Items 121 to 130 of 265 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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SL 0101-1 | 77307-50-7 | sc-204287 sc-204287A sc-204287B sc-204287C sc-204287D | 1 mg 10 mg 25 mg 50 mg 100 mg | $200.00 $353.00 $772.00 $1230.00 $2070.00 | 3 | |
SL 0101-1 is a novel compound that modulates signal transduction by selectively targeting intracellular pathways. Its unique ability to form stable complexes with specific protein kinases enhances phosphorylation events, leading to altered gene expression. The compound exhibits rapid kinetics in binding, facilitating swift cellular responses. Additionally, SL 0101-1's distinct molecular interactions promote the activation of secondary messengers, amplifying its signaling effects within the cell. | ||||||
SQ-29548 | 98672-91-4 | sc-201332 sc-201332A | 1 mg 10 mg | $190.00 $1200.00 | 5 | |
SQ-29548 is a distinctive compound that influences signal transduction through its selective interaction with G-protein coupled receptors. It exhibits a high affinity for specific receptor subtypes, leading to the modulation of downstream signaling cascades. The compound's unique structural features allow for enhanced receptor dimerization, which significantly alters cellular responses. Furthermore, SQ-29548 demonstrates a remarkable ability to stabilize transient signaling complexes, prolonging the activation of key pathways. | ||||||
ML-9 | 105637-50-1 | sc-200519 sc-200519A sc-200519B sc-200519C | 10 mg 50 mg 100 mg 250 mg | $110.00 $440.00 $660.00 $1200.00 | 2 | |
ML-9 is a notable compound that modulates signal transduction by selectively inhibiting myosin light chain kinase, thereby impacting actin-myosin interactions. This inhibition leads to alterations in cellular contractility and motility. Its unique binding dynamics facilitate the disruption of specific phosphorylation events, influencing various downstream signaling pathways. Additionally, ML-9's ability to affect cytoskeletal organization highlights its role in regulating cellular architecture and dynamics. | ||||||
AAL-993 | 269390-77-4 | sc-221195 sc-221195A | 5 mg 25 mg | $255.00 $816.00 | ||
AAL-993 is a potent modulator of signal transduction, acting primarily through the inhibition of specific kinases involved in cellular signaling cascades. Its unique structural features enable selective interactions with target proteins, leading to altered phosphorylation states that influence gene expression and cellular responses. The compound's kinetics reveal a rapid onset of action, allowing for precise temporal control over signaling events, thereby affecting cellular processes such as proliferation and differentiation. | ||||||
PD 168393 | 194423-15-9 | sc-222138 | 1 mg | $162.00 | 4 | |
PD 168393 is a selective inhibitor that disrupts signal transduction pathways by targeting specific protein interactions. Its unique binding affinity allows it to modulate the activity of key enzymes involved in cellular communication, leading to significant alterations in downstream signaling events. The compound exhibits distinct reaction kinetics, facilitating a swift engagement with its targets, which can result in profound changes in cellular behavior and regulatory mechanisms. | ||||||
Isoniazid | 54-85-3 | sc-205722 sc-205722A sc-205722B | 5 g 50 g 100 g | $25.00 $99.00 $143.00 | ||
Isoniazid acts as a modulator in signal transduction by influencing the activity of specific enzymes and receptors. Its unique ability to form covalent bonds with target proteins alters their conformation, impacting downstream signaling cascades. This compound exhibits selective reactivity, allowing it to engage in distinct molecular interactions that can enhance or inhibit cellular responses. The kinetics of isoniazid's interactions contribute to its role in fine-tuning regulatory pathways within the cell. | ||||||
Cantharidin | 56-25-7 | sc-201321 sc-201321A | 25 mg 100 mg | $81.00 $260.00 | 6 | |
Cantharidin functions in signal transduction by selectively inhibiting protein phosphatases, particularly PP2A, which plays a crucial role in regulating various cellular processes. Its unique structure allows for specific binding, leading to altered phosphorylation states of target proteins. This modulation can significantly impact cellular signaling pathways, influencing processes such as cell growth and apoptosis. The compound's interaction kinetics are characterized by a rapid onset, facilitating immediate cellular responses. | ||||||
Probenecid | 57-66-9 | sc-202773 sc-202773A sc-202773B sc-202773C | 1 g 5 g 25 g 100 g | $27.00 $38.00 $98.00 $272.00 | 28 | |
Probenecid acts in signal transduction by modulating the activity of transport proteins, particularly those involved in the renal excretion of uric acid. Its unique ability to inhibit anion transporters alters the intracellular concentration of various metabolites, thereby influencing downstream signaling pathways. This compound exhibits distinct interaction kinetics, allowing for prolonged effects on cellular homeostasis and metabolic regulation, ultimately affecting processes like inflammation and oxidative stress responses. | ||||||
Acenaphthenone | 2235-15-6 | sc-337506 | 100 mg | $102.00 | ||
Acenaphthenone plays a role in signal transduction by interacting with specific receptors and influencing cellular pathways. Its unique structure allows for selective binding to proteins involved in cellular communication, modulating their activity. This compound can alter phosphorylation states of target proteins, impacting downstream signaling cascades. Additionally, its reactivity with nucleophiles can lead to the formation of adducts, further diversifying its effects on cellular processes and regulatory mechanisms. | ||||||
PTP Inhibitor I | 2491-38-5 | sc-204220 sc-204220A | 10 mg 100 mg | $102.00 $204.00 | 6 | |
PTP Inhibitor I functions as a pivotal modulator in signal transduction by selectively targeting protein tyrosine phosphatases, which are crucial for regulating phosphorylation dynamics. Its unique binding affinity alters the conformation of these enzymes, enhancing substrate availability and promoting specific signaling pathways. This compound's kinetic profile allows for rapid interaction with target proteins, facilitating immediate cellular responses and influencing various regulatory networks within the cell. |