產(chǎn)品名稱：PIK-75, Hydrochloride Salt 產(chǎn)品貨號：LC P-7050 產(chǎn)品規(guī)格：100 MG PIK-75 is a preferential inhibitor of the p110α/γ forms of phosphatidylinositol 3-kinase (PI3K), which comprise a class of lipid kinases that phosphorylate phosphatidylinositol 4,5-bisphosphate (PIP2) to generate phosphatidylinositol 3,4,5-trisphosphate (PIP3). PIP3 activates Akt and mTOR, and plays important roles in cell growth and survival. PIK-75-mediated anti-inflammatory effects are associated with dramatic inhibition of AKT phosphorylation, IKK activation and NF-κB transcription. Dagia, N.M., et al. "A Preferential p110α/γ PI3K Inhibitor Attenuates Experimental Inflammation by Suppressing the Production of Proinflammatory Mediators in NF-κB Dependent Manner." Am. J. Physiol. Cell Physiol. 298: C929-C941 (2010). PIK-75 completely inhibited adipocyte differentiation. Kim, J.E., et al. "Investigating the role of class-IA PI 3-kinase isoforms in adipocyte differentiation." Biochem. Biophys. Res. Commun. 379: 830-834 (2009). Insulin-like growth factor-1 (IGF-1) potentiates PAR-1-mediated platelet aggregation. PIK-75 and PI-103 completely inhibited this potentiation, indicating PI3Kα; is essential for the enhancement by IGF-1 of platelet responses. Hers, I. "Insulin-like growth factor-1 potentiates platelet activation via the IRS/PI3Kalpha pathway." Blood 110: 4243-4252 (2007). In addition to the p110α isotype of PI3K , p110β and p110δ can also play a role in insulin signalling. Chaussade, C., et al. "Evidence for functional redundancy of class IA PI3K isoforms in insulin signalling." Biochem. J. 404: 449-458 (2007). Our PIK-75 product, whose CAS number appears above, is the hydrochloride salt. The CAS number for the free base is 372196-67-3. Storage: Store at or below -20 ºC. Solubility: Soluble in DMSO. Disposal: A
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