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RK-24466
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。
RK-24466图片
CAS NO:213743-31-8
包装与价格:
包装价格(元)
1 mg电议
5 mg电议
10 mg电议
25 mg电议
50 mg电议
100 mg电议
200 mg电议
1 mL*10 mM(in DMSO)电议

产品名称
KIN 001-51
产品介绍
RK-24466 是高效的、选择性的Lck抑制剂,对 Lck (64-509) 和 LckCD 亚型的 IC50 值分别为小于 1 和2 nM。

产品描述

RK-24466 is a selective and potent inhibitor of Lck, inhibits Lck (64-509) and LckCD isoforms with IC50s of less than 1 and 2 nM, respectively.

体外活性

RK-24466, a lymphocyte-specific protein tyrosine kinase (Lck) inhibitor, significantly inhibited both VSMC proliferation and migration. RK-24466 suppresses VSMC proliferation and migration via down-regulating the protein kinase B (Akt) and extracellular signal regulated kinase (ERK) pathways, and it significantly decreased the expression of proliferating cell nuclear antigen (PCNA) and cyclin D1 and, the phosphorylation of retinoblastoma protein (pRb). Additionally, RK-24466 suppressed the migration of VSMCs from endothelium-removed aortic rings, as well as neointima formation following rat carotid balloon injury. The present study identified RK-24466 as a potent VSMC proliferation and migration inhibitor and warrants further studies to elucidate its more detailed molecular mechanisms, such as its primary target, and to further validate its in vivo efficacy as a therapeutic agent for pathologic vascular conditions, such as restenosis and atherosclerosis[1].

Cas No.

213743-31-8

分子式

C23H22N4O

分子量

370.45

别名

KIN 001-51

储存和溶解度

DMSO:40 mg/mL (107.97 mM),Need ultrasonic
Powder: -20°C for 3 years
In solvent: -80°C for 2 years