Items 1 to 10 of 138 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
D-Sorbitol | 50-70-4 | sc-203278A sc-203278 | 100 g 1 kg | $28.00 $68.00 | ||
D-Sorbitol is a sugar alcohol that exhibits unique interactions with cellular membranes and proteins, influencing osmotic balance and cellular hydration. Its hydroxyl groups facilitate hydrogen bonding, enhancing solubility and stability in aqueous environments. D-Sorbitol participates in metabolic pathways, acting as a substrate for various enzymes, which can modulate energy production and carbohydrate metabolism. Its ability to form complexes with other biomolecules further underscores its role in biochemical processes. | ||||||
Thymoquinone | 490-91-5 | sc-215986 sc-215986A | 1 g 5 g | $46.00 $130.00 | 21 | |
Thymoquinone is a bioactive compound derived from the seeds of Nigella sativa, known for its distinctive antioxidant properties. It engages in redox reactions, scavenging free radicals and modulating oxidative stress. Thymoquinone can influence signaling pathways, particularly those related to inflammation and apoptosis, by interacting with specific receptors and enzymes. Its lipophilic nature allows it to permeate cell membranes, enhancing its bioavailability and efficacy in various biological contexts. | ||||||
p-Coumaric acid | 501-98-4 | sc-215648 sc-215648A sc-215648B sc-215648C sc-215648D | 1 g 5 g 25 g 100 g 500 g | $27.00 $40.00 $80.00 $290.00 $918.00 | 5 | |
p-Coumaric acid is a phenolic compound that plays a significant role in plant metabolism and defense mechanisms. It participates in the phenylpropanoid pathway, contributing to the synthesis of flavonoids and lignin, which are crucial for plant structure and protection. Its ability to form hydrogen bonds enhances its solubility in polar solvents, facilitating interactions with various biomolecules. Additionally, p-Coumaric acid exhibits antioxidant activity, effectively neutralizing reactive oxygen species and stabilizing cellular environments. | ||||||
D(+)Glucose, Anhydrous | 50-99-7 | sc-211203 sc-211203B sc-211203A | 250 g 5 kg 1 kg | $37.00 $194.00 $64.00 | 5 | |
D(+)Glucose, Anhydrous is a simple sugar that serves as a primary energy source in various biological processes. It participates in glycolysis, where it undergoes enzymatic conversion to produce ATP, highlighting its role in cellular respiration. The molecule's hydroxyl groups enable extensive hydrogen bonding, enhancing its solubility in water and facilitating interactions with proteins and enzymes. Its structural configuration allows for diverse isomerization, influencing metabolic pathways and energy dynamics in living organisms. | ||||||
Rutin trihydrate | 250249-75-3 | sc-204897 sc-204897A sc-204897B | 5 g 50 g 100 g | $56.00 $71.00 $124.00 | 7 | |
Rutin trihydrate is a flavonoid glycoside known for its complex interactions with cellular components. Its unique structure allows for strong antioxidant activity, scavenging free radicals and modulating oxidative stress pathways. The molecule's ability to form stable complexes with metal ions enhances its role in cellular signaling. Additionally, its solubility in water, attributed to multiple hydroxyl groups, facilitates its transport across biological membranes, influencing various physiological processes. | ||||||
β-Eudesmol | 473-15-4 | sc-235107 sc-235107A | 10 mg 1 g | $218.00 $10914.00 | 1 | |
β-Eudesmol is a sesquiterpene alcohol characterized by its unique structural conformation, which enables it to engage in specific hydrophobic interactions with lipid membranes. This compound exhibits notable volatility, contributing to its role in plant defense mechanisms. Its ability to influence gene expression through modulation of signaling pathways highlights its importance in plant physiology. Furthermore, β-Eudesmol's distinct stereochemistry allows for selective binding to receptors, impacting various biological processes. | ||||||
Cyanidin chloride | 528-58-5 | sc-202559 sc-202559A | 10 mg 50 mg | $227.00 $897.00 | 7 | |
Cyanidin chloride is a flavonoid compound known for its vibrant pigmentation, which arises from its unique chromophore structure. This compound exhibits strong antioxidant properties, engaging in electron transfer reactions that neutralize free radicals. Its interactions with metal ions can enhance stability and solubility, influencing its behavior in various environments. Additionally, cyanidin chloride can modulate cellular signaling pathways, affecting plant responses to stress and environmental changes. | ||||||
β-Carotene | 7235-40-7 | sc-202485 sc-202485A sc-202485B sc-202485C | 1 g 25 g 50 g 5 kg | $68.00 $297.00 $502.00 $12246.00 | 5 | |
β-Carotene is a carotenoid pigment characterized by its distinctive conjugated double bond system, which contributes to its vibrant orange color. This structure allows for efficient light absorption, playing a crucial role in photosynthesis. As a potent antioxidant, β-Carotene can quench singlet oxygen and scavenge free radicals, thereby protecting cellular components. Its lipophilic nature facilitates incorporation into lipid membranes, influencing membrane fluidity and functionality. | ||||||
Phytic acid sodium salt | 14306-25-3 | sc-250718 sc-250718A | 10 g 25 g | $57.00 $90.00 | ||
Phytic acid sodium salt, a naturally occurring phytochemical, exhibits unique chelating properties, binding metal ions such as calcium, magnesium, and iron. This interaction can modulate mineral bioavailability, influencing nutrient absorption in biological systems. Its ability to form stable complexes enhances its role in various biochemical pathways, while its hydrophilic nature allows for solubility in aqueous environments, facilitating diverse applications in food chemistry and plant biology. | ||||||
(-)-Perillyl Alcohol | 18457-55-1 | sc-205798 sc-205798A | 10 g 50 g | $154.00 $462.00 | ||
(-)-Perillyl Alcohol is a monoterpene alcohol known for its distinctive structural features that enable it to interact with cellular membranes and proteins. Its hydrophobic character allows it to integrate into lipid bilayers, potentially influencing membrane fluidity and permeability. Additionally, it can modulate signaling pathways by interacting with specific receptors, impacting gene expression and cellular responses. Its unique stereochemistry contributes to its reactivity and potential for diverse biological interactions. | ||||||