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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 360.347
MOL 文件 152121-53-4.mol
更新日期 2025/01/22 01:45:32
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(diǎn)583.1±50.0 °C(Predicted)
密度1.354±0.06 g/cm3(Predicted)
儲(chǔ)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

安全數(shù)據(jù)

危險(xiǎn)性符號(hào)(GHS)GHS hazard pictogramsGHS hazard pictograms
GHS05,GHS06
警示詞危險(xiǎn)
危險(xiǎn)性描述H301-H315-H318-H335
危險(xiǎn)品標(biāo)志Xn
危險(xiǎn)類別碼22-37/38-41
安全說(shuō)明26-39
危險(xiǎn)品運(yùn)輸編號(hào)UN 2811 6.1/PG 3
WGK Germany3
海關(guān)編碼2933399990
4-[4-(4-氟苯基)-2-(4-硝基苯基)-1H-咪唑-5-基]吡啶價(jià)格(試劑級(jí))
報(bào)價(jià)日期產(chǎn)品編號(hào)產(chǎn)品名稱CAS號(hào)包裝價(jià)格
2024/11/08P2532PD 169316
PD 169316
152121-53-410mg290元
2024/11/08S51834-[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
2024/11/08P31614-[4-(4-氟苯基)-2-(4-硝基苯基)-1H-咪唑-5-基]吡啶
PD 169316 [Optimized for Cell Culture]
152121-53-41MG690元

常見(jiàn)問(wèn)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(hào)傳導(dǎo)。 PD169316對(duì) Enterovirus71 具有抗病毒活性。
靶點(diǎn)
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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