402088

Indirubin-3′-monoxime-5-sulphonic Acid

A potent, reversible, and selective inhibitor of Cdk1 (IC₅₀ = 5 nM) and Cdk5 (IC₅₀ = 7 nM) and glycogen synthase kinase-3β (GSK-3β; IC₅₀ = 80 nM).

• 别名: Indirubin-3′-monoxime-5-sulphonic Acid
• 经验公式（希尔记法）: C₁₆H₁₁N₃O₅S
• CAS号: 331467-05-1
• 分子量: 357.34
• 分類程式碼代碼: 12352106
• 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: dark red
• 溶解度: DMSO: 50 mg/mL
• 運輸包裝: ambient
• 儲存溫度: −20°C
• InChI: 1S/C16H11N3O5S/c20-16-13(10-7-8(25(22,23)24)5-6-12(10)18-16)15-14(19-21)9-3-1-2-4-11(9)17-15/h1-7,17,19,21H,(H,22,23,24)
• InChI 密鑰: IZDNACYDKBNHHC-UHFFFAOYSA-N

说明

一般說明

A highly potent, reversible, and selective inhibitor of cyclin-dependent kinases 1 and 5 (IC₅₀ = 5 nM for CDK1; IC₅₀ = 7 nM for CDK5). Reported to act by competing with ATP for binding to the catalytic site of the kinase. Also acts as a potent inhibitor of glycogen synthase kinase-3β (GSK-3β; IC₅₀ = 80 nM).

A potent, reversible, and selective inhibitor of Cdk1 (IC₅₀ = 5 nM) and Cdk5 (IC₅₀ = 7 nM) and glycogen synthase kinase-3β (GSK-3β; IC₅₀ = 80 nM). The inhibition is competitive with respect to ATP.

生化／生理作用

Cell permeable: no

Primary Target
CDK1

Product competes with ATP.

Reversible: yes

Target IC₅₀: 5 nM, 7 nM, 80 nM, against Cdk1, Cdk5, and glycogen synthase kinase-3β (GSK-3β), respectively

包裝

Packaged under inert gas

警告

Toxicity: Standard Handling (A)

重構

Following reconstitution, aliquot and freeze at -20°C. Stock solutions are stable for up to 4 months at -20°C.

其他說明

Leclerc, S., et al. 2001. J. Biol. Chem.276, 251.

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 1
• 閃點（°F）: Not applicable
• 閃點（°C）: Not applicable