Items 91 to 100 of 145 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Necrosis Inhibitor, IM-54 | 861891-50-1 | sc-222053A sc-222053 | 1 mg 5 mg | $47.00 $186.00 | 6 | |
Necrosis Inhibitor, IM-54, acts as a selective modulator of oxidative stress by disrupting key signaling pathways involved in cellular damage. Its unique ability to form stable adducts with reactive species alters the kinetics of oxidative reactions, effectively reducing the accumulation of harmful byproducts. The compound's interactions with cellular components can influence redox homeostasis, providing insights into the mechanisms of necrosis and cellular resilience under stress conditions. | ||||||
MitoPBN | 652968-37-1 | sc-221946 | 10 mg | $366.00 | ||
MitoPBN is a potent antioxidant that engages in specific interactions with reactive oxygen species, effectively scavenging free radicals and mitigating oxidative damage. Its unique structure allows it to penetrate mitochondrial membranes, where it modulates mitochondrial function and enhances cellular defense mechanisms. By influencing electron transport chain dynamics, MitoPBN alters the balance of reactive species, promoting a more favorable redox environment and supporting cellular integrity under oxidative stress. | ||||||
GERI-BP002-A | 119-47-1 | sc-221667 sc-221667A | 100 mg 1 g | $43.00 $102.00 | ||
GERI-BP002-A is a novel compound that exhibits remarkable properties in the context of oxidative stress. It selectively interacts with key cellular components, facilitating the modulation of redox-sensitive signaling pathways. Its unique reactivity profile allows it to form stable adducts with reactive oxygen species, effectively reducing their availability. Additionally, GERI-BP002-A influences the kinetics of oxidative reactions, enhancing the resilience of cellular systems against oxidative challenges. | ||||||
PPA | 13159-16-5 | sc-222185 sc-222185A | 500 µg 1 mg | $96.00 $150.00 | ||
PPA is a distinctive compound that plays a significant role in oxidative stress by engaging in specific interactions with biomolecules. It acts as a potent scavenger of free radicals, altering the dynamics of oxidative processes. Its ability to form transient intermediates with reactive species leads to a modulation of cellular redox states. Furthermore, PPA influences electron transfer mechanisms, thereby impacting the overall oxidative stress response in various biological systems. | ||||||
8,12-iso-iPF2α-VI 1,5- lactone | sc-221153 sc-221153A | 25 µg 50 µg | $123.00 $237.00 | |||
8,12-iso-iPF2α-VI 1,5-lactone is a unique compound that significantly contributes to oxidative stress through its intricate molecular interactions. It participates in the formation of lipid peroxidation products, which can disrupt cellular membranes and signaling pathways. This compound exhibits distinct reactivity with nucleophiles, influencing the stability of cellular components. Additionally, its kinetic behavior in redox reactions highlights its role in modulating oxidative damage and cellular responses. | ||||||
Azelaoyl-PAF | 354583-69-0 | sc-221278 sc-221278A | 1 mg 5 mg | $200.00 $440.00 | ||
Azelaoyl-PAF is a notable compound in the context of oxidative stress, characterized by its ability to engage in complex redox reactions. It interacts with various biomolecules, leading to the generation of reactive oxygen species that can compromise cellular integrity. Its unique structural features facilitate specific binding to lipid membranes, altering their fluidity and function. The compound's reactivity with thiols and other nucleophiles further underscores its role in modulating oxidative pathways and cellular signaling. | ||||||
9-(2-Biphenylyl)-10-methylacridinium Perchlorate | sc-291756 sc-291756A | 1 g 5 g | $242.00 $746.00 | |||
9-(2-Biphenylyl)-10-methylacridinium Perchlorate is a distinctive compound in oxidative stress research, known for its potent electron-accepting properties. It readily participates in one-electron transfer reactions, generating reactive intermediates that can initiate lipid peroxidation. Its planar structure enhances π-π stacking interactions with nucleic acids, potentially disrupting cellular processes. Additionally, its ability to form stable complexes with metal ions can influence redox homeostasis, impacting cellular signaling pathways. | ||||||
9-(2,5-Dimethylphenyl)-10-methylacridinium Perchlorate | sc-291758 sc-291758A | 1 g 5 g | $242.00 $726.00 | |||
9-(2,5-Dimethylphenyl)-10-methylacridinium Perchlorate is a notable compound in oxidative stress studies, characterized by its strong propensity to engage in redox cycling. This compound can facilitate the generation of reactive oxygen species through its unique electron transfer dynamics, leading to oxidative damage in biomolecules. Its bulky aromatic structure promotes hydrophobic interactions, potentially altering membrane integrity and influencing cellular signaling cascades. Furthermore, its reactivity with thiols can disrupt antioxidant defenses, exacerbating oxidative stress conditions. | ||||||
9-Mesityl-2,7,10-trimethylacridinium Perchlorate | sc-291767 | 1 g | $471.00 | |||
9-Mesityl-2,7,10-trimethylacridinium Perchlorate is a significant player in oxidative stress research, exhibiting a unique ability to undergo rapid electron transfer processes. Its intricate molecular structure enhances its interaction with cellular components, promoting the formation of reactive oxygen species. This compound's distinctive hydrophobic characteristics can disrupt lipid bilayers, affecting membrane fluidity and cellular homeostasis. Additionally, its reactivity with various biomolecules can lead to the depletion of critical antioxidants, intensifying oxidative stress responses. | ||||||
Ammonium cerium(IV) nitrate on silica gel | sc-319820 | 25 g | $390.00 | |||
Ammonium cerium(IV) nitrate on silica gel serves as a potent oxidative stress agent, characterized by its ability to facilitate electron transfer reactions. This compound exhibits a strong affinity for hydroxyl radicals, promoting their generation and enhancing oxidative damage to cellular structures. Its unique interaction with biomolecules can lead to the modification of proteins and lipids, disrupting cellular signaling pathways. The solid-state form on silica gel also influences its reactivity, allowing for controlled release and targeted oxidative effects. | ||||||