The designation LOC441461 Activators refers to a class of chemical compounds that have been designed to specifically interact with and increase the activity of the product encoded by the genetic locus LOC441461. The LOC prefix usually denotes a 'locus,' which is a specific location within the genome that has been identified and cataloged, but for which detailed functional information might not be fully established. An 'activator' in this context is a molecule that increases the functional output of the gene product, which could manifest through a variety of biological mechanisms. These could include the upregulation of gene expression, enhancement of mRNA stability, promotion of protein translation, stabilization of the protein once synthesized, or an increase in the protein's catalytic activity if it functions as an enzyme. The development of such activators would hinge on a comprehensive understanding of the structure and regulatory mechanisms of the LOC441461 gene product, requiring a detailed map of its expression patterns, cellular localization, and interaction within cellular pathways.
To create LOC441461 activators, scientists would embark on a multi-disciplinary approach that integrates computational biology, chemistry, and molecular biology techniques. Initially, researchers would need to characterize the LOC441461 gene product, potentially using sequence analysis to predict its structure and function, and experimental methods to confirm these predictions. Structural studies, such as X-ray crystallography or NMR spectroscopy, might reveal the three-dimensional conformation of the protein, highlighting potential binding sites for small-molecule activators. Once these sites are identified, a library of candidate activators would be designed and synthesized. This library would include diverse chemical structures, possibly based on a common scaffold known to interact with similar proteins, or novel compounds identified through virtual screening techniques. These compounds would then be tested for their ability to bind to and activate the LOC441461 gene product using in vitro assays, such as binding affinity studies or functional assays that measure the activation of the protein's biological activity. Hits from these screens would then enter a phase of iterative optimization, where their chemical structures are refined to improve their effectiveness as activators, enhance their specificity to reduce off-target effects, and optimize their physicochemical properties to ensure proper cellular distribution. Through this rigorous process, a refined set of LOC441461 activators could be developed, each designed to engage with the protein product of LOC441461 in a way that maximizes its intended biological activity.
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产品名称 | CAS # | 产品编号 | 数量 | 价格 | 应用 | 排名 |
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5-Aza-2′-Deoxycytidine | 2353-33-5 | sc-202424 sc-202424A sc-202424B | 25 mg 100 mg 250 mg | ¥2414.00 ¥3565.00 ¥4716.00 | 7 | |
一种 DNA 甲基转移酶抑制剂,可导致 DNA 去甲基化,从而可能改变基因表达。 | ||||||
β-Estradiol | 50-28-2 | sc-204431 sc-204431A | 500 mg 5 g | ¥699.00 ¥2008.00 | 8 | |
一种主要的女性性激素,可通过雌激素受体介导的转录调节基因表达。 | ||||||
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 | ¥1681.00 ¥5303.00 ¥6995.00 ¥13527.00 ¥23579.00 | 33 | |
组蛋白去乙酰化酶抑制剂,可改变染色质结构,从而影响基因表达。 | ||||||
Sodium Butyrate | 156-54-7 | sc-202341 sc-202341B sc-202341A sc-202341C | 250 mg 5 g 25 g 500 g | ¥338.00 ¥519.00 ¥925.00 ¥2459.00 | 19 | |
一种短链脂肪酸,可作为组蛋白去乙酰化酶抑制剂,可能影响转录。 | ||||||
Mithramycin A | 18378-89-7 | sc-200909 | 1 mg | ¥609.00 | 6 | |
一种能与 DNA 结合并抑制转录的药物,可非特异性地改变各种转录物的表达。 | ||||||
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 | ¥824.00 ¥2685.00 ¥8089.00 ¥28453.00 ¥241660.00 | 53 | |
与 DNA 相互作用,抑制 RNA 合成,可能影响转录物的表达模式。 | ||||||
Ademetionine | 29908-03-0 | sc-278677 sc-278677A | 100 mg 1 g | ¥2031.00 ¥7390.00 | 2 | |
在生物甲基化反应中用作甲基供体,可影响基因表达。 | ||||||
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 | ¥293.00 ¥1038.00 ¥1354.00 ¥3497.00 ¥5641.00 ¥10244.00 ¥20545.00 | 46 | |
一种植物雌激素,可通过与雌激素受体的相互作用调节基因表达。 | ||||||
Histone Lysine Methyltransferase Inhibitor 抑制剂 | 935693-62-2 free base | sc-202651 | 5 mg | ¥1670.00 | 4 | |
组蛋白甲基转移酶抑制剂,可改变染色质结构并影响基因表达。 | ||||||
RG 108 | 48208-26-0 | sc-204235 sc-204235A | 10 mg 50 mg | ¥1444.00 ¥5697.00 | 2 | |
另一种 DNA 甲基转移酶抑制剂,可能导致基因表达发生变化。 |