The designation C14orf124 inhibitors pertains to a specific category of chemical compounds that interact with the product of the gene symbolized as C14orf124. This nomenclature suggests that the gene is situated on chromosome 14 and is characterized as an 'open reading frame' (orf), which is a segment of DNA potentially coding for a protein; 124 serves as a distinctive identifier within this genomic location. The term inhibitors in this context implies that these compounds are designed to bind to the protein encoded by C14orf124 and impede its activity. The discovery and development of such inhibitors would be based on comprehensive research that delves into the protein's structure, function, and its role in cellular processes, although the specific functions of such genes are often not immediately apparent based solely on their genomic location and open reading frame status.
Developing a class of inhibitors for a protein like that encoded by C14orf124 would require a meticulous approach to understand the protein's role at the molecular level. This would include studies to determine the protein's structure, possibly through crystallography or other imaging techniques, to identify potential active or binding sites. Chemists would then design small molecules that can specifically bind to these sites on the protein. These molecules would be engineered to have a high affinity for the target protein, ensuring that they effectively impede its function. The process of designing these inhibitors is characterized by a cyclical pattern of synthesis, testing, and refinement. This cycle is driven by the need to create a compound with the desired specificity and an ability to stably interact with the protein in question, without adversely affecting other proteins. Once an initial compound is synthesized, it undergoes rigorous testing to confirm its efficacy and specificity. Adjustments are made based on the results of these tests, with the dual goals of maximizing the inhibitor's interaction with the C14orf124 protein while minimizing unintended interactions with other molecular structures.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Cycloheximide | 66-81-9 | sc-3508B sc-3508 sc-3508A | 100 mg 1 g 5 g | $40.00 $82.00 $256.00 | 127 | |
Cycloheximide inhibits eukaryotic protein synthesis by interfering with the translocation step in protein elongation, which could reduce SDR39U1 levels. | ||||||
Fostriecin | 87860-39-7 | sc-202160 | 50 µg | $260.00 | 9 | |
Fostriecin selectively inhibits protein phosphatase 2A, which may affect various signaling pathways and potentially decrease SDR39U1 expression. | ||||||
Camptothecin | 7689-03-4 | sc-200871 sc-200871A sc-200871B | 50 mg 250 mg 100 mg | $57.00 $182.00 $92.00 | 21 | |
Camptothecin inhibits DNA topoisomerase I, leading to DNA damage and potentially affecting transcription and expression of SDR39U1. | ||||||
Flavopiridol | 146426-40-6 | sc-202157 sc-202157A | 5 mg 25 mg | $78.00 $254.00 | 41 | |
Flavopiridol is a cyclin-dependent kinase inhibitor, which can modify cell cycle progression and potentially downregulate SDR39U1 expression. | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | $132.00 $1064.00 | 115 | |
Bortezomib inhibits the 26S proteasome, potentially leading to altered protein turnover and expression levels, including that of SDR39U1. | ||||||
Betulinic Acid | 472-15-1 | sc-200132 sc-200132A | 25 mg 100 mg | $115.00 $337.00 | 3 | |
Betulinic acid can trigger various cellular responses, such as apoptosis, possibly affecting SDR39U1 expression indirectly. | ||||||
Geldanamycin | 30562-34-6 | sc-200617B sc-200617C sc-200617 sc-200617A | 100 µg 500 µg 1 mg 5 mg | $38.00 $58.00 $102.00 $202.00 | 8 | |
Geldanamycin binds to heat shock protein 90 (Hsp90) and disrupts its function, which could impact the stability and expression of client proteins like SDR39U1. | ||||||
Anisomycin | 22862-76-6 | sc-3524 sc-3524A | 5 mg 50 mg | $97.00 $254.00 | 36 | |
Anisomycin interferes with protein synthesis by inhibiting peptidyl transferase activity on the 60S ribosomal subunit, potentially reducing SDR39U1 levels. | ||||||
MG-132 [Z-Leu- Leu-Leu-CHO] | 133407-82-6 | sc-201270 sc-201270A sc-201270B | 5 mg 25 mg 100 mg | $56.00 $260.00 $980.00 | 163 | |
MG-132 is a proteasome inhibitor, which can lead to increased protein levels but also affect the transcription of certain genes. | ||||||
Rocaglamide | 84573-16-0 | sc-203241 sc-203241A sc-203241B sc-203241C sc-203241D | 100 µg 1 mg 5 mg 10 mg 25 mg | $270.00 $465.00 $1607.00 $2448.00 $5239.00 | 4 | |
Rocaglamide inhibits translation initiation and could thereby decrease the synthesis of proteins, including SDR39U1. |