Cell Signaling
Items 241 to 250 of 496 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
MAZ51 | 163655-37-6 | sc-202703 | 2 mg | $110.00 | 2 | |
MAZ51 functions as a critical cell signaling agent by engaging specific receptors that initiate a cascade of intracellular events. Its unique structure allows for selective binding to target proteins, influencing downstream signaling pathways. The compound exhibits rapid kinetics, promoting swift cellular responses through conformational changes in receptor complexes. Additionally, its ability to modulate ion channel activity enhances excitability in target cells, further diversifying its signaling capabilities. | ||||||
YC-1 | 170632-47-0 | sc-202856 sc-202856A sc-202856B sc-202856C | 1 mg 5 mg 10 mg 50 mg | $33.00 $124.00 $218.00 $947.00 | 9 | |
YC-1 acts as a pivotal cell signaling molecule by selectively interacting with key regulatory proteins, thereby modulating various intracellular pathways. Its distinct molecular configuration facilitates the formation of stable complexes, which can alter gene expression and protein activity. The compound exhibits unique allosteric effects, enhancing the sensitivity of target proteins to other signaling molecules. This dynamic interplay contributes to its role in fine-tuning cellular responses and maintaining homeostasis. | ||||||
SC 560 | 188817-13-2 | sc-202805 | 5 mg | $77.00 | 1 | |
SC 560 functions as a critical cell signaling agent by engaging with specific receptors, leading to the activation of downstream signaling cascades. Its unique structural features allow for precise binding interactions, influencing the phosphorylation states of target proteins. This modulation can result in altered cellular behaviors, such as changes in metabolism and growth. Additionally, SC 560's kinetic properties enable rapid responses to cellular stimuli, enhancing its role in dynamic signaling networks. | ||||||
IU1 | 314245-33-5 | sc-361215 sc-361215A sc-361215B | 10 mg 50 mg 100 mg | $138.00 $607.00 $866.00 | 2 | |
IU1 acts as a pivotal cell signaling molecule by selectively interacting with intracellular pathways, particularly influencing the activity of kinases and phosphatases. Its unique conformation facilitates the formation of transient complexes, which can modulate gene expression and cellular responses. The compound exhibits distinct reaction kinetics, allowing for swift activation or inhibition of signaling cascades, thereby fine-tuning cellular processes such as differentiation and apoptosis. | ||||||
SC 57461A | 423169-68-0 | sc-204266 sc-204266A | 5 mg 25 mg | $151.00 $577.00 | 1 | |
SC 57461A serves as a crucial modulator in cell signaling by engaging with specific receptor sites, leading to the activation of downstream signaling cascades. Its unique structural features enable it to form stable complexes with target proteins, influencing their conformational states and activity. The compound demonstrates selective binding affinity, which enhances its ability to regulate cellular functions, including metabolic pathways and stress responses, through precise kinetic interactions. | ||||||
PP242 | 1092351-67-1 | sc-301606A sc-301606 | 1 mg 5 mg | $57.00 $172.00 | 8 | |
PP242 is a potent inhibitor that selectively targets the mTOR pathway, crucial for regulating cell growth and metabolism. Its unique ability to disrupt the interaction between mTOR and its substrates leads to altered phosphorylation states, impacting downstream signaling events. The compound exhibits a distinct binding profile, allowing for effective modulation of cellular responses to nutrient availability and stress, thereby influencing various metabolic processes through specific kinetic mechanisms. | ||||||
1-Naphthohydroxamic Acid | 6953-61-3 | sc-364388 sc-364388A | 5 mg 25 mg | $87.00 $337.00 | ||
1-Naphthohydroxamic Acid serves as a critical regulator in cellular signaling pathways, particularly through its ability to chelate metal ions, influencing enzyme activity and gene expression. Its unique hydroxamic acid moiety facilitates specific interactions with metalloproteins, modulating their function. The compound exhibits distinct reaction kinetics, allowing for precise control over signaling cascades, thereby impacting cellular responses to environmental changes. | ||||||
Tyrphostin 9 | 10537-47-0 | sc-200568 sc-200568A | 50 mg 250 mg | $108.00 $469.00 | 5 | |
Tyrphostin 9 acts as a potent inhibitor of receptor tyrosine kinases, disrupting key cell signaling pathways. Its structure allows for selective binding to the ATP-binding site of these kinases, effectively blocking phosphorylation events crucial for cellular communication. This compound exhibits unique kinetics, enabling rapid modulation of signaling cascades, which can lead to altered cellular behaviors. Its specificity for certain kinases highlights its role in fine-tuning cellular responses. | ||||||
Fluvoxamine maleate | 61718-82-9 | sc-203582 sc-203582A | 10 mg 50 mg | $51.00 $224.00 | ||
Fluvoxamine maleate functions as a modulator of intracellular signaling by influencing serotonin receptor activity. Its unique molecular structure facilitates interactions with specific receptor subtypes, leading to alterations in downstream signaling pathways. This compound exhibits distinct binding affinities, which can affect the dynamics of neurotransmitter release and synaptic plasticity. The kinetics of its receptor engagement allow for nuanced regulation of cellular responses, impacting various physiological processes. | ||||||
Ac-DEVD-pNA | 189950-66-1 | sc-311275 sc-311275A sc-311275B sc-311275C | 1 mg 5 mg 25 mg 250 mg | $97.00 $286.00 $734.00 $4692.00 | 14 | |
Ac-DEVD-pNA is a synthetic peptide substrate that selectively targets caspase-3, a key enzyme in the apoptotic pathway. Its unique structure allows for specific cleavage by caspase-3, resulting in the release of a chromogenic moiety that can be quantitatively measured. This interaction provides insights into the kinetics of apoptosis, enabling the study of cellular responses to various stimuli. The compound's specificity and sensitivity make it a valuable tool for dissecting apoptotic signaling mechanisms. | ||||||