Items 71 to 80 of 147 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Oxythiamine chloride hydrochloride | 614-05-1 | sc-236265 sc-236265A sc-236265B | 1 g 5 g 25 g | $39.00 $119.00 $437.00 | 2 | |
Oxythiamine chloride hydrochloride is a derivative of thiamine, playing a crucial role in carbohydrate metabolism. It enhances the activity of enzymes involved in the decarboxylation of alpha-keto acids, facilitating energy production. This compound also exhibits unique interactions with thiamine transporters, influencing its bioavailability. Furthermore, its chloride component may enhance solubility, promoting efficient absorption in biological systems, thereby impacting metabolic pathways. | ||||||
Riboflavin Tetrabutyrate | 752-56-7 | sc-296266 sc-296266A | 5 g 25 g | $60.00 $277.00 | ||
Riboflavin Tetrabutyrate is a derivative of riboflavin that showcases unique interactions with cellular membranes, enhancing lipid solubility and facilitating its transport across biological barriers. This compound participates in various metabolic pathways, particularly in the oxidation-reduction reactions essential for energy production. Its butyrate moieties may influence gene expression and cellular signaling, contributing to its distinct biochemical behavior. Additionally, it exhibits stability under diverse conditions, making it an intriguing subject for further study. | ||||||
Pterine-6-carboxylic acid | 948-60-7 | sc-215760 | 100 mg | $173.00 | ||
Pterine-6-carboxylic acid is a pivotal compound in the biosynthesis of folate derivatives, playing a crucial role in one-carbon metabolism. Its carboxylic acid group enhances solubility in aqueous environments, promoting effective interactions with enzymes involved in metabolic pathways. This compound can participate in various enzymatic reactions, influencing the kinetics of folate synthesis. Its structural features allow for specific binding interactions, potentially modulating cellular processes and signaling pathways. | ||||||
α-CEHC | sc-222430 sc-222430A | 1 mg 5 mg | $44.00 $146.00 | |||
α-CEHC is a potent antioxidant that exhibits unique interactions with lipid membranes, enhancing their fluidity and stability. It participates in redox reactions, effectively scavenging free radicals and mitigating oxidative stress. This compound also influences gene expression by modulating transcription factors, thereby impacting metabolic pathways. Its lipophilic nature allows for efficient incorporation into cellular structures, promoting cellular resilience and functionality. | ||||||
O-Phosphorylethanolamine | 1071-23-4 | sc-215612 sc-215612A sc-215612B | 1 g 5 g 25 g | $27.00 $37.00 $115.00 | ||
O-Phosphorylethanolamine is a significant compound in cellular signaling and membrane dynamics. Its phosphoryl group facilitates interactions with lipid bilayers, enhancing membrane fluidity and stability. This compound is involved in the regulation of phospholipid metabolism, influencing the synthesis of key membrane components. Its unique structure allows for specific binding to proteins, potentially modulating enzymatic activity and cellular communication pathways. | ||||||
Folinic acid calcium salt | 1492-18-8 | sc-252837 sc-252837A | 100 mg 500 mg | $92.00 $368.00 | 3 | |
Folinic acid calcium salt plays a crucial role in one-carbon metabolism, acting as a cofactor in various enzymatic reactions. Its unique structure allows it to participate in the synthesis of nucleotides and amino acids, influencing cellular growth and division. The calcium salt form enhances solubility and stability, facilitating its transport across biological membranes. This compound also exhibits distinct interactions with folate receptors, impacting cellular uptake and bioavailability. | ||||||
Choline Bromide | 1927-06-6 | sc-294026 | 25 g | $98.00 | ||
Choline bromide is a quaternary ammonium compound that serves as a vital source of choline, essential for neurotransmitter synthesis and lipid metabolism. Its unique ionic structure enhances solubility in aqueous environments, promoting efficient cellular uptake. The bromide ion contributes to its stability and reactivity, facilitating interactions with various biological molecules. This compound also plays a role in methylation processes, influencing gene expression and cellular signaling pathways. | ||||||
D-α-Tocopheryl Succinate | 4345-03-3 | sc-200141 sc-200141A sc-200141B sc-200141C sc-200141D | 1 g 5 g 25 g 100 g 1 kg | $42.00 $49.00 $112.00 $333.00 $3066.00 | ||
D-α-Tocopheryl Succinate is a derivative of vitamin E, characterized by its esterified form that enhances its stability and bioavailability. This compound exhibits unique antioxidant properties, effectively scavenging free radicals and protecting cellular membranes from oxidative stress. Its lipophilic nature allows for integration into lipid bilayers, influencing membrane fluidity and function. Additionally, it participates in cellular signaling pathways, modulating gene expression and promoting cellular health. | ||||||
Retinyl propionate | 7069-42-3 | sc-236667 sc-236667A | 25 g 100 g | $104.00 $330.00 | 1 | |
Retinyl propionate is an ester of retinol, notable for its role in skin health and cellular processes. This compound undergoes hydrolysis to release retinol, which then interacts with nuclear receptors, influencing gene transcription related to cell differentiation and proliferation. Its lipophilic characteristics facilitate incorporation into lipid environments, enhancing its stability and absorption. The compound also exhibits unique photochemical properties, making it responsive to light, which can affect its reactivity and efficacy in biological systems. | ||||||
Inositol | 6917-35-7 | sc-394417 | 100 g | $77.00 | ||
Inositol is a versatile carbohydrate that plays a crucial role in cellular signaling and membrane formation. Its unique stereochemistry allows it to interact with phospholipids, influencing membrane fluidity and integrity. Inositol is involved in the synthesis of inositol phosphates, which act as secondary messengers in various signaling pathways. This compound also participates in lipid metabolism, contributing to the regulation of fat storage and energy balance within cells. |