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103141-09-9

中文名称 N-(4-甲氧苯基)-1-苯基-1H-吡唑-3-胺
英文名称 FPL 62064
CAS 103141-09-9
分子式 C16H15N3O
分子量 265.31
MOL 文件 103141-09-9.mol
更新日期 2024/07/21 13:45:55
103141-09-9 结构式 103141-09-9 结构式

基本信息

中文别名
N-(4-甲氧苯基)-1-苯基-1H-吡唑-3-胺
英文别名
FPL 62064
N-(4-Methoxyphenyl)-1-phenyl-1H-pyrazol-3-amine
1H-Pyrazol-3-amine,N-(4-methoxyphenyl)-1-phenyl-

物理化学性质

沸点442.6±25.0 °C(Predicted)
密度1.15±0.1 g/cm3(Predicted)
储存条件Keep in dark place,Sealed in dry,Room Temperature
溶解度DMSO: 250 mg/mL (942.29 mM)
酸度系数(pKa)2.42±0.50(Predicted)
形态Solid
颜色Light yellow to yellow

安全数据

危险性符号(GHS)
GHS08
警示词警告
危险性描述H341
N-(4-甲氧苯基)-1-苯基-1H-吡唑-3-胺价格(试剂级)
报价日期产品编号产品名称CAS号包装价格
2024/04/30HY-105024N-(4-甲氧苯基)-1-苯基-1H-吡唑-3-胺
FPL 62064
103141-09-95mg1500元
2024/04/30S0759N-(4-甲氧苯基)-1-苯基-1H-吡唑-3-胺
FPL 62064
103141-09-95mg1570.85元
2024/04/30HY-105024N-(4-甲氧苯基)-1-苯基-1H-吡唑-3-胺
FPL 62064
103141-09-910mM * 1mLin DMSO1666元

常见问题列表

生物活性
FPL 62064 是一种 5-lipoxygenase (5-LOX) 和 prostaglandin synthetase (cyclooxygenase, COX) 的有效双重抑制剂,对RBL-1胞质5-LOX和精囊prostaglandin synthetase的IC50值分别为3.5 μM和3.1 μM。FPL 62064 具有有效的抗炎活性。
靶点
TargetValue
seminal vesicle prostaglandin synthetase
(Cell-free assay)
3.1 μM
RBL-1 cytosolic 5-LOX
(Cell-free assay)
3.5 μM
体外研究

FPL 62064 inhibits both 5-1ipoxygenase (IC 50 of 3.5 μM for RBL-1 cytosolic 5-1ipoxygenase) and prostaglandin synthetase (IC 50 of 3.1 μM for seminal vesicle prostaglandin synthetase ) with equal facility in the isolated enzyme screens. However in the intact RBL-I cell prostaglandin synthetase (IC 50 of 3.6 μM) is more readily inhibited by FPL 62064 than is 5-1ipoxygenase (IC 50 of 31 μM). This difference in sensitivity is not reflected in the mouse macrophage where the IC 50 s for leukotriene (IC 50 of 0.72 μM) and prostaglandin (IC 50 of 0.43 μM) production are similar.

体内研究

FPL 62064 (5-20 mg/kg; intraperitoneal injection; female LACA mice) treatment inhibits peritoneal inflammation induced by immune-complex.

Animal Model: Female LACA mice (20-30 g) injected with immune complex.
Dosage: 5 mg/kg, 10 mg/kg, 20 mg/kg
Administration: Intraperitoneal injection
Result: Produced a dose-related inhibition of dye extravasation, leukotriene C 4 (LTC 4 ) and prostaglandin E 2 (PGE 2 ) formation.
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