Items 11 to 20 of 185 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Hyaluronic Acid, Sodium Salt | 9067-32-7 | sc-204004A sc-204004B sc-204004C sc-204004D sc-204004 | 100 mg 1 g 25 g 100 g 500 mg | $82.00 $360.00 $700.00 $1715.00 $235.00 | 1 | |
Hyaluronic Acid, Sodium Salt is a polysaccharide renowned for its exceptional water retention capacity, enabling it to maintain hydration in various environments. Its unique structure allows for extensive hydrogen bonding, promoting viscoelasticity and contributing to its gel-like consistency. This compound interacts with cell membranes, facilitating cellular communication and influencing tissue hydration dynamics. Its high molecular weight enhances its ability to form stable complexes, impacting its behavior in diverse biochemical pathways. | ||||||
Pirlimycin hydrochloride (Mixture of Diastereomers) | 78822-40-9 | sc-212565 sc-212565A | 500 µg 5 mg | $405.00 $2550.00 | ||
Pirlimycin hydrochloride, a mixture of diastereomers, exhibits intriguing molecular interactions due to its unique stereochemistry. This compound engages in specific hydrogen bonding and hydrophobic interactions, influencing its solubility and reactivity in various environments. Its distinct conformational flexibility allows for diverse binding affinities, which can modulate its kinetic behavior in biochemical pathways. Additionally, the presence of functional groups enhances its ability to participate in complexation reactions, affecting its overall stability and reactivity. | ||||||
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
5-Azacytidine is a nucleoside analog that exhibits unique interactions with nucleic acids, influencing gene expression and epigenetic regulation. Its structure allows for incorporation into RNA, disrupting normal base pairing and altering transcriptional dynamics. This compound can modulate cellular pathways by affecting RNA stability and processing, leading to distinct kinetic profiles in biochemical reactions. Its ability to mimic natural nucleotides enables it to engage in specific molecular interactions that impact cellular function. | ||||||
λ-Carrageenan | 9064-57-7 | sc-216084 sc-216084B sc-216084A sc-216084C sc-216084D | 5 g 10 g 25 g 50 g 100 g | $97.00 $173.00 $352.00 $520.00 $622.00 | 6 | |
λ-Carrageenan is a sulfated polysaccharide known for its unique gel-forming properties, which arise from its helical structure and the presence of sulfate groups. These features facilitate strong intermolecular interactions, including ionic and hydrogen bonding, leading to the formation of stable gels in aqueous solutions. Its ability to undergo conformational changes in response to temperature and ionic strength allows for dynamic viscosity modulation, making it a versatile agent in various applications. | ||||||
D-myo-Inositol-1-phosphate, sodium salt | sc-223909 sc-223909A | 500 µg 1 mg | $77.00 $115.00 | |||
D-myo-Inositol-1-phosphate, sodium salt, is a carbohydrate derivative characterized by its role in cellular signaling and metabolic pathways. Its phosphate group facilitates interactions with proteins and lipids, influencing membrane dynamics and cellular communication. This compound participates in the inositol phosphate signaling cascade, impacting various physiological processes. Additionally, its solubility in aqueous environments enhances its reactivity and bioavailability, making it a key player in cellular metabolism. | ||||||
H-Trisaccharide | sc-300786 | 1 mg | $250.00 | |||
H-Trisaccharide is a complex carbohydrate that exhibits unique structural properties, enabling it to form specific hydrogen bonds and hydrophobic interactions. Its branched configuration allows for diverse molecular recognition events, influencing enzyme-substrate interactions and facilitating glycosylation processes. The compound's solubility in polar solvents enhances its kinetic reactivity, promoting rapid participation in carbohydrate metabolism and energy transfer pathways within biological systems. | ||||||
D-Mannose-6-phosphate, Disodium Salt | 33068-18-7 | sc-203019 sc-203019A | 50 mg 1 g | $154.00 $740.00 | ||
D-Mannose-6-phosphate, Disodium Salt is a phosphorylated sugar that plays a pivotal role in cellular metabolism. Its phosphate group enhances solubility and facilitates specific enzyme interactions, promoting efficient energy transfer. This compound participates in the mannose metabolic pathway, influencing glycoprotein synthesis and cellular signaling. Its unique structural conformation allows for effective binding with lectins, impacting cell recognition processes and intercellular communication. | ||||||
D-myo-Inositol-1,2,3,5,6-pentaphosphate, sodium salt | sc-223913 sc-223913A | 100 µg 500 µg | $220.00 $992.00 | |||
D-myo-Inositol-1,2,3,5,6-pentaphosphate, sodium salt is a highly phosphorylated carbohydrate that serves as a key regulator in various cellular processes. Its multiple phosphate groups confer a high degree of negative charge, enhancing its interaction with metal ions and proteins. This compound is integral in signaling pathways, particularly inositol phosphate signaling, where it modulates enzyme activity and influences cellular responses. Its unique structure allows for specific binding to proteins, impacting cellular dynamics and metabolic regulation. | ||||||
D-myo-Inositol-1,2,4,5,6-pentaphosphate, sodium salt | sc-223916 sc-223916A | 100 µg 500 µg | $220.00 $992.00 | |||
D-myo-Inositol-1,2,4,5,6-pentaphosphate, sodium salt is a complex carbohydrate characterized by its extensive phosphorylation, which facilitates intricate interactions with cellular components. The presence of multiple phosphate groups enhances its solubility and reactivity, allowing it to participate in diverse biochemical pathways. This compound plays a pivotal role in cellular signaling, influencing processes such as calcium mobilization and protein phosphorylation, thereby affecting metabolic pathways and cellular homeostasis. Its structural versatility enables it to act as a molecular scaffold, promoting specific protein interactions and modulating enzymatic functions. | ||||||
DL-Glyceraldehyde | 56-82-6 | sc-218255 sc-218255A | 1 g 5 g | $148.00 $444.00 | 2 | |
DL-Glyceraldehyde is a triose sugar that serves as a key intermediate in various metabolic pathways, particularly glycolysis. Its unique aldehyde functional group allows for rapid isomerization and participation in aldol reactions, influencing carbohydrate metabolism. The compound exhibits distinct stereochemistry, leading to different reactivity profiles in enzymatic processes. Additionally, its ability to form hemiacetals with alcohols enhances its role in carbohydrate chemistry, contributing to the formation of more complex sugars. | ||||||