Cot Inhibitors
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Tpl2 Kinase Inhibitor Inhibitor | 871307-18-5 | sc-204351 | 1 mg | $250.00 | 6 | |
Tpl2 Kinase Inhibitor is a selective modulator of Tpl2 kinase activity, characterized by its ability to disrupt specific protein-protein interactions within signaling cascades. This compound exhibits unique binding affinity, stabilizing an inactive conformation of the kinase, which alters downstream signaling pathways. Its kinetic profile reveals a competitive inhibition mechanism, providing insights into the regulatory networks influenced by Tpl2, and highlighting its role in cellular responses. | ||||||
Luteolin | 491-70-3 | sc-203119 sc-203119A sc-203119B sc-203119C sc-203119D | 5 mg 50 mg 500 mg 5 g 500 g | $26.00 $50.00 $99.00 $150.00 $1887.00 | 40 | |
Luteolin, a flavonoid compound, exhibits remarkable interactions with various cellular targets, influencing multiple signaling pathways. Its unique ability to modulate enzyme activity stems from its capacity to form hydrogen bonds and π-π stacking interactions with key residues in target proteins. This results in altered reaction kinetics, enhancing or inhibiting enzymatic functions. Additionally, Luteolin's antioxidant properties contribute to its role in cellular homeostasis, impacting redox-sensitive pathways. | ||||||
3′,4′,7-Trihydroxyisoflavone | 485-63-2 | sc-206722 | 200 mg | $295.00 | 1 | |
3',4',7-Trihydroxyisoflavone is a flavonoid that demonstrates significant binding affinity to specific receptors, facilitating unique molecular interactions that can influence gene expression. Its structural features allow for effective chelation of metal ions, which can modulate oxidative stress responses. The compound's hydrophilic nature enhances solubility in biological systems, promoting its bioavailability and interaction with cellular membranes, thereby affecting permeability and transport mechanisms. | ||||||