Items 171 to 180 of 185 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
D-myo-Inositol-2,3,4,5-tetraphosphate, ammonium salt | sc-223929 sc-223929A | 100 µg 500 µg | $220.00 $992.00 | |||
D-myo-Inositol-2,3,4,5-tetraphosphate, ammonium salt, is a polyphosphate carbohydrate that exhibits unique binding properties due to its multiple phosphate groups. These groups enable it to participate in intricate signaling pathways, influencing cellular processes such as calcium mobilization and enzyme activation. Its structural conformation allows for specific interactions with proteins, modulating their activity and stability, thereby playing a pivotal role in cellular metabolism and regulatory mechanisms. | ||||||
4-Methoxyphenyl 2-Azido-3,6-di-O-benzyl-2-deoxy-beta-D-glucopyranoside | sc-290396 | 1 g | $960.00 | |||
4-Methoxyphenyl 2-Azido-3,6-di-O-benzyl-2-deoxy-beta-D-glucopyranoside is a sophisticated carbohydrate featuring azido and benzyl substituents that enhance its reactivity and solubility. The azido group allows for versatile click chemistry applications, facilitating conjugation with various biomolecules. Its unique structural configuration promotes selective interactions with specific receptors, influencing molecular recognition and binding dynamics in complex biological systems. | ||||||
GlcNAc beta(1-2)Man alpha-1-Ethylazide | sc-295009 | 100 mg | $2215.00 | |||
GlcNAc beta(1-2)Man alpha-1-Ethylazide is a distinctive carbohydrate characterized by its unique glycosidic linkage and ethylazide modification. This structure enhances its reactivity in glycosylation reactions, promoting selective interactions with lectins and other carbohydrate-binding proteins. The ethylazide group introduces a site for further functionalization, enabling the exploration of diverse synthetic pathways. Its specific stereochemistry influences molecular recognition, impacting binding affinities in various biochemical contexts. | ||||||
N-GlcNAc-Biotin | sc-295719 | 50 mg | $1140.00 | |||
N-GlcNAc-Biotin is a specialized carbohydrate featuring a biotin moiety that enhances its affinity for specific proteins. This compound exhibits unique molecular interactions due to its ability to form stable complexes with avidin and streptavidin, facilitating targeted binding in biochemical assays. The presence of the N-acetylglucosamine unit contributes to its solubility and stability in aqueous environments, while its structural conformation influences enzymatic recognition and activity in glycosylation processes. | ||||||
1,2-Dipalmitoylphosphatidylinositol 3,4,5-trisphosphate tetrasodium salt | sc-297914 | 100 µg | $149.00 | |||
1,2-Dipalmitoylphosphatidylinositol 3,4,5-trisphosphate tetrasodium salt is a phospholipid that plays a crucial role in cellular signaling pathways. Its unique structure allows for specific interactions with proteins involved in signal transduction, particularly in the activation of kinases. The presence of multiple phosphate groups enhances its hydrophilicity, promoting membrane association and influencing lipid bilayer dynamics. This compound also participates in the regulation of cellular processes through its involvement in lipid rafts and membrane microdomains. | ||||||
(2,6-Di-O-)ethyl-β-cyclodextrin | sc-298647 | 1 g | $1600.00 | |||
(2,6-Di-O-)ethyl-β-cyclodextrin is a modified cyclodextrin that exhibits unique host-guest chemistry due to its hydrophobic cavity, which can encapsulate various guest molecules. This encapsulation enhances solubility and stability of the guest compounds. Its ethyl substitutions increase lipophilicity, facilitating interactions with lipid membranes. The compound's ability to form inclusion complexes can influence reaction kinetics and molecular transport, making it a versatile tool in various chemical processes. | ||||||
D-myo-Inositol 1,4,5-tris-phosphate trisodium salt | sc-300413 | 1 mg | $240.00 | |||
D-myo-Inositol 1,4,5-tris-phosphate trisodium salt is a key signaling molecule involved in cellular processes, particularly in calcium mobilization and phosphoinositide metabolism. Its unique structure allows it to interact specifically with various proteins, influencing pathways such as cell proliferation and differentiation. The compound's trisodium form enhances its solubility in aqueous environments, facilitating rapid diffusion and interaction with target receptors, thereby modulating intracellular signaling cascades effectively. | ||||||
1,5-Anhydro-D-mannitol | 492-93-3 | sc-220557 | 50 mg | $350.00 | ||
1,5-Anhydro-D-mannitol is a unique carbohydrate derivative known for its ability to stabilize molecular structures through intramolecular hydrogen bonding. This compound can influence the solubility and crystallization behavior of polysaccharides, affecting their physical properties. Its anhydro form allows for distinct reactivity in glycosidic bond formation, facilitating specific enzymatic interactions and altering metabolic pathways in carbohydrate chemistry. | ||||||
Methyl 2-Acetamido-2-deoxy-β-D-glucopyranoside | 3946-01-8 | sc-221893 | 100 mg | $180.00 | ||
Methyl 2-Acetamido-2-deoxy-β-D-glucopyranoside is a notable carbohydrate characterized by its unique glycosidic linkage, which influences its solubility and reactivity in aqueous environments. The presence of the acetamido group enhances hydrogen bonding capabilities, facilitating specific interactions with other biomolecules. This compound can undergo enzymatic hydrolysis, impacting its stability and reactivity in biochemical pathways, while its structural conformation allows for diverse molecular recognition events. | ||||||
D-Ribulose o-nitrophenylhydrazone | 6155-41-5 | sc-214829 | 25 mg | $62.00 | ||
D-Ribulose o-nitrophenylhydrazone is a distinctive carbohydrate derivative known for its ability to form stable hydrazone linkages, which significantly influence its reactivity and interaction with other biomolecules. The nitrophenyl group enhances electron-withdrawing properties, affecting the compound's reactivity in condensation reactions. Its unique structural arrangement allows for specific binding interactions, making it a valuable tool in studying carbohydrate metabolism and enzymatic processes. | ||||||