Items 11 to 20 of 89 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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5(S)-HETE | 70608-72-9 | sc-200939 | 50 µg | $226.00 | ||
5(S)-HETE is a notable eicosanoid that participates in intricate cellular signaling processes, primarily through its interaction with specific receptors involved in inflammatory pathways. Its stereochemistry allows for unique conformational dynamics, influencing its binding affinity and selectivity. The compound exhibits distinct reaction kinetics, facilitating the formation of lipid mediators that can modulate cellular responses. Additionally, its role in regulating gene expression highlights its importance in cellular homeostasis. | ||||||
(±)12-HETE | 71030-37-0 | sc-204982 sc-204982A sc-204982B | 25 µg 50 µg 250 µg | $120.00 $220.00 $700.00 | ||
(±)12-HETE is an eicosanoid that plays a crucial role in modulating cellular functions through its interactions with various G-protein coupled receptors. Its unique stereochemical configuration contributes to diverse signaling pathways, influencing processes such as cell migration and proliferation. The compound is involved in lipid peroxidation reactions, generating secondary messengers that can amplify inflammatory responses. Its ability to alter membrane fluidity further impacts receptor activity and cellular communication. | ||||||
8(S)-HETE | 98462-03-4 | sc-200940 | 50 µg | $226.00 | ||
8(S)-HETE is an eicosanoid characterized by its specific stereochemistry, which influences its binding affinity to various receptors, particularly in the context of inflammatory responses. It participates in lipid metabolism, acting as a precursor for other bioactive lipids. The compound is known to modulate nitric oxide production and can affect vascular tone. Its unique interactions with cellular membranes can alter lipid raft dynamics, impacting signal transduction pathways and cellular responses. | ||||||
Lipoxin A4, 15-epi | 171030-11-8 | sc-202695 | 25 µg | $248.00 | ||
Lipoxin A4, 15-epi is an eicosanoid that plays a crucial role in the resolution of inflammation. Its unique stereochemistry allows for selective receptor engagement, influencing downstream signaling pathways. This compound is involved in the regulation of leukocyte trafficking and can modulate the production of pro-inflammatory cytokines. Additionally, it exhibits distinct kinetics in its biosynthesis, often generated from arachidonic acid through specific enzymatic pathways, highlighting its role in cellular homeostasis. | ||||||
AM-404 | 198022-70-7 | sc-200363B sc-200363 sc-200363C sc-200363A | 5 mg 10 mg 25 mg 50 mg | $46.00 $65.00 $147.00 $242.00 | ||
AM-404 is an eicosanoid derivative that exhibits unique interactions with cannabinoid receptors, influencing neurotransmitter release and synaptic plasticity. Its structure allows for selective binding, modulating intracellular signaling cascades. AM-404 is also involved in the regulation of lipid metabolism, impacting the synthesis of other bioactive lipids. The compound's stability and reactivity in biological systems contribute to its role in cellular signaling and homeostasis, showcasing its intricate biochemical behavior. | ||||||
Prostaglandin D3 | 71902-47-1 | sc-205449 sc-205449A | 50 µg 100 µg | $107.00 $270.00 | ||
Prostaglandin D3 is a significant eicosanoid that plays a crucial role in cellular signaling and homeostasis. It is synthesized through distinct enzymatic pathways, particularly from arachidonic acid, and exhibits unique interactions with G-protein coupled receptors. This compound influences various physiological processes by modulating intracellular calcium levels and cyclic AMP production. Its structural features enable it to participate in diverse lipid-mediated signaling cascades, impacting cellular responses and tissue dynamics. | ||||||
(S)-Bromoenol lactone | 478288-94-7 | sc-222281 sc-222281A sc-222281B sc-222281C | 500 µg 1 mg 5 mg 10 mg | $51.00 $92.00 $326.00 $561.00 | 1 | |
(S)-Bromoenol lactone is a notable eicosanoid analog that engages in specific molecular interactions, particularly with enzymes involved in lipid metabolism. Its unique structure facilitates the formation of reactive intermediates, influencing the kinetics of enzymatic reactions. This compound can modulate the synthesis of various lipid mediators, impacting inflammatory pathways. Additionally, its reactivity as an acid halide allows for selective acylation reactions, further diversifying its biochemical roles. | ||||||
5-oxo-ETE | 106154-18-1 | sc-203783 sc-203783A | 25 µg 50 µg | $113.00 $205.00 | 2 | |
5-oxo-ETE is a notable eicosanoid characterized by its role in mediating inflammatory responses and immune cell activation. It is derived from the metabolism of arachidonic acid and engages with specific receptors, influencing cellular migration and adhesion. The compound exhibits unique reactivity patterns, facilitating the formation of lipid peroxides and altering membrane dynamics. Its interactions with various signaling pathways underscore its importance in modulating cellular behavior and tissue responses. | ||||||
Arachidonic Acid (20:4, n-6) | 506-32-1 | sc-200770 sc-200770A sc-200770B | 100 mg 1 g 25 g | $90.00 $235.00 $4243.00 | 9 | |
Arachidonic acid serves as a crucial precursor in the biosynthesis of eicosanoids, which are signaling molecules that play pivotal roles in various physiological processes. It undergoes enzymatic conversion through cyclooxygenase and lipoxygenase pathways, leading to the production of prostaglandins and leukotrienes. These metabolites exhibit distinct affinities for specific receptors, influencing vascular tone, platelet aggregation, and immune responses. The rapid turnover and diverse metabolic fates of arachidonic acid highlight its dynamic role in cellular signaling and homeostasis. | ||||||
Dihomo-γ-linolenic Acid (20:3, n-6) | 1783-84-2 | sc-200780 sc-200780A | 100 mg 1 g | $150.00 $975.00 | 2 | |
Dihomo-γ-linolenic acid is an important polyunsaturated fatty acid that acts as a precursor in the synthesis of eicosanoids, particularly in the formation of prostaglandins and leukotrienes. Its unique structure allows for specific enzymatic interactions, particularly with lipoxygenase, leading to the production of bioactive lipids that modulate inflammatory responses. The acid's incorporation into cell membranes influences membrane fluidity and receptor signaling, thereby impacting cellular communication and function. |