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AS1517499
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
AS1517499图片
CAS NO:919486-40-1
包装:10mg, 50mg
包装与价格:
包装价格(元)
10mg询价
50mg询价

生物活性

体外研究:AS1517499抑制IL-4诱导的小鼠脾脏T细胞向Th2分化,但对IL-12诱导的Th1分化没有影响。AS1517499能够阻止IL-4激活的、由STAT6介导的原代PCa细胞形成克隆潜力的增加。浓度为300 nM时,AS1517499降低了原代基底PCa细胞的形成克隆潜能。

体内研究:在小鼠体内进行AS1517499处理,AS1517499可通过抑制气管平滑肌中RhoA的上调,减缓抗原诱导的气管平滑肌高反应性,这可能是由于AS1517499降低了小鼠气管中IL-13的产生。AS1517499可通过抑制PPARγ来减少凋亡细胞灌注对bleomycin诱导的肺纤维化的预防效果。


化学数据

分子量397.86
分子式C20H20ClN5O2
CAS号919486-40-1
纯度>98%
溶解性(25°C)79 mg/mL in DMSO
储存和运输条件固体粉末: -20°C 冷藏长期储存
常温运输及临时存放

实验操作 来自于公开的文献,仅供相同实验参考(如实验材料、目的不同,请参考其他文献)

细胞实验
细胞系Normal human BSM cells
方法Cells are maintained in SmBM medium supplemented with 5% fetal bovine serum, 0.5 ng/ml human epidermal growth factor (hEGF), 5 mg/ml insulin, 2 ng/ml human fibroblast growth factor-basic (hFGF-b), 50 mg/ml gentamicin, and 50 ng/ml amphotericin B. Cells are maintained at 37℃ in a humidified atmosphere (5% CO2), fed every 48 to 72 hours, and passaged when cells reached 90 to 95% confluence. Then the hBSMCs (passages 7-9) are seeded in 6-well plates and 8-well chamber slides at a density of 3,500 cells/cm2 and, when 80 to 85% confluence is observed, cells are cultured without serum for 24 hours before addition of recombinant human IL-13. AS1517499, or its vehicle (0.3% DMSO) is treated 30 minutes before the addition of IL-13 (100 ng/ml). In some experiments, AS1517499 is treated 0 (co-incubation), 3, or 12 hours after the addition of IL-13. In another series of experiments, a selective Rho-kinase inhibitor Y-27632 or its vehicle (0.3% DMSO) is also applied 15 minutes before the IL-13 application. At the indicated time after the IL-13 treatment, cells are washed with PBS, immediately collected, and disrupted with 1×SDS sample buffer (250 μl/well), and used for Western blot analyses.
浓度100 nM
处理时间30 min

动物实验
动物模型A murine model of allergic bronchial asthma (Male BALB/c mice)
配制20% DMSO in saline
剂量1 or 10 mg/kg/d
给药处理i.p.

不同实验动物依据体表面积的等效剂量转换表(数据来源于FDA指南)

小鼠大鼠豚鼠仓鼠
重量 (kg)0.020.151.80.40.0810
体表面积 (m2)0.0070.0250.150.050.020.5
Km系数36128520
动物 A (mg/kg) = 动物 B (mg/kg) × 动物 B的Km系数
动物 A的Km系数

例如,依据体表面积折算法,将化合物用于小鼠的剂量20 mg/kg 换算成大鼠的剂量,需要将20 mg/kg 乘以小鼠的Km系数(3),再除以大鼠的Km系数(6),得到化合物用于大鼠的等效剂量为10 mg/kg。


储备液配制

以下数据基于产品分子量,对于特殊产品,请参照COA中的储备液配制条件和说明进行操作。

Concentration / Solvent Volume / Mass1 mg5 mg10 mg
1 mM2.5134 mL12.5672 mL25.1345 mL
5 mM0.5027 mL2.5134 mL5.0269 mL
10 mM0.2513 mL1.2567 mL2.5134 mL
 
 
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