Oxidative Stress
Items 131 to 140 of 145 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
DMNQ | 6956-96-3 | sc-202586 | 10 mg | $245.00 | ||
DMNQ is a potent redox-active compound that plays a critical role in oxidative stress studies. It engages in electron transfer reactions, facilitating the generation of reactive oxygen species (ROS) that can modify cellular components. Its unique ability to interact with various biomolecules, including lipids and proteins, can disrupt cellular homeostasis. Furthermore, DMNQ's kinetics in redox cycling contribute to its effectiveness in altering cellular signaling pathways, underscoring its significance in oxidative stress research. | ||||||
DAF-2 | 205391-01-1 | sc-205910 | 1 mg | $379.00 | 2 | |
DAF-2 is a fluorescent probe that selectively reacts with reactive oxygen species, particularly in oxidative stress contexts. Its unique design allows for specific interactions with cellular components, leading to the formation of stable adducts. The probe's reaction kinetics are finely tuned, enabling real-time monitoring of oxidative changes within cells. DAF-2's distinct photophysical properties enhance its sensitivity, making it a valuable tool for studying oxidative stress dynamics in biological systems. | ||||||
N-Oxalyl-L-alanine | 5302-46-5 | sc-205959 sc-205959A | 10 mg 50 mg | $42.00 $125.00 | ||
N-Oxalyl-L-alanine is a compound that plays a significant role in modulating oxidative stress through its ability to interact with various cellular pathways. It exhibits unique reactivity with free radicals, facilitating the formation of transient intermediates that can influence cellular redox states. The compound's structural features allow it to engage in specific molecular interactions, potentially altering enzyme activities and metabolic processes. Its behavior as an acid halide contributes to its reactivity profile, making it a noteworthy subject in oxidative stress research. | ||||||
14(S)-HDoHE | 119433-37-3 | sc-489491 sc-489491A | 25 µg 50 µg | $88.00 $126.00 | ||
14(S)-HDoHE is a bioactive lipid that significantly influences oxidative stress by modulating cellular signaling pathways. Its unique structure allows for specific interactions with lipid membranes, enhancing the formation of reactive oxygen species. This compound participates in lipid peroxidation processes, leading to the generation of secondary metabolites that can further impact cellular redox balance. Its distinct reactivity and ability to engage in complex molecular interactions make it a critical player in oxidative stress dynamics. | ||||||
2-Thioxanthine | 2487-40-3 | sc-280287 sc-280287A | 1 g 5 g | $147.00 $480.00 | ||
2-Thioxanthine is a heterocyclic compound that plays a significant role in oxidative stress through its ability to scavenge free radicals and modulate redox-sensitive signaling pathways. Its unique sulfur atom enhances electron donation, facilitating interactions with reactive species. This compound can influence the stability of cellular membranes and alter the kinetics of oxidative reactions, contributing to the overall balance of oxidative and reductive processes within cells. | ||||||
L-Buthionine-(S,R)-Sulfoximine | 83730-53-4 | sc-218630 sc-218630A sc-218630B sc-218630C | 500 mg 1 g 5 g 10 g | $222.00 $414.00 $1638.00 $2760.00 | 2 | |
L-Buthionine-(S,R)-Sulfoximine is a potent inhibitor of gamma-glutamylcysteine synthetase, crucial for glutathione synthesis. By disrupting this pathway, it elevates oxidative stress levels, leading to increased reactive oxygen species. Its unique sulfoximine group enhances its reactivity, allowing it to interact with thiol groups in proteins, potentially altering their function. This compound's influence on cellular redox state can significantly impact metabolic processes and stress responses. | ||||||
2′-Deoxyguanosine-13C10,15N5 | 961-07-9 (unlabeled) | sc-500624 | 1 mg | $700.00 | ||
2′-Deoxyguanosine-13C10,15N5 is a nucleoside analog that exhibits unique behavior in oxidative stress contexts by participating in DNA repair mechanisms. Its isotopic labeling allows for precise tracking of metabolic pathways and interactions with reactive oxygen species. This compound can influence the stability of nucleic acids, potentially altering the kinetics of oxidative damage and repair processes. Its incorporation into DNA may affect gene expression and cellular responses to oxidative challenges. | ||||||
(R)-3-Hydroxymyristic Acid | 28715-21-1 | sc-208231A sc-208231B sc-208231C sc-208231 sc-208231D sc-208231E | 10 mg 25 mg 50 mg 100 mg 500 mg 1 g | $138.00 $199.00 $301.00 $403.00 $1637.00 $2861.00 | 2 | |
(R)-3-Hydroxymyristic Acid is a fatty acid that plays a significant role in modulating oxidative stress through its unique interactions with cellular membranes and signaling pathways. Its hydroxyl group enhances hydrogen bonding, promoting fluidity and altering membrane dynamics. This compound can influence lipid peroxidation processes, leading to the generation of reactive oxygen species. Additionally, it may affect the activity of antioxidant enzymes, thereby impacting cellular redox balance and stress response mechanisms. | ||||||
Chromone | 491-38-3 | sc-234357 | 5 g | $49.00 | ||
Chromone is a versatile compound that plays a critical role in oxidative stress through its ability to form adducts with reactive oxygen species. Its unique structure facilitates interactions with various biomolecules, influencing redox signaling pathways. Chromone can enhance the activity of certain enzymes involved in oxidative processes, thereby altering reaction kinetics. Additionally, it exhibits properties that can stabilize free radicals, impacting cellular homeostasis and stress responses. | ||||||
(±)5-iPF2α-VI-d11 | 936565-17-2 | sc-221031 sc-221031A | 10 µg 25 µg | $600.00 $1405.00 | ||
(±)5-iPF2α-VI-d11 is a potent marker of oxidative stress, engaging in specific interactions with lipid peroxidation products. This compound can modulate signaling pathways related to inflammation and cellular response to oxidative damage. Its unique isotopic labeling facilitates the study of reactive species dynamics, providing insights into the kinetics of oxidative processes. Additionally, it may influence cellular redox states, impacting overall cellular homeostasis. | ||||||