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甘珀酸钠
产品纠错
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
中文名称 甘珀酸钠
英文名称 Carbenoxolone disodium
CAS号 7421-40-1
分子式 C34H48Na2O7
分子量 614.72
EINECS号 231-044-0
物化性质
熔点 >275°C (dec.)
LogP 7.083 (est)
溶解度 甲醇(微溶)、水(微溶)
形态 固体
酸度系数(pKa) pKa1 4.18; pKa2 5.52(at 25℃)
颜色 白色至类白色
水溶解性 Soluble in water to 100 mM.
稳定性 吸湿性
安全信息
危险品标志 Xn,Xi
危险类别码 22-36
安全说明 26-36
WGK Germany 3
RTECS号 RK0250000
毒性 LD50 in male mice (mg/kg): 198 i.v.; 120 i.p.; in male rats (mg/kg): 3200 orally (Robson, Sullivan)
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

Cell Line: HaCaT cells
Concentration: 6 μM, 12 μM, 30 μM, 60 μM, 150 μM
Incubation Time: Pre-treatment 1 hour
Result: Had no toxicity until 48 hours at high dose in virus-infected cells.

Western Blot Analysis

Cell Line: HaCaT cells
Concentration: 30 μM
Incubation Time: Pre-treatment 1 hour
Result: Presented an obvious upregulation of A27.

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).

Animal Model: Male BALB/c mice
Dosage: 100, 200 and 300 mg/kg
Administration: Intraperitoneal injection; 30, 60 and 60 min before Pentylenetetrazole
Result: Significantly increased the sleeping time in mice.
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
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