Date published: 2026-4-26

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Fgr Inhibitors

Santa Cruz Biotechnology now offers a broad range of Fgr Inhibitors for use in various applications. Fgr Inhibitors are a specialized category of chemical compounds extensively utilized in scientific research, particularly within the fields of molecular biology and biochemistry. Fgr, a member of the Src family kinases, plays a crucial role in regulating various cellular processes, including signal transduction, cell adhesion, and cytoskeletal organization. By inhibiting Fgr activity, researchers can gain deeper insights into the mechanisms by which cells communicate and coordinate their activities. Fgr Inhibitors are invaluable for dissecting the specific pathways and interactions that Fgr is involved in, thereby helping to map out the complex networks of intracellular signaling. These inhibitors are particularly important for studying the dynamic processes of cell movement, differentiation, and growth, as well as understanding the molecular basis of cell-cell interactions. In experimental settings, Fgr Inhibitors allow for precise control over kinase activity, enabling detailed investigations into the enzyme's substrate specificity, regulatory mechanisms, and impact on cellular functions. Additionally, these inhibitors are used in structural biology to study the three-dimensional structure of Fgr and its complexes, providing critical information about its functional sites and interaction domains. This detailed understanding is fundamental for advancing knowledge in cell biology, facilitating the exploration of how alterations in kinase activity affect broader cellular behaviors. Fgr Inhibitors thus serve as essential tools for researchers aiming to uncover the intricacies of cellular signaling and function. View detailed information on our available Fgr Inhibitors by clicking on the product name.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Staurosporine

62996-74-1sc-3510
sc-3510A
sc-3510B
100 µg
1 mg
5 mg
$82.00
$153.00
$396.00
113
(4)

Staurosporine is a potent inhibitor that interacts with various protein kinases, exhibiting a unique ability to bind to the ATP-binding site. Its complex structure allows for multiple hydrogen bonding and hydrophobic interactions, enhancing its affinity for target proteins. The compound's kinetic behavior is characterized by a slow dissociation rate, which prolongs its inhibitory effects. Staurosporine's diverse solubility properties enable it to penetrate cellular membranes effectively, influencing a range of signaling pathways.

PKC-412

120685-11-2sc-200691
sc-200691A
1 mg
5 mg
$52.00
$114.00
10
(1)

PKC-412 is a selective inhibitor that targets specific protein kinases, particularly within the PKC family. Its unique structure facilitates strong electrostatic interactions with the active site, promoting a high degree of specificity. The compound exhibits a rapid association rate, allowing for swift modulation of kinase activity. Additionally, PKC-412's solubility profile enhances its distribution in various environments, impacting cellular signaling dynamics and regulatory mechanisms.