Olfr507, a member of the olfactory receptor family, plays a crucial role in initiating the neuronal response responsible for the perception of smell. This receptor, characterized by its 7-transmembrane domain structure typical of G-protein-coupled receptors (GPCRs), is encoded by single coding-exon genes. As a part of the largest gene family in the genome, Olfr507 is involved in the recognition and G protein-mediated transduction of odorant signals. Its function lies in the intricate orchestration of events that occur upon interaction with odorant molecules within the nose. This complex process ultimately triggers a neuronal response, leading to the perception of a specific smell. The specific function of Olfr507 can be delineated by its role as a GPCR involved in olfactory signal transduction. As odorant molecules bind to Olfr507, the receptor undergoes conformational changes that activate downstream signaling pathways. These pathways, shared with neurotransmitter and hormone receptors, contribute to the transduction of odorant signals through G protein mediation. Olfr507's involvement in this intricate process highlights its significance in the initial stages of olfactory perception. The nomenclature assigned to Olfr507 is unique to the organism, emphasizing its distinct identity within the olfactory receptor gene family.
Inhibition of Olfr507 involves a nuanced approach, considering both direct and indirect mechanisms. Direct inhibitors targeting Olfr507 may interfere with its structural conformation, impeding its ability to bind with odorant molecules effectively. On the other hand, indirect inhibitors may influence the specific signaling pathways associated with Olfr507, disrupting the transduction of odorant signals. For instance, chemicals that modulate GABA-gated chloride channels, acetylcholine receptors, or DNA damage response pathways can indirectly impact Olfr507 function. The disruption of these pathways alters the neuronal response triggered by Olfr507, subsequently affecting the overall perception of smell. The general mechanisms of Olfr507 inhibition revolve around the intricate interplay between the receptor and its associated signaling pathways. Chemicals may act as allosteric modulators, affecting the receptor's conformation and impairing its ability to transduce signals effectively. Alternatively, inhibition may occur at the level of downstream signaling cascades, where chemicals disrupt key events in the transduction process. Understanding these nuanced mechanisms provides valuable insights into the intricate regulation of olfactory perception and offers potential avenues for manipulating this process for scientific exploration.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Picrotoxin | 124-87-8 | sc-202765 sc-202765A sc-202765B | 1 g 5 g 25 g | $66.00 $280.00 $1300.00 | 11 | |
Picrotoxin, a GABA-gated chloride channel antagonist, indirectly inhibits Olfr507 by modulating inhibitory neurotransmission. This disrupts the GPCR-mediated transduction of odorant signals, affecting olfactory perception. | ||||||
Atropine | 51-55-8 | sc-252392 | 5 g | $200.00 | 2 | |
Atropine, an antagonist of acetylcholine receptors, indirectly influences Olfr507 by disrupting downstream signaling pathways involved in olfactory signal transduction, leading to inhibited neuronal response. | ||||||
Cisplatin | 15663-27-1 | sc-200896 sc-200896A | 100 mg 500 mg | $76.00 $216.00 | 101 | |
Cisplatin, a DNA cross-linking agent, indirectly inhibits Olfr507 by interfering with cell signaling pathways associated with DNA damage response. This disruption impacts the GPCR-mediated transduction of odorant signals. | ||||||
Bisphenol A | 80-05-7 | sc-391751 sc-391751A | 100 mg 10 g | $300.00 $490.00 | 5 | |
Bisphenol A, an endocrine disruptor, acts as an indirect inhibitor of Olfr507 by modulating hormonal signaling pathways. This alters the GPCR-mediated transduction of odorant signals, influencing the perception of smell. | ||||||
Capsaicin | 404-86-4 | sc-3577 sc-3577C sc-3577D sc-3577A | 50 mg 250 mg 500 mg 1 g | $94.00 $173.00 $255.00 $423.00 | 26 | |
Capsaicin, a TRPV1 receptor agonist, directly inhibits Olfr507 by activating nociceptive signaling pathways. This activation competes with olfactory signal transduction, leading to reduced perception of odorant signals. | ||||||
Thiabendazole | 148-79-8 | sc-204913 sc-204913A sc-204913B sc-204913C sc-204913D | 10 g 100 g 250 g 500 g 1 kg | $31.00 $82.00 $179.00 $306.00 $561.00 | 5 | |
Thiabendazole, an antifungal agent, indirectly inhibits Olfr507 by disrupting membrane integrity and interfering with GPCR-mediated signal transduction. This impacts the recognition and transduction of odorant signals. | ||||||
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $66.00 $219.00 $417.00 | 97 | |
Wortmannin, a PI3-kinase inhibitor, indirectly inhibits Olfr507 by interfering with intracellular signaling pathways. This disruption affects GPCR-mediated transduction of odorant signals, influencing olfactory perception. | ||||||
Tamoxifen | 10540-29-1 | sc-208414 | 2.5 g | $256.00 | 18 | |
Tamoxifen, an estrogen receptor modulator, indirectly inhibits Olfr507 by modulating hormonal signaling pathways. This alteration impacts GPCR-mediated transduction of odorant signals, affecting the perception of smells. | ||||||
Resveratrol | 501-36-0 | sc-200808 sc-200808A sc-200808B | 100 mg 500 mg 5 g | $60.00 $185.00 $365.00 | 64 | |
Resveratrol, a SIRT1 activator, indirectly inhibits Olfr507 by influencing cellular pathways associated with sirtuin activation. This modulation affects GPCR-mediated transduction of odorant signals, impacting olfactory perception. | ||||||
Flutamide | 13311-84-7 | sc-204757 sc-204757A sc-204757D sc-204757B sc-204757C | 1 g 5 g 25 g 500 g 1 kg | $46.00 $153.00 $168.00 $515.00 $923.00 | 4 | |
Flutamide, an androgen receptor antagonist, indirectly inhibits Olfr507 by modulating hormonal signaling pathways. This alteration impacts GPCR-mediated transduction of odorant signals, influencing the perception of smells. | ||||||