耗材描述
Tagraxofusp
产品活性:Tagraxofusp (SL-401) 是一种有效的 IL-3 受体抑制剂,可抑制多发性骨髓瘤 (MM) 骨髓 (BM) 微环境中浆细胞样树突状细胞 (pDCs) 的生长。Tagraxofusp 与 Bortezomib (HY-10227)、Pomalidomide (HY-10984) 有协同抑制多发性骨髓瘤的作用。
产品来源: https://www.medchemexpress.cn/tagraxofusp.html
研究领域:Immunology/Inflammation
作用靶点:Interleukin Related
In Vitro: Tagraxofusp (0-1367 pM; 72 h) inhibits pDCs viability, as well as pDC-induced proliferation of MM cells.
Tagraxofusp (0-136.7 pM; 2-3 weeks) inhibits osteoclast formation and bone resorption, as well as stabilizes osteoblast formation.
Tagraxofusp (0-13.67 nM; 48 h) targets tumor-initiating stem-like cells in MM.
In Vivo: Tagraxofusp (12-50 μg/kg; i.v.; 5 times per week for 3 weeks) blocks pDC-induced tumor growth and prolongs SCID-hu mice survival in subcutaneous INA-6 MM xenograft model.
Tagraxofusp (16 μg/kg; i.v.; 5 times per week for 1 weeks) enhances the anti-MM activity of 2.5 mg/kg Pomalidomide in CB-17 mice of subcutaneous MM xenograft model.
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