Cell Signaling
Items 491 to 496 of 496 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
JAK3 Inhibitor IV | 58753-54-1 | sc-295217 | 10 mg | $431.00 | ||
JAK3 Inhibitor IV is a specialized compound that selectively disrupts Janus kinase 3-mediated signaling pathways. Its unique binding affinity allows it to effectively compete with ATP at the active site, inhibiting downstream phosphorylation events. This selective inhibition alters the dynamics of cytokine receptor signaling, impacting transcription factor activation. The compound's structural features promote stability in complex environments, enhancing its role in modulating cellular communication networks. | ||||||
Procaterol hydrochloride | 62929-91-3 | sc-203667 sc-203667A | 10 mg 50 mg | $235.00 $700.00 | ||
Procaterol hydrochloride is a selective beta-2 adrenergic agonist that engages with specific G-protein coupled receptors, initiating a cascade of intracellular signaling. Its unique interaction with the receptor promotes the activation of adenylate cyclase, leading to increased cyclic AMP levels. This modulation of second messenger systems influences various cellular responses, including smooth muscle relaxation and metabolic regulation. The compound's stereochemistry enhances receptor affinity, contributing to its distinct signaling profile. | ||||||
SKF 83959 | 67287-95-0 | sc-204285 sc-204285A | 10 mg 50 mg | $187.00 $786.00 | ||
SKF 83959 is a potent modulator of dopamine receptor signaling, specifically targeting D2-like receptors. Its unique binding affinity alters receptor conformation, promoting downstream signaling pathways that influence neuronal activity. By selectively inhibiting certain G-proteins, SKF 83959 fine-tunes intracellular calcium levels and cyclic nucleotide signaling, thereby impacting synaptic transmission and plasticity. This compound's distinct molecular interactions contribute to its nuanced effects on cellular communication and behavior. | ||||||
SR 57227 hydrochloride | 77145-61-0 | sc-204301 sc-204301A | 10 mg 50 mg | $151.00 $570.00 | ||
SR 57227 hydrochloride acts as a selective modulator of cell signaling pathways, particularly influencing the activity of specific G-protein coupled receptors. Its unique structural features facilitate high-affinity interactions with target proteins, leading to altered phosphorylation states and modulation of second messenger systems. This compound exhibits distinct kinetics in receptor activation, enabling precise regulation of intracellular signaling cascades that govern cellular responses and adaptations. | ||||||
L-165041 | 79558-09-1 | sc-203094 | 5 mg | $156.00 | ||
L-165041 functions as a potent modulator of cell signaling by selectively engaging with intracellular pathways. Its unique chemical structure allows for specific interactions with key signaling proteins, influencing their conformational states and activity. This compound demonstrates remarkable kinetics in binding, promoting or inhibiting downstream signaling events. By altering the dynamics of protein-protein interactions, L-165041 plays a crucial role in fine-tuning cellular responses to various stimuli. | ||||||
(−)-Huperzine A | 102518-79-6 | sc-200183 sc-200183A | 1 mg 5 mg | $143.00 $362.00 | 1 | |
(-)-Huperzine A acts as a significant player in cell signaling by selectively inhibiting acetylcholinesterase, leading to increased levels of acetylcholine. This elevation enhances neurotransmission and modulates synaptic plasticity. Its unique stereochemistry allows for specific binding to the active site of the enzyme, resulting in altered reaction kinetics. This compound's ability to influence cholinergic signaling pathways highlights its role in regulating cellular communication and response mechanisms. | ||||||