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152121-53-4

中文名稱 4-[4-(4-氟苯基)-2-(4-硝基苯基)-1H-咪唑-5-基]吡啶
英文名稱 PD 169316
CAS 152121-53-4
分子式 C20H13FN4O2
分子量 360.34
MOL 文件 152121-53-4.mol
更新日期 2026/05/26 12:43:09
152121-53-4 結(jié)構(gòu)式 152121-53-4 結(jié)構(gòu)式

基本信息

中文別名
4-[4-(4-氟苯基)-2-(4-硝基苯基)-1H-咪唑-5-基]吡啶
英文別名
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]-

物理化學(xué)性質(zhì)

沸點583.1±50.0 °C(Predicted)
密度1.354±0.06 g/cm3(Predicted)
儲存條件2-8°C
溶解度二甲基亞砜:>10mg/mL
酸度系數(shù)(pKa)9.09±0.10(Predicted)
形態(tài)固體
顏色淺橙色
InChI1S/C20H13FN4O2/c21-16-5-1-13(2-6-16)18-19(14-9-11-22-12-10-14)24-20(23-18)15-3-7-17(8-4-15)25(26)27/h1-12H,(H,23,24)
InChIKeyBGIYKDUASORTBB-UHFFFAOYSA-N
SMILES[O-][N+](=O)c1ccc(cc1)-c2nc(-c3ccc(F)cc3)c([nH]2)-c4ccncc4

安全數(shù)據(jù)

危險性符號(GHS)腐蝕 (GHS05)有毒 (GHS06)
GHS05,GHS06
警示詞危險
危險性描述H301-H315-H318-H335
危險品標(biāo)志Xn
危險類別碼22-37/38-41
安全說明26-39
危險品運輸編號UN 2811 6.1/PG 3
WGK Germany3
海關(guān)編碼2933399990
存儲類別6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
危險性類別Acute Tox. 3 Oral
Eye Dam. 1
Skin Irrit. 2
STOT SE 3
4-[4-(4-氟苯基)-2-(4-硝基苯基)-1H-咪唑-5-基]吡啶價格(試劑級)
報價日期產(chǎn)品編號產(chǎn)品名稱CAS號包裝價格
2026/03/03S51834-[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
2026/03/03S51834-[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
2025/12/22P2532PD 169316
PD 169316
152121-53-410mg290元

常見問題列表

生物活性
PD 169316 是一種有效的、細(xì)胞可滲透的選擇性 p38 MAP kinase 抑制劑,IC50值為89 nM。 PD169316 可消除 TGFbeta 和 Activin A 引發(fā)的信號傳導(dǎo)。 PD169316對 Enterovirus71 具有抗病毒活性。
靶點
TargetValue
TGF-β
()
Activin A
()
Enterovirus71
()
p38 MAPK
(Cell-free assay)
89 nM
體外研究

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.
體內(nèi)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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