The term C14orf152 inhibitors would refer to a class of chemical compounds designed to interact with and inhibit the function of the protein encoded by the gene denoted as C14orf152. This naming convention indicates that the gene in question is located on chromosome 14 and is the 152nd open reading frame identified within this region. Open reading frames (orfs) are sequences in the genome that are predicted to encode proteins, and they are commonly identified through genomic sequencing efforts. The inhibitors that fall under this class would be molecules that specifically bind to the protein product of C14orf152, inhibiting its normal biological activity. The pathway to discovering such inhibitors typically commences with a comprehensive understanding of the protein's structure, function, and the role it plays within cellular or biochemical pathways.
In the quest to develop C14orf152 inhibitors, a multidisciplinary approach is often employed. This starts with a detailed study of the protein itself, leveraging a combination of molecular biology, bioinformatics, and structural biology techniques to understand its three-dimensional conformation, functional domains, and interactions with other cellular components. With this knowledge, molecular designers and chemists begin the process of creating molecules capable of binding to the protein. These molecules can be engineered to fit into the active site of the enzyme or protein, potentially mimicking the shape and charge of the natural substrate or ligand, but with the intent to block the protein's activity. Alternatively, these compounds might bind to allosteric sites on the protein, which are regions that, when occupied by certain molecules, can induce a change in the protein's activity. The development of such inhibitors is usually a rigorous process, involving iterative rounds of modification and testing to enhance the inhibitor's affinity, specificity, and stability.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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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 | |
Actinomycin D intercalates into DNA and prevents the transcription elongation by RNA polymerase, which could lead to reduced FAM181A mRNA synthesis. | ||||||
Triptolide | 38748-32-2 | sc-200122 sc-200122A | 1 mg 5 mg | $88.00 $200.00 | 13 | |
Triptolide has been shown to inhibit the transcription of various genes by affecting RNA polymerase II activity, potentially decreasing FAM181A expression. | ||||||
α-Amanitin | 23109-05-9 | sc-202440 sc-202440A | 1 mg 5 mg | $260.00 $1029.00 | 26 | |
α-Amanitin is a potent inhibitor of RNA polymerase II, the enzyme responsible for mRNA synthesis, which could lower FAM181A expression levels. | ||||||
DRB | 53-85-0 | sc-200581 sc-200581A sc-200581B sc-200581C | 10 mg 50 mg 100 mg 250 mg | $42.00 $185.00 $310.00 $650.00 | 6 | |
DrB inhibits RNA synthesis by targeting RNA polymerase II and III, which could suppress FAM181A transcription. | ||||||
Cordycepin | 73-03-0 | sc-203902 | 10 mg | $99.00 | 5 | |
Cordycepin terminates mRNA elongation by acting as an adenosine analog, potentially reducing FAM181A expression. | ||||||
Homoharringtonine | 26833-87-4 | sc-202652 sc-202652A sc-202652B | 1 mg 5 mg 10 mg | $51.00 $123.00 $178.00 | 11 | |
Homoharringtonine inhibits the initiation step of protein elongation, which could reduce the translation of FAM181A protein. | ||||||
Mycophenolic acid | 24280-93-1 | sc-200110 sc-200110A | 100 mg 500 mg | $68.00 $261.00 | 8 | |
Mycophenolic acid inhibits inosine monophosphate dehydrogenase, which is necessary for the synthesis of guanosine nucleotides, affecting RNA and DNA synthesis. | ||||||
Leflunomide | 75706-12-6 | sc-202209 sc-202209A | 10 mg 50 mg | $20.00 $81.00 | 5 | |
Leflunomide inhibits dihydroorotate dehydrogenase, leading to decreased pyrimidine synthesis, which can subsequently decrease RNA and DNA synthesis, including that of FAM181A. | ||||||
Trichostatin A | 58880-19-6 | sc-3511 sc-3511A sc-3511B sc-3511C sc-3511D | 1 mg 5 mg 10 mg 25 mg 50 mg | $149.00 $470.00 $620.00 $1199.00 $2090.00 | 33 | |
Trichostatin A is an inhibitor of histone deacetylase (HDAC), which can change chromatin structure and gene expression, potentially affecting FAM181A. | ||||||
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
5-Azacytidine incorporates into RNA and DNA and can cause demethylation of DNA, which might result in altered gene expression patterns, including FAM181A. |