Items 21 to 30 of 138 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Ergosterol | 57-87-4 | sc-205313 sc-205313A | 5 g 10 g | $128.00 $209.00 | ||
Ergosterol is a vital phytochemical characterized by its unique role in cellular membranes, particularly in fungi and plants. It interacts with membrane lipids, influencing fluidity and permeability, which is crucial for maintaining cellular integrity. Ergosterol also participates in the biosynthesis of steroid hormones, impacting growth and development. Its distinct double bonds contribute to its reactivity, allowing it to engage in photochemical processes that can affect plant responses to light and stress. | ||||||
Stigmasterol | 83-48-7 | sc-281156 | 1 g | $44.00 | 7 | |
Stigmasterol is a notable phytochemical recognized for its structural similarity to cholesterol, which allows it to integrate into cell membranes, enhancing their stability and fluidity. This compound plays a significant role in plant signaling pathways, influencing growth and stress responses. Its unsaturated bonds facilitate unique interactions with reactive oxygen species, potentially modulating oxidative stress. Additionally, stigmasterol's hydrophobic nature aids in its role as a precursor in the biosynthesis of various plant sterols, contributing to overall plant health and resilience. | ||||||
Vanillic acid | 121-34-6 | sc-251422 sc-251422A | 25 g 50 g | $44.00 $88.00 | 2 | |
Vanillic acid is a distinctive phytochemical characterized by its aromatic structure, which enables it to engage in hydrogen bonding and π-π stacking interactions. This compound is involved in various metabolic pathways, influencing phenolic compound synthesis and plant defense mechanisms. Its antioxidant properties allow it to scavenge free radicals, thereby protecting cellular components. Furthermore, vanillic acid's solubility in polar solvents enhances its bioavailability and interaction with other phytochemicals, promoting synergistic effects in plant systems. | ||||||
Xanthophyll | 127-40-2 | sc-220391 sc-220391A | 25 mg 100 mg | $566.00 $1163.00 | 2 | |
Xanthophyll is a carotenoid pigment notable for its role in light absorption and energy transfer within photosynthetic organisms. Its unique structure allows for specific interactions with chlorophyll, enhancing the efficiency of photosynthesis. Xanthophylls play a crucial role in photoprotection by dissipating excess light energy as heat, thus preventing oxidative damage. Additionally, their lipid solubility facilitates integration into thylakoid membranes, optimizing their functional dynamics in light-harvesting complexes. | ||||||
Alginic acid calcium salt from brown algae | 9005-35-0 | sc-233828 | 50 g | $28.00 | ||
Alginic acid calcium salt, derived from brown algae, exhibits unique gel-forming properties due to its ability to interact with water molecules, creating viscous solutions. This polysaccharide's structure allows for ionic interactions with divalent cations, leading to the formation of stable gels. Its high molecular weight contributes to its thickening and stabilizing capabilities, making it an effective emulsifier. Additionally, its biocompatibility and biodegradability enhance its appeal in various applications. | ||||||
Polydatin | 65914-17-2 | sc-203203 | 10 mg | $92.00 | 5 | |
Polydatin, a natural phenolic compound, showcases remarkable antioxidant properties through its ability to scavenge free radicals and chelate metal ions. Its unique structure facilitates interactions with cellular signaling pathways, influencing gene expression and modulating inflammatory responses. The compound's solubility in various solvents enhances its bioavailability, while its stability under different pH conditions allows for diverse applications in research. Polydatin's role in plant defense mechanisms further underscores its ecological significance. | ||||||
Polyphenon 60 from green tea | 138988-88-2 | sc-250743 | 25 g | $97.00 | ||
Polyphenon 60, derived from green tea, is a complex mixture of catechins that exhibits potent antioxidant activity by neutralizing reactive oxygen species. Its unique polyphenolic structure enables it to interact with various cellular receptors, potentially influencing metabolic pathways. The compound's high solubility in water and organic solvents enhances its reactivity, while its stability across a range of pH levels allows for versatile applications in biochemical studies. Additionally, its role in plant defense highlights its ecological importance. | ||||||
(−)-trans-Caryophyllene | 87-44-5 | sc-251281 sc-251281A sc-251281B sc-251281C | 1 ml 5 ml 25 ml 1 L | $79.00 $157.00 $437.00 $2861.00 | 1 | |
(-)-trans-Caryophyllene is a bicyclic sesquiterpene known for its unique ability to selectively bind to cannabinoid receptors, influencing signaling pathways in various biological systems. Its lipophilic nature facilitates membrane interactions, enhancing its permeability across cellular barriers. This compound exhibits notable stability under diverse environmental conditions, contributing to its role in plant defense mechanisms. Its distinct aroma and flavor profile also play a significant role in ecological interactions, attracting pollinators and deterring herbivores. | ||||||
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 characterized by its complex structure, which allows it to engage in specific interactions with cellular enzymes and receptors. This compound is known for its antioxidant properties, influencing redox reactions and cellular signaling pathways. Its hydrophobic characteristics enable it to integrate into lipid membranes, potentially affecting membrane fluidity and function. Additionally, matairesinol's role in plant metabolism highlights its significance in ecological dynamics and plant resilience. | ||||||
Benzyl isothiocyanate | 622-78-6 | sc-204641 sc-204641A | 5 g 25 g | $46.00 $153.00 | 1 | |
Benzyl isothiocyanate is a phytochemical notable for its reactive isothiocyanate group, which facilitates nucleophilic attack on electrophilic centers in biological systems. This compound exhibits unique interactions with proteins, potentially altering enzyme activity and influencing metabolic pathways. Its lipophilic nature allows for effective partitioning into cellular membranes, impacting membrane dynamics and permeability. Furthermore, its role in plant defense mechanisms underscores its ecological importance. | ||||||