您好,欢迎来到试剂信息网! [登录] [免费注册]
试剂信息网
位置:首页 > 产品库 > PD-089828
立即咨询
咨询类型:
     
*姓名:
*电话:
*单位:
Email:
*留言内容:
请详细说明您的需求。
*验证码:
 
PD-089828
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。
PD-089828图片
CAS NO:179343-17-0
包装与价格:
包装价格(元)
5mg电议
10mg电议

产品介绍
PD-089828 是 ATP 竞争性FGFR-1PDGFR-βEGFR(IC50分别为 0.15, 1.76, 5.47 μM) 抑制剂和c-Src酪氨酸激酶非竞争性抑制剂 (IC50=0.18 μM)。PD-089828 也抑制MAPKIC50值为 7.1 μM。PD-089828 体外抑制 PDGF-、EGF- 和 bFGF 介导的酪氨酸激酶受体的自磷酸化。PD-089828 具有持久的细胞活性。
生物活性

PD-089828 is an ATP competitive inhibitor ofFGFR-1,PDGFR-βandEGFR(IC50s=0.15, 1.76, and 5.47 μM, respectively) and a noncompetitive inhibitor ofc-Srctyrosine kinase (IC50=0.18 μM). PD-089828 also inhibitsMAPKwith anIC50of 7.1 μM. PD-089828 inhibits PDGF-, EGF- and bFGF-mediated tyrosine kinase receptor autophosphorylation in vitro. PD-089828 has a long-lasting cellular activity[1].

IC50& Target[1]

FGFR1

0.15 μM (IC50)

PDGFR-β

1.76 μM (IC50)

EGFR

5.47 μM (IC50)

c-Src

0.18 μM (IC50)

FGFR1

0.14 μM (Ki)

PDGFR-β

2.38 μM (Ki)

EGFR

3.16 μM (Ki)

c-Src

0.1 μM (Ki)

体外研究
(In Vitro)

PD-089828 (0.5-20 μM; 2 hours) inhibits PDGFR autophosphorylation with an IC50of 0.82 μM[1].
PD-089828 (1-50 μM; 2 hours) inhibits EGFR autophosphorylation with an IC50value of 10.9 μM[1].
In A121(p) cells, PD 089828 potently inhibits the phosphorylation of FGFR-1 with an IC50value of 0.63 μM[1]. PD-089828 (10 μM; 8 days) produces a concentration-related inhibition of serum-stimulated cell growth with an IC50value of 1.8 μM[1].
PD-089828 inhibits increases in DNA synthesis stimulated by all three growth factors, with IC50values of 0.8 for PDGF-, 1.7 for EGF- and 0.48 μM for bFGF-induced mitogenesis[1].

Cell Proliferation Assay[1]

Cell Line:Vascular smooth muscle cells (serum-stimulated growth)
Concentration:10 μM
Incubation Time:8 consecutive days
Result:Produced a concentration-related inhibition of serum-stimulated cell growth with an IC50 value of 1.8 μM.

Western Blot Analysis[1]

Cell Line:Vascular smooth muscle cells (stimulated with PDGF-BB 30 ng/ml)
Concentration:0.5-20 μM
Incubation Time:2 hours
Result:Inhibited PDGFR autophosphorylation with an IC50of 0.82 μM.
分子量

405.28

Formula

C18H18Cl2N6O

CAS 号

179343-17-0

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.