OR4F15 inhibitors belong to a unique class of chemical compounds that target and interact with the OR4F15 gene product, a specific olfactory receptor protein. The OR4F15 gene is part of the olfactory receptor family, a group of genes encoding G protein-coupled receptors (GPCRs) responsible for the detection of odor molecules. The structure and function of these receptors are incredibly diverse, allowing a wide array of volatile compounds to be detected and discriminated. Inhibitors of OR4F15 are designed to bind selectively to the receptor encoded by this gene, thereby modulating its activity. These compounds can be small molecules or larger peptide-based entities, the specificity and affinity of which are crucial for their interaction with the OR4F15 receptor. The design of such inhibitors often involves a deep understanding of the receptor's ligand-binding domain, which is typically elucidated through techniques such as X-ray crystallography or NMR spectroscopy. The development of OR4F15 inhibitors is informed by a comprehensive knowledge of the receptor's three-dimensional structure and the dynamic conformational changes it undergoes upon ligand binding.
The research into OR4F15 inhibitors is driven by the complexity of olfactory receptor-ligand interactions and the vast potential to understand molecular recognition and signaling pathways. These compounds are synthesized using advanced organic chemistry techniques, which may involve multiple steps of chemical reactions, purification, and characterization. Each inhibitor is typically assessed for its binding efficiency, selectivity, and stability, which are critical parameters in their interaction with the OR4F15 receptor. The specificity of OR4F15 inhibitors is of paramount importance, as it determines their ability to modulate the receptor without off-target effects on other olfactory receptors, which could lead to unintended consequences. Research in this field is interdisciplinary, combining aspects of biochemistry, molecular biology, structural biology, and computational chemistry to optimize the interaction of these inhibitors with their target receptor. Additionally, the study of OR4F15 inhibitors contributes to the broader understanding of olfactory receptor function and the molecular basis of olfaction.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Eugenol | 97-53-0 | sc-203043 sc-203043A sc-203043B | 1 g 100 g 500 g | $31.00 $61.00 $214.00 | 2 | |
Eugenol is a phenylpropene, similar in structure to compounds that activate olfactory receptors. It could inhibit OR4F15 through competitive binding or causing a conformational change in the receptor that reduces its activity. | ||||||
Isopentyl acetate | 123-92-2 | sc-250190 sc-250190A | 100 ml 500 ml | $105.00 $221.00 | ||
This compound is a known flavor and fragrance agent that could inhibit OR4F15 by mimicking its natural ligands, binding to the receptor and preventing activation. | ||||||
Methimazole | 60-56-0 | sc-205747 sc-205747A | 10 g 25 g | $69.00 $110.00 | 4 | |
Methimazole is known to interact with olfactory receptors and could inhibit OR4F15 by binding to the receptor's active site or nearby allosteric sites, inducing a conformational change that leads to decreased activity. | ||||||
Naphthalene | 91-20-3 | sc-215533 sc-215533A | 250 mg 5 g | $20.00 $36.00 | ||
This polycyclic aromatic hydrocarbon could inhibit OR4F15 by non-competitive inhibition, binding to a site other than the receptor's active site, leading to a change in receptor conformation that decreases its activity. | ||||||
Acetophenone | 98-86-2 | sc-239189 | 5 g | $20.00 | ||
Acetophenone, a fragrant compound, could inhibit OR4F15 by competitive binding to its ligand-binding site, thus preventing the receptor from interacting with its natural ligands and subsequent signal transduction. | ||||||