538498

RGS4 Inhibitor, CCG-

• 別名: RGS4 Inhibitor, CCG-, 4-Butyl-2-ethyl-1,2,4-thiadiazolidine-3,5-dione, CCG203769
• 実験式（ヒル表記法）: C₈H₁₄N₂O₂S
• 分子量: 202.27
• UNSPSCコード: 12352200
• NACRES: NA.77

特性

• アッセイ: ≥98% (HPLC)
• 品質水準: 100
• フォーム: oil
• メーカー／製品名: Calbiochem^®
• 保管条件: OK to freeze; protect from light
• 色: colorless
• 溶解性: DMSO: 100 mg/mL
• 輸送温度: wet ice
• 保管温度: 2-8°C

詳細

詳細

A cell-permeable, thiadiazolidinone based, thiol reactive compound that covalently binds to the regulator of G protein signaling 4 (RGS4) and irreversibly inhibits its activity (IC₅₀ = 17 nM). Exhibits high selectivity over RGS19 and RGS16 (IC₅₀ = 140 nM and 6 µM, respectively) and has negligible effects towards RGS7, RGS8, and papain IC₅₀ = 100, 70, and 100 µM, respectively). Displays ~300-fold greater selectivity over GSK-3beta (IC₅₀ = 5.4 µM). Shown to disrupt RGS4/Gαo interaction and reverse the Gαo-induced membrane translocation of GFP-tagged RGS4 in HEK293 cells (~3 µM). Enhances Gαq-dependent Ca2+ signaling activated by the M3 muscarinic receptor. Potentiates Gαi-dependent muscarinic bradycardia and reverses D2 antagonist raclopride-induced akinesia and bradykinesia in a murine model of the movement disorder in Parkinson′s disease.

生物化学的／生理学的作用

Cell permeable: yes

Primary Target
RGS4

Reversible: no

Target IC₅₀: 17 nM for RGS4 inhibition

包装

Packaged under inert gas

警告

Toxicity: Standard Handling (A)

再構成

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.

その他情報

Blazer, L.L., et al. 2015. ACS Chem. Neurosci.6, 311.

Turner, E., et al. 2012. ACS Med. Chem. Lett..3, 146.

法的情報

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

安全性情報

• 保管分類コード: 10 - Combustible liquids
• WGK: WGK 3
• 引火点(°F): Not applicable
• 引火点(℃): Not applicable