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152121-53-4

中文名称 4-[4-(4-氟苯基)-2-(4-硝基苯基)-1H-咪唑-5-基]吡啶
英文名称 PD 169316
CAS 152121-53-4
分子式 C20H13FN4O2
分子量 360.347
MOL 文件 152121-53-4.mol
更新日期 2024/05/25 01:05:48
152121-53-4 结构式 152121-53-4 结构式

基本信息

中文别名
4-[4-(4-氟苯基)-2-(4-硝基苯基)-1H-咪唑-5-基]吡啶
英文别名
CS-497
PD169317
PD 169316, >97%
PD 169316, >=98%
PD169316(hanDMSO)
PD169316/PD-169316
PD 169316 - CAS 152121-53-4 - Calbiochem
4-[5-(4-fluorophenyl)-2-(4-nitrophenyl)-1H-iMidazol-4-yl]pyridine
4-[4-(4-Fluorophenyl)-2-(4-nitrophenyl)-1H-imidazol-5-yl]pyridine
Pyridine, 4-[4-(4-fluorophenyl)-2-(4-nitrophenyl)-1H-iMidazol-5-yl]-

物理化学性质

沸点583.1±50.0 °C(Predicted)
密度1.354±0.06 g/cm3(Predicted)
储存条件2-8°C
溶解度二甲基亚砜:>10mg/mL
酸度系数(pKa)9.09±0.10(Predicted)
形态固体
颜色浅橙色

安全数据

危险性符号(GHS)
GHS05,GHS06
警示词危险
危险性描述H301-H315-H318-H335
危险品标志Xn
危险类别码22-37/38-41
安全说明26-39
危险品运输编号UN 2811 6.1/PG 3
WGK Germany3
海关编码2933399990
4-[4-(4-氟苯基)-2-(4-硝基苯基)-1H-咪唑-5-基]吡啶价格(试剂级)
报价日期产品编号产品名称CAS号包装价格
2024/04/30P2532PD 169316
PD 169316
152121-53-410mg290元
2024/04/30S51834-[4-(4-氟苯基)-2-(4-硝基苯基)-1H-咪唑-5-基]吡啶
PD 169316
152121-53-45mg570.25元
2024/04/30S51834-[4-(4-氟苯基)-2-(4-硝基苯基)-1H-咪唑-5-基]吡啶
PD 169316
152121-53-425mg1570.48元

常见问题列表

生物活性
PD 169316 是一种有效的、细胞可渗透的选择性 p38 MAP kinase 抑制剂,IC50值为89 nM。 PD169316 可消除 TGFbeta 和 Activin A 引发的信号传导。 PD169316对 Enterovirus71 具有抗病毒活性。
靶点
TargetValue
TGF-β
()
Activin A
()
Enterovirus71
()
p38 MAPK
(Cell-free assay)
89 nM
体外研究

PD169316 (10 μM) inhibits TGFβ and Activin A, but not BMP4 signaling in CaOV3 cells. PD169316 (0.2-20 μM) inhibits TGFβ-induced Smad2 nuclear translocation, Smad7 mRNA induction, and reporter gene activity in CaOV3 cells. PD169316 (10 μM) shows a significantly increased rate of proliferation in Nestin knockdown cells, and can rescue the effect of Nestin knockdown on cell viability in the absence of EGF. PD169316 significantly inhibits p38 MAP kinase activity with no significant change in ERK activity in PC12 cells. PD169316 (10 μM) blocks apoptosis induced by trophic factor withdrawal in differentiated PC12 cells.PD169316 (10 μM, 30 min) selectively inhibits the kinase activity of the phosphorylated p38 without hindering upstream kinases to phosphorylate p38. Increased phospho p-38 levels in the presence of PD169316 are most likely due to blockade of negative feedback loop of dephosphorylation of p38 MAPK by MAPK phosphatases.

Western Blot Analysis

Cell Line: Ishikawa PRB or PRA cells.
Concentration: 10 μM.
Incubation Time: 30 min.
Result: Did not inhibit MEKK1-induced p38 phosphorylation.
体内研究

PD169316 (1 mg/kg, intramuscular injection every day for 14 consecutive days) shows antiviral activity in a suckling mouse model.

Animal Model: EV71-challenged suckling mouse model (7-day-old Kunming mice).
Dosage: 1 mg/kg.
Administration: Intramuscular injection every day for 14 consecutive days.
Result: Showed antiviral activity.
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