The chemical class known as LysRS inhibitors refers to a group of compounds designed to selectively target and inhibit the activity of the enzyme Lysyl-tRNA synthetase (LysRS). LysRS is an essential enzyme involved in protein synthesis, specifically in the charging of transfer RNA (tRNA) molecules with the amino acid lysine. This process is a fundamental step in the translation of genetic information from DNA to proteins. LysRS ensures the accurate pairing of lysine with its corresponding tRNA, a critical step for maintaining the fidelity of protein synthesis. LysRS inhibitors are designed to disrupt the enzymatic activity of LysRS by binding to its active site or other key regions. By inhibiting LysRS, these compounds aim to modulate protein synthesis and potentially impact cellular processes that rely on accurate and timely protein production.
The chemical structures of LysRS inhibitors can vary widely, with modifications that allow for specific interactions with the enzyme's active site residues. These inhibitors are often developed through a combination of computational modeling, structural analysis, and experimental validation to ensure their effectiveness and specificity. Understanding the intricacies of LysRS inhibition at the molecular level is crucial for designing compounds that can selectively disrupt its function. The development of LysRS inhibitors contributes to the broader field of enzymology and molecular biology, shedding light on the mechanisms governing protein synthesis and its regulation. Ongoing research aims to refine the design and effectiveness of LysRS inhibitors, with the ultimate goal of advancing our understanding of cellular processes and potentially revealing new avenues for targeted interventions in various contexts.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Tranylcypromine | 13492-01-8 | sc-200572 sc-200572A | 1 g 5 g | $175.00 $599.00 | 5 | |
One of the first identified LSD1 inhibitors, it binds to the active site of LSD1. | ||||||
1,3,5-Tri(9H-carbazol-9-yl)benzene | 148044-07-9 | sc-476484 | 1 g | $129.00 | ||
Tranylcypromine analogs like 2-PCPA and 3-PCPA are competitive LSD1 inhibitors used in research. | ||||||
SP2509 | 1423715-09-6 | sc-492604 | 5 mg | $284.00 | ||
Developed as a selective LSD1 inhibitor, it exhibits anti-tumor effects in research studies. | ||||||
OG-L002 | 1357302-64-7 | sc-478221 | 5 mg | $270.00 | ||
A selective LSD1 inhibitor, showing efficacy in acute myeloid leukemia. | ||||||