Items 31 to 40 of 192 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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cis-Resveratrol Solution (in Ethanol) | 61434-67-1 | sc-205254 sc-205254A | 5 mg 10 mg | $120.00 $228.00 | 2 | |
Cis-Resveratrol Solution in Ethanol is a naturally derived compound recognized for its unique structural configuration, which allows it to engage in specific molecular interactions with various cellular receptors. Its dual hydroxyl groups enable strong hydrogen bonding, influencing signaling pathways related to cellular stress responses. The compound's lipophilic characteristics enhance its permeability across cell membranes, facilitating its role in modulating gene expression and antioxidant activity. Its stability in ethanol further supports its reactivity in diverse biochemical environments. | ||||||
Thaxtomin A | 122380-18-1 | sc-358702 sc-358702A | 1 mg 5 mg | $241.00 $979.00 | 1 | |
Thaxtomin A is a natural product characterized by its unique ability to inhibit cellulose synthesis in plant cells, disrupting cell wall formation. This compound interacts specifically with cellulose synthase, leading to altered plant growth and development. Its structural features allow for effective binding to target enzymes, influencing metabolic pathways. Thaxtomin A's stability in various environments enhances its reactivity, making it a significant player in plant-microbe interactions. | ||||||
Sesamol | 533-31-3 | sc-253552 | 5 g | $27.00 | ||
Sesamol is a natural phenolic compound known for its antioxidant properties, which arise from its ability to scavenge free radicals and chelate metal ions. Its unique structure facilitates interactions with cellular membranes, potentially altering membrane fluidity and permeability. Sesamol also participates in redox reactions, influencing various biochemical pathways. Additionally, its solubility in organic solvents enhances its reactivity, making it a versatile compound in natural product chemistry. | ||||||
Cholecalciferol | 67-97-0 | sc-205630 sc-205630A sc-205630B | 1 g 5 g 10 g | $70.00 $160.00 $290.00 | 2 | |
Cholecalciferol, a natural form of vitamin D, is synthesized in the skin through UVB radiation, showcasing its unique photochemical pathway. This compound interacts with specific receptors, modulating gene expression and influencing calcium homeostasis. Its lipophilic nature allows for efficient incorporation into lipid membranes, affecting membrane dynamics. Cholecalciferol also exhibits distinct solubility characteristics, enhancing its bioavailability and interaction with various biological systems. | ||||||
Questiomycin A | 1916-59-2 | sc-391695 sc-391695A | 1 mg 5 mg | $62.00 $288.00 | ||
Questiomycin A is a natural product characterized by its unique structural features that facilitate specific molecular interactions. It exhibits remarkable affinity for certain protein targets, influencing cellular signaling pathways. The compound's stability under various conditions allows for prolonged activity, while its hydrophobic regions enhance membrane penetration. Additionally, Questiomycin A demonstrates distinct kinetic properties in its reactions, contributing to its role in complex biochemical processes. | ||||||
L-(+)-Arabinose | 5328-37-0 | sc-221794 sc-221794A sc-221794B | 10 g 25 g 100 g | $29.00 $67.00 $165.00 | 2 | |
L-(+)-Arabinose is a naturally occurring sugar that plays a pivotal role in various metabolic pathways. Its unique stereochemistry allows for specific interactions with enzymes, influencing carbohydrate metabolism. The compound's ability to form hydrogen bonds enhances its solubility in water, facilitating its participation in biochemical reactions. Furthermore, L-(+)-Arabinose exhibits distinct reactivity patterns, making it a key player in polysaccharide synthesis and degradation processes. | ||||||
Deoxynojirimycin | 19130-96-2 | sc-201369 sc-201369A | 1 mg 5 mg | $72.00 $142.00 | ||
Deoxynojirimycin is a naturally occurring imino sugar that exhibits unique interactions with glycosidases, inhibiting their activity through competitive binding. This compound's structural conformation allows it to mimic natural substrates, disrupting carbohydrate processing pathways. Its solubility in aqueous environments promotes effective diffusion in biological systems, while its ability to form stable complexes with enzymes highlights its role in modulating glycosylation processes. | ||||||
Silybin | 22888-70-6 | sc-202812 sc-202812A sc-202812B sc-202812C | 1 g 5 g 10 g 50 g | $54.00 $112.00 $202.00 $700.00 | 6 | |
Silybin, a flavonoid derived from milk thistle, showcases remarkable antioxidant properties through its ability to scavenge free radicals and chelate metal ions. Its unique polyphenolic structure facilitates interactions with cellular membranes, enhancing its bioavailability. Silybin also influences various signaling pathways, modulating gene expression and enzyme activity. Its solubility in lipids allows for effective incorporation into lipid bilayers, impacting membrane fluidity and function. | ||||||
Antimycin A2 | 27220-57-1 | sc-391740 | 500 µg | $250.00 | 1 | |
Antimycin A2, a natural product derived from Streptomyces species, is notable for its potent inhibition of the mitochondrial electron transport chain, specifically targeting complex III. This interaction disrupts the proton gradient, leading to a decrease in ATP synthesis. Its unique structure allows for specific binding to the ubiquinone site, altering electron flow and generating reactive oxygen species. Additionally, Antimycin A2 exhibits distinct solubility characteristics, influencing its distribution in biological systems. | ||||||
Umckalin | 43053-62-9 | sc-296680 sc-296680A | 5 mg 20 mg | $630.00 $1215.00 | ||
Umckalin, a natural product isolated from the roots of Pelargonium sidoides, exhibits intriguing interactions with cellular signaling pathways. It modulates the activity of various transcription factors, influencing gene expression related to stress responses. Its unique molecular structure facilitates specific binding to target proteins, enhancing its bioactivity. Furthermore, Umckalin demonstrates distinctive solubility properties, affecting its bioavailability and interaction dynamics within complex biological environments. |