Pinch-3 inhibitors belong to a class of chemical compounds that have garnered attention in the fields of molecular biology and pharmacology due to modulating specific cellular processes. Pinch-3, also known as particularly interesting new cysteine-histidine-rich protein 3, is a scaffolding protein that plays a pivotal role in cell adhesion, signal transduction, and cytoskeletal organization. It is a crucial component of the integrin signaling pathway, where it bridges the connection between integrin receptors on the cell membrane and the actin cytoskeleton, thereby facilitating cell adhesion and migration. Pinch-3 inhibitors are designed to interact with the active site or binding domain of the Pinch-3 protein, effectively inhibiting its function and influencing cellular processes dependent on Pinch-3-mediated interactions.
Structurally, Pinch-3 inhibitors are engineered to selectively target the active site of Pinch-3, ensuring high specificity for this particular scaffolding protein. By inhibiting Pinch-3, these compounds may disrupt its role in linking integrin receptors to the actin cytoskeleton, ultimately affecting cell adhesion and signaling events. The study of Pinch-3 inhibitors is of significant interest to researchers as it provides insights into the regulatory mechanisms governing essential cellular functions, particularly those related to cell adhesion and migration. This knowledge contributes to our understanding of basic cell biology and may have implications in various research areas, including cancer biology, tissue development, and immune response modulation. However, further research is required to fully explore the extent of their applications and their impact on cellular physiology in the context of Pinch-3-mediated signaling.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
CCG-1423 | 285986-88-1 | sc-205241 sc-205241A | 1 mg 5 mg | $30.00 $90.00 | 8 | |
A RhoA/ROCK pathway inhibitor, indirectly affecting cell adhesion and migration processes linked with LIMS1. | ||||||
Thiazovivin | 1226056-71-8 | sc-361380 sc-361380A | 10 mg 25 mg | $284.00 $634.00 | 15 | |
A ROCK inhibitor, could indirectly modify LIMS1 functionality in cell adhesion and migration. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
Another JNK inhibitor, may indirectly affect LIMS1 through stress-activated protein kinase pathways. | ||||||