Understanding the Application of Dactolisib in Cancer Research & Drug Discovery
The landscape of cancer research is continuously evolving, driven by a deeper understanding of cellular pathways and the development of targeted therapeutic agents. Central to many oncogenic processes is the PI3K/AKT/mTOR signaling pathway, which governs critical cellular functions like proliferation, metabolism, and survival. Consequently, inhibitors of this pathway are of immense interest. Dactolisib (CAS 915019-65-7) is a prominent example of a potent dual PI3K and mTOR inhibitor that has found widespread application in cancer research and drug discovery. This article delves into the key applications of Dactolisib and highlights its importance for scientists and researchers looking to purchase this vital compound.
Dactolisib's primary application lies in its role as a research tool to investigate the PI3K/mTOR pathway. As a dual inhibitor, it provides a powerful means to dissect the complex cross-talk between PI3K and mTOR signaling. Researchers utilize Dactolisib to study how inhibiting these kinases affects cancer cell growth, induces apoptosis (programmed cell death), and influences other cellular processes. The compound's ability to achieve low nanomolar IC50 values against multiple PI3K isoforms and mTOR underscores its potency and effectiveness in blocking this crucial signaling cascade. For institutions and companies aiming to purchase Dactolisib, selecting a supplier that guarantees high purity is essential for achieving accurate and reproducible experimental results.
In the realm of drug discovery, Dactolisib serves as a foundational molecule and a critical fine chemical intermediate. Its well-defined mechanism of action and demonstrated efficacy in preclinical models make it a valuable component in the development of novel anticancer drugs. Scientists use Dactolisib to screen for synergistic drug combinations, to validate new therapeutic targets, and to understand resistance mechanisms that may arise against other targeted therapies. When considering a bulk purchase of Dactolisib for drug development programs, partnering with an experienced China manufacturer can ensure a consistent supply and cost-effectiveness, facilitating the progression of research from lab bench to potential clinical trials.
Beyond direct inhibition of tumor cell proliferation, Dactolisib's application extends to the study of tumor microenvironment modulation, particularly angiogenesis. By inhibiting VEGF-induced angiogenesis, Dactolisib can impede the formation of new blood vessels that support tumor growth. This makes it a subject of study for its role in combination therapies aimed at both targeting tumor cells directly and disrupting their blood supply. Researchers investigating these complex biological interactions can effectively buy Dactolisib to explore these multifaceted therapeutic strategies. The availability of such compounds from reliable chemical suppliers is crucial for driving innovation in oncology.
In summary, Dactolisib (CAS 915019-65-7) is an indispensable research chemical with broad applications in understanding cancer biology and developing new treatments. Its potent dual inhibition of PI3K and mTOR, coupled with its ability to influence angiogenesis, makes it a valuable tool for scientists worldwide. We are a leading manufacturer and supplier, committed to providing high-quality Dactolisib to support your critical research and drug discovery endeavors. Inquire about our product specifications and purchase options today.
Perspectives & Insights
Logic Thinker AI
“In summary, Dactolisib (CAS 915019-65-7) is an indispensable research chemical with broad applications in understanding cancer biology and developing new treatments.”
Molecule Spark 2025
“Its potent dual inhibition of PI3K and mTOR, coupled with its ability to influence angiogenesis, makes it a valuable tool for scientists worldwide.”
Alpha Pioneer 01
“We are a leading manufacturer and supplier, committed to providing high-quality Dactolisib to support your critical research and drug discovery endeavors.”