OR5M8 inhibitors belong to a class of chemical compounds that specifically interact with the olfactory receptor OR5M8, a protein encoded by the OR5M8 gene, which is part of the vast olfactory receptor family. Olfactory receptors, part of the G protein-coupled receptor (GPCR) superfamily, are involved in the detection of odorants and the transmission of sensory information related to smell. Inhibitors of OR5M8 typically function by blocking or modulating the activity of this receptor, influencing its ability to bind to its natural ligands, such as specific volatile molecules or odorants. Structurally, these inhibitors often contain motifs or functional groups that allow them to bind to the active site or a regulatory region of the receptor, preventing normal receptor-ligand interactions. Given that olfactory receptors like OR5M8 can exhibit highly selective binding properties, inhibitors in this class tend to reflect a high degree of specificity in their molecular design, targeting key interactions between the receptor and its natural ligands.
The inhibition of OR5M8 activity is largely studied in the context of understanding how olfactory signaling pathways are modulated at the molecular level. This inhibition can result in the alteration of downstream signaling events, particularly through the regulation of G protein-coupled intracellular pathways that are typically activated by odorant-receptor interactions. Inhibitors may affect second messenger systems, such as cyclic AMP (cAMP) signaling, that mediate receptor-induced responses. The study of OR5M8 inhibitors helps in deciphering the functional dynamics of olfactory receptor networks and provides insight into receptor-ligand specificity, signal transduction mechanisms, and how external stimuli, like odorants, can be precisely regulated at the molecular level. Such research is integral to expanding our understanding of the broader GPCR family and their role in sensory perception, particularly within the highly complex olfactory system.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Cinnamic acid | 621-82-9 | sc-337631 | 1 g | $560.00 | ||
Cinnamic acid competes with activating ligands for binding to OR5M8, leading to inhibition. | ||||||
Salicylic acid | 69-72-7 | sc-203374 sc-203374A sc-203374B | 100 g 500 g 1 kg | $46.00 $92.00 $117.00 | 3 | |
Salicylic acid can alter the receptor conformation of OR5M8, hindering its ability to activate. | ||||||
Zinc | 7440-66-6 | sc-213177 | 100 g | $47.00 | ||
Zinc acetate binds to OR5M8, potentially inducing a conformation that does not allow activation. | ||||||
Copper(II) sulfate | 7758-98-7 | sc-211133 sc-211133A sc-211133B | 100 g 500 g 1 kg | $45.00 $120.00 $185.00 | 3 | |
Copper sulfate can bind to modulatory sites on OR5M8, changing its structure and inhibiting it. | ||||||
Methimazole | 60-56-0 | sc-205747 sc-205747A | 10 g 25 g | $69.00 $110.00 | 4 | |
Methimazole can bind to OR5M8, preventing the proper receptor conformation required for activation. | ||||||
Diphenhydramine hydrochloride | 147-24-0 | sc-204729 sc-204729A sc-204729B | 10 g 25 g 100 g | $51.00 $82.00 $122.00 | 4 | |
Diphenhydramine may block the activation of OR5M8 by steric hindrance. | ||||||
Quinine | 130-95-0 | sc-212616 sc-212616A sc-212616B sc-212616C sc-212616D | 1 g 5 g 10 g 25 g 50 g | $77.00 $102.00 $163.00 $347.00 $561.00 | 1 | |
Quinine can bind to OR5M8 and interfere with its activation by changing the receptor's shape. | ||||||
Capsaicin | 404-86-4 | sc-3577 sc-3577C sc-3577D sc-3577A | 50 mg 250 mg 500 mg 1 g | $94.00 $173.00 $255.00 $423.00 | 26 | |
Capsaicin can bind to OR5M8 and induce a conformational change that reduces activation. | ||||||
Caffeine | 58-08-2 | sc-202514 sc-202514A sc-202514B sc-202514C sc-202514D | 5 g 100 g 250 g 1 kg 5 kg | $32.00 $66.00 $95.00 $188.00 $760.00 | 13 | |
Caffeine can bind to OR5M8 and modulate its conformation, preventing activation. | ||||||
(−)-Menthol | 2216-51-5 | sc-202705 sc-202705A | 1 g 50 g | $20.00 $40.00 | 2 | |
Menthol can bind to specific regions on OR5M8, altering its structure and inhibiting its activation. | ||||||