Items 341 to 350 of 392 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Conjugated Linoleic Acid, 90%(Mixture of Isomers) | 22880-03-1 | sc-217949 | 50 mg | $360.00 | ||
Conjugated Linoleic Acid, 90% (Mixture of Isomers) showcases potent antioxidant capabilities by engaging in lipid peroxidation inhibition, effectively disrupting the propagation of free radical chains. Its unique isomeric composition allows for selective interactions with cellular membranes, enhancing membrane fluidity and integrity. This compound also modulates signaling pathways related to oxidative stress, contributing to cellular defense mechanisms through its multifaceted reactivity and structural versatility. | ||||||
Balsalazide | 80573-04-2 | sc-210858 | 10 mg | $200.00 | ||
Balsalazide exhibits remarkable antioxidant properties through its ability to scavenge reactive oxygen species, thereby mitigating oxidative damage. Its unique structure facilitates interactions with various biomolecules, promoting stabilization of cellular components. The compound influences redox signaling pathways, enhancing the cellular antioxidant defense system. Additionally, its distinct molecular interactions can alter enzyme activity, further contributing to its protective role against oxidative stress. | ||||||
2-Phenyl-4-quinolinecarboxylic acid | 132-60-5 | sc-225531 | 50 g | $80.00 | ||
2-Phenyl-4-quinolinecarboxylic acid demonstrates significant antioxidant capabilities by effectively neutralizing free radicals and reducing oxidative stress. Its unique quinoline structure allows for strong π-π stacking interactions with other aromatic compounds, enhancing its stability and reactivity. This compound can modulate cellular signaling pathways, influencing gene expression related to oxidative stress response. Furthermore, its ability to chelate metal ions may prevent catalysis of harmful oxidative reactions, reinforcing its protective effects. | ||||||
3,4,5-Trihydroxybenzamide | 618-73-5 | sc-214175 sc-214175A | 5 g 25 g | $50.00 $190.00 | ||
3,4,5-Trihydroxybenzamide exhibits remarkable antioxidant properties through its ability to scavenge reactive oxygen species and inhibit lipid peroxidation. The presence of multiple hydroxyl groups enhances its electron-donating capacity, facilitating the formation of stable radical intermediates. This compound can disrupt oxidative chain reactions by acting as a hydrogen donor, while its structural flexibility allows for effective interactions with various biomolecules, promoting cellular resilience against oxidative damage. | ||||||
Calcium L-ascorbate dihydrate | 5743-28-2 | sc-257212 | 100 g | $42.00 | ||
Calcium L-ascorbate dihydrate serves as a potent antioxidant by stabilizing free radicals through its unique calcium salt structure, which enhances solubility and bioavailability. Its dual role as a vitamin C derivative allows it to regenerate other antioxidants, amplifying its protective effects. The compound's ability to chelate metal ions further reduces oxidative stress, while its dihydrate form contributes to improved stability and prolonged activity in various environments, making it an effective agent in combating oxidative damage. | ||||||
4-Hydroxy-3-methoxycinnamaldehyde | 458-36-6 | sc-232757 sc-232757A | 1 g 5 g | $87.00 $311.00 | ||
4-Hydroxy-3-methoxycinnamaldehyde exhibits remarkable antioxidant properties through its ability to scavenge reactive oxygen species, effectively neutralizing free radicals. Its unique structure allows for specific interactions with lipid membranes, enhancing cellular protection. The compound's electron-rich aromatic system facilitates rapid reaction kinetics, promoting efficient electron transfer. Additionally, it can modulate signaling pathways related to oxidative stress, contributing to its overall protective role in biological systems. | ||||||
Mangostin | 6147-11-1 | sc-211773 | 10 mg | $245.00 | ||
Mangostin is a potent antioxidant characterized by its ability to inhibit lipid peroxidation and protect cellular integrity. Its unique xanthone structure allows for strong interactions with cellular membranes, enhancing stability against oxidative damage. The compound's capacity to chelate metal ions further reduces oxidative stress by preventing the formation of harmful free radicals. Additionally, Mangostin influences gene expression related to antioxidant defense mechanisms, showcasing its multifaceted role in cellular protection. | ||||||
Conjugated Linoleic Acid (10E,12Z) | 2420-56-6 | sc-223898 sc-223898A sc-223898B | 10 mg 25 mg 50 mg | $238.00 $378.00 $672.00 | ||
Conjugated Linoleic Acid (10E,12Z) exhibits remarkable antioxidant properties through its unique conjugated double bond system, which enhances its ability to scavenge free radicals. This compound interacts with lipid membranes, promoting fluidity and stability while mitigating oxidative stress. Its distinct molecular structure facilitates the modulation of signaling pathways involved in inflammation and oxidative damage, contributing to its protective effects at the cellular level. | ||||||
Salvianolic Acid B | 121521-90-2 | sc-212911B sc-212911 sc-212911A sc-212911C | 5 mg 10 mg 25 mg 100 mg | $235.00 $306.00 $551.00 $1837.00 | 6 | |
Salvianolic Acid B is a potent antioxidant characterized by its ability to chelate metal ions, thereby preventing oxidative damage. Its unique polyphenolic structure allows for effective hydrogen atom transfer, stabilizing free radicals and disrupting oxidative chain reactions. This compound also influences cellular signaling pathways, enhancing the expression of endogenous antioxidant enzymes. Its solubility in various solvents further aids in its interaction with biological membranes, promoting cellular resilience against oxidative stress. | ||||||
(S)-ar-Turmerone | 532-65-0 | sc-491935A sc-491935B sc-491935 | 1 mg 5 mg 10 mg | $140.00 $750.00 $800.00 | ||
(S)-ar-Turmerone exhibits remarkable antioxidant properties through its ability to scavenge free radicals and inhibit lipid peroxidation. Its unique structure facilitates electron donation, effectively neutralizing reactive oxygen species. Additionally, (S)-ar-Turmerone can modulate redox-sensitive signaling pathways, enhancing cellular defense mechanisms. Its lipophilic nature allows for efficient integration into lipid membranes, promoting stability and resilience against oxidative challenges. |