Date published: 2026-5-5

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PITSLRE Inhibitors

Santa Cruz Biotechnology now offers a broad range of PITSLRE Inhibitors for use in various applications. PITSLRE Inhibitors are essential tools for studying the PITSLRE family of protein kinases, which are part of the larger cyclin-dependent kinase (CDK) family. These kinases play crucial roles in regulating cell cycle progression, apoptosis, and gene expression. By inhibiting PITSLRE kinases, researchers can investigate their specific functions and understand their contributions to cellular processes and signaling pathways. In scientific research, PITSLRE Inhibitors are used to explore the mechanisms by which these kinases regulate cellular responses to various stimuli, including DNA damage and stress signals. Researchers employ these inhibitors to study the downstream effects on cellular processes such as cell proliferation, differentiation, and programmed cell death. Additionally, PITSLRE Inhibitors are valuable for dissecting the roles of these kinases in transcriptional regulation and RNA processing. By providing a means to selectively inhibit PITSLRE kinase activity, these inhibitors facilitate the development of experimental models to study the intricate regulatory networks that control cell cycle dynamics and cellular homeostasis. Furthermore, PITSLRE Inhibitors are used in high-throughput screening assays to identify novel modulators of kinase activity, aiding in the discovery of new regulatory mechanisms and potential research targets. The use of PITSLRE Inhibitors enhances our understanding of kinase function and regulation, contributing to the broader field of cell biology and molecular signaling. View detailed information on our available PITSLRE Inhibitors by clicking on the product name.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

2-Aminopurine Dihydrochloride

76124-64-6sc-201524
sc-201524A
100 mg
500 mg
$73.00
$301.00
7
(1)

2-Aminopurine Dihydrochloride exhibits intriguing properties as a pitslre, characterized by its ability to form hydrogen bonds that enhance molecular interactions. This compound participates in unique tautomeric equilibria, influencing its reactivity and stability in various environments. Its dual protonation states allow for versatile participation in acid-base reactions, while its crystalline structure contributes to distinct solubility profiles, impacting its behavior in diverse chemical contexts.