产品
编 号:F322331
分子式:C27H29NO4
分子量:431.52
产品类型
结构图
CAS No: 330834-54-3
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产品详情
生物活性:
AGX51 is a first-in-class pan-Id (inhibitors of DNA-binding/differentiation proteins) antagonist and degrader. AGX51 inhibits the Id1-E47 interaction, leading to ubiquitin-mediated degradation of Ids, cell growth arrest, and reduces viability. AGX51 inhibits the TNBC cell lines with IC50s of nearly 25 μM. AGX51 can be used for the research of cancer.
体内研究:
AGX51 (50 mg/kg;ip 每天两次,持续 4 周) 抑制肺转移。 AGX51 (15 mg/kg;ip 每天两次,持续 3 周) 表现出抗-具有自发性癌症的肿瘤活动。Animal Model:Balb/c mice with luciferase-labeled 4T1 cells
Dosage:50 mg/kg
Administration:Intraperitoneal injection; 60 mg/kg twice a day; for 4 weeks
Result:Inhibited lung metastasis development.
Animal Model:A/J mice with AOM colon tumor model
Dosage:15 mg/kg
Administration:Intraperitoneal injection; 15 mg/kg twice a day; for 3 weeks
Result:Dreased the colon tumors and exhibited anti-tumor activity in AOM colon tumor mice.
体外研究:
AGX51 (0 -80 μM;24 小时) 降低 4T1 细胞中的 ID1 蛋白水平。 AGX51 (40 μM;0-72 小时) 降低 40 μM 的 ID1 蛋白水平4T1细胞浓度。 AGX51 (40 μM;24 h) 影响4T1细胞、ER+、HER2+、TNBC和三种乳腺癌PDX细胞基因。 AGX51 (0 -80 μM;24-48 h) 影响 4T1 细胞周期。 AGX51 (40 μM;4-24 h)) 影响 4T1 细胞中的磷酸组蛋白 H3 水平。 AGX51 (40 μM;24 h) 影响 4T1 细胞中的 ROS 水平。