PTPκ Inhibitors are a class of chemical compounds that target and inhibit the activity of protein tyrosine phosphatase kappa (PTPκ), an enzyme belonging to the protein tyrosine phosphatase (PTP) family. PTPκ is a transmembrane receptor-type phosphatase that plays a critical role in cellular signaling pathways by dephosphorylating specific tyrosine residues on target proteins. This dephosphorylation process is essential for regulating various cellular functions, including cell adhesion, migration, and signaling cascades involved in cell growth and differentiation. PTPκ is particularly noted for its involvement in the regulation of cadherin-mediated cell-cell adhesion, a fundamental process in maintaining tissue architecture and integrity.
The use of PTPκ Inhibitors in research allows scientists to investigate the complex signaling networks that PTPκ influences, particularly those related to cell-cell communication and the maintenance of epithelial cell integrity. By inhibiting PTPκ activity, researchers can explore the downstream effects on cadherin-mediated adhesion and how disruptions in this process can affect cellular behavior. These inhibitors are valuable tools for studying the dynamics of cell adhesion molecules and their role in tissue morphogenesis, wound healing, and cellular response to environmental changes. Additionally, PTPκ Inhibitors provide insights into the broader regulatory mechanisms of tyrosine phosphorylation and dephosphorylation in cellular signaling networks, offering a deeper understanding of how cells coordinate their functions and maintain homeostasis. Overall, PTPκ Inhibitors are critical for advancing knowledge in cell biology, particularly in areas related to cell adhesion, signaling, and the intricate balance of phosphorylation states that govern cellular processes.
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产品名称 | CAS # | 产品编号 | 数量 | 价格 | 应用 | 排名 |
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Deferoxamine | 70-51-9 | sc-507390 | 5 mg | ¥2821.00 | ||
螯合铁,可能间接影响PTPR的酶活性。 | ||||||
3-(3-Hydroxyphenyl)propionic acid | 621-54-5 | sc-275695 | 5 g | ¥1207.00 | ||
可作为某些PTP的抑制剂,可能影响PTPR的功能。 | ||||||
Perphenazine | 58-39-9 | sc-208161 | 100 mg | ¥2144.00 | ||
作为一种抗精神病药,它会影响各种细胞通路,可能对PTPR产生脱靶效应。 | ||||||
Ethacrynic acid | 58-54-8 | sc-257424 sc-257424A | 1 g 5 g | ¥553.00 ¥2584.00 | 5 | |
已知可抑制某些PTP,可能对PTPR有抑制作用。 | ||||||
Troglitazone | 97322-87-7 | sc-200904 sc-200904B sc-200904A | 5 mg 10 mg 25 mg | ¥1218.00 ¥2256.00 ¥4806.00 | 9 | |
一种抗糖尿病药物,可影响多种细胞通路,可能间接影响PTPR。 | ||||||
Zoledronic acid, anhydrous | 118072-93-8 | sc-364663 sc-364663A | 25 mg 100 mg | ¥1015.00 ¥2832.00 | 5 | |
一种双膦酸盐,可能对蛋白酪氨酸磷酸酶(包括PTPR活性)有脱靶效应。 |