Items 61 to 70 of 192 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Ratjadone C (native) | sc-204876 | 5 µg | $207.00 | 1 | ||
Ratjadone C (native) is a fascinating natural product characterized by its unique structural features that enable specific molecular interactions with biological membranes. Its distinct hydrophobic regions facilitate integration into lipid bilayers, influencing membrane fluidity and permeability. Additionally, Ratjadone C exhibits selective binding affinities, which can modulate enzymatic pathways and cellular signaling. This compound's intricate stereochemistry contributes to its reactivity, making it a subject of interest in studies of natural product chemistry and ecological interactions. | ||||||
WP631 dimethanesulfonate | sc-222419 | 500 µg | $169.00 | 1 | ||
WP631 dimethanesulfonate is a notable natural product distinguished by its ability to engage in specific ionic interactions, enhancing solubility in polar environments. Its unique sulfonate groups facilitate strong hydrogen bonding, which can influence molecular aggregation and stability. The compound's reactivity is further characterized by its participation in nucleophilic substitution reactions, allowing it to act as a versatile building block in synthetic pathways. Its distinct physical properties, such as high polarity, contribute to its behavior in various chemical contexts, making it an intriguing subject for research in natural product chemistry. | ||||||
Purpurin | 81-54-9 | sc-205822 sc-205822A sc-205822B sc-205822C | 5 g 25 g 100 g 250 g | $47.00 $164.00 $406.00 $884.00 | ||
Purpurin is a fascinating natural product known for its vibrant red hue, derived from the madder plant. It exhibits strong chelating properties, forming stable complexes with metal ions, which can influence its reactivity and stability in various environments. The compound's unique conjugated structure allows for efficient light absorption, contributing to its role in photochemical processes. Additionally, Purpurin's ability to participate in electron transfer reactions highlights its significance in redox chemistry, making it a compelling subject for exploration in natural product studies. | ||||||
Lauric Acid ethyl ester | 106-33-2 | sc-204790 sc-204790A | 100 mg 500 mg | $15.00 $17.00 | ||
Lauric acid ethyl ester is a notable natural product characterized by its unique esterification of lauric acid. This compound exhibits distinct hydrophobic interactions due to its long carbon chain, influencing solubility and phase behavior in various environments. Its reactivity is enhanced by the presence of the ester functional group, facilitating transesterification and hydrolysis reactions. Additionally, the compound's molecular structure allows for specific interactions with lipid membranes, making it an intriguing subject for studies on lipid dynamics and membrane permeability. | ||||||
Methyl Salicylate | 119-36-8 | sc-204802 sc-204802A | 250 ml 500 ml | $47.00 $70.00 | ||
Methyl salicylate is a fascinating natural product known for its distinctive aromatic properties and ability to engage in hydrogen bonding due to its hydroxyl group. This compound exhibits unique solubility characteristics, allowing it to interact effectively with both polar and nonpolar environments. Its ester functionality contributes to its reactivity in transesterification processes, while its volatile nature enhances its role in scent profiles, making it a subject of interest in studies of olfactory perception and environmental interactions. | ||||||
Viridicatin | 129-24-8 | sc-202385 | 1 mg | $187.00 | 4 | |
Viridicatin is a notable natural product characterized by its complex molecular structure, which facilitates unique interactions with biological membranes. This compound exhibits significant hydrophobicity, influencing its partitioning behavior in various environments. Its ability to form stable complexes with metal ions enhances its reactivity in catalysis. Additionally, Viridicatin's distinct stereochemistry plays a crucial role in its interaction with enzymes, potentially affecting metabolic pathways in diverse organisms. | ||||||
Shikimic acid | 138-59-0 | sc-208387 sc-208387A | 250 mg 1 g | $80.00 $198.00 | 1 | |
Shikimic acid is a naturally occurring compound known for its role in the shikimic acid pathway, a crucial biosynthetic route in plants and microorganisms. Its unique structure allows for specific hydrogen bonding interactions, influencing solubility and reactivity. The compound's ability to act as a chiral building block enables the synthesis of various derivatives, while its participation in metabolic processes highlights its importance in ecological interactions and plant defense mechanisms. | ||||||
1-Kestose | 470-69-9 | sc-255837A sc-255837B sc-255837C sc-255837 | 100 mg 250 mg 1 g 25 mg | $124.00 $246.00 $737.00 $52.00 | ||
1-Kestose is a naturally occurring oligosaccharide that plays a significant role in plant metabolism and energy storage. Its unique glycosidic linkages facilitate specific interactions with enzymes, influencing its digestibility and fermentation properties. This compound exhibits prebiotic effects, promoting beneficial gut microbiota. Additionally, its structural diversity allows for various interactions with water molecules, enhancing its solubility and functionality in different biological systems. | ||||||
Icariin | 489-32-7 | sc-279198 sc-279198A sc-279198B | 1 g 5 g 10 g | $145.00 $421.00 $830.00 | ||
Icariin is a flavonoid glycoside derived from various plants, particularly Epimedium species. It exhibits unique interactions with cellular signaling pathways, notably influencing nitric oxide production and cyclic GMP levels. This compound's structural complexity allows it to engage in diverse molecular interactions, enhancing its stability and bioavailability. Furthermore, its antioxidant properties contribute to its ability to scavenge free radicals, showcasing its dynamic behavior in biological environments. | ||||||
Asterric acid | 577-64-0 | sc-202474 | 1 mg | $196.00 | ||
Asterric acid is a natural product characterized by its unique structural features that facilitate specific molecular interactions. As an acid halide, it exhibits reactivity that allows for the formation of acyl derivatives through nucleophilic acyl substitution. Its distinct carbonyl group enhances electrophilicity, promoting rapid reaction kinetics with various nucleophiles. Additionally, its hydrophobic nature influences solubility and partitioning behavior in biological systems, affecting its distribution and interaction with biomolecules. | ||||||