Oxidative Stress
Items 31 to 40 of 145 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
N-Oxalylglycine | 5262-39-5 | sc-202720 sc-202720A | 10 mg 100 mg | $53.00 $153.00 | 5 | |
N-Oxalylglycine is a compound that influences oxidative stress through its ability to chelate metal ions, thereby reducing the availability of catalysts for reactive oxygen species formation. Its unique structure allows it to interact with various cellular components, modulating enzymatic activities linked to oxidative pathways. By altering the kinetics of redox reactions, N-Oxalylglycine can impact cellular homeostasis and stress response mechanisms, showcasing its role in maintaining oxidative balance. | ||||||
(+)-Taxifolin | 17654-26-1 | sc-202829 sc-202829A | 10 mg 50 mg | $38.00 $130.00 | ||
(+)-Taxifolin is a flavonoid that exhibits potent antioxidant properties, effectively scavenging free radicals and mitigating oxidative stress. Its unique hydroxyl groups facilitate strong interactions with reactive species, enhancing its ability to stabilize and neutralize them. Additionally, (+)-Taxifolin can modulate signaling pathways related to oxidative stress, influencing gene expression and cellular defense mechanisms. This compound's dynamic reactivity contributes to its role in cellular protection against oxidative damage. | ||||||
Diethyldithiocarbamic acid sodium salt trihydrate | 20624-25-3 | sc-202576 sc-202576A | 5 g 25 g | $19.00 $59.00 | 2 | |
Diethyldithiocarbamic acid sodium salt trihydrate is a versatile compound known for its ability to chelate metal ions, which plays a crucial role in modulating oxidative stress. By forming stable complexes with transition metals, it inhibits Fenton-type reactions that generate harmful free radicals. Its unique dithiocarbamate structure allows for selective interactions with various biological targets, influencing redox balance and cellular signaling pathways. This compound's kinetic properties enhance its reactivity, making it a significant player in oxidative stress modulation. | ||||||
12(S)-HHT | 54397-84-1 | sc-200969 sc-200969A | 50 µg 250 µg | $332.00 $1665.00 | ||
12(S)-HHT is a bioactive lipid that plays a pivotal role in oxidative stress through its unique interactions with cellular signaling pathways. It is known to influence the production of reactive oxygen species by modulating the activity of specific enzymes involved in lipid peroxidation. Its distinct stereochemistry allows for selective binding to receptors, impacting inflammatory responses and cellular redox states. The compound's reactivity is characterized by rapid kinetics, facilitating its role in cellular defense mechanisms against oxidative damage. | ||||||
Trihydroxyethylrutin | 7085-55-4 | sc-203301 sc-203301A sc-203301B sc-203301C | 5 g 25 g 100 g 1 kg | $30.00 $74.00 $300.00 $800.00 | 1 | |
Trihydroxyethylrutin is a flavonoid derivative that exhibits significant antioxidant properties by scavenging free radicals and chelating metal ions, thereby mitigating oxidative stress. Its unique hydroxyl groups enhance its ability to interact with lipid membranes, promoting stability and reducing lipid peroxidation. The compound also influences gene expression related to oxidative stress response, engaging in complex signaling pathways that regulate cellular homeostasis and protect against oxidative damage. | ||||||
(±)20-HDoHE | 90906-41-5 | sc-205101 sc-205101A | 25 µg 50 µg | $80.00 $154.00 | ||
(±)20-HDoHE is a bioactive lipid mediator that plays a pivotal role in modulating oxidative stress through its unique interactions with cellular membranes. It participates in the formation of reactive oxygen species, influencing lipid peroxidation and cellular signaling pathways. Its distinct structure allows for specific binding to proteins involved in oxidative stress responses, thereby altering their activity and contributing to the regulation of inflammatory processes. | ||||||
FDMPO | sc-221609 | 10 mg | $275.00 | |||
FDMPO is a chemical that acts as a potent modulator of oxidative stress, engaging in specific interactions with cellular components. It facilitates the generation of reactive species, impacting redox signaling pathways. Its unique structure enables it to interact with various biomolecules, influencing their conformation and function. This interaction can lead to alterations in cellular responses to oxidative damage, highlighting its role in the intricate balance of oxidative and reductive processes within biological systems. | ||||||
Tetrahydro Curcumin | 36062-04-1 | sc-391609 | 1 g | $297.00 | 1 | |
Tetrahydro Curcumin is a unique compound that exhibits significant antioxidant properties, effectively scavenging free radicals and reducing oxidative stress. Its molecular structure allows for enhanced electron donation, facilitating interactions with reactive oxygen species. This compound influences cellular signaling pathways by modulating the activity of key enzymes involved in redox homeostasis. Additionally, its stability and solubility in biological systems enhance its capacity to mitigate oxidative damage, contributing to cellular resilience. | ||||||
Neobavaisoflavone | 41060-15-5 | sc-202728 | 1 mg | $142.00 | ||
Neobavaisoflavone is a distinctive compound known for its ability to modulate oxidative stress through specific interactions with cellular components. It engages in redox cycling, promoting the reduction of reactive species while stabilizing free radicals. Its unique structural features enable it to influence gene expression related to oxidative stress responses. Furthermore, Neobavaisoflavone's affinity for metal ions enhances its role in chelating harmful oxidants, thereby contributing to cellular protection mechanisms. | ||||||
Trimethylamine N-oxide dihydrate | 62637-93-8 | sc-296626 sc-296626A | 25 g 500 g | $87.00 $713.00 | ||
Trimethylamine N-oxide dihydrate is a notable compound that influences oxidative stress by participating in electron transfer processes. Its unique structure allows it to interact with various biomolecules, facilitating the modulation of redox states within cells. This compound can enhance the stability of reactive oxygen species, thereby influencing cellular signaling pathways. Additionally, its hydrophilic nature aids in solvation dynamics, impacting reaction kinetics and the overall oxidative environment. | ||||||