Items 101 to 110 of 264 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Phosphoramidon | 119942-99-3 | sc-201283 sc-201283A | 5 mg 25 mg | $195.00 $620.00 | 8 | |
Phosphoramidon is a selective inhibitor of metalloproteinases, influencing signal transduction pathways by modulating the activity of matrix metalloproteinases (MMPs). Its unique ability to bind to the active site of these enzymes alters proteolytic processes, impacting cellular signaling cascades. This interaction can lead to changes in extracellular matrix remodeling and cell migration, highlighting its role in regulating cellular responses and maintaining tissue homeostasis. | ||||||
Carboxy-PTIO, potassium salt | 148819-94-7 | sc-202985 sc-202985A sc-202985B | 10 mg 50 mg 250 mg | $95.00 $299.00 $950.00 | 10 | |
Carboxy-PTIO, potassium salt, acts as a potent modulator in signal transduction by selectively scavenging reactive nitrogen species. Its unique ability to interact with nitric oxide facilitates the regulation of various signaling pathways, influencing cellular responses. The compound exhibits distinct reaction kinetics, allowing for rapid modulation of oxidative stress levels, which can alter downstream signaling events. This dynamic behavior underscores its role in fine-tuning cellular communication and responses to environmental stimuli. | ||||||
RS 102895 Hydrochloride | 300815-41-2 | sc-204243 sc-204243A | 10 mg 50 mg | $125.00 $495.00 | 5 | |
RS 102895 Hydrochloride functions as a selective antagonist in signal transduction, primarily targeting specific receptors involved in cellular communication. Its unique molecular interactions disrupt the binding of endogenous ligands, thereby modulating downstream signaling cascades. The compound exhibits distinct kinetics, allowing for precise temporal control over receptor activity, which can significantly influence cellular behavior and adaptive responses to stimuli. This specificity enhances its role in elucidating complex signaling networks. | ||||||
NNC 55-0396 | 357400-13-6 | sc-203647A sc-203647 | 5 mg 10 mg | $245.00 $413.00 | 2 | |
NNC 55-0396 acts as a modulator in signal transduction by selectively influencing intracellular pathways. Its unique ability to interact with specific protein targets alters phosphorylation states, thereby impacting the activation of key signaling molecules. The compound demonstrates distinct reaction kinetics, facilitating rapid changes in cellular responses. By fine-tuning these interactions, NNC 55-0396 provides insights into the dynamics of cellular signaling and the regulation of physiological processes. | ||||||
5-Aminosalicylic acid | 89-57-6 | sc-202890 | 5 g | $26.00 | 4 | |
5-Aminosalicylic acid plays a pivotal role in signal transduction by engaging with various cellular receptors and enzymes, leading to modulation of downstream signaling cascades. Its structural features enable it to form hydrogen bonds and hydrophobic interactions, influencing protein conformation and activity. This compound exhibits unique kinetics, allowing for precise temporal regulation of signaling events, thereby contributing to the intricate balance of cellular communication and response mechanisms. | ||||||
N-Butyldeoxynojirimycin·HCl | 210110-90-0 | sc-201398 sc-201398A sc-201398B | 5 mg 25 mg 50 mg | $148.00 $492.00 $928.00 | 4 | |
N-Butyldeoxynojirimycin·HCl is a notable compound that modulates signal transduction pathways by selectively inhibiting glycosidases, which play a crucial role in glycoprotein processing. This inhibition alters the glycosylation patterns of proteins, impacting cellular signaling and recognition processes. Its unique interaction with specific enzyme active sites leads to distinct kinetic profiles, influencing downstream signaling cascades and cellular responses. | ||||||
BAPTA tetrapotassium salt | 73630-08-7 | sc-202076A sc-202076 | 100 mg 1 g | $112.00 $223.00 | 13 | |
BAPTA tetrapotassium salt is a potent calcium chelator that plays a critical role in modulating intracellular calcium levels, thereby influencing various signal transduction pathways. By binding to calcium ions with high affinity, it disrupts calcium-dependent processes, such as enzyme activation and neurotransmitter release. This selective interaction alters the kinetics of calcium-mediated signaling, providing insights into cellular responses and the dynamics of calcium signaling networks. | ||||||
Compound E | 209986-17-4 | sc-221433 sc-221433A sc-221433B | 250 µg 1 mg 5 mg | $122.00 $335.00 $948.00 | 12 | |
Compound E functions as a pivotal modulator in signal transduction by acting as an acid halide that selectively interacts with specific protein targets. Its unique reactivity allows it to form covalent bonds with nucleophilic residues, thereby influencing protein conformation and activity. This interaction can initiate distinct signaling cascades, altering downstream effects and cellular responses. The compound's rapid kinetics facilitate swift modulation of pathways, making it a key player in dynamic cellular environments. | ||||||
PGF2α (Prostaglandin F2α) | 38562-01-5 | sc-201227 sc-201227B sc-201227A sc-201227C | 1 mg 5 mg 10 mg 25 mg | $41.00 $165.00 $294.00 $651.00 | 5 | |
PGF2α serves as a crucial signaling molecule in cellular communication, engaging with G-protein coupled receptors to activate various intracellular pathways. Its ability to induce conformational changes in receptor proteins leads to the activation of second messengers, such as cyclic AMP and calcium ions. This cascade of events can modulate gene expression and cellular responses, highlighting its role in regulating physiological processes. The compound's specificity and rapid action underscore its importance in fine-tuning cellular signaling networks. | ||||||
Ganglioside GM3 sodium salt | 54827-14-4 | sc-202628 sc-202628A sc-202628B | 1 mg 10 mg 50 mg | $315.00 $2250.00 $9200.00 | ||
Ganglioside GM3 sodium salt plays a pivotal role in cellular signal transduction by interacting with membrane receptors and modulating lipid raft dynamics. Its unique structure allows for specific binding to glycoproteins, influencing receptor clustering and activation. This interaction initiates downstream signaling cascades, including the activation of kinases and phosphatases, which can alter cellular behavior and gene expression. The compound's ability to facilitate cell-cell communication underscores its significance in maintaining cellular homeostasis. | ||||||