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TG101209
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。
TG101209图片
CAS NO:936091-14-4
包装:5mg, 10mg, 25mg
包装与价格:
包装价格(元)
Free Sample (0.5-1 mg)电议
5mg电议
10mg电议
25mg电议

产品介绍

生物活性

TG101209是一种选择性的JAK2抑制剂,IC50为6 nM,对Flt3和RET作用效果稍弱,IC50分别为25 nM和17 nM,作用于JAK2比作用于JAK3选择性高30倍左右,对JAK2V617F和MPLW515L/K突变型敏感。


化学数据

分子量509.67
分子式C26H35N7O2S
CAS号936091-14-4
纯度99.01%
溶解性(25°C)DMSO 72 mg/mL
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Ba/F3 cells, MPLW515L, CTLL-2 cells and HEL and K562 cells
方法XTT assay for cell proliferation.
In brief, approximately 2*103cells were plated into microtiterplate wells in 100 ml RPMI-1640 growth media with indicated concentrations of inhibitor. The relative growth of cells was quantified at 24-h intervals using Cell Proliferation Kit II (XTT) as per manufacturer’s guidelines (Roche, Indianapolis, IN, USA). After incubation, 20 ml of XTT was added to the wells and allowed to incubate for 4–6 h. The colored formazan product was measured spectrophotometrically at 450 nm with correction at 650 nm, and IC50 values were determined using the GraphPad Prism 4.0 software. Data were subjected to a non-linear regression-fit analysis and IC50 values were determined as the concentration, that inhibited proliferation by 50%. All experiments were done in triplicate and the results normalized to growth of untreated cells.
浓度0~100 μ M
处理时间24 h

动物实验
动物模型JAK2V617F-induced hematopoietic disease in a nude mouse model
配制DMSO
剂量10, 30 and 100mg/kg bid
给药处理oral gavage

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 mM1.9621 mL9.8103 mL19.6205 mL
5 mM0.3924 mL1.9621 mL3.9241 mL
10 mM0.1962 mL0.981 mL1.9621 mL