Items 71 to 80 of 185 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
D-myo-Inositol-1,3,4,6-tetraphosphate, ammonium salt | 142507-74-2 | sc-223922 sc-223922A | 100 µg 500 µg | $68.00 $406.00 | ||
D-myo-Inositol-1,3,4,6-tetraphosphate, ammonium salt, is a phosphoinositide derivative that plays a crucial role in cellular signaling pathways. Its unique structure allows for specific interactions with proteins and enzymes, influencing intracellular processes. The compound exhibits distinct binding affinities, which can modulate signal transduction mechanisms. Additionally, its solubility in aqueous environments enhances its reactivity, facilitating rapid participation in biochemical reactions. | ||||||
D-Lyxonic Acid, Potassium Salt | 78138-87-1 | sc-218028 | 5 g | $950.00 | ||
D-Lyxonic Acid, Potassium Salt is a carbohydrate derivative characterized by its unique stereochemistry, which influences its reactivity and interaction with biological systems. This compound participates in various metabolic pathways, acting as a substrate for enzymatic reactions. Its ionic nature enhances solubility, promoting efficient transport across cellular membranes. The presence of potassium ions can also affect the stability and reactivity of the acid, facilitating specific molecular interactions that are essential for carbohydrate metabolism. | ||||||
N,N′,N′′,N′′′-Tetraacetylchitotetraose | 2706-65-2 | sc-222017A sc-222017B sc-222017 | 1 mg 2 mg 10 mg | $104.00 $166.00 $416.00 | 1 | |
N,N',N'',N'''-Tetraacetylchitotetraose is a complex carbohydrate composed of multiple acetylated chito-oligosaccharide units. Its unique acetylation pattern enhances solubility and stability, allowing for specific interactions with lectins and other carbohydrate-binding proteins. This compound exhibits distinct reactivity in glycosylation reactions, influencing the synthesis of glycoproteins. Its structural conformation plays a critical role in modulating biological recognition processes, impacting various biochemical pathways. | ||||||
1,4-Anhydro-D-sorbitol | 27299-12-3 | sc-220552 | 1 g | $385.00 | ||
1,4-Anhydro-D-sorbitol is a unique carbohydrate characterized by its anhydro structure, which influences its reactivity and stability in various chemical environments. This compound participates in specific hydrogen bonding interactions, enhancing its solubility in polar solvents. Its distinct configuration allows for selective enzymatic recognition, making it a valuable model for studying carbohydrate metabolism and enzymatic pathways. Additionally, its low molecular weight contributes to rapid diffusion in biological systems. | ||||||
PtdIns-(3,4,5)-P3 (1,2-dipalmitoyl) (sodium salt) | 1628353-02-5 | sc-222208 sc-222208A | 100 µg 500 µg | $53.00 $315.00 | ||
PtdIns-(3,4,5)-P3 (1,2-dipalmitoyl) (sodium salt) is a phosphoinositide that plays a crucial role in cellular signaling. Its unique structure allows for specific interactions with proteins containing pleckstrin homology domains, facilitating signal transduction pathways. The presence of multiple phosphate groups enhances its hydrophilicity, promoting membrane association and localization. This compound's dynamic behavior in lipid bilayers influences membrane curvature and cellular responses, making it integral to various biological processes. | ||||||
Tetraglycol | 31692-85-0 | sc-215954 sc-215954A sc-215954B | 100 g 250 g 1 kg | $84.00 $124.00 $349.00 | ||
Tetraglycol is a carbohydrate characterized by its unique polyol structure, which allows for extensive hydrogen bonding and solvation effects in aqueous solutions. This compound exhibits a high degree of viscosity and low volatility, influencing its behavior in various chemical environments. Its ability to participate in multiple reaction pathways, including esterification and etherification, enhances its reactivity and versatility in synthetic applications. The presence of hydroxyl groups contributes to its strong affinity for polar solvents, facilitating interactions with biomolecules. | ||||||
D-myo-Inositol-3,4,5-triphosphate (sodium salt) | sc-221512 sc-221512A | 100 µg 500 µg | $65.00 $390.00 | |||
D-myo-Inositol-3,4,5-triphosphate (sodium salt) is a key signaling molecule involved in intracellular calcium release and phosphoinositide metabolism. Its triphosphate structure enables it to bind with high affinity to specific receptors, triggering diverse cellular responses. The compound's ability to modulate enzyme activity and influence cytoskeletal dynamics highlights its role in regulating cellular architecture. Additionally, its solubility in aqueous environments facilitates rapid diffusion and interaction within cellular compartments. | ||||||
PtdIns-(4,5)-P2 (1,2-dipalmitoyl) (sodium salt) | sc-224241 sc-224241A | 100 µg 500 µg | $194.00 $673.00 | |||
PtdIns-(4,5)-P2 (1,2-dipalmitoyl) (sodium salt) is a phosphoinositide that serves as a key regulator in cellular signaling. Its distinct diacylglycerol backbone facilitates membrane anchoring, allowing it to participate in lipid bilayer dynamics. The compound's ability to undergo phosphorylation and dephosphorylation reactions enables it to modulate protein interactions and activate downstream signaling cascades. Its amphipathic nature enhances membrane fluidity, influencing cellular processes such as endocytosis and cytoskeletal organization. | ||||||
1,2,3,4,6-Penta-O-trimethylsilyl α-D-galactose | sc-213469 | 1 g | $408.00 | |||
1,2,3,4,6-Penta-O-trimethylsilyl α-D-galactose is a highly silylated carbohydrate that exhibits unique solubility and reactivity profiles due to its trimethylsilyl groups. These modifications enhance its stability and facilitate selective reactions, making it a versatile intermediate in glycosylation processes. The steric bulk of the silyl groups influences molecular interactions, promoting specific binding affinities and altering reaction kinetics in carbohydrate chemistry. Its structural features enable it to participate in diverse synthetic pathways, contributing to the complexity of carbohydrate derivatives. | ||||||
1,4:3,6-Dianhydro-D-mannitol | 641-74-7 | sc-255945 | 25 g | $86.00 | ||
1,4:3,6-Dianhydro-D-mannitol is a unique carbohydrate characterized by its anhydro structure, which enhances its stability and alters its reactivity. This compound exhibits distinctive hydrogen bonding capabilities, influencing its solubility and interaction with other molecules. The absence of hydroxyl groups at specific positions leads to unique reaction pathways, allowing it to participate in selective condensation reactions. Its rigid conformation also affects molecular dynamics, making it an intriguing subject in carbohydrate chemistry. | ||||||