Items 141 to 147 of 147 total
Display:
Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
---|---|---|---|---|---|---|
DL-α-Tocopherol acetate | 7695-91-2 | sc-214934D sc-214934 sc-214934A sc-214934B sc-214934C | 5 g 25 g 100 g 500 g 10 g | $20.00 $55.00 $139.00 $475.00 $26.00 | ||
DL-α-Tocopherol acetate, a derivative of vitamin E, exhibits unique antioxidant properties by scavenging free radicals and protecting cellular membranes from oxidative damage. Its lipophilic nature allows it to integrate into lipid bilayers, enhancing membrane stability. Additionally, it participates in the regulation of gene expression related to cellular defense mechanisms. The acetate form provides a stable reservoir, facilitating gradual release and bioavailability in biological systems. | ||||||
Canola oil | 120962-03-0 | sc-211009 sc-211009A sc-211009B | 1 g 10 g 100 g | $74.00 $153.00 $260.00 | ||
Canola oil, rich in unsaturated fatty acids, plays a crucial role in cellular health by supporting the absorption of fat-soluble vitamins. Its unique composition promotes the formation of lipid rafts, enhancing membrane fluidity and facilitating protein interactions. The oil's high levels of omega-3 and omega-6 fatty acids contribute to anti-inflammatory pathways, while its antioxidant compounds help mitigate oxidative stress, promoting overall cellular integrity and function. | ||||||
(+)-δ-Tocopherol | 119-13-1 | sc-216082 sc-216082A | 25 g 100 g | $241.00 $776.00 | ||
(+)-δ-Tocopherol, a form of vitamin E, exhibits potent antioxidant properties, effectively scavenging free radicals and protecting cellular membranes from oxidative damage. Its lipophilic nature allows it to integrate into lipid bilayers, enhancing membrane stability and fluidity. This compound also plays a role in modulating gene expression related to cellular defense mechanisms, influencing pathways that regulate inflammation and cellular aging, thereby supporting overall cellular resilience. | ||||||
Vitamin K5 Hydrochloride | 130-24-5 | sc-296697 sc-296697A | 1 g 5 g | $668.00 $2300.00 | 1 | |
Vitamin K5 Hydrochloride, a synthetic derivative of vitamin K, is notable for its role in promoting electron transfer reactions within biological systems. Its unique structure facilitates interactions with various enzymes involved in the carboxylation of proteins, crucial for blood coagulation. Additionally, it exhibits distinct solubility characteristics, allowing it to participate in diverse biochemical pathways. The compound's reactivity with metal ions can influence its stability and bioavailability, impacting its overall behavior in physiological contexts. | ||||||
(±)-α-Tocopherol nicotinate | 51898-34-1 | sc-216078 sc-216078A | 5 g 25 g | $66.00 $148.00 | ||
(±)-α-Tocopherol nicotinate, a derivative of vitamin E, is distinguished by its antioxidant properties, which stem from its ability to scavenge free radicals and protect cellular membranes. Its unique ester linkage enhances lipid solubility, facilitating its incorporation into biological membranes. This compound also engages in specific molecular interactions that modulate gene expression related to oxidative stress response, contributing to cellular homeostasis and metabolic regulation. | ||||||
DL Carnitine-d9 Chloride | 1219386-75-0 | sc-218251 sc-218251A sc-218251B sc-218251C | 10 mg 25 mg 50 mg 100 mg | $302.00 $567.00 $1123.00 $1995.00 | ||
DL Carnitine-d9 Chloride is a unique compound that plays a pivotal role in fatty acid metabolism. Its structure allows for efficient transport of long-chain fatty acids into mitochondria, where they undergo β-oxidation. The presence of deuterium enhances its stability and alters reaction kinetics, potentially influencing metabolic pathways. Additionally, its ionic nature facilitates interactions with cellular membranes, promoting effective uptake and utilization in energy production processes. | ||||||
Acetic acid | 64-19-7 | sc-214462 sc-214462A | 500 ml 2.5 L | $62.00 $104.00 | 5 | |
Acetic acid, a simple carboxylic acid, plays a pivotal role in metabolic pathways, particularly in the synthesis of acetyl-CoA, a key molecule in energy production. Its ability to donate protons influences pH levels in biological systems, affecting enzyme activity and metabolic rates. The compound's polar nature enhances solubility in water, facilitating its participation in biochemical reactions. Additionally, acetic acid can form esters through condensation reactions, contributing to various biosynthetic processes. |