217720

Cdk1/5 Inhibitor

The Cdk1/5 Inhibitor, also referenced under CAS 40254-90-8, controls the biological activity of Cdk1/5. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.

• 別名: Cdk1/5 Inhibitor, 3-Amino-1H-pyrazolo[3,4-b]quinoxaline
• 実験式（ヒル表記法）: C₉H₇N₅
• CAS番号: 40254-90-8
• 分子量: 185.19
• UNSPSCコード: 12352200

特性

• 品質水準: 100
• アッセイ: ≥95% (HPLC)
• フォーム: solid
• メーカー／製品名: Calbiochem^®
• 保管条件: OK to freeze; protect from light
• 色: red
• 溶解性: DMSO: 5 mg/mL
• 輸送温度: ambient
• 保管温度: 2-8°C
• InChI: 1S/C9H7N5/c10-8-7-9(14-13-8)12-6-4-2-1-3-5(6)11-7/h1-4H,(H3,10,12,13,14)
• InChI Key: DWHVZCLBMTZRQM-UHFFFAOYSA-N

詳細

詳細

A 3-amino substituted pyrazoloquinoxaline compound that acts as a selective inhibitor of cyclin-dependent kinases 1 and 5 (Cdks; IC₅₀ = 0.6 µM and 0.4 µM for Cdk1/cyclin B and Cdk5/p25, respectively). Also shown to inhibit GSK-3β with (IC₅₀ = 1 µM). Does not inhibit Cdc25 phosphatase activity (IC₅₀ >10 µM).

A selective inhibitor of cyclin-dependent kinases 1 and 5 (Cdk1/Cdk5) (IC₅₀ = 600 nM for Cdk1/cyclin B and 400 nM for Cdk5/p25). Also shown to inhibit glycogen synthase kinase-3β (GSK-3β) (IC₅₀ = 1 µM). Does not inhibit Cdc25 phosphatase activity (IC₅₀ >10 µM).

生物化学的／生理学的作用

Cell permeable: no

Primary Target
Cdk1/cyclin B, Cdk5/p25

Product does not compete with ATP.

Reversible: no

Target IC₅₀: 0.6 µM and 0.4 µM for Cdk1/cyclin B and Cdk5/p25, respectively

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

Ortega, M.A., et al. 2002. Bioorg. Med. Chem.10, 2177.

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: 11 - Combustible Solids
• WGK: WGK 1