Ionophores
Items 91 to 100 of 263 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Sisomicin sulfate salt | 53179-09-2 | sc-236885 sc-236885A | 250 mg 1 g | $92.00 $309.00 | ||
Sisomicin sulfate salt acts as an ionophore by facilitating the transport of cations across lipid membranes through specific binding interactions. Its structure allows for the formation of transient complexes with ions, enhancing their solubility in the hydrophobic environment of the membrane. This compound exhibits distinct reaction kinetics, characterized by a swift exchange of ions, which can lead to alterations in membrane potential and ionic gradients, impacting cellular processes. | ||||||
Tiamulin | 55297-95-5 | sc-237107 | 100 mg | $372.00 | 1 | |
Tiamulin, a member of the pleuromutilin class, acts as an ionophore by forming complexes with cations, particularly affecting calcium and magnesium ions. Its unique structure allows for specific interactions with lipid membranes, enhancing permeability and ion transport. The compound exhibits distinct reaction kinetics, characterized by a gradual release of bound ions, which can modulate cellular ion concentrations. Its amphipathic nature aids in membrane integration, influencing ion dynamics and cellular processes. | ||||||
Trinactin | 7561-71-9 | sc-202370 | 1 mg | $420.00 | ||
Trinactin functions as an ionophore by facilitating the transport of cations across biological membranes through its unique structural conformation. Its ability to form transient complexes with metal ions enhances their solubility and mobility, allowing for rapid ion exchange. The compound's interaction with lipid bilayers alters membrane permeability, leading to significant changes in ionic flux and cellular signaling pathways. This dynamic behavior highlights its influence on ion distribution and cellular electrochemical balance. | ||||||
Coumarin 343 | 55804-65-4 | sc-252639 | 100 mg | $32.00 | ||
Coumarin 343 functions as an ionophore by facilitating the transport of cations across biological membranes. Its unique molecular structure enables it to selectively bind to metal ions, promoting their translocation through lipid bilayers. This compound exhibits rapid kinetics in ion exchange, allowing for swift modulation of intracellular ion levels. Additionally, its photophysical properties enhance its interaction with membranes, influencing ion flux and cellular signaling pathways. | ||||||
Spiramycin | 8025-81-8 | sc-251064 sc-251064A sc-251064B | 1 g 5 g 10 g | $81.00 $176.00 $317.00 | 1 | |
Spiramycin acts as an ionophore by selectively binding to cations, promoting their translocation across lipid membranes. Its unique cyclic structure allows for the formation of stable complexes with divalent and monovalent ions, enhancing their diffusion rates. This interaction modifies membrane fluidity and alters ion gradients, which can significantly impact cellular homeostasis and metabolic processes. The compound's affinity for specific ions underscores its role in modulating ionic environments within cells. | ||||||
Gramicidin A | 11029-61-1 | sc-203061 sc-203061A | 1 mg 5 mg | $82.00 $151.00 | 7 | |
Gramicidin A acts as an ionophore by forming a channel in lipid membranes, allowing selective passage of monovalent cations, particularly sodium and potassium ions. Its unique helical structure stabilizes ion binding through specific interactions, promoting rapid ion translocation. The dynamic nature of these channels enables a swift response to concentration gradients, significantly affecting membrane potential and ionic homeostasis. This behavior underscores its role in modulating electrochemical environments. | ||||||
Enniatin complex | 11113-62-5 | sc-202152 | 10 mg | $459.00 | ||
Enniatin complex functions as an ionophore by forming a unique cyclic structure that facilitates the transport of cations across lipid membranes. Its ability to selectively bind to divalent and monovalent ions is attributed to its hydrophobic and polar regions, which create a favorable environment for ion solvation. The complex exhibits rapid kinetics in ion exchange, significantly influencing cellular ionic balance and membrane potential, thereby impacting electrochemical gradients. | ||||||
PGB1 (Prostaglandin B1) | 13345-51-2 | sc-201217 sc-201217A | 1 mg 10 mg | $37.00 $232.00 | ||
PGB1 operates as an ionophore through its distinctive ability to interact with lipid bilayers, promoting the translocation of ions. Its molecular structure allows for specific binding to cations, enhancing their solubility in the membrane environment. The compound exhibits notable reaction kinetics, facilitating swift ion transport and influencing cellular homeostasis. Additionally, PGB1's unique conformational flexibility enables it to modulate ion selectivity, impacting membrane dynamics and ionic equilibrium. | ||||||
N-Benzylidenebenzenesulfonamide | 13909-34-7 | sc-250446 | 5 g | $77.00 | ||
N-Benzylidenebenzenesulfonamide functions as an ionophore by engaging in selective ion binding through its sulfonamide group, which enhances its affinity for cations. This compound exhibits unique conformational flexibility, allowing it to adapt its structure for optimal interaction with target ions. Its hydrophobic benzylidene moiety promotes partitioning into lipid environments, facilitating ion transport across membranes and modulating electrochemical gradients, thereby influencing cellular ionic dynamics. | ||||||
Monensin A | 17090-79-8 | sc-362032 sc-362032A | 5 mg 25 mg | $155.00 $525.00 | ||
Monensin A functions as an ionophore by facilitating the transport of monovalent cations across biological membranes. Its unique structure allows it to form cyclic complexes with sodium and potassium ions, enhancing ion mobility. The presence of a carboxylic acid group contributes to its solubility in lipophilic environments, while its hydrophobic regions promote interaction with lipid bilayers. This selective ion transport alters membrane potential and influences cellular ionic homeostasis. | ||||||