SHIP-1 inhibitors belong to a specific chemical class of compounds meticulously designed to modulate the activity of the SHIP-1 protein. SHIP-1, or Src homology 2 domain-containing inositol 5-phosphatase 1, is a critical enzyme involved in intracellular signaling pathways that regulate immune cell activation, cellular responses, and phosphoinositide metabolism. These inhibitors are thoughtfully crafted molecules engineered to interact with the SHIP-1 protein, influencing its normal function. Through these interactions, they might impact various cellular processes associated with immune cell signaling, cellular activation, and phosphoinositide-mediated responses, without directly altering its interactions with substrate molecules or its involvement in downstream signaling cascades.
The design of SHIP-1 inhibitors is grounded in a comprehensive understanding of the structural and functional attributes of the SHIP-1 protein. Typically developed using advanced chemical synthesis methods and informed by insights from molecular biology, these inhibitors are characterized by their ability to selectively bind to SHIP-1. This selectivity enables focused modulation of cellular pathways that rely on the activity of this specific enzyme. Unraveling the intricacies of immune regulation, cellular responses, and intracellular signaling often employ SHIP-1 inhibitors as valuable tools. The development and utilization of SHIP-1 inhibitors contribute to advancing our knowledge of the complex interplay between cellular components and intracellular signaling dynamics, offering insights into the fundamental molecular mechanisms that govern immune responses and contribute to cellular behavior.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
myo-Inositol | 87-89-8 | sc-202714 sc-202714A sc-202714B sc-202714C | 100 g 250 g 1 kg 5 kg | $78.00 $148.00 $270.00 $821.00 | ||
D-myo-Inositol-1,4,5-triphosphate, sodium salt is a synthetic inositol phosphate that functions as a competitive inhibitor of SHIP-1. By binding to the inositol phosphate binding site of SHIP-1, it prevents the enzyme from hydrolyzing PI(3,4,5)P3, leading to increased PI3K signaling and potentially modulating immune cell responses. | ||||||