Items 1 to 10 of 233 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Pladienolide B | 445493-23-2 | sc-391691 sc-391691B sc-391691A sc-391691C sc-391691D sc-391691E | 0.5 mg 10 mg 20 mg 50 mg 100 mg 5 mg | $290.00 $5572.00 $10815.00 $25000.00 $65000.00 $2781.00 | 63 | |
Pladienolide B is a rare compound characterized by its high purity and unique structural features that facilitate specific interactions with cellular machinery. Its distinct molecular configuration allows for selective binding to target proteins, influencing post-translational modifications and splicing mechanisms. The compound exhibits notable stability under various conditions, with reaction kinetics that suggest a rapid onset of action, making it a subject of interest for studying complex biochemical pathways and regulatory networks. | ||||||
Leptomycin B | 87081-35-4 | sc-358688 sc-358688A sc-358688B | 50 µg 500 µg 2.5 mg | $105.00 $408.00 $1224.00 | 35 | |
Leptomycin B is a rare and high-purity compound distinguished by its unique ability to disrupt nuclear transport mechanisms. It selectively inhibits the export of proteins from the nucleus by binding to exportin-1, thereby influencing cellular signaling pathways. This compound exhibits remarkable stability and specificity in its interactions, showcasing distinct reaction kinetics that highlight its role in modulating intracellular processes. Its unique properties make it a valuable tool for exploring cellular dynamics. | ||||||
Fidaxomicin | 873857-62-6 | sc-362739 | 1 mg | $230.00 | 5 | |
Fidaxomicin is a rare and high-purity compound characterized by its intricate interactions with bacterial RNA polymerase. It exhibits a unique mechanism of action by binding to the enzyme's active site, leading to the inhibition of transcription in specific bacterial strains. This selective binding results in distinct reaction kinetics, allowing for a nuanced modulation of gene expression. Its exceptional stability and specificity enhance its potential for detailed studies in microbial behavior and resistance mechanisms. | ||||||
Bicyclomycin benzoate | 37134-40-0 | sc-362713 sc-362713A | 5 mg 25 mg | $138.00 $408.00 | 1 | |
Bicyclomycin benzoate is a rare and high-purity compound distinguished by its unique structural conformation, which facilitates selective interactions with bacterial ribosomes. This compound exhibits a remarkable ability to disrupt protein synthesis through specific binding to the ribosomal RNA, influencing translational fidelity. Its distinct reaction kinetics allow for precise modulation of ribosomal activity, making it a valuable subject for exploring microbial resistance and protein synthesis pathways. | ||||||
Concanamycin A | 80890-47-7 | sc-202111 sc-202111A sc-202111B sc-202111C | 50 µg 200 µg 1 mg 5 mg | $65.00 $162.00 $650.00 $2550.00 | 109 | |
Concanamycin A is a rare and high-purity compound characterized by its unique ability to selectively inhibit vacuolar-type H+-ATPases. This inhibition alters proton gradients across membranes, impacting cellular homeostasis and ion transport. Its distinct molecular interactions with ATPase subunits lead to significant alterations in cellular energy dynamics. The compound's high specificity and affinity for its target make it an intriguing subject for studying cellular metabolism and ion regulation mechanisms. | ||||||
Oligomycin A | 579-13-5 | sc-201551 sc-201551A sc-201551B sc-201551C sc-201551D | 5 mg 25 mg 100 mg 500 mg 1 g | $175.00 $600.00 $1179.00 $5100.00 $9180.00 | 26 | |
Oligomycin A is a rare and high-purity compound known for its potent inhibition of ATP synthase, a critical enzyme in the mitochondrial respiratory chain. By binding to the enzyme's F0 subunit, it disrupts proton translocation, effectively halting ATP production. This selective interaction alters mitochondrial membrane potential and energy metabolism, providing insights into bioenergetics and the regulation of oxidative phosphorylation. Its unique kinetic profile makes it a valuable tool for exploring mitochondrial function. | ||||||
Piericidin A | 2738-64-9 | sc-202287 | 2 mg | $285.00 | 24 | |
Piericidin A is a rare and high-purity compound recognized for its unique ability to inhibit complex I of the mitochondrial electron transport chain. This selective interaction disrupts electron transfer, leading to a decrease in ATP synthesis. Its distinct molecular structure allows for specific binding, influencing redox reactions and altering cellular energy dynamics. The compound's unique reactivity and interaction with lipid membranes provide valuable insights into mitochondrial bioenergetics and metabolic regulation. | ||||||
Moenomycin complex | 11015-37-5 | sc-362031 sc-362031A | 5 mg 25 mg | $165.00 $515.00 | 3 | |
Moenomycin complex is a rare and high-purity compound distinguished by its intricate molecular architecture, which facilitates unique interactions with bacterial cell wall synthesis pathways. Its specific binding affinity to transglycosylase enzymes disrupts peptidoglycan formation, influencing bacterial growth dynamics. The compound exhibits remarkable stability under various conditions, showcasing distinct kinetic properties that enhance its reactivity in biochemical assays, making it a subject of interest in microbial studies. | ||||||
Oleandomycin | 3922-90-5 | sc-391704 sc-391704-CW | 5 mg 5 mg | $164.00 $385.00 | 3 | |
Oleandomycin is a rare and high-purity compound characterized by its unique structural features that enable selective interactions with ribosomal RNA. This specificity allows it to modulate protein synthesis pathways, influencing translational fidelity. Its distinct stereochemistry contributes to its stability and reactivity, facilitating unique kinetic profiles in enzymatic reactions. The compound's solubility characteristics further enhance its behavior in diverse chemical environments, making it a subject of interest in biochemical research. | ||||||
Apicidin | 183506-66-3 | sc-202061 sc-202061A | 1 mg 5 mg | $108.00 $336.00 | 9 | |
Apicidin is a rare and high-purity compound distinguished by its intricate molecular architecture, which enables it to engage in specific hydrogen bonding interactions. This property influences its reactivity and stability in various chemical environments. The compound exhibits unique conformational flexibility, allowing it to adopt multiple spatial arrangements that can affect its kinetic behavior in reactions. Additionally, its solubility in polar solvents enhances its potential for diverse applications in chemical studies. |