sc-205654A | 50 g 100 g | $52.00 $87.00 | 7 | |
An inhibitor of aldehyde dehydrogenase that has been shown to modulate NF-κB activity and could indirectly affect gene expression. | ||||||
Genistein | 446-72-0 | sc-3515 sc-3515A sc-3515B sc-3515C sc-3515D sc-3515E sc-3515F | 100 mg 500 mg 1 g 5 g 10 g 25 g 100 g | $26.00 $92.00 $120.00 $310.00 $500.00 $908.00 $1821.00 | 46 | |
A tyrosine kinase inhibitor that may also modulate epigenetic marks, thus affecting gene expression. | ||||||
Retinoic Acid, all trans | 302-79-4 | sc-200898 sc-200898A sc-200898B sc-200898C | 500 mg 5 g 10 g 100 g | $65.00 $319.00 $575.00 $998.00 | 28 | |
A metabolite of vitamin A that regulates gene transcription by activating nuclear receptors. | ||||||
Actinomycin D | 50-76-0 | sc-200906 sc-200906A sc-200906B sc-200906C sc-200906D | 5 mg 25 mg 100 mg 1 g 10 g | $73.00 $238.00 $717.00 $2522.00 $21420.00 | 53 | |
A compound that intercalates into DNA and prevents RNA synthesis, thus inhibiting gene expression. | ||||||
Methotrexate | 59-05-2 | sc-3507 sc-3507A | 100 mg 500 mg | $92.00 $209.00 | 33 | |
A dihydrofolate reductase inhibitor that affects nucleotide synthesis and can indirectly impact gene expression. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
A PI3K inhibitor that can alter AKT signaling and potentially downstream gene expression patterns. | ||||||
Triptolide | 38748-32-2 | sc-200122 sc-200122A | 1 mg 5 mg | $88.00 $200.00 | 13 | |
A diterpene triepoxide that has been shown to inhibit transcriptional activity and may affect gene expression. | ||||||
Flavopiridol | 146426-40-6 | sc-202157 sc-202157A | 5 mg 25 mg | $78.00 $254.00 | 41 | |
A CDK inhibitor that can affect cell cycle regulation and transcriptional processes, indirectly influencing gene expression. | ||||||