CNGB1 inhibitors are a class of chemical compounds that specifically target and inhibit the function of the CNGB1 protein, a critical subunit of cyclic nucleotide-gated (CNG) ion channels. CNGB1 is primarily found in the rod photoreceptor cells of the retina, where it plays a significant role in visual signal transduction. CNG channels are essential for converting light-induced changes in cyclic guanosine monophosphate (cGMP) levels into electrical signals, which are then processed by the brain to produce vision. In rod photoreceptors, the CNGB1 subunit combines with CNGA1 subunits to form functional heteromeric CNG channels, which allow the influx of sodium and calcium ions into the cell in response to cGMP binding. This ion influx is a crucial part of the phototransduction cascade, which ultimately leads to changes in the membrane potential of photoreceptors and signal generation for visual perception.
Inhibitors of CNGB1 disrupt this ion flow by preventing the proper functioning of the CNG channels, thereby modulating the activity of photoreceptors. The CNGB1 subunit is also known to influence the stability and localization of the CNG channel in the plasma membrane, making it a key player in channel regulation and maintenance. By inhibiting CNGB1, researchers can study the specific contributions of this subunit to visual processes, as well as its broader role in the structural and functional integrity of CNG channels. These inhibitors are important tools in elucidating the molecular mechanisms of phototransduction, and they allow for a more detailed understanding of how CNG channels control cellular excitability and response to environmental stimuli, particularly in the context of vision.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Psoralen | 66-97-7 | sc-205965 sc-205965A | 25 mg 100 mg | $103.00 $321.00 | 1 | |
Psoralen inhibits cyclic nucleotide gated channel subunit beta 1 by binding to the channel pore and altering its permeability. | ||||||
Zinc | 7440-66-6 | sc-213177 | 100 g | $48.00 | ||
Zinc inhibits cyclic nucleotide gated channel subunit beta 1 by altering the channel's conformation and reducing conductivity. | ||||||
Copper(II) sulfate | 7758-98-7 | sc-211133 sc-211133A sc-211133B | 100 g 500 g 1 kg | $46.00 $122.00 $189.00 | 3 | |
Copper(II) sulfate can inhibit cyclic nucleotide gated channel subunit beta 1 by binding to the channel and interfering with ion transport. | ||||||
Chlorpromazine | 50-53-3 | sc-357313 sc-357313A | 5 g 25 g | $61.00 $110.00 | 21 | |
Chlorpromazine inhibits cyclic nucleotide gated channel subunit beta 1 by blocking the channel and reducing ion permeability. | ||||||
1-Adamantylamine | 768-94-5 | sc-251475 sc-251475A | 1 g 25 g | $39.00 $147.00 | ||
Amantadine inhibits cyclic nucleotide gated channel subunit beta 1 by blocking the ion-conducting pore of the channel. | ||||||
Quinine | 130-95-0 | sc-212616 sc-212616A sc-212616B sc-212616C sc-212616D | 1 g 5 g 10 g 25 g 50 g | $79.00 $104.00 $166.00 $354.00 $572.00 | 1 | |
Quinine inhibits cyclic nucleotide gated channel subunit beta 1 by altering channel gating and blocking ion flow. | ||||||
Propranolol | 525-66-6 | sc-507425 | 100 mg | $180.00 | ||
Propranolol inhibits cyclic nucleotide gated channel subunit beta 1 by binding to the channel and obstructing the ion pathway. | ||||||
Verapamil | 52-53-9 | sc-507373 | 1 g | $374.00 | ||
Verapamil inhibits cyclic nucleotide gated channel subunit beta 1 by directly binding and blocking the channel's ion-conducting pore. | ||||||
Trifluoperazine Dihydrochloride | 440-17-5 | sc-201498 sc-201498A | 1 g 5 g | $57.00 $101.00 | 9 | |
Trifluoperazine inhibits cyclic nucleotide gated channel subunit beta 1 by binding to the channel and preventing ion permeability. | ||||||
Phenothiazine | 92-84-2 | sc-250686 sc-250686A | 50 g 250 g | $23.00 $44.00 | ||
Phenothiazine inhibits cyclic nucleotide gated channel subunit beta 1 by interacting with the channel and altering its structure. | ||||||