Indirubin-3'-monoxime

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Chemical Structure| 160807-49-8 同义名 : 靛玉红-3' -单肟 ;Indirubin-3'-oxime
CAS号 : 160807-49-8
货号 : A738539
分子式 : C16H11N3O2
纯度 : 99%+
分子量 : 277.28
MDL号 : MFCD02683594
存储条件:

Pure form Sealed in dry, 2-8°C

In solvent -20°C:3-6个月-80°C:12个月

溶解度 : -
动物实验配方:
生物活性
描述 Indirubin-3'-monoxime is an antagonist to GSK-3β by competing with ATP, displaying a Ki of 0.85 μM, and a Km of 110 μM. Furthermore, it deters the phosphorylation of tau by GSK-3β, showing an IC50 roughly around 100 nM, and fully obstructs the phosphorylation at the AT100 epitope[1]. Additionally, Indirubin-3'-monoxime impedes the proliferation of vascular smooth muscle cells (VSMC) with an IC50 approximately 2 µM. It mitigates the PDGF-induced migration of VSMC and hinders the migratory response in VSMCs, while also diminishing the production of pro-migratory LT in monocytes. Indirubin-3'-monoxime equally curbs the synthesis of 5-lipoxygenase (5-LO) products in monocytes and neutrophils, with IC50 values of 5.0±1.1 and 3.7±1.2 µM, respectively, and it stands as a 5-LO inhibitor with an IC50 between 7.8-10 µM in assays free of cells[3].
实验方案
1mg 5mg 10mg

1 mM

5 mM

10 mM

3.61mL

0.72mL

0.36mL

18.03mL

3.61mL

1.80mL

36.06mL

7.21mL

3.61mL

参考文献

[1]Leclerc S, et al. Indirubins inhibit glycogen synthase kinase-3 beta and CDK5/p25, two protein kinases involved in abnormal tau phosphorylation in Alzheimer's disease. A property common to most cyclin-dependent kinase inhibitors? J Biol Chem. 2001 Jan 5;2

[2]Sharma S, et al. Neuroprotective role of Indirubin-3'-monoxime, a GSKβ inhibitor in high fat diet induced cognitive impairment in mice. Biochem Biophys Res Commun. 2014 Oct 3;452(4):1009-15.

[3]Blazevic T, et al. Indirubin-3'-monoxime exerts a dual mode of inhibition towards leukotriene-mediated vascular smooth muscle cell migration. Cardiovasc Res. 2014 Mar 1;101(3):522-32.