Items 91 to 93 of 93 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 exhibits intriguing properties as a cannabinoid analog, primarily through its selective binding to cannabinoid receptors. Its deuterated structure enhances stability and tracking in metabolic studies, allowing for precise analysis of lipid signaling pathways. The compound's unique hydrophobic interactions facilitate its incorporation into lipid bilayers, potentially influencing membrane dynamics and receptor conformation. This behavior underscores its role in modulating cellular responses and signaling cascades. | ||||||
N-Palmitoyl Taurine | 83982-06-3 | sc-205408 sc-205408A | 1 mg 5 mg | $96.00 $578.00 | ||
N-Palmitoyl Taurine is characterized by its unique ability to modulate lipid metabolism and cellular signaling through interactions with G-protein coupled receptors. Its amphiphilic nature promotes integration into cellular membranes, influencing membrane fluidity and receptor accessibility. The compound's distinct molecular structure allows for selective engagement with various signaling pathways, potentially altering intracellular calcium levels and impacting neurotransmitter release. This multifaceted behavior positions it as an intriguing candidate for further investigation in biochemical studies. | ||||||
N-Stearoyl Taurine | 63155-80-6 | sc-205410 sc-205410A | 1 mg 5 mg | $115.00 $475.00 | ||
N-Stearoyl Taurine demonstrates unique characteristics as a cannabinoid derivative, particularly through its ability to form stable micelles in aqueous environments. This amphiphilic nature promotes effective interactions with lipid membranes, influencing membrane fluidity and permeability. Additionally, its taurine moiety may enhance neuroprotective signaling pathways, while the stearoyl group contributes to its hydrophobic interactions, potentially modulating protein-lipid interactions and cellular signaling mechanisms. | ||||||