CB2 Activators
Items 21 to 25 of 25 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Palmitoyl Ethanolamide-d4 | 1159908-45-8 | sc-224199 sc-224199A | 100 µg 500 µg | $29.00 $130.00 | ||
Palmitoyl Ethanolamide-d4 is characterized by its unique ability to engage with the CB2 receptor through a distinct mechanism of action. Its deuterated structure enhances stability and alters interaction dynamics, allowing for precise modulation of receptor conformations. This compound exhibits a unique affinity profile, promoting selective receptor activation while minimizing off-target effects. The kinetic behavior indicates a balanced rate of binding and unbinding, contributing to its prolonged presence in biological systems. | ||||||
JTE 907 | 282089-49-0 | sc-203616 sc-203616A | 10 mg 50 mg | $283.00 $1100.00 | ||
JTE-907 is a selective CB2 inverse agonist. At lower concentrations, it can act as a partial agonist and enhance the functional activity of CB2 by binding to the receptor and triggering intracellular signaling events, thus enhancing CB2's immunomodulatory effects. | ||||||
Arachidonoyl 2′-fluoroethylamide | 166100-37-4 | sc-202469 | 5 mg | $200.00 | ||
Arachidonoyl 2'-fluoroethylamide exhibits a remarkable selectivity for the CB2 receptor, driven by its unique fluorinated ethylamide moiety. This modification enhances lipophilicity, facilitating deeper membrane penetration and altering receptor binding kinetics. The compound's interactions promote specific conformational changes in the receptor, leading to distinct signaling pathways. Its stability in biological environments allows for sustained engagement, influencing downstream effects with precision. | ||||||
Dihomo-γ-linolenylethanolamide | 150314-34-4 | sc-202137 | 5 mg | $55.00 | ||
Dihomo-γ-linolenylethanolamide is characterized by its unique structural features that enhance its affinity for the CB2 receptor. The compound's elongated carbon chain facilitates unique hydrophobic interactions, promoting effective receptor engagement. Its ability to modulate receptor conformations leads to selective activation of signaling cascades. Additionally, the compound's stability in lipid environments supports prolonged receptor interaction, influencing cellular responses with specificity and efficiency. | ||||||
Yangonin | 500-62-9 | sc-205889 sc-205889A | 5 mg 10 mg | $268.00 $510.00 | 1 | |
Yangonin exhibits a distinctive molecular architecture that allows it to selectively bind to the CB2 receptor, primarily through its aromatic ring system, which enhances π-π stacking interactions. This compound's unique stereochemistry contributes to its ability to induce specific conformational changes in the receptor, activating downstream signaling pathways. Furthermore, Yangonin's lipophilic nature aids in its membrane permeability, facilitating rapid cellular uptake and interaction with lipid rafts, thereby influencing receptor dynamics and cellular signaling. | ||||||