|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
![]()
CAS号:7421-40-1
|
英文名称:Carbenoxolone disodium
分子式
C34H48Na2O7
分子量
615
EINECS号
231-044-0
MDL
MFCD03840711
Smiles
InChIKey
乙二醇化学百科
基本信息
物化性质
安全信息
生产及用途
Carbenoxolone disodium 是甘草酸 (HY-N0184) 的活性代谢物和人 11β-HSD 和细菌 3α, 20β-HSD 的抑制剂。Carbenoxolone disodium 是一种缝隙连接的解耦剂 (gap junctions) 和并且可以有效抑制牛痘病毒生长。Carbenoxolone disodium 可用于研究消化性、食道和口腔溃疡和炎症的相关研究。 IC50: human 11β-HSD; bacterial 3α, 20β-HSD; gap junction; Vaccinia virus Carbenoxolone disodium (6-150 μM; pre-treatment 1 hour) inhibits Vaccinia virus (VACV) replication in a gap junction-independent in HaCaT cells, and it has toxicity effects on VACV-A5L-EGFP infected cells at 48 h.Carbenoxolone (30 μM; pre-treatment 1 hour) does not upregulate PP2A expression, but induces the late protein A27 expression in hacat cells.
Cell Viability Assay
Western Blot Analysis
Carbenoxolone (intraperitoneal injection; 100, 200 and 300 mg/kg; 30, 60 and 60 min before Diazepam) does not induce a muscle relaxant activity and shows muscle relaxant activity compared to normal saline, and this effect was more than diazepam in the traction test.Carbenoxolone (intraperitoneal injection; 100, 200 and 300 mg/kg; 30, 60 and 60 min before Pentylenetetrazole) significantly increases sleeping time and decreases latency in mice as a dose-dependent manner in Pentylenetetrazole (PTZ) Seizure model. The ED 50 value is 83.3 mg/kg (%95 CL:556.29).
类别 有毒物质毒性分级 中毒急性毒性 口服-大鼠 LD50: 2450 毫克/公斤; 腹腔-小鼠 LD50: 120 毫克/公斤可燃性危险特性 热分解排出有毒氧化钠烟雾储运特性 库房低温通风干燥灭火剂 水, 二氧化碳, 泡沫, 干粉
上下游产品
相关产品
产品供应商
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||