Vmn1r137 Inhibitors would represent a theoretical class of chemical entities designed to selectively bind to and inhibit the activity of the Vmn1r137 protein, presuming it is a chemosensory receptor within the vomeronasal type-1 receptor (Vmn1r) family. As these receptors are typically involved in detecting specific pheromonal cues, the inhibitors would likely function by blocking the receptor's ligand-binding site, preventing the natural ligand from interacting with the receptor and thereby inhibiting the signal transduction normally initiated upon ligand binding. Alternatively, these inhibitors might bind to other critical sites on the receptor, known as allosteric sites, to induce a conformational change in the receptor that results in decreased sensitivity or complete inactivation of the receptor's signaling ability.
The development of Vmn1r137 inhibitors would commence with an extensive study of the receptor's structure to identify key binding domains and to understand the molecular dynamics of ligand interaction. Advanced techniques such as crystallography or cryo-electron microscopy could be employed to ascertain the three-dimensional structure of Vmn1r137 at an atomic level. With this structural knowledge, a combination of in silico modeling and medicinal chemistry would be instrumental in designing and synthesizing inhibitors that are both specific to Vmn1r137 and highly effective at preventing receptor activation. These molecules might resemble the natural ligand's structure to compete for the binding site or might be entirely different in structure, designed to bind to distinct regions of the receptor to modulate its function. Investigating Vmn1r137 inhibitors would offer a way to understand the role of this receptor in the complex network of chemical communication through pheromones. By inhibiting Vmn1r137, researchers could dissect the pathways involved in pheromone detection and signaling, revealing the physiological processes that underlie these essential aspects of animal behavior. Such research could contribute significantly to the basic scientific understanding of sensory reception and signal transduction. It's crucial to note that the purpose of these inhibitors would be as tools for research, allowing scientists to probe the functions of chemosensory systems and to expand our foundational knowledge of molecular recognition and sensory biology.
Items 1 to 10 of 12 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Retinoic Acid, all trans | 302-79-4 | sc-200898 sc-200898A sc-200898B sc-200898C | 500 mg 5 g 10 g 100 g | $65.00 $319.00 $575.00 $998.00 | 28 | |
It may regulate gene expression by activating nuclear retinoic acid receptors, which bind to specific DNA response elements. | ||||||
Forskolin | 66575-29-9 | sc-3562 sc-3562A sc-3562B sc-3562C sc-3562D | 5 mg 50 mg 1 g 2 g 5 g | $76.00 $150.00 $725.00 $1385.00 $2050.00 | 73 | |
Could elevate cAMP levels, leading to the activation of cAMP-dependent transcription factors, potentially affecting gene expression. | ||||||
Sodium Butyrate | 156-54-7 | sc-202341 sc-202341B sc-202341A sc-202341C | 250 mg 5 g 25 g 500 g | $30.00 $46.00 $82.00 $218.00 | 19 | |
As an HDAC inhibitor, it might increase the transcription of certain genes by altering chromatin accessibility. | ||||||
Trichostatin A | 58880-19-6 | sc-3511 sc-3511A sc-3511B sc-3511C sc-3511D | 1 mg 5 mg 10 mg 25 mg 50 mg | $149.00 $470.00 $620.00 $1199.00 $2090.00 | 33 | |
This HDAC inhibitor may lead to histone acetylation changes, potentially influencing gene expression. | ||||||
β-Estradiol | 50-28-2 | sc-204431 sc-204431A | 500 mg 5 g | $62.00 $178.00 | 8 | |
Through binding to estrogen receptors, it could modulate the transcription of various genes, including those for chemosensory receptors. | ||||||
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
A DNA methyltransferase inhibitor that might activate gene expression through the demethylation of DNA. | ||||||
Dexamethasone | 50-02-2 | sc-29059 sc-29059B sc-29059A | 100 mg 1 g 5 g | $76.00 $82.00 $367.00 | 36 | |
This glucocorticoid could influence gene transcription by interacting with glucocorticoid response elements in the genome. | ||||||
(−)-Epigallocatechin Gallate | 989-51-5 | sc-200802 sc-200802A sc-200802B sc-200802C sc-200802D sc-200802E | 10 mg 50 mg 100 mg 500 mg 1 g 10 g | $42.00 $72.00 $124.00 $238.00 $520.00 $1234.00 | 11 | |
Known to modulate gene expression via epigenetic pathways and signaling molecules, potentially influencing receptor gene transcription. | ||||||
Curcumin | 458-37-7 | sc-200509 sc-200509A sc-200509B sc-200509C sc-200509D sc-200509F sc-200509E | 1 g 5 g 25 g 100 g 250 g 1 kg 2.5 kg | $36.00 $68.00 $107.00 $214.00 $234.00 $862.00 $1968.00 | 47 | |
May alter transcription factor activity, influencing the expression of a variety of genes including those for sensory receptors. | ||||||
Resveratrol | 501-36-0 | sc-200808 sc-200808A sc-200808B | 100 mg 500 mg 5 g | $60.00 $185.00 $365.00 | 64 | |
By affecting sirtuin proteins and signaling pathways, it could have an impact on gene expression. | ||||||