您好,欢迎来到试剂仪器网! [登录] [免费注册]
试剂仪器网
位置:首页 > 产品库 > SRPIN340(SRPK inhibitor)
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:
 
SRPIN340(SRPK inhibitor)
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。
SRPIN340(SRPK inhibitor)图片
CAS NO:218156-96-8
规格:≥98%
包装与价格:
包装价格(元)
1mg电议
2mg电议
5mg电议
10mg电议
25mg电议
50mg电议
100mg电议
250mg电议
500mg电议

产品介绍
理化性质和储存条件
Molecular Weight (MW)349.35
FormulaC18H18F3N3O
CAS No.218156-96-8
Storage-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)DMSO: 70 mg/mL (200.4 mM)
Water: <1 mg/mL
Ethanol: 70 mg/mL (200.4 mM)
Solubility (In vivo)1% DMSO+30% polyethylene glycol+1% Tween 80: 8 mg/mL
SynonymsSRPIN340; SRPIN-340; SRPIN 340
实验参考方法
In Vitro

In vitro activity: SRPIN340 inhibits SR phosphorylation by SRPK in Flp-In293 cells and promotes degradation of SRp75 in a dose-dependent manner, which subsequently inhibits HIV production. SRPIN340 dose (5 mg/mL) produces no abnormalities in chromosomal structure and chromosome number of CHO cells. SRPIN340 suppresses in a dose-dependent fashion expression of a HCV subgenomic replicon and replication of the HCV-JFH1 clone in vitro.


Cell Assay: SRPIN340 has been revealed to inhibit replication of HIV-1 and other viruses that require SR protein-dependent RNA processing for the propagation in HIV-1 transfected or infected Flp-In293 cell lines. In addition, SRPIN340 has been reported to significantly inhibit SRPK1 and SRPK2 kinase activity but not potently inhibit other SRPKs, such as Clk1 and Clk4 with a Ki value of 0.89μM for SRPK1. Besides, SRPIN340 has been exhibited to dose-dependently promote degradation of SRp75 which is necessary for HIV expression. Moreover, SRPIN340 has shown the inhibition of propagation of Sindbis virus with an IC50 of 60μM and the protection against the cytopathic effect of Sindbis virus.

In VivoSRPIN340 inhibits CNV formation in a dose-dependent manner in vivo. SRPIN340 significantly decreases the protein levels of VEGF, MCP-1, ICAM-1, and consequently inhibits macrophage infiltration.
Animal modelA mouse model with choroidal neovascularization (CNV)
Formulation & DosageDissolved in DMSO; ~20 pmol; i.v.
References

Proc Natl Acad Sci U S A. 2006 Jul 25;103(30):11329-33; Antimicrob Agents Chemother. 2010 Aug;54(8):3179-86; Mol Vis. 2013;19:536-43.