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PDK1-IN-RS2
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。
PDK1-IN-RS2图片
CAS NO:1643958-89-7
包装与价格:
包装价格(元)
5mg电议
10mg电议
25mg电议
50mg电议
100mg电议

产品介绍
PDK1-IN-RS2 是一种肽对接基序 (PIFtide) 的模拟物,也是一种底物选择性 PDK1 抑制剂,Kd 为 9 μM。PDK1-IN-RS2 抑制 PDK1 对下游激酶 S6K1 的激活。
Cas No.1643958-89-7
分子式C15H9ClN2O2S3
分子量380.89
溶解度DMSO : 125 mg/mL (328.18 mM; Need ultrasonic)
储存条件Store at -20°C
General tipsFor obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.
Shipping ConditionEvaluation sample solution : ship with blue ice
All other available size: ship with RT , or blue ice upon request
产品描述

PDK1-IN-RS2 is a mimic of peptide docking motif (PIFtide) and is a substrate-selectivePDK1inhibitor with aKdof 9 μM. PDK1-IN-RS2 suppresses the activation of the downstream kinases S6K1 byPDK1[1].

PDK1-IN-RS2 stimulates the catalytic activity of PDK1 toward a peptide substrate by sixfold. The sulfonyl group of PDK1-IN-RS2 interacts with Arg131 through a salt bridge, because the sulfonamide is likely ionized under the crystallization conditions[1].