Oxidative Stress
Items 81 to 90 of 145 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
(±)9-HODE | 98524-19-7 | sc-205184 sc-205184A | 100 µg 500 µg | $155.00 $523.00 | ||
(±)9-HODE is a lipid peroxidation product derived from the oxidation of linoleic acid, playing a significant role in cellular oxidative stress. It interacts with various cellular components, including proteins and lipids, leading to the formation of adducts that can alter membrane fluidity and function. This compound is involved in signaling pathways that modulate inflammation and apoptosis, highlighting its impact on cellular homeostasis and stress responses. | ||||||
Nitisinone | 104206-65-7 | sc-208100 | 10 mg | $98.00 | ||
Nitisinone is a compound that influences oxidative stress by modulating the levels of reactive oxygen species (ROS) within cells. It interacts with key enzymes involved in the oxidative stress response, potentially altering their activity and stability. This modulation can affect cellular redox balance and impact metabolic pathways, leading to changes in energy production and antioxidant defense mechanisms. Its unique structure allows for specific binding interactions that can influence cellular signaling cascades related to oxidative damage. | ||||||
Zinc (II) Deuteroporphyrin IX-2,4-bisethyleneglycol | 119700-81-1 | sc-222426 | 1 mg | $150.00 | ||
Zinc (II) Deuteroporphyrin IX-2,4-bisethyleneglycol plays a significant role in oxidative stress by acting as a potent chelator of metal ions, particularly zinc. This interaction can disrupt metal-dependent enzymatic processes, influencing the generation of reactive oxygen species. Its unique porphyrin structure facilitates electron transfer reactions, enhancing oxidative damage in cellular components. Additionally, it can modulate the activity of antioxidant enzymes, thereby affecting the overall redox state within biological systems. | ||||||
U-83836E | 122003-11-6 | sc-200805 | 100 mg | $109.00 | 1 | |
U-83836E exhibits unique properties in oxidative stress through its ability to form reactive intermediates that engage in selective oxidation reactions. Its structure allows for specific interactions with cellular lipids and proteins, leading to the formation of lipid peroxides and protein carbonyls. This compound can influence signaling pathways by altering redox-sensitive transcription factors, thereby modulating cellular responses to oxidative damage. Its kinetic profile suggests rapid reactivity, contributing to its role in oxidative processes. | ||||||
U-74389G | 153190-29-5 | sc-200804 | 100 mg | $108.00 | 2 | |
U-74389G is a potent antioxidant that modulates oxidative stress through its ability to scavenge free radicals and inhibit lipid peroxidation. Its unique structure allows for selective interactions with reactive species, stabilizing them and preventing cellular damage. The compound also influences signaling pathways related to oxidative stress, enhancing the expression of protective enzymes. Its kinetic profile reveals a rapid reaction with peroxides, effectively mitigating oxidative damage in biological systems. | ||||||
3,3′,5,5′-Tetramethylbenzidine dihydrochloride dihydrate | 207738-08-7 | sc-205527 sc-205527A | 100 mg 1 g | $41.00 $88.00 | ||
3,3',5,5'-Tetramethylbenzidine dihydrochloride dihydrate is a versatile compound that plays a significant role in oxidative stress modulation. Its unique electron-rich structure facilitates rapid redox reactions, allowing it to engage with various reactive oxygen species. The compound exhibits distinct colorimetric properties, enabling real-time monitoring of oxidative processes. Additionally, it can form stable complexes with metal ions, influencing catalytic pathways and enhancing the understanding of oxidative mechanisms in biological systems. | ||||||
ZnAF-2 DA | 357339-96-9 | sc-202858 | 1 mg | $471.00 | 1 | |
ZnAF-2 DA is a distinctive compound that exhibits remarkable reactivity in oxidative stress contexts. Its unique structural features enable it to interact selectively with specific reactive oxygen species, promoting targeted redox reactions. The compound's ability to form transient intermediates enhances its kinetic profile, allowing for rapid electron transfer processes. Furthermore, ZnAF-2 DA's solubility characteristics facilitate its diffusion in biological environments, influencing oxidative pathways and cellular responses. | ||||||
ROS Probe, HPF | 359010-69-8 | sc-222262 | 1 mg | $520.00 | ||
ROS Probe, HPF is a specialized chemical designed to detect and quantify reactive oxygen species in biological systems. Its unique fluorescence properties allow it to emit light upon reaction with specific oxidants, providing a sensitive readout of oxidative stress levels. The probe undergoes selective oxidation, leading to a distinct change in its spectral characteristics. This specificity enhances its utility in studying cellular redox states and the dynamics of oxidative stress responses. | ||||||
APF | 359010-70-1 | sc-202468 | 1 mg | $665.00 | ||
APF is a selective probe that reacts with peroxynitrite, a key player in oxidative stress pathways. Upon interaction, APF undergoes a transformation that enhances its fluorescence, allowing for real-time monitoring of reactive species. This chemical exhibits unique reaction kinetics, with a rapid response to oxidative environments, making it an effective tool for studying cellular mechanisms. Its distinct molecular interactions provide insights into the dynamics of oxidative damage and cellular signaling. | ||||||
9-Mesityl-10-methylacridinium Tetrafluoroborate | 1442433-71-7 | sc-291766 sc-291766A | 1 g 5 g | $210.00 $860.00 | ||
9-Mesityl-10-methylacridinium Tetrafluoroborate serves as a potent indicator of oxidative stress through its unique electron transfer properties. This compound engages in specific redox reactions, facilitating the generation of reactive oxygen species. Its distinctive photophysical characteristics enable it to exhibit enhanced luminescence in oxidative conditions, allowing for the observation of cellular oxidative states. The compound's reactivity with various oxidants highlights its role in elucidating oxidative pathways and mechanisms. | ||||||