Items 161 to 170 of 192 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
11(R)-HETE | 73347-43-0 | sc-204974 sc-204974A | 25 µg 50 µg | $140.00 $266.00 | ||
11(R)-HETE is a bioactive lipid derived from arachidonic acid, known for its role in cellular signaling and inflammation. It engages in specific interactions with G-protein coupled receptors, influencing various physiological responses. This compound is involved in distinct metabolic pathways, including the modulation of vascular tone and platelet aggregation. Its unique stereochemistry allows for selective binding, impacting reaction kinetics and enhancing its biological efficacy in cellular processes. | ||||||
Mycalolide B | 122752-21-0 | sc-358736 sc-358736A | 20 µg 100 µg | $418.00 $2050.00 | 4 | |
Mycalolide B is a natural product characterized by its unique ability to interact with actin filaments, promoting depolymerization and influencing cytoskeletal dynamics. This compound exhibits distinct binding affinities that alter the stability of actin structures, thereby affecting cellular motility and morphology. Its specific molecular interactions can modulate cellular signaling pathways, leading to changes in cell shape and movement, showcasing its role in regulating cytoskeletal integrity. | ||||||
Harpagoside | 19210-12-9 | sc-203073 sc-203073A | 5 mg 25 mg | $111.00 $428.00 | 2 | |
Harpagoside is a natural product notable for its ability to modulate oxidative stress responses in cells. It interacts with various signaling molecules, influencing pathways related to inflammation and cellular defense mechanisms. This compound exhibits unique solubility properties, allowing it to penetrate cellular membranes effectively. Its distinct molecular interactions can alter redox states, impacting cellular metabolism and energy production, thereby highlighting its role in maintaining cellular homeostasis. | ||||||
Eicosatrienoic Acid (5Z,11Z,14Z) | 7019-85-4 | sc-205307 sc-205307A | 100 µg 500 µg | $92.00 $227.00 | ||
Eicosatrienoic Acid (5Z,11Z,14Z) is a polyunsaturated fatty acid characterized by its unique triple cis-double bond configuration, which influences its fluidity and membrane incorporation. This compound participates in lipid metabolism, serving as a precursor for bioactive lipids that modulate cellular signaling pathways. Its distinct structural features facilitate specific interactions with proteins, potentially affecting enzyme activity and gene expression, thereby playing a role in cellular communication and homeostasis. | ||||||
15-epi Prostaglandin A1 | 20897-92-1 | sc-205020 sc-205020A | 1 mg 5 mg | $49.00 $222.00 | ||
15-epi Prostaglandin A1 is a naturally occurring compound known for its unique stereochemistry, which enhances its binding affinity to specific receptors. This compound is involved in various signaling pathways, influencing cellular responses through its interactions with G-protein coupled receptors. Its distinct molecular conformation allows for selective modulation of downstream effects, impacting processes such as inflammation and vascular tone regulation. The compound's reactivity and stability are also notable, contributing to its role in biological systems. | ||||||
Geranyl acetate | 105-87-3 | sc-235243 | 25 g | $40.00 | ||
Geranyl acetate is a naturally occurring ester characterized by its fruity aroma and unique structural features. It exhibits interesting interactions with lipid membranes, influencing fluidity and permeability. The compound participates in various biosynthetic pathways, particularly in the formation of terpenes, and its reactivity allows for diverse transformations in natural product synthesis. Its distinct volatility and solubility properties enhance its role in ecological signaling and plant communication. | ||||||
12-Deoxywithastramonolide | 60124-17-6 | sc-490055 | 10 mg | $610.00 | ||
12-Deoxywithastramonolide is a natural product notable for its complex molecular structure and unique stereochemistry. It engages in specific interactions with cellular membranes, potentially affecting membrane dynamics and signaling pathways. This compound is involved in intricate biosynthetic routes, contributing to the diversity of secondary metabolites. Its distinctive solubility characteristics facilitate its role in ecological interactions, influencing plant defense mechanisms and ecological balance. | ||||||
14-Deoxy-11,12-didehydroandrographolide | 42895-58-9 | sc-490074 | 5 mg | $269.00 | ||
14-Deoxy-11,12-didehydroandrographolide is a natural product characterized by its intriguing structural features and unique reactivity. It exhibits selective binding affinities, which may influence protein interactions and cellular processes. The compound participates in diverse biosynthetic pathways, showcasing its role in the synthesis of various secondary metabolites. Its distinct solubility and stability profiles allow it to engage in complex ecological interactions, impacting plant resilience and adaptation. | ||||||
3-O-Acetyl-α-boswellic acid | 89913-60-0 | sc-490075 | 5 mg | $466.00 | ||
3-O-Acetyl-α-boswellic acid is a natural product notable for its unique structural configuration and reactivity. It demonstrates specific interactions with cellular membranes, influencing permeability and transport mechanisms. This compound is involved in various metabolic pathways, contributing to the biosynthesis of other bioactive compounds. Its distinctive solubility characteristics enhance its ecological role, facilitating interactions within diverse biological systems and promoting adaptive responses in plants. | ||||||
Andrograpanin | 82209-74-3 | sc-490076 sc-490076A sc-490076B | 10 mg 50 mg 100 mg | $378.00 $1705.00 $2765.00 | ||
Andrograpanin is a natural product characterized by its intriguing molecular structure, which allows for selective binding to various protein targets. This compound exhibits unique solubility properties, enabling it to traverse lipid membranes effectively. Its interactions with cellular signaling pathways can modulate gene expression, influencing metabolic processes. Additionally, Andrograpanin's stability under varying environmental conditions highlights its potential role in ecological interactions and plant resilience. | ||||||