Date published: 2025-10-13

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OR8H1 Activators

OR8H1 can be understood through their interactions with olfactory receptors and the consequent biochemical signaling pathways. Menthol interacts with the TRPM8 receptors, which are also present in olfactory sensory neurons, and through this interaction, it can lead to the activation of OR8H1 by stimulating the same sensory pathways that perceive cold. Similarly, eugenol, with its capacity to bind to specific sites on olfactory receptors, is capable of initiating a cascade of intracellular events culminating in the activation of OR8H1. This binding is likely due to the structural compatibility of eugenol with the active site of OR8H1, resulting in the receptor's conformational change and activation. Isoamyl acetate and benzaldehyde, both of which serve as odorant molecules for various olfactory receptors, can activate OR8H1 through direct binding, taking advantage of the structural specificity that olfactory receptors have for their ligands.

2-Phenylethanol's floral scent profile implies its ability to activate olfactory receptors and, by extension, suggests its interaction with OR8H1. Anethole's structural resemblance to other olfactory activators enables it to induce activation of OR8H1. Geraniol and citronellol both contribute to the activation of olfactory receptors via their characteristic scents and can activate OR8H1 by integrating into the receptor's ligand-binding domain. Cinnamaldehyde, with its unique cinnamon scent, and limonene, recognized for its citrus aroma, can both activate OR8H1 by directly binding to the receptor, causing an activation response due to the receptor's affinity for specific scent molecules. Alpha-Pinene and methyl salicylate, each with distinctive pine and wintergreen scents, respectively, activate olfactory receptors in a manner that suggests they can also activate OR8H1 by engaging with the sensory mechanisms inherent to olfaction, resulting in the receptor's active state. These chemicals, with their diverse structural properties, are all capable of activating the OR8H1 receptor through direct molecular interactions that trigger the receptor's innate sensory functions.

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