Vmn2r49 function in diverse ways to modulate the receptor's activity indirectly through various mechanisms. Phosphoramidon, a metalloprotease inhibitor, can increase the concentration of peptide ligands by inhibiting their breakdown, which can lead to receptor desensitization or downregulation due to sustained activation. Alpha-methylserotonin, as a serotonin receptor agonist, activates serotonin receptors, which can alter neurotransmitter signaling and thereby inhibit Vmn2r49 by changing the neural activity context. Bicuculline, which is an antagonist of GABA receptors, can increase neuronal excitability by reducing inhibitory neurotransmission. This change in the balance of excitatory and inhibitory inputs in the olfactory system can impact the Vmn2r49 receptor's activity. Similarly, methoctramine blocks muscarinic acetylcholine receptors, which can disrupt cholinergic signaling and thus modulate the activity of Vmn2r49.
Tetrodotoxin, by blocking sodium channels, inhibits action potential propagation, which can reduce the activity of neural pathways involving the Vmn2r49 receptor. Ondansetron, being a selective 5-HT3 receptor antagonist, can alter serotonergic signaling pathways, which might indirectly inhibit Vmn2r49. Hexamethonium and methyllycaconitine, both nicotinic acetylcholine receptor antagonists, can influence cholinergic input to the olfactory bulb, thereby affecting the receptor's function. Atropine, another muscarinic antagonist, can similarly modulate the cholinergic system, impacting the circuits in which Vmn2r49 is involved. SCH-23390, as a dopamine D1 receptor antagonist, can modify dopaminergic signaling, which can also affect the receptor's activity. Ketanserin, mainly a 5-HT2 receptor antagonist, can change the modulation of neural pathways including Vmn2r49. Lastly, dihydro-β-erythroidine, by blocking nicotinic acetylcholine receptors, can alter neural network activity and thus inhibit the Vmn2r49 receptor. Each chemical, through its unique interaction with different neurotransmitter systems, can modulate the activity of Vmn2r49, demonstrating the complexity of receptor regulation within the olfactory system.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Phosphoramidon | 119942-99-3 | sc-201283 sc-201283A | 5 mg 25 mg | $199.00 $632.00 | 8 | |
Phosphoramidon is a metalloprotease inhibitor that prevents the breakdown of peptides by inhibiting neprilysin. Since Vmn2r49 is a receptor involved in pheromone detection, inhibition of peptide metabolism may increase levels of ligands, thus potentially inhibiting the Vmn2r49 signaling due to receptor desensitization or downregulation. | ||||||
(+)-Bicuculline | 485-49-4 | sc-202498 sc-202498A | 50 mg 250 mg | $82.00 $281.00 | ||
Bicuculline is a GABA receptor antagonist that can increase neuronal excitability. By influencing GABAergic neurotransmission, it may affect the neural circuits that modulate the activity of Vmn2r49 by changing the overall balance of excitatory and inhibitory inputs in the olfactory system. | ||||||
Ondansetron | 99614-02-5 | sc-201127 sc-201127A | 10 mg 50 mg | $82.00 $333.00 | 1 | |
Ondansetron is a selective 5-HT3 receptor antagonist, which can alter serotonin signaling. By blocking 5-HT3 receptors, it may change the serotonergic modulation of the olfactory system where Vmn2r49 operates, thus indirectly inhibiting the functional activity of Vmn2r49. | ||||||
Hexamethonium bromide | 55-97-0 | sc-205712 sc-205712A | 10 g 25 g | $46.00 $64.00 | ||
Hexamethonium is a nicotinic acetylcholine receptor antagonist. By blocking nicotinic receptors, it could influence the cholinergic input to the olfactory bulb and related pathways, potentially leading to an indirect functional inhibition of Vmn2r49 by altering the neural circuitry it is part of. | ||||||
Atropine | 51-55-8 | sc-252392 | 5 g | $204.00 | 2 | |
Atropine is a competitive antagonist for the muscarinic acetylcholine receptors. By inhibiting these receptors, it may affect the cholinergic system, which could lead to changes in the neural circuits of the olfactory system and indirectly inhibit the function of Vmn2r49 as part of these circuits. | ||||||
SCH 23390 | 125941-87-9 | sc-200408 sc-200408A | 5 mg 25 mg | $179.00 $733.00 | 2 | |
SCH-23390 is a dopamine D1 receptor antagonist, and by inhibiting D1 receptors, it can modify dopaminergic signaling. This modification has the potential to indirectly inhibit Vmn2r49 by affecting the neural pathways it is involved in within the olfactory system. | ||||||
Ketanserin | 74050-98-9 | sc-279249 | 1 g | $700.00 | ||
Ketanserin is a serotonin antagonist that primarily blocks 5-HT2 receptors. By altering serotonergic signaling, ketanserin could change the modulation of neural pathways within the olfactory system where Vmn2r49 is active, resulting in its indirect functional inhibition. | ||||||