Items 31 to 40 of 103 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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AM 92016 hydrochloride | 178894-81-0 | sc-203506 sc-203506A | 10 mg 50 mg | $230.00 $1148.00 | ||
AM 92016 hydrochloride functions as a potassium channel modulator by engaging with distinct allosteric sites on the channel protein, inducing structural rearrangements that modify ion flow. Its unique chemical architecture promotes specific interactions with surrounding lipid bilayers, enhancing membrane fluidity. This compound also exhibits differential kinetics in ion conductance, impacting the overall ionic balance and influencing cellular homeostasis and signaling pathways. | ||||||
Aprindine hydrochloride | 33237-74-0 | sc-252383 | 10 mg | $125.00 | ||
Aprindine hydrochloride acts as a potassium channel modulator by selectively binding to specific sites on the channel, leading to conformational changes that alter ion permeability. Its unique structure facilitates interactions with membrane components, potentially affecting channel gating dynamics. The compound demonstrates varied reaction kinetics, influencing the rate of ion transport and contributing to the modulation of electrical activity across cellular membranes. | ||||||
L-364,373 | 103342-82-1 | sc-204036 sc-204036B sc-204036C | 2.5 mg 5 mg 10 mg | $240.00 $469.00 $877.00 | ||
L-364,373 functions as a potassium channel modulator by engaging with distinct allosteric sites, inducing specific conformational shifts that enhance or inhibit channel activity. Its unique molecular architecture allows for selective interactions with lipid bilayers, influencing membrane fluidity and channel accessibility. The compound exhibits unique kinetic profiles, affecting the timing and magnitude of ion flux, thereby playing a critical role in cellular excitability and signaling pathways. | ||||||
CP 339818 hydrochloride | 185855-91-8 | sc-203903 sc-203903A | 10 mg 50 mg | $155.00 $660.00 | ||
CP 339818 hydrochloride acts as a potassium channel modulator by selectively binding to specific sites on the channel protein, leading to alterations in ion conductance. Its unique structural features facilitate interactions with surrounding lipid environments, potentially stabilizing channel conformations. The compound demonstrates distinct reaction kinetics, influencing the rate of ion transport and contributing to the modulation of electrical signaling in various cellular contexts. | ||||||
UCL 1684 ditrifluoroacetate | 201147-19-5 | sc-253818 | 5 mg | $281.00 | 1 | |
UCL 1684 ditrifluoroacetate functions as a potassium channel modulator through its ability to interact with the channel's gating mechanisms. Its unique trifluoroacetate groups enhance hydrophobic interactions, promoting conformational changes in the channel protein. This compound exhibits specific binding affinities that influence ion selectivity and permeability, thereby affecting the overall electrochemical gradients across membranes. Its kinetic profile reveals a nuanced impact on channel activation and inactivation dynamics. | ||||||
Paxillinol | sc-205792 | 2 mg | $153.00 | |||
Paxillinol acts as a potassium channel modulator by selectively binding to specific sites on the channel protein, altering its conformational state. This compound's unique structural features facilitate enhanced interactions with lipid bilayers, influencing channel stability and function. Its modulation of ion flow is characterized by distinct reaction kinetics, which can lead to variations in channel responsiveness under different physiological conditions. The compound's ability to fine-tune ion conductance plays a crucial role in cellular excitability. | ||||||
Tertiapin LQ | sc-362807 | 1 mg | $175.00 | |||
Tertiapin LQ functions as a potassium channel modulator through its specific binding to the channel's pore region, leading to a unique alteration in ion selectivity. Its distinct molecular structure allows for enhanced affinity towards certain channel subtypes, influencing gating mechanisms. The compound exhibits unique reaction kinetics, resulting in prolonged channel inhibition, which can significantly affect cellular signaling pathways and excitability. Its interactions with membrane components further modulate channel dynamics. | ||||||
Rutaecarpine | 84-26-4 | sc-205846 sc-205846A | 10 mg 25 mg | $123.00 $359.00 | 1 | |
Rutaecarpine acts as a potassium channel modulator by selectively interacting with the channel's voltage-sensing domains, which alters the conformational state of the channel. This compound exhibits a unique ability to stabilize specific channel states, influencing the kinetics of ion flow. Its distinct molecular interactions can lead to differential modulation of various potassium channel subtypes, thereby impacting cellular excitability and signaling cascades in a nuanced manner. | ||||||
Doxapram | 309-29-5 | sc-279007 | 5 mg | $100.00 | ||
Doxapram functions as a potassium channel modulator by engaging with the channel's pore region, facilitating alterations in ion permeability. Its unique binding dynamics can enhance or inhibit channel activity, depending on the specific subtype involved. This compound exhibits a rapid onset of action, with reaction kinetics that allow for swift modulation of membrane potential. Additionally, its interactions can influence downstream signaling pathways, contributing to a complex regulatory network within cellular environments. | ||||||
Adenosine 5′-Triphosphate, disodium salt | 987-65-5 | sc-202040 sc-202040A | 1 g 5 g | $38.00 $74.00 | 9 | |
Adenosine 5'-Triphosphate, disodium salt acts as a potassium channel modulator by interacting with specific binding sites on the channel, leading to conformational changes that affect ion flow. Its unique structure allows for differential modulation of various potassium channel subtypes, influencing their gating mechanisms. The compound's rapid hydrolysis in cellular environments results in dynamic shifts in energy states, impacting cellular excitability and signaling cascades. |