Items 1 to 10 of 35 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
UK 5099 | 56396-35-1 | sc-361394 sc-361394A | 10 mg 50 mg | $154.00 $633.00 | 5 | |
UK 5099 functions as a specialized ion pump reagent, characterized by its ability to modulate ion transport through selective interactions with membrane proteins. Its unique structure allows for specific binding to ion channels, influencing their conformational states and enhancing ion flux. The compound exhibits distinct kinetic properties, facilitating rapid ion exchange and contributing to the regulation of electrochemical gradients, thereby impacting cellular ionic homeostasis. | ||||||
Esomeprazole magnesium dihydrate | 217087-10-0 | sc-252785 | 50 mg | $69.00 | ||
Esomeprazole magnesium dihydrate serves as a sophisticated ion pump reagent, distinguished by its capacity to interact with proton pumps at a molecular level. Its unique stereochemistry enables selective inhibition of H+/K+ ATPase, altering the dynamics of ion transport. This compound exhibits notable reaction kinetics, promoting efficient ion exchange and stabilizing membrane potential. Its solubility characteristics enhance bioavailability, facilitating targeted interactions within cellular environments. | ||||||
Ouabain Octahydrate | 11018-89-6 | sc-201548 sc-201548A | 1 g 5 g | $190.00 $720.00 | 11 | |
Ouabain Octahydrate functions as a potent ion pump reagent, characterized by its ability to selectively inhibit Na+/K+ ATPase. This inhibition disrupts the electrochemical gradient across cell membranes, influencing cellular ion homeostasis. The compound's unique binding affinity and conformational changes in the enzyme facilitate distinct signaling pathways. Additionally, its hydrophilic nature enhances solubility, promoting effective interaction with membrane proteins and modulating cellular responses. | ||||||
ZD 7288 | 133059-99-1 | sc-361419 sc-361419A | 10 mg 50 mg | $207.00 $541.00 | ||
ZD 7288 serves as a specialized ion pump reagent, primarily acting as a selective blocker of hyperpolarization-activated cyclic nucleotide-gated (HCN) channels. Its unique molecular structure allows for specific interactions with the channel's binding sites, altering ion flow and impacting cellular excitability. The compound exhibits distinct kinetic properties, enabling rapid onset and offset of action, which is crucial for studying dynamic ion transport processes in various cellular environments. | ||||||
DK-AH 269 | 186097-54-1 | sc-252761 | 5 mg | $180.00 | ||
DK-AH 269 functions as an innovative ion pump reagent, characterized by its ability to modulate ion transport through specific interactions with membrane proteins. Its unique structural features facilitate selective binding to target sites, influencing ion permeability and cellular signaling pathways. The compound demonstrates remarkable stability and solubility, enhancing its efficacy in experimental setups. Additionally, its distinct reaction kinetics allow for precise control over ion flow dynamics, making it a valuable tool in electrochemical studies. | ||||||
Kainic acid monohydrate | 58002-62-3 | sc-269283 | 10 mg | $270.00 | ||
Kainic acid monohydrate serves as a specialized ion pump reagent, exhibiting unique interactions with ion channels and transporters. Its structural conformation enables it to effectively alter ion gradients, thereby influencing cellular excitability and signaling mechanisms. The compound's high solubility and stability contribute to its reliability in experimental conditions. Furthermore, its distinct kinetic profile allows for the fine-tuning of ion transport processes, making it an essential component in electrochemical research. | ||||||
Clopamide | 636-54-4 | sc-201553 | 500 mg | $32.00 | ||
Clopamide functions as a distinctive ion pump reagent, characterized by its ability to modulate ion transport dynamics through specific binding interactions with membrane proteins. Its unique molecular structure facilitates selective inhibition of sodium-potassium pumps, leading to altered ion homeostasis. The compound's favorable solubility enhances its accessibility in various experimental setups, while its reaction kinetics allow for precise manipulation of ion flow, making it a valuable tool in studies of cellular ion regulation. | ||||||
Tenatoprazole | 113712-98-4 | sc-204909 sc-204909A | 100 mg 500 mg | $153.00 $408.00 | 1 | |
Tenatoprazole serves as a notable ion pump reagent, distinguished by its capacity to interact with proton pumps at a molecular level. Its unique structural features enable it to effectively disrupt the proton gradient across cellular membranes, influencing intracellular pH. The compound exhibits rapid kinetics, allowing for swift modulation of ion transport processes. Additionally, its stability in diverse environments enhances its utility in experimental investigations of ion channel behavior and cellular signaling pathways. | ||||||
Pantoprazole Sodium | 138786-67-1 | sc-204831 sc-204831A | 1 g 5 g | $61.00 $153.00 | ||
Pantoprazole Sodium functions as a potent ion pump reagent, characterized by its selective binding to the H+/K+ ATPase enzyme. This interaction alters the conformational dynamics of the enzyme, leading to a significant reduction in proton transport efficiency. The compound's unique ability to form stable complexes with the enzyme facilitates detailed studies of ion exchange mechanisms. Its solubility in various solvents allows for versatile applications in biochemical assays and membrane studies. | ||||||
Glycine sodium salt anhydrous | 6000-44-8 | sc-257565 sc-257565A | 100 g 500 g | $65.00 $252.00 | ||
Glycine sodium salt anhydrous serves as an effective ion pump reagent, exhibiting unique interactions with cellular membranes and ion channels. Its zwitterionic nature enhances its solubility and facilitates electrostatic interactions, promoting the modulation of ion transport processes. The compound's ability to stabilize charged intermediates can influence reaction kinetics, making it a valuable tool for exploring ion dynamics in various biochemical environments. Its low toxicity and compatibility with diverse experimental setups further enhance its utility in research. | ||||||