Oxidative Stress
Items 11 to 20 of 145 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
D609 | 83373-60-8 | sc-201403 sc-201403A | 5 mg 25 mg | $189.00 $575.00 | 7 | |
D609 is a synthetic compound that exhibits unique properties in the context of oxidative stress. It functions as a selective inhibitor of certain phospholipases, modulating lipid signaling pathways that are crucial in cellular responses to oxidative damage. By altering membrane dynamics and influencing the production of reactive species, D609 can impact cellular signaling cascades. Its ability to interact with specific lipid substrates highlights its role in regulating oxidative stress at the molecular level. | ||||||
2′,7′-Dichlorodihydrofluorescein Diacetate | 4091-99-0 | sc-359840 sc-359840A sc-359840B | 100 mg 250 mg 500 mg | $124.00 $286.00 $416.00 | 40 | |
2′,7′-Dichlorodihydrofluorescein Diacetate is a fluorescent probe that serves as a sensitive indicator of oxidative stress within biological systems. Upon oxidation, it undergoes a transformation that enhances its fluorescence, allowing for real-time monitoring of reactive oxygen species. This compound's unique ability to permeate cell membranes and react with various oxidants makes it a valuable tool for studying redox biology and cellular responses to oxidative challenges. Its reaction kinetics are influenced by the local microenvironment, providing insights into the dynamics of oxidative processes. | ||||||
S-Methyl-L thiocitrulline, Dihydrochloride | 209589-59-3 | sc-3571 | 10 mg | $56.00 | 1 | |
S-Methyl-L thiocitrulline, Dihydrochloride is a compound that plays a significant role in modulating oxidative stress through its unique interactions with thiol groups and reactive nitrogen species. It participates in redox reactions, influencing cellular signaling pathways and the balance of reactive species. Its distinct chemical structure allows for specific binding to target molecules, affecting reaction kinetics and enhancing our understanding of oxidative damage mechanisms in biological systems. | ||||||
Zinc Protoporphyrin-9 | 15442-64-5 | sc-200329 sc-200329A | 25 mg 100 mg | $78.00 $213.00 | 31 | |
Zinc Protoporphyrin-9 is a complex that acts as a potent indicator of oxidative stress, primarily through its ability to chelate metal ions and modulate heme metabolism. Its unique structure facilitates interactions with reactive oxygen species, influencing cellular redox states. By altering electron transfer processes, it impacts various signaling pathways, providing insights into the dynamics of oxidative damage and the cellular response to stressors. | ||||||
Amlodipine | 88150-42-9 | sc-200195 sc-200195A | 100 mg 1 g | $74.00 $166.00 | 2 | |
Amlodipine exhibits unique properties in the context of oxidative stress by modulating calcium channels, which influences intracellular calcium levels and subsequently affects reactive oxygen species production. Its interactions with cellular membranes can alter lipid peroxidation processes, impacting mitochondrial function. Additionally, amlodipine's ability to stabilize endothelial function may mitigate oxidative damage, highlighting its role in cellular redox balance and signaling pathways related to oxidative stress. | ||||||
Dihydrorhodamine 123 | 109244-58-8 | sc-203027 | 10 mg | $175.00 | 25 | |
Dihydrorhodamine 123 serves as a sensitive probe for oxidative stress, undergoing oxidation to form a fluorescent product in the presence of reactive oxygen species. This transformation allows for real-time monitoring of oxidative conditions within cells. Its unique interaction with cellular components enhances its ability to detect changes in redox status, while its rapid reaction kinetics facilitate immediate responses to oxidative stimuli, making it a valuable tool for studying cellular oxidative processes. | ||||||
MnTMPyP pentachloride | 100012-18-8 | sc-221956 sc-221956B sc-221956A | 10 mg 25 mg 50 mg | $57.00 $67.00 $109.00 | 8 | |
MnTMPyP pentachloride is a potent redox-active compound that interacts with reactive oxygen species, facilitating electron transfer processes. Its unique porphyrin structure allows for effective binding to metal ions, influencing oxidative pathways. The compound exhibits distinct reaction kinetics, promoting the generation of reactive intermediates that can amplify oxidative stress responses. Additionally, its ability to modulate cellular signaling pathways highlights its role in redox homeostasis and stress response mechanisms. | ||||||
Methylene blue trihydrate | 7220-79-3 | sc-203744 sc-203744A | 5 g 25 g | $32.00 $62.00 | 3 | |
Methylene blue trihydrate is a versatile redox-active dye that engages in complex electron transfer reactions, significantly impacting oxidative stress dynamics. Its unique structure enables it to act as a photosensitizer, generating reactive oxygen species upon light exposure. This compound can alter cellular redox states, influencing various biochemical pathways. Its affinity for cellular components allows it to modulate oxidative damage, showcasing its role in cellular stress responses. | ||||||
Potassium hexacyanoferrate(III) | 13746-66-2 | sc-203355 sc-203355A sc-203355B sc-203355C sc-203355D sc-203355E | 100 g 250 g 1 kg 2.5 kg 5 kg 10 kg | $43.00 $97.00 $119.00 $234.00 $411.00 $779.00 | ||
Potassium hexacyanoferrate(III) is a potent oxidizing agent that participates in intricate redox reactions, influencing oxidative stress mechanisms. Its unique coordination chemistry allows it to interact with various biomolecules, facilitating electron transfer processes. This compound can stabilize reactive intermediates, affecting reaction kinetics and promoting oxidative pathways. Its distinct ability to form complexes with metal ions enhances its reactivity, contributing to cellular oxidative environments. | ||||||
L-Selenomethionine | 3211-76-5 | sc-204050 sc-204050A | 250 mg 1 g | $223.00 $597.00 | 1 | |
L-Selenomethionine is a naturally occurring amino acid that plays a significant role in modulating oxidative stress through its unique selenium content. It participates in redox reactions, acting as a potent antioxidant by scavenging free radicals. The presence of selenium allows it to influence enzymatic pathways, particularly those involving glutathione metabolism. Its molecular structure enables specific interactions with thiol groups, enhancing its protective effects against oxidative damage. | ||||||