Olr210 inhibitors represent a specific chemical class that targets the Olr210 protein, a member of the olfactory receptor family, which is known to play a role in signal transduction mechanisms associated with olfaction. These inhibitors are designed to modulate the activity of the Olr210 receptor by binding to its active site or allosteric regions, thereby influencing the receptor's conformational dynamics. The olfactory receptors, including Olr210, are G-protein-coupled receptors (GPCRs) that initiate a cascade of intracellular events upon binding to specific ligands. This interaction is typically characterized by conformational changes in the receptor, leading to the activation or inhibition of downstream signaling pathways. Olr210 inhibitors, by their design, disrupt these molecular interactions, which can be crucial for understanding the basic biological processes governed by this receptor.
The development and study of Olr210 inhibitors are essential in the context of molecular biology and biochemistry, as they provide insights into the structural and functional aspects of olfactory receptors. These compounds are valuable tools for probing the signaling mechanisms of the Olr210 receptor, enabling researchers to dissect the receptor's role in cellular communication and sensory perception. By modulating the receptor's activity, Olr210 inhibitors help elucidate the specificity and selectivity of olfactory signal transduction, contributing to a broader understanding of GPCR function in various physiological processes. Additionally, the exploration of these inhibitors may reveal new aspects of receptor-ligand interactions, which are fundamental to the field of structural biology and receptor chemistry.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Verapamil | 52-53-9 | sc-507373 | 1 g | $367.00 | ||
Calcium channel blocker, can influence cardiovascular and smooth muscle function, impacting Olr210. | ||||||