Signal Transduction
Items 131 to 140 of 264 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
NFAT Activation Inhibitor III | 3519-82-2 | sc-203160 | 10 mg | $115.00 | 2 | |
NFAT Activation Inhibitor III functions as a critical modulator in signal transduction by selectively interfering with calcium-dependent signaling pathways. It uniquely binds to regulatory proteins, altering their conformation and preventing the activation of NFAT transcription factors. This inhibition affects the transcriptional response to stimuli, thereby fine-tuning cellular signaling networks. Its rapid interaction with target proteins allows for immediate modulation of cellular processes, showcasing its dynamic role in cellular communication. | ||||||
Coumermycin A1 | 4434-05-3 | sc-507271 | 5 mg | $1250.00 | 1 | |
Coumermycin A1 is an activator of JAK2 and Raf-1 | ||||||
Sanguinarine chloride | 5578-73-4 | sc-202800 | 5 mg | $184.00 | 4 | |
Sanguinarine chloride functions as a significant player in signal transduction by engaging with specific receptors and modulating intracellular pathways. Its unique ability to influence calcium ion flux and reactive oxygen species generation can lead to altered cellular responses. By interacting with various kinases, it can affect phosphorylation states of target proteins, thereby impacting downstream signaling events and cellular homeostasis. This compound's distinct molecular interactions contribute to its role in regulating cellular communication. | ||||||
Ginkgolide B | 15291-77-7 | sc-201037B sc-201037 sc-201037C sc-201037A | 5 mg 10 mg 25 mg 50 mg | $45.00 $63.00 $112.00 $197.00 | 8 | |
Ginkgolide B is a notable modulator in signal transduction, primarily through its interaction with specific G-protein coupled receptors. This compound can influence the activation of various signaling cascades, including those involving phospholipase C and protein kinase C. Its unique ability to alter membrane fluidity enhances receptor-ligand interactions, facilitating rapid signal propagation. Additionally, Ginkgolide B's role in modulating nitric oxide pathways underscores its impact on cellular signaling dynamics. | ||||||
Zinc Protoporphyrin-9 | 15442-64-5 | sc-200329 sc-200329A | 25 mg 100 mg | $76.00 $209.00 | 31 | |
Zinc Protoporphyrin-9 serves as a critical regulator in signal transduction by acting as a competitive inhibitor of heme oxygenase. This interaction leads to the modulation of intracellular signaling pathways, particularly those involving reactive oxygen species and nitric oxide synthesis. Its unique coordination with metal ions influences the stability of protein complexes, thereby affecting downstream signaling events. The compound's ability to alter cellular redox states further enhances its role in mediating various physiological responses. | ||||||
(−)-Arctiin | 20362-31-6 | sc-202064 | 25 mg | $63.00 | 1 | |
(-)-Arctiin plays a significant role in signal transduction by modulating the activity of specific receptors and enzymes involved in cellular communication. Its unique structural features allow it to interact with various signaling molecules, influencing pathways related to inflammation and cellular stress responses. The compound's ability to form hydrogen bonds and engage in hydrophobic interactions enhances its affinity for target proteins, thereby affecting downstream signaling cascades and cellular outcomes. | ||||||
PPARγ Antagonist III, G3335 | 36099-95-3 | sc-202771 sc-202771A | 50 mg 100 mg | $100.00 $200.00 | 3 | |
PPARγ Antagonist III, G3335, functions as a pivotal modulator in signal transduction by selectively disrupting the interaction between PPARγ and its coactivators. This compound exhibits unique binding dynamics, characterized by its ability to stabilize inactive receptor conformations, thereby inhibiting transcriptional activity. Its distinct molecular architecture facilitates specific interactions with regulatory proteins, influencing metabolic pathways and cellular differentiation processes. | ||||||
Fluoxetine hydrochloride | 56296-78-7 | sc-201125 sc-201125A sc-201125B sc-201125C | 50 mg 250 mg 1 g 5 g | $75.00 $209.00 $399.00 $849.00 | 14 | |
Fluoxetine hydrochloride acts as a modulator in signal transduction by selectively inhibiting the reuptake of serotonin, leading to increased synaptic availability. Its unique molecular structure allows for specific interactions with serotonin transporters, altering their conformational states. This compound exhibits distinct kinetic properties, influencing neurotransmitter dynamics and downstream signaling pathways, ultimately affecting neuronal communication and plasticity. | ||||||
Equisetin | 57749-43-6 | sc-202153 | 1 mg | $153.00 | 4 | |
Equisetin functions as a signal transduction agent by engaging in specific interactions with cellular receptors, modulating intracellular signaling cascades. Its unique structural features facilitate the formation of stable complexes with target proteins, influencing their activity and downstream effects. The compound exhibits distinctive reaction kinetics, allowing for rapid activation of signaling pathways, which can lead to alterations in gene expression and cellular responses. Its behavior as an acid halide further enhances its reactivity in biological systems. | ||||||
Citalopram, Hydrobromide Salt | 59729-32-7 | sc-201123 sc-201123A | 10 mg 50 mg | $108.00 $433.00 | 4 | |
Citalopram, Hydrobromide Salt operates in signal transduction by selectively binding to serotonin transporters, inhibiting their reuptake and thereby enhancing synaptic serotonin levels. This modulation of neurotransmitter dynamics initiates a cascade of intracellular signaling events, influencing second messenger systems. Its unique hydrobromide structure contributes to its solubility and stability, facilitating effective interactions with membrane proteins and altering cellular signaling networks. | ||||||