Date published: 2025-10-31

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Vmn1r224 Activators

Vomeronasal 1 receptor 224 activators encompass a range of compounds that indirectly influence the receptor's activity by modulating the intracellular signaling environment of GPCRs. Forskolin, by increasing cAMP, enhances PKA activity, which can then lead to the phosphorylation of proteins within the signaling pathways that Vmn1r224 might utilize, potentially resulting in an enhanced receptor response. Similarly, isoproterenol elevates cAMP levels, creating a signaling milieu that can amplify Vmn1r224 function through increased GPCR activity.

On the other hand, ionomycin and pilocarpine alter intracellular calcium levels, which can lead to the activation of PKC. PKC plays a pivotal role in the phosphorylation of proteins that are part of the GPCR signaling machinery, which in turn could enhance the signaling pathways involving Vmn1r224. Moreover, compounds such as carbachol and nicotine, by increasing PKC activity through cholinergic receptor activation, can further potentiate GPCR-mediated signaling pathways, which may include those related to Vmn1r224. Adenosine and bradykinin also contribute to this activation cascade by binding to their respective receptors and promoting the activities of cAMP and PKC, thereby fostering an environment conducive to the enhancement of Vmn1r224 signaling. Lastly, L-Arginine, through its role in the production of nitric oxide and subsequent activation of guanylyl cyclase, increases cGMP levels, which has the potential to modulate GPCR signaling pathways, including those associated with Vmn1r224, leading to an enhanced receptor activity.

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