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172733-42-5

中文名称 LY-315920
英文名称 NATRIUM[(1-BENZYL-2-ETHYL-3-OXAMOYLINDOOL-4-YL)OXY]ACETAAT
CAS 172733-42-5
分子式 C21H19N2NaO5
分子量 402.376
MOL 文件 172733-42-5.mol
172733-42-5 结构式 172733-42-5 结构式

基本信息

中文别名
伐瑞拉迪钠
英文别名
LY 315920Na
LY 315920 sodium
Varespladib sodium
LY315920 sodiuM salt
NATRIUM[(1-BENZYL-2-ETHYL-3-OXAMOYLINDOOL-4-YL)OXY]ACETAAT
[[3-(Aminooxoacetyl)-2-ethyl-1-(phenylmethyl)-1H-indol-4-yl]oxy]acetic acid monosodium salt

物理化学性质

形态Solid
颜色Off-white to light yellow

常见问题列表

生物活性
Varespladib sodium (LY315920 sodium) 是一种有效且具有选择性的 group IIA, secretory phospholipase A2 (sPLA2) 抑制剂,其 IC50 值为 9 nM。Varespladib sodium 对大鼠,兔,豚鼠和人等各种物种血清的 sPLA2 活性具有明显的抑制作用,IC50 分别为 8.1 nM,5.0 nM,3.2 nM 和 6.2 nM。
靶点

sPLA2

9 nM (IC 50 )

体外研究

Varespladib sodium (10 μM; 24 and 48 hours; HCjE cells) treatment results in complete inhibition of the RA-induced increase in MUC16 protein detected in cell lysates at both time points.
Varespladib sodium (10 μM; 24 and 48 hours; HCjE cells) treatment significantly inhibits RA-induced MUC16 expression by 100% at 24 hours and 99% at 48 hours.

Western Blot Analysis

Cell Line: HCjE cells
Concentration: 10 μM
Incubation Time: 24 hours, 48 hours
Result: Significantly inhibited the RA-induced MUC16 protein expression at both time points.

RT-PCR

Cell Line: HCjE cells
Concentration: 10 μM
Incubation Time: 24 hours, 48 hours
Result: Significantly inhibited RA-induced MUC16 expression by 100% at 24 hours and 99% at 48 hours.
体内研究

Varespladib sodium treatment inhibits human sPLA 2 -induced release of thromboxane A 2 (TXA 2 ) from isolated guinea pig lung bronchoalveolar lavage cells with an IC 50 of 0.79 μM. And the ED 50 for Varespladib sodium is 16.1 mg/kg.

Animal Model: Male Hartley guinea pigs (300-500 g)
Dosage: 3 mg/kg, 10 mg/kg, and 30 mg/kg
Administration: Intravenous injection (Pharmacokinetic study)
Result: Consistent inhibition of sPLA2 activity in BAL fluid was observed. Reduced the human sPLA2-induced generation of TXA2 on BAL cells from guinea pigs.
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