Vmn1r165 Inhibitors would comprise a class of specialized chemical compounds designed to bind to and inhibit the Vmn1r165 receptor, if we are to assume that Vmn1r165 is a member of the vomeronasal type-1 receptor family involved in the detection of pheromonal signals. These inhibitors would function by preventing the interaction between the receptor and its natural ligands, hindering the receptor's ability to initiate the cellular response typically triggered by such an interaction. The inhibition could occur through direct competition with the ligand for binding sites on the receptor or by binding to alternative sites on the receptor to induce conformational changes that impede its function.
Creating Vmn1r165 inhibitors would involve a detailed investigation of the receptor's structure and the biochemistry of its interaction with ligands. This exploration would likely utilize techniques such as X-ray crystallography or cryo-electron microscopy to map the three-dimensional structure of the receptor, particularly focusing on the ligand-binding domain. Research into the function of Vmn1r165 and its interaction with potential inhibitors would provide deeper insights into the molecular mechanisms of chemosensory perception. By exploring how Vmn1r165 inhibitors affect the receptor's activity, scientists could better understand its role in the complex web of chemosensory signaling, including how it contributes to the detection of specific chemical cues.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Lithium | 7439-93-2 | sc-252954 | 50 g | $214.00 | ||
An inhibitor of GSK-3, which might affect transcription factors and influence the expression of certain genes. | ||||||
Tunicamycin | 11089-65-9 | sc-3506A sc-3506 | 5 mg 10 mg | $169.00 $299.00 | 66 | |
Induces the unfolded protein response and can affect gene expression through this stress response pathway. | ||||||