中文名称: L48H37
英文名称: L48H37
CAS No: 343307-76-6
分子式: C27H33NO7
分子量: 483.55
L11416 L48H37 ≥97% (psaitong)
包装规格:
2mg 5mg 10mg 25mg 50mg 100mg in glass bottle
产品简介:
L48H37 是一种化学稳定性提高了的姜黄素 (HY-N0005) 类似物。L48H37 是一种有效且特异性的髓系分化蛋白 2 (MD2) 抑制剂,抑制 LPS-TLR4/MD2 的相互作用和信号转导。L48H37 用于脓毒症或肺损伤的相关研究。
溶解性:
DMSO :50 mg/mL (103.40 mM; Need ultrasonic)
储备液保存:
-80°C, 6 months
-20°C, 1 month
(protect from light)
靶点:
TLR4
体外研究:
L48H37 inhibits LPS-induced inflammation, particularly TNF-α and IL-6 production and gene expression in mouse macrophages.
L48H37 (0-20 µM; 24 hours) decreases the viability of A549 and H460 cells with IC50 values of 5.3 µM and 2.3 µM, respectively, which is more effective compared to curcumin in lung cancer cells. It shows a low cytotoxicity on normal human lung epithelial cells (BEAS-2B) with IC50 of 21 μM.
L48H37 (1, 2, or 4 µM; 16 hours) dose‐dependently inhibited the expression of p‐Cdc2 and Cdc2, and increases the expression of p53. It also shows increased levels of cleaved poly (ADP‐ribosyl) polymerase (PARP) and reduced levels of anti‐apoptotic protein Bcl‐2 in H460 and A549 cells.
L48H37 (4 µM; 16 hours) rapidly induces intracellular ROS levels dose-dependently as detected by increased DCF levels in H460 and A549 cells.
体内研究:
L48H37 (intraperitoneal injection; 5 mg or 10 mg/kg; once daily; 11‐day ) inhibits H460 xenograft tumor growth and exhibits anti‐tumor activity in mice.
注意事项:
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2、以上信息仅做参考交流之用。
保存条件:
2-8°C 避光
UN码:
HazardClass:
危害声明:
安全说明:
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