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Palupiprant

CAS No. : 1369489-71-3

MCE 站：Palupiprant

产品活性：Palupiprant (E7046) 是一种口服有效的，特异性的 EP4 拮抗剂，IC₅₀ 值为 13.5 nM， K_i 值为 23.14 nM；Palupiprant 具有抗肿瘤活性。

研究领域：GPCR/G Protein

作用靶点：Prostaglandin Receptor

In Vitro: Palupiprant (E7046) reverses the immunosuppressive effects of PGE2 on activation ａnd differentiation of human myeloid cells through selective EP4 antagonism.

In Vivo: In the CT-26 tumor model, the Palupiprant/RT combination causes the anti-tumor memory response of 9 animals. In the 4T1 model, the combination of Palupiprant ａnd RT also produces significant better tumor growth inhibition activity compared with each treatment alone. The combination significantly improves survival by inhibiting the subsequent spontaneous lung metastasis of 4T1 tumors. Palupiprant (150 mg/kg) inhibits the growth of multiple syngeneic tumor models. Blockade of EP4 signaling promotes anti-tumor DC differentiation ａnd slows tumor growth in mice. Palupiprant treatment reduces the growth or even rejected established tumors in vivo in a manner dependent on both myeloid ａnd CD8C T cells. Furthermore, co-administration of Palupiprant ａnd E7777, an IL-2-diphtheria toxin fusion protein that preferentially kills Tregs, synergistically disrupts the myeloid ａnd Treg immunosuppressive networks, resulting in effective ａnd durable anti-tumor immune responses in mouse tumor models.

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