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AS-604850

CAS No. : 648449-76-7

MCE 站：AS-604850

产品活性：AS-604850 是一种有效的，具有选择性的和 ATP 竞争性的 PI3Kγ 抑制剂，IC₅₀ 值为 0.25 μM，K_i 值为 0.18 μM。AS-604850 是 PI3Kγ 的同工型选择性抑制剂，对 PI3Kγ 的选择性是 PI3Kδ/β 的 30 倍以上，是 PI3Kα 的 18 倍以上。

研究领域：PI3K/Akt/mTOR

作用靶点：PI3K

In Vitro: AS-604850 inhibits C5a-mediated PKB phosphorylation with an IC₅₀ of 10 μM in RAW264 mouse macrophages.
AS-604850 blocks PKB phosphorylation induced by MCP-1 and has little or no effect after stimulation with CSF-1 in in primary monocytes from Pik3cg^+/+ or Pik3cg^–/– mice.
AS-604850 (0-30 μM; 15 minutes; primary monocytes from Pik3cg^+/+ mice) treatment inhibits MCP-1-mediated phosphorylation of PKB and its downstream substrates GSK3α andβ in a concentration-dependent manner. MCP-1-induced phosphorylation of p44/42 ERK (ERK1/2) MAPKs is also reduced, in a concentration dependent manner in primary monocytes from Pik3cg^+/+ mice.

In Vivo: AS-604850 (10-100 mg/kg; oral administration; for 4.5 or 4.25 hours; Balb/C or C3H mice) treatment reduces RANTES-induced peritoneal neutrophil recruitment with an ED₅₀ value of 42.4 mg/kg. In the thioglycollate-induced peritonitis model, oral administration of 10 mg/kg AS-604850 results in a 31% reduction of neutrophil recruitment.

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