Items 231 to 240 of 392 total
Display:
Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
---|---|---|---|---|---|---|
PAPA NONOate | 146672-58-4 | sc-202272 sc-202272A | 5 mg 25 mg | $37.00 $109.00 | 8 | |
PAPA NONOate functions as a robust antioxidant through its ability to scavenge free radicals, effectively mitigating oxidative damage. Its distinctive molecular architecture facilitates the formation of stable adducts with reactive species, thereby interrupting harmful chain reactions. Furthermore, PAPA NONOate can modulate redox-sensitive signaling pathways, promoting cellular resilience against oxidative stress. Its interactions with lipid membranes also contribute to its protective effects, enhancing overall cellular stability. | ||||||
Secoisolariciresinol diglucoside | 148244-82-0 | sc-286769 sc-286769A | 5 mg 10 mg | $360.00 $600.00 | ||
Secoisolariciresinol diglucoside exhibits potent antioxidant properties by engaging in electron donation, which neutralizes free radicals and reduces oxidative stress. Its unique glycosidic structure allows for effective interaction with lipid peroxidation products, stabilizing cellular membranes. Additionally, it influences gene expression related to antioxidant defense mechanisms, enhancing the body's natural resilience. The compound's ability to form complexes with metal ions further contributes to its protective role against oxidative damage. | ||||||
U-74389G | 153190-29-5 | sc-200804 | 100 mg | $108.00 | 2 | |
U-74389G functions as a robust antioxidant by scavenging reactive oxygen species through its unique ability to donate electrons, thereby interrupting oxidative chain reactions. Its distinctive molecular structure facilitates interactions with lipid bilayers, promoting membrane integrity. Furthermore, U-74389G modulates signaling pathways associated with oxidative stress responses, enhancing cellular resilience. Its kinetic profile allows for rapid engagement with free radicals, optimizing its protective effects in various environments. | ||||||
dimethoxy Curcumin | 160096-59-3 | sc-205217 sc-205217A sc-205217B | 1 mg 5 mg 10 mg | $45.00 $171.00 $265.00 | 1 | |
Dimethoxy Curcumin exhibits potent antioxidant properties through its ability to chelate metal ions, thereby reducing oxidative stress. Its unique molecular configuration allows for effective interaction with cellular membranes, enhancing stability and fluidity. Additionally, it influences gene expression related to antioxidant defenses, promoting a balanced redox state. The compound's reactivity with free radicals is characterized by a rapid kinetic response, ensuring timely protection against oxidative damage. | ||||||
Ro 48-8071 | 161582-11-2 | sc-205492 sc-205492A | 5 mg 10 mg | $50.00 $125.00 | 2 | |
Ro 48-8071 functions as a robust antioxidant by engaging in electron transfer mechanisms that neutralize reactive oxygen species. Its unique structural features facilitate strong interactions with lipid bilayers, enhancing membrane integrity. The compound exhibits selective reactivity with specific radicals, leading to a cascade of protective responses at the cellular level. Furthermore, its stability under various conditions allows for sustained antioxidant activity, contributing to its effectiveness in mitigating oxidative stress. | ||||||
Sauchinone | 177931-17-8 | sc-222288 sc-222288A | 1 mg 5 mg | $36.00 $192.00 | ||
Sauchinone acts as a potent antioxidant through its ability to scavenge free radicals, effectively disrupting oxidative chain reactions. Its unique molecular structure allows for specific interactions with metal ions, which can enhance its reactivity and stability. Additionally, Sauchinone influences cellular signaling pathways, modulating the expression of antioxidant enzymes. This compound's lipophilic nature enables it to integrate into cellular membranes, providing localized protection against oxidative damage. | ||||||
EUK 118 | 186299-34-3 | sc-205319 sc-205319A | 5 mg 50 mg | $50.00 $400.00 | ||
EUK 118 functions as a robust antioxidant by mimicking the activity of superoxide dismutase and catalase, facilitating the conversion of harmful reactive oxygen species into less harmful molecules. Its unique dual-enzyme-like properties allow it to engage in rapid redox cycling, enhancing its efficiency in neutralizing oxidative stress. The compound's amphiphilic characteristics enable it to interact with both hydrophilic and lipophilic environments, promoting widespread cellular protection. | ||||||
Succinobucol | 216167-82-7 | sc-391465 sc-391465A sc-391465B sc-391465C | 50 mg 100 mg 250 mg 500 mg | $360.00 $573.00 $1380.00 $2290.00 | 1 | |
Succinobucol acts as a potent antioxidant through its ability to scavenge free radicals and inhibit lipid peroxidation. Its unique structure allows for effective electron donation, stabilizing reactive species and preventing cellular damage. The compound's interactions with cellular membranes enhance its bioavailability, while its capacity to modulate redox signaling pathways contributes to its protective effects against oxidative stress. This multifaceted behavior underscores its significance in maintaining cellular integrity. | ||||||
SOTS-1 | 223507-96-8 | sc-205511 sc-205511A sc-205511B sc-205511C | 500 µg 1 mg 5 mg 10 mg | $37.00 $52.00 $225.00 $375.00 | 2 | |
SOTS-1 exhibits remarkable antioxidant properties by engaging in specific electron transfer mechanisms that neutralize reactive oxygen species. Its unique molecular architecture facilitates strong interactions with lipid bilayers, enhancing its stability and distribution within biological systems. Additionally, SOTS-1 influences key signaling pathways by modulating the activity of redox-sensitive proteins, thereby playing a crucial role in cellular defense against oxidative damage. Its kinetic profile allows for rapid reaction with oxidants, further amplifying its protective capabilities. | ||||||
(+)-Catechin monohydrate | 225937-10-0 | sc-202523 | 1 g | $69.00 | ||
(+)-Catechin monohydrate serves as a potent antioxidant through its ability to scavenge free radicals via hydrogen atom transfer, effectively disrupting oxidative chain reactions. Its polyphenolic structure enables strong chelation of metal ions, reducing their pro-oxidant activity. The compound also exhibits a unique capacity to stabilize lipid peroxidation products, thereby preserving cellular integrity. Furthermore, its solubility in aqueous environments enhances its bioavailability, promoting efficient interaction with cellular components. |