Chloride Channel Modulators
Items 11 to 15 of 15 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Chromanol 293B | 163163-23-3 | sc-203889 sc-203889A | 10 mg 50 mg | $182.00 $774.00 | 1 | |
Chromanol 293B acts as a chloride channel modulator by engaging with the channel's regulatory sites, leading to alterations in ion permeability. Its unique structural features allow for specific interactions with amino acid residues, which can shift the channel's activation thresholds. The compound's kinetic profile reveals a rapid onset of action, influencing the channel's response to voltage changes. Additionally, its hydrophobic characteristics promote effective membrane integration, impacting cellular ionic balance. | ||||||
SFK1 | 678997-25-6 | sc-215849 | 10 mg | $159.00 | ||
SFK1 functions as a chloride channel modulator by selectively binding to allosteric sites on the channel, inducing conformational changes that enhance chloride ion flow. Its unique molecular architecture facilitates specific hydrogen bonding and hydrophobic interactions with channel proteins, fine-tuning their gating mechanisms. The compound exhibits a distinct reaction kinetics profile, characterized by a delayed onset, allowing for prolonged modulation of channel activity under varying physiological conditions. | ||||||
PG 01 | 853138-65-5 | sc-358839 sc-358839A | 5 mg 25 mg | $500.00 $750.00 | ||
PG 01 acts as a chloride channel modulator through its ability to interact with specific binding domains on the channel proteins, promoting alterations in their structural dynamics. This compound showcases unique electrostatic interactions that stabilize intermediate states of the channel, influencing ion permeability. Its kinetic behavior is marked by a rapid onset of action, enabling swift adjustments in chloride ion transport, which can be critical in various cellular environments. | ||||||
Etbicyphat | 1005-93-2 | sc-294479 | 100 mg | $439.00 | ||
Etbicyphat functions as a chloride channel modulator by selectively engaging with allosteric sites on channel proteins, leading to conformational changes that enhance chloride ion flow. Its unique hydrophobic interactions facilitate the stabilization of channel open states, optimizing ion conductance. The compound exhibits distinctive reaction kinetics, characterized by a gradual activation phase that allows for fine-tuning of chloride transport in response to cellular signals, thereby influencing physiological processes. | ||||||
Duramycin | 1391-36-2 | sc-239840 | 10 mg | $590.00 | 2 | |
Duramycin acts as a chloride channel modulator by binding to specific sites on channel proteins, inducing structural alterations that promote chloride ion permeability. Its unique ability to form hydrogen bonds enhances the stability of the channel's open conformation, facilitating efficient ion transport. The compound demonstrates a rapid onset of action, with a pronounced effect on ion flux, allowing for dynamic regulation of chloride flow in response to varying cellular conditions. | ||||||