681641

Wee1 Inhibitor II

The Wee1 Inhibitor II, also referenced under CAS 622855-50-9, controls the biological activity of Wee1. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.

• 别名: Wee1 Inhibitor II, 6-Butyl-4-(2-chlorophenyl)-9-hydroxypyrrolo[3,4-c]carbazole-1,3-(2H,6H)-dione
• 经验公式（希尔记法）: C₂₄H₁₉ClN₂O₃
• CAS号: 622855-50-9
• 分子量: 418.87
• MDL號碼: MFCD28138108
• 分類程式碼代碼: 12352200
• NACRES: NA.77

属性

• 品質等級: 100
• 化驗: ≥97% (HPLC)
• 形狀: solid
• 製造商／商標名: Calbiochem^®
• 儲存條件: OK to freeze; protect from light
• 顏色: brown
• 溶解度: DMSO: 10 mg/mL; ethanol: 10 mg/mL
• 運輸包裝: ambient
• 儲存溫度: −20°C
• SMILES 字串: Clc1c(cccc1)c2c3c(c4c([n](c5c4cc(cc5)O)CCCC)c2)[c]([nH][c]3=O)=O
• InChI: 1S/C24H19ClN2O3/c1-2-3-10-27-18-9-8-13(28)11-16(18)20-19(27)12-15(14-6-4-5-7-17(14)25)21-22(20)24(30)26-23(21)29/h4-9,11-12,28H,2-3,10H2,1H3,(H,26,29,30)
• InChI 密鑰: HLSZACLAFZWCCS-UHFFFAOYSA-N

说明

一般說明

A pyrrolocarbazole compound that acts as a potent, ATP-binding site-targeting inhibitor of Wee1 (IC₅₀ = 59 nM) with a ~590-fold selectivity over the related checkpoint kinase Chk1 (IC₅₀ = 35 µM).

生化／生理作用

Cell permeable: no

Primary Target
Wee1

Product does not compete with ATP.

Reversible: no

Target IC₅₀: 59 nM against Wee1

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 6 months at -20°C.

其他說明

Palmer, B.D., et al. 2006. J. Med. Chem.49, 4896.

法律資訊

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

安全信息

• 儲存類別代碼: 11 - Combustible Solids
• 水污染物質分類（WGK）: WGK 2
• 閃點（°F）: Not applicable
• 閃點（°C）: Not applicable