The chemical class referred to as LOC100041119 Inhibitors encompasses a series of compounds specifically engineered to target and inhibit the activity of the gene product associated with LOC100041119. This gene, uncovered through rigorous genomic and molecular analysis, plays a crucial role in various cellular processes. The functionality of LOC100041119 is notably context-sensitive, meaning its functional role within the cell can significantly vary depending on the cellular environment and external stimuli. The inhibitors designed for LOC100041119 are characterized by their ability to selectively bind to the proteins or enzymes that result from the gene's expression. This selective binding is key to the functionality of these inhibitors, as it directly influences the biochemical pathways involving the LOC100041119 gene product. By modulating the activity of this gene product, the inhibitors aim to alter the corresponding cellular processes, potentially impacting specific cellular functions and mechanisms.
The development of LOC100041119 Inhibitors is an intricate and interdisciplinary process, requiring expertise in molecular biology, chemistry, and structural biology. The initial stage of developing these inhibitors involves attaining an in-depth understanding of the structure and function of the LOC100041119 gene product. Techniques such as X-ray crystallography, nuclear magnetic resonance (NMR) spectroscopy, and computational molecular modeling are employed to gain detailed insights into the target molecule. This comprehensive understanding is critical for the rational design of inhibitors that are both effective in their interaction with the target and exhibit high specificity. Typically, these inhibitors are small molecules, designed for efficient penetration into cellular membranes and to establish a stable and potent interaction with their target. The molecular design of these inhibitors is meticulously optimized to ensure robust interactions with the target molecule, often involving hydrogen bonds, hydrophobic interactions, and van der Waals forces. The effectiveness of these inhibitors is evaluated through various biochemical assays in vitro. These assays are crucial for assessing the inhibitors' potency, specificity, and overall behavior under controlled experimental conditions. This research is vital for understanding the inhibitors' mechanism of action and for further exploration into their potential impact on the complex network of cellular pathways influenced by LOC100041119.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Cordycepin | 73-03-0 | sc-203902 | 10 mg | $99.00 | 5 | |
Cordycepin, an adenosine analog, can terminate RNA synthesis by inhibiting RNA polymerase, leading to decreased gene 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, resulting in DNA damage that could reduce transcription and gene expression. | ||||||
Nitrofurantoin | 67-20-9 | sc-212399 | 10 g | $82.00 | ||
Nitrofurantoin can interfere with bacterial RNA and protein synthesis, potentially affecting gene expression. | ||||||
Chloramphenicol | 56-75-7 | sc-3594 | 25 g | $53.00 | 10 | |
Chloramphenicol binds to the bacterial 50S ribosomal subunit, inhibiting peptidyl transferase and thus protein synthesis. | ||||||
Fusidic acid | 6990-06-3 | sc-215065 | 1 g | $292.00 | ||
Fusidic acid prevents the turnover of elongation factor G (EF-G) from the ribosome, inhibiting protein synthesis. | ||||||
Neomycin sulfate | 1405-10-3 | sc-3573 sc-3573A | 1 g 5 g | $26.00 $34.00 | 20 | |
Neomycin binds to rRNA and interferes with the initiation complex, ribosomal proofreading, and translocation, impacting protein synthesis. | ||||||
Emetine | 483-18-1 | sc-470668 sc-470668A sc-470668B sc-470668C | 1 mg 10 mg 50 mg 100 mg | $352.00 $566.00 $1331.00 $2453.00 | ||
Emetine inhibits the elongation step of protein synthesis by affecting the ribosomal movement along mRNA. | ||||||
Rifampicin | 13292-46-1 | sc-200910 sc-200910A sc-200910B sc-200910C | 1 g 5 g 100 g 250 g | $95.00 $322.00 $663.00 $1438.00 | 6 | |
Rifampicin binds to the bacterial RNA polymerase, inhibiting the initiation of RNA synthesis and gene expression. | ||||||
Novobiocin | 303-81-1 | sc-362034 sc-362034A | 5 mg 25 mg | $96.00 $355.00 | ||
Novobiocin inhibits DNA gyrase, which is necessary for DNA replication and transcription, thus affecting gene expression. | ||||||