Date published: 2025-10-27

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Olfr464 Activators

Chemical activators of Olfr464 modulate the gene's activity through distinct intracellular pathways and mechanisms. These chemicals have been selected based on their potential to influence Olfr464, a member of the olfactory receptor family, without inducing generalized effects. Forskolin acts as an activator by elevating intracellular cyclic adenosine monophosphate (cAMP) levels. This increase in cAMP, in turn, stimulates Olfr464 gene expression, as cAMP serves as a critical second messenger in olfactory receptor signaling. Similarly, 8-Bromo-cGMP impacts cGMP-dependent pathways, indirectly influencing Olfr464 activation. By altering intracellular cGMP levels, it can facilitate the functional activation of Olfr464, contributing to olfactory receptor-mediated processes. Phorbol 12,13-Dibutyrate serves as an activator by modulating protein kinase C (PKC), which plays a role in olfactory receptor signaling. This chemical enhances PKC activity, which can ultimately influence Olfr464 gene function. Additionally, Retinoic Acid interacts with retinoic acid receptors, potentially leading to the functional activation of Olfr464 gene expression. Thapsigargin influences calcium homeostasis, indirectly affecting Olfr464 activation by altering calcium-dependent signaling pathways critical for olfactory receptor function.

Ionomycin, a calcium ionophore, can activate Olfr464 by modulating calcium signaling pathways essential for olfactory receptor function. 3-Isobutyl-1-methylxanthine inhibits phosphodiesterases, leading to increased cAMP levels, which, in turn, activate Olfr464 gene function. Moreover, 1,2-Dioleoyl-sn-glycerol serves as a PKC activator, enhancing PKC activity, which is linked to olfactory receptor signaling and gene activation. Quercetin interacts with intracellular signaling pathways connected to olfactory receptors, potentially influencing Olfr464 gene activity. Dibutyryl cAMP, a cell-permeable cAMP analog, directly elevates intracellular cAMP levels, leading to the activation of Olfr464 signaling. Lastly, 1-Oleoyl-2-acetyl-sn-glycerol influences the diacylglycerol (DAG) pathway, connected to olfactory receptor activation, enhancing Olfr464 function. These chemicals offer insights into potential mechanisms for activating Olfr464, each targeting specific pathways or cellular processes associated with olfactory receptor gene expression. Further experimental studies are essential to validate these effects and explore the intricate details of Olfr464 activation by these chemical modulators.

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