Olr23 inhibitors represent a specific class of chemical compounds that function by modulating the activity of the Olr23 receptor, a member of the olfactory receptor family. Olfactory receptors, typically associated with the detection of odorants in the olfactory system, are G protein-coupled receptors (GPCRs) characterized by their seven transmembrane domains. These receptors are not only limited to the olfactory epithelium but have been identified in various tissues throughout the body, where they are thought to play diverse roles in cellular signaling pathways. Olr23, in particular, has been a focus of scientific interest due to its unique binding sites and structural configuration, which distinguish it from other olfactory receptors. Inhibitors of Olr23 typically work by binding to these specific sites, effectively blocking the receptor's ability to interact with its natural ligands or agonists.
The chemical structure of Olr23 inhibitors varies widely, ranging from small organic molecules to more complex synthetic compounds. These inhibitors are often designed to mimic the structural motifs of the natural ligands of Olr23, allowing them to occupy the receptor's active site without activating it. The design and synthesis of these inhibitors require a deep understanding of the receptor's three-dimensional structure, which is often elucidated using techniques such as X-ray crystallography or nuclear magnetic resonance (NMR) spectroscopy. Once the structural information is obtained, computational modeling and molecular docking studies are employed to predict how different chemical structures might interact with Olr23. Through these approaches, researchers can design inhibitors with high specificity and affinity for the receptor, enabling precise control over its activity in various experimental settings. The study of Olr23 inhibitors continues to provide valuable insights into the broader understanding of olfactory receptor function and the intricate signaling mechanisms they are involved in.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Propranolol | 525-66-6 | sc-507425 | 100 mg | $180.00 | ||
Beta-adrenergic antagonist, might modulate GPCR activity, potentially affecting Olr23. | ||||||
Carvedilol | 72956-09-3 | sc-200157 sc-200157A sc-200157B sc-200157C sc-200157D | 100 mg 1 g 10 g 25 g 100 g | $122.00 $235.00 $520.00 $979.00 $1500.00 | 2 | |
Beta-adrenergic antagonist with alpha-1 blocking activity, could impact Olr23 signaling indirectly. | ||||||
Yohimbine hydrochloride | 65-19-0 | sc-204412 sc-204412A sc-204412B | 1 g 5 g 25 g | $50.00 $168.00 $520.00 | 2 | |
Alpha-2 adrenergic receptor antagonist, may affect GPCR signaling pathways related to Olr23. | ||||||
Labetalol | 36894-69-6 | sc-484723 | 50 mg | $176.00 | ||
Combined alpha and beta blocker, could indirectly affect GPCR pathways including Olr23. | ||||||
Pindolol | 13523-86-9 | sc-204847 sc-204847A | 100 mg 1 g | $194.00 $760.00 | ||
Beta-adrenergic antagonist, may influence GPCR-mediated signaling pathways related to Olr23. | ||||||
Isoproterenol Hydrochloride | 51-30-9 | sc-202188 sc-202188A | 100 mg 500 mg | $27.00 $37.00 | 5 | |
Beta-adrenergic agonist, could indirectly affect Olr23 through GPCR modulation. | ||||||
Atropine | 51-55-8 | sc-252392 | 5 g | $200.00 | 2 | |
Muscarinic acetylcholine receptor antagonist, may influence GPCR signaling pathways including Olr23. | ||||||
Salmeterol | 89365-50-4 | sc-224277 sc-224277A | 10 mg 50 mg | $186.00 $562.00 | 1 | |
Beta-2 adrenergic agonist, potentially affecting GPCR pathways related to Olr23. | ||||||
Alprenolol | 13655-52-2 | sc-507469 | 50 mg | $130.00 | ||
Beta blocker, could indirectly influence GPCR signaling pathways including Olr23. | ||||||