Signal Transduction
Items 191 to 200 of 264 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Clozapine N-oxide Methanol Adduct | 34233-69-7 | sc-201111 sc-201111A | 5 mg 25 mg | $66.00 $351.00 | 1 | |
Clozapine N-oxide Methanol Adduct serves as a potent modulator of signal transduction by engaging in specific molecular interactions that influence cellular pathways. Its unique structure facilitates selective binding to target proteins, altering conformational states and impacting downstream signaling events. The compound exhibits distinctive reaction kinetics, enabling fine-tuning of cellular responses through modulation of protein-protein interactions and post-translational modifications, thereby shaping cellular behavior. | ||||||
Formoterol fumarate | 43229-80-7 | sc-203050 sc-203050A sc-203050B sc-203050C sc-203050D | 10 mg 50 mg 100 mg 500 mg 1 g | $143.00 $663.00 $1224.00 $3060.00 $5100.00 | 4 | |
Formoterol fumarate acts as a significant player in signal transduction by selectively interacting with beta-adrenergic receptors, leading to the activation of adenylate cyclase. This interaction enhances cyclic AMP levels, triggering a cascade of intracellular signaling pathways. Its unique stereochemistry allows for prolonged receptor engagement, influencing downstream effects such as gene expression and cellular metabolism. The compound's kinetic profile supports rapid onset and sustained modulation of signaling, impacting various cellular functions. | ||||||
Astemizole | 68844-77-9 | sc-201088 sc-201088A | 10 mg 50 mg | $113.00 $404.00 | 5 | |
Astemizole functions in signal transduction by selectively inhibiting histamine H1 receptors, which modulates intracellular calcium levels and affects phospholipase C activity. This inhibition disrupts the normal signaling cascade, leading to altered cellular responses. Its unique binding affinity and prolonged receptor occupancy result in significant downstream effects on neurotransmitter release and cellular communication. The compound's interaction dynamics contribute to its distinct influence on cellular signaling pathways. | ||||||
Bepridil hydrochloride | 74764-40-2 | sc-202974 sc-202974A | 10 mg 25 mg | $52.00 $104.00 | 2 | |
Bepridil hydrochloride acts as a modulator in signal transduction by influencing calcium channel dynamics, particularly through its interaction with L-type calcium channels. This modulation alters intracellular calcium flux, impacting various downstream signaling pathways. Its unique binding characteristics allow for prolonged channel inhibition, which can lead to significant alterations in cellular excitability and contractility. The compound's kinetic profile and interaction with membrane proteins further define its role in cellular signaling networks. | ||||||
DL-2-Amino-5-phosphonovaleric acid (AP5) | 76326-31-3 | sc-201503 sc-201503A | 10 mg 50 mg | $80.00 $316.00 | 7 | |
DL-2-Amino-5-phosphonovaleric acid (AP5) serves as a competitive antagonist at NMDA receptors, crucial for synaptic plasticity and neurotransmission. By selectively inhibiting glutamate binding, it disrupts calcium influx and downstream signaling cascades. This interference can modulate neuronal excitability and synaptic strength, influencing pathways involved in learning and memory. Its unique structural features allow for specific interactions with receptor sites, shaping its role in cellular communication. | ||||||
Syntide-2, Protein Kinase Substrate | 108334-68-5 | sc-201151 | 1 mg | $183.00 | ||
Syntide-2 is a synthetic peptide that acts as a substrate for various protein kinases, playing a pivotal role in signal transduction pathways. Its unique sequence allows for specific phosphorylation events, influencing cellular responses to external stimuli. The kinetics of its interaction with kinases can vary, affecting the rate of signal propagation. By modulating protein activity through phosphorylation, Syntide-2 contributes to the regulation of diverse cellular processes, including growth and differentiation. | ||||||
MJ33 | 1135306-36-3 | sc-221947 | 5 mg | $261.00 | 3 | |
MJ33 is a novel compound that functions as a modulator in signal transduction, specifically targeting G-protein coupled receptors (GPCRs). Its unique structure facilitates selective binding, leading to the activation of downstream signaling cascades. The compound exhibits distinct reaction kinetics, influencing the duration and intensity of the signaling response. By altering the conformational dynamics of receptor interactions, MJ33 plays a critical role in fine-tuning cellular communication and response mechanisms. | ||||||
Aminopurvalanol A | 220792-57-4 | sc-223775 sc-223775A | 1 mg 5 mg | $51.00 $118.00 | ||
Aminopurvalanol A is an innovative compound that acts as a signal transduction modulator, primarily influencing kinase pathways. Its unique molecular architecture allows for specific interactions with protein targets, enhancing phosphorylation events. This compound exhibits distinctive binding affinities, which can alter the kinetics of signal propagation, thereby impacting cellular responses. By stabilizing certain protein conformations, Aminopurvalanol A effectively shapes the dynamics of intracellular signaling networks. | ||||||
NVP-AUY922 | 747412-49-3 | sc-364551 sc-364551A sc-364551B sc-364551C sc-364551D sc-364551E | 5 mg 25 mg 100 mg 250 mg 1 g 5 g | $150.00 $263.00 $726.00 $1400.00 $2900.00 $11000.00 | 3 | |
NVP-AUY922 is a selective inhibitor that modulates signal transduction by targeting specific chaperone proteins involved in the folding and stabilization of client proteins. Its unique binding mechanism disrupts the interaction between heat shock proteins and their substrates, leading to altered protein homeostasis. This compound exhibits distinct kinetic profiles, influencing the rate of signal transmission and cellular responses by affecting the stability and activity of key signaling molecules. | ||||||
SH-6 | 701976-55-8 | sc-205974 sc-205974A | 0.5 mg 1 mg | $466.00 $818.00 | 8 | |
SH-6 is a potent modulator of signal transduction pathways, primarily acting through the inhibition of specific kinases that regulate cellular signaling cascades. Its unique ability to selectively bind to the ATP-binding site of target kinases alters phosphorylation dynamics, thereby impacting downstream signaling events. The compound exhibits rapid reaction kinetics, facilitating swift modulation of cellular responses and influencing the overall balance of signaling networks within the cell. | ||||||