Antioxidants
Items 131 to 140 of 392 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Necrox-2 | sc-391057 sc-391057A | 1 mg 5 mg | $143.00 $491.00 | 5 | ||
Necrox-2 functions as a potent antioxidant by engaging in complex electron transfer processes that neutralize free radicals. Its unique structural features enable it to form stable complexes with metal ions, thereby preventing oxidative catalysis. The compound's ability to interact with various biomolecules enhances its protective effects against oxidative stress. Furthermore, Necrox-2 modulates key signaling pathways, influencing cellular responses to oxidative challenges. | ||||||
Naringenin | 480-41-1 | sc-219338 | 25 g | $245.00 | 11 | |
Naringenin is a flavonoid that exhibits potent antioxidant properties by modulating cellular oxidative stress. Its unique structure facilitates interactions with lipid membranes, enhancing membrane fluidity and stability. Naringenin can chelate metal ions, reducing their availability for catalyzing harmful oxidative reactions. Furthermore, it influences the expression of antioxidant enzymes, promoting a cellular environment that mitigates oxidative damage and supports overall cellular health. | ||||||
Didox | 69839-83-4 | sc-221539 sc-221539A | 1 mg 5 mg | $20.00 $72.00 | ||
Didox acts as a robust antioxidant through its ability to scavenge reactive oxygen species, effectively disrupting oxidative chain reactions. Its distinctive molecular structure allows for the formation of hydrogen bonds with cellular components, enhancing its stability and reactivity. Additionally, Didox exhibits a unique capacity to regenerate other antioxidants, amplifying its protective role. This compound also influences redox-sensitive signaling pathways, contributing to cellular resilience against oxidative damage. | ||||||
Matairesinol | 580-72-3 | sc-205379 sc-205379A sc-205379B | 1 mg 5 mg 25 mg | $56.00 $170.00 $795.00 | ||
Matairesinol is a lignan known for its antioxidant capabilities, primarily through its ability to scavenge free radicals and inhibit lipid peroxidation. Its unique phenolic structure allows for effective electron donation, stabilizing reactive species. Additionally, matairesinol can modulate signaling pathways related to oxidative stress, enhancing the expression of protective proteins. This compound also exhibits synergistic effects with other antioxidants, amplifying its protective role in biological systems. | ||||||
D-saccharic acid calcium salt tetrahydrate | 5793-89-5 | sc-205336 sc-205336A | 25 g 100 g | $136.00 $366.00 | 1 | |
D-saccharic acid calcium salt tetrahydrate functions as an antioxidant by chelating metal ions, thereby preventing oxidative damage caused by free radicals. Its unique calcium salt form enhances solubility and bioavailability, facilitating its interaction with cellular components. The compound can disrupt lipid peroxidation pathways, reducing the formation of harmful byproducts. Additionally, it may influence redox balance, promoting cellular resilience against oxidative stress. | ||||||
Neohesperidin dihydrochalcone | 20702-77-6 | sc-219345 sc-219345A | 1 g 5 g | $117.00 $535.00 | ||
Neohesperidin dihydrochalcone acts as an antioxidant through its ability to scavenge free radicals and inhibit oxidative stress. Its unique structure allows for effective interaction with lipid membranes, stabilizing them against oxidative damage. The compound can modulate enzymatic pathways involved in oxidative processes, enhancing cellular defense mechanisms. Furthermore, its solubility properties facilitate its integration into various biological systems, promoting overall antioxidant activity. | ||||||
Etretinate | 54350-48-0 | sc-205689 sc-205689A | 25 mg 100 mg | $92.00 $224.00 | ||
Etretinate exhibits antioxidant properties by engaging in redox reactions that neutralize reactive oxygen species. Its distinctive molecular structure allows for strong interactions with cellular membranes, enhancing their resilience to oxidative damage. The compound can influence signaling pathways related to oxidative stress, potentially altering gene expression linked to antioxidant defenses. Additionally, its lipophilic nature aids in its distribution within lipid-rich environments, optimizing its protective effects. | ||||||
AK-7 | 420831-40-9 | sc-364096 sc-364096A sc-364096B | 5 mg 25 mg 100 mg | $54.00 $221.00 $880.00 | ||
AK-7 functions as an antioxidant by effectively scavenging free radicals through its unique electron-donating capabilities. Its molecular configuration facilitates specific interactions with lipid peroxidation products, stabilizing cellular membranes against oxidative stress. The compound also modulates enzymatic pathways involved in the antioxidant response, potentially enhancing the activity of endogenous protective mechanisms. Its hydrophobic characteristics promote integration into lipid bilayers, further amplifying its protective role. | ||||||
3,4-dihydroxy Hydrocinnamic acid (L-Aspartic acid dibenzyl ester) amide | 615264-62-5 | sc-223562 sc-223562A sc-223562B sc-223562C | 5 mg 10 mg 50 mg 100 mg | $42.00 $106.00 $336.00 $588.00 | ||
3,4-dihydroxy Hydrocinnamic acid (L-Aspartic acid dibenzyl ester) amide exhibits antioxidant properties through its ability to chelate metal ions, thereby preventing oxidative damage. Its structural features allow for effective interaction with reactive oxygen species, leading to the formation of stable adducts. Additionally, it influences redox signaling pathways, enhancing cellular resilience against oxidative stress. The compound's amphiphilic nature aids in its distribution within biological membranes, optimizing its protective effects. | ||||||
Vialinin A | 858134-23-3 | sc-205539 | 1 mg | $128.00 | ||
Vialinin A functions as a potent antioxidant by engaging in electron transfer reactions that neutralize free radicals. Its unique structural configuration facilitates the formation of hydrogen bonds with reactive species, enhancing its stability and reactivity. This compound also modulates cellular signaling pathways, promoting adaptive responses to oxidative stress. Furthermore, its lipophilic characteristics enable efficient integration into lipid membranes, amplifying its protective capabilities against oxidative damage. | ||||||