538498

RGS4 Inhibitor, CCG-

• 别名: RGS4 Inhibitor, CCG-, 4-Butyl-2-ethyl-1,2,4-thiadiazolidine-3,5-dione, CCG203769
• 经验公式（希尔记法）: C₈H₁₄N₂O₂S
• 分子量: 202.27
• 分類程式碼代碼: 12352200
• NACRES: NA.77

属性

• 化驗: ≥98% (HPLC)
• 品質等級: 100
• 形狀: oil
• 製造商／商標名: Calbiochem^®
• 儲存條件: OK to freeze; protect from light
• 顏色: colorless
• 溶解度: DMSO: 100 mg/mL
• 運輸包裝: wet ice
• 儲存溫度: 2-8°C

说明

一般說明

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.

生化／生理作用

Cell permeable: yes

Primary Target
RGS4

Reversible: no

Target IC₅₀: 17 nM for RGS4 inhibition

包裝

Packaged under inert gas

警告

Toxicity: Standard Handling (A)

重構

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

其他說明

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

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

法律資訊

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

安全信息

• 儲存類別代碼: 10 - Combustible liquids
• 水污染物質分類（WGK）: WGK 3
• 閃點（°F）: Not applicable
• 閃點（°C）: Not applicable