Chemical activators of Vmn2r16 can influence the protein's activity through various biochemical pathways. Sodium fluoride, by mimicking the structure of GTP, can directly engage G-protein coupled receptors, triggering a cascade that results in the activation of Vmn2r16. Similarly, Forskolin, by stimulating adenylate cyclase, increases cAMP levels, leading to protein kinase A (PKA) activation. PKA then phosphorylates target proteins within the cellular pathways that Vmn2r16 is a part of, leading to its activation. Ionomycin, as a calcium ionophore, raises intracellular calcium levels, which activates calcium-dependent protein kinases that, in turn, can activate Vmn2r16. Phorbol 12-myristate 13-acetate (PMA) also plays a role in the activation of Vmn2r16 through its action on protein kinase C (PKC), which phosphorylates proteins that are part of the same signaling pathways as Vmn2r16.
In concert with these chemicals, Isoproterenol functions as a beta-adrenergic agonist to activate adenylate cyclase and raise cAMP levels, thus activating PKA and influencing the activity of Vmn2r16. The cAMP analog 8-Bromoadenosine 3',5'-cyclic monophosphate (8-Br-cAMP) activates PKA, which then phosphorylates proteins in pathways that include Vmn2r16, leading to its activation. Another calcium ionophore, A23187, increases intracellular calcium and activates kinases that can activate Vmn2r16. Nitric oxide donors, such as Sodium nitroprusside, release nitric oxide which increases cGMP levels and activates protein kinases that can lead to the activation of Vmn2r16. Kainic acid, as a glutamate receptor agonist, prompts calcium influx and activates calcium-dependent signaling pathways that can activate Vmn2r16. Acetylcholine, through its action on muscarinic and nicotinic receptors, triggers downstream signaling pathways that activate Vmn2r16. Histamine, by binding to its cell surface receptors, activates phospholipase C involved pathways, culminating in the activation of Vmn2r16. Lastly, ATP, by acting on purinergic receptors, can initiate signaling cascades that activate Vmn2r16. Each of these chemicals plays a pivotal role in the direct or indirect activation of Vmn2r16 through specific and well-established cellular mechanisms.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Sodium Fluoride | 7681-49-4 | sc-24988A sc-24988 sc-24988B | 5 g 100 g 500 g | $39.00 $45.00 $98.00 | 26 | |
Sodium fluoride activates G-protein coupled receptors by mimicking the structure of GTP, leading to an activation of downstream signaling molecules, including Vmn2r16. | ||||||
Forskolin | 66575-29-9 | sc-3562 sc-3562A sc-3562B sc-3562C sc-3562D | 5 mg 50 mg 1 g 2 g 5 g | $76.00 $150.00 $725.00 $1385.00 $2050.00 | 73 | |
Forskolin directly stimulates adenylate cyclase, increasing cAMP levels, which in turn activates PKA. PKA phosphorylates various targets, which can include components of pathways that Vmn2r16 is part of, leading to its activation. | ||||||
Ionomycin | 56092-82-1 | sc-3592 sc-3592A | 1 mg 5 mg | $76.00 $265.00 | 80 | |
Ionomycin is a calcium ionophore that increases intracellular calcium concentrations, which can activate calcium-dependent protein kinases that then activate Vmn2r16. | ||||||
PMA | 16561-29-8 | sc-3576 sc-3576A sc-3576B sc-3576C sc-3576D | 1 mg 5 mg 10 mg 25 mg 100 mg | $40.00 $129.00 $210.00 $490.00 $929.00 | 119 | |
PMA activates protein kinase C (PKC), which phosphorylates target proteins. PKC-mediated phosphorylation can lead to the activation of pathways involving Vmn2r16. | ||||||
Isoproterenol Hydrochloride | 51-30-9 | sc-202188 sc-202188A | 100 mg 500 mg | $27.00 $37.00 | 5 | |
Isoproterenol is a beta-adrenergic agonist that activates adenylate cyclase via G-protein coupled receptors, raising cAMP levels and activating PKA which can lead to activation of Vmn2r16. | ||||||
8-Bromo-cAMP | 76939-46-3 | sc-201564 sc-201564A | 10 mg 50 mg | $97.00 $224.00 | 30 | |
8-Br-cAMP is a cAMP analog that activates PKA. Activated PKA can phosphorylate proteins within the signaling pathways that include Vmn2r16, resulting in its activation. | ||||||
A23187 | 52665-69-7 | sc-3591 sc-3591B sc-3591A sc-3591C | 1 mg 5 mg 10 mg 25 mg | $54.00 $128.00 $199.00 $311.00 | 23 | |
A23187 is another calcium ionophore that increases intracellular calcium, potentially activating calcium-dependent kinases that can activate Vmn2r16. | ||||||
Sodium nitroprusside dihydrate | 13755-38-9 | sc-203395 sc-203395A sc-203395B | 1 g 5 g 100 g | $42.00 $83.00 $155.00 | 7 | |
Sodium nitroprusside releases nitric oxide which activates guanylate cyclase, increasing cGMP levels. Elevated cGMP can activate protein kinases that can lead to the activation of Vmn2r16. | ||||||
Kainic acid | 487-79-6 | sc-200454 sc-200454A sc-200454B sc-200454C sc-200454D | 5 mg 25 mg 100 mg 1 g 5 g | $85.00 $370.00 $1350.00 $7650.00 $24480.00 | 12 | |
Kainic acid is an agonist for glutamate receptors, which can lead to calcium influx and activation of calcium-dependent signaling pathways, potentially leading to the activation of Vmn2r16. | ||||||
Histamine, free base | 51-45-6 | sc-204000 sc-204000A sc-204000B | 1 g 5 g 25 g | $92.00 $277.00 $969.00 | 7 | |
Histamine binds to its receptors on the cell surface, which can activate signaling pathways involving phospholipase C, leading to the activation of Vmn2r16. | ||||||