Items 101 to 110 of 263 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Sulfate-ionophore I | 37042-63-0 | sc-255626 | 50 mg | $112.00 | ||
Sulfate-ionophore I functions as an ionophore by forming stable complexes with sulfate ions, promoting their transport across biological membranes. Its unique structural features enable it to interact selectively with anionic species, enhancing ion mobility. The compound's ability to alter membrane potential and ionic balance is influenced by its dynamic conformation, which facilitates rapid ion exchange. This behavior is crucial for modulating electrochemical gradients in various systems. | ||||||
Trifloxystrobin | 141517-21-7 | sc-229576 | 100 mg | $103.00 | ||
Trifloxystrobin functions as a potent ionophore, facilitating the selective transport of specific ions across biological membranes. Its unique molecular structure allows for effective binding with target ions, promoting their translocation through lipid bilayers. The compound exhibits distinct reaction kinetics, characterized by rapid ion exchange rates, which can significantly alter ionic gradients. This behavior influences various cellular processes, including energy metabolism and signaling pathways, underscoring its role in ion regulation. | ||||||
Cephradine | 38821-53-3 | sc-234296 | 500 mg | $130.00 | ||
Cephradine acts as an ionophore by selectively binding to cationic species, facilitating their translocation through lipid bilayers. Its unique cyclic structure allows for specific interactions with metal ions, enhancing their solubility and mobility. The compound's kinetic properties enable swift ion exchange, which can significantly influence cellular ionic homeostasis. Additionally, its conformational flexibility plays a key role in optimizing binding affinities, thereby affecting transport efficiency across membranes. | ||||||
Ferutinin | 41743-44-6 | sc-221610 sc-221610A | 1 mg 5 mg | $38.00 $107.00 | 3 | |
Ferutinin functions as an ionophore by forming stable complexes with cations, promoting their passage across biological membranes. Its distinctive polycyclic framework enables strong coordination with various metal ions, enhancing their permeability. The compound exhibits rapid ion transport kinetics, which can alter electrochemical gradients. Furthermore, its ability to adopt multiple conformations allows for tailored interactions with different ions, optimizing transport dynamics in diverse environments. | ||||||
2-NP-AMOZ | 183193-59-1 | sc-238185 | 10 mg | $150.00 | ||
2-NP-AMOZ is a distinctive ionophore known for its selective ion transport capabilities, particularly in mediating the movement of cations through lipid bilayers. Its unique structural features enable strong interactions with target ions, enhancing selectivity and binding affinity. The compound's kinetic profile allows for swift ion exchange, contributing to its effectiveness in altering membrane potential and influencing electrochemical gradients. This dynamic interaction with ions underscores its role in cellular ionic regulation. | ||||||
A23187 (Mixed Calcium-Magnesium Salt) | 52665-69-7 | sc-221193 sc-221193A | 5 mg 10 mg | $94.00 $166.00 | ||
A23187, a mixed calcium-magnesium salt, functions as an ionophore by forming stable complexes with divalent cations, promoting their passage across biological membranes. Its unique ability to alter membrane permeability is attributed to its hydrophobic regions, which interact favorably with lipid bilayers. The compound exhibits rapid ion transport kinetics, enabling efficient calcium and magnesium influx, which can significantly influence cellular signaling pathways and ionic homeostasis. | ||||||
Narasin from Streptomyces auriofaciens | 55134-13-9 | sc-253180 sc-253180A sc-253180B sc-253180C sc-253180D | 5 mg 25 mg 100 mg 500 mg 1 g | $173.00 $615.00 $2346.00 $9884.00 $13525.00 | 1 | |
Narasin, derived from Streptomyces auriofaciens, functions as an ionophore by selectively binding to monovalent cations, particularly sodium and potassium. Its unique cyclic structure promotes the formation of stable ion complexes, enabling efficient ion transport across lipid bilayers. This compound exhibits notable reaction kinetics, with rapid ion exchange rates that can disrupt ionic homeostasis, influencing cellular signaling pathways and metabolic functions. Its hydrophobic characteristics enhance interaction with membrane components, facilitating ion mobility. | ||||||
Cefmetazole sodium salt | 56796-39-5 | sc-234292 sc-234292A | 250 mg 1 g | $52.00 $133.00 | ||
Cefmetazole sodium salt acts as an ionophore by forming stable complexes with cations, enhancing their mobility across lipid membranes. Its distinctive molecular architecture allows for specific interactions with various metal ions, facilitating their transport through hydrophobic environments. The compound exhibits notable reaction kinetics, enabling efficient ion exchange processes. Furthermore, its solubility characteristics contribute to its ability to influence ionic gradients, impacting cellular homeostasis. | ||||||
CA 1001 | 58801-34-6 | sc-202512 | 25 mg | $163.00 | 2 | |
CA 1001 functions as an ionophore by selectively binding to cations, promoting their translocation through lipid bilayers. Its unique structural features enable it to interact with a range of metal ions, optimizing their passage through nonpolar regions. The compound demonstrates rapid reaction kinetics, which enhances its ion transport efficiency. Additionally, its distinctive solubility profile allows it to modulate ionic concentrations, thereby influencing electrochemical gradients within cellular systems. | ||||||
Erythromycin A dihydrate | 59319-72-1 | sc-234871 | 250 mg | $79.00 | ||
Erythromycin A dihydrate acts as an ionophore by facilitating the transport of cations across biological membranes. Its unique macrolide structure allows for specific interactions with various metal ions, enhancing their mobility through hydrophobic environments. The compound exhibits notable selectivity and affinity for certain ions, which can alter membrane potential and ionic balance. Its ability to form stable complexes with cations contributes to its effectiveness in modulating cellular ionic dynamics. | ||||||