INDIRUBIN-3'-MONOXIME-5-SULPHONIC ACID
INDIRUBIN-3'-MONOXIME-5-SULPHONIC ACID Basic information
- Product Name:
- INDIRUBIN-3'-MONOXIME-5-SULPHONIC ACID
- Synonyms:
-
- 1H-Indole-5-sulfonic acid, 3-[1,3-dihydro-3-(hydroxyimino)-2H-indol-2-ylidene]-2,3-dihydro-2-oxo-
- Indirubin3'monoxime5sulphonic acid,Indirubin 3' monoxime 5 sulphonic acid
- Indirubin-3'-monoxime-5-sulphonic acid
- Indirubin-3'-monoxime-5-sulphonic acid
- CAS:
- 331467-05-1
- MF:
- C16H11N3O5S
- MW:
- 357.34
- Mol File:
- Mol File
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INDIRUBIN-3'-MONOXIME-5-SULPHONIC ACID Chemical Properties
- storage temp.
- Store at -20°C
- solubility
- Soluble in DMSO
- form
- solid
- color
- dark red
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INDIRUBIN-3'-MONOXIME-5-SULPHONIC ACID Usage And Synthesis
Uses
Indirubin-3'-monoxime-5-sulphonic acid is a potent and selective inhibitor of CDK1, CDK5, and GSK-3β with IC50s of 5 nM, 7 nM, and 80 nM, respectively[1].
Biological Activity
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
IC 50
CDK1: 5 nM (IC50); CDK5: 7 nM (IC50); GSK-3β: 80 nM (IC50)
References
[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;276(1):251-60. DOI:10.1074/jbc.M002466200
INDIRUBIN-3'-MONOXIME-5-SULPHONIC ACIDSupplier
Beijing Jin Ming Biotechnology Co., Ltd.
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Beijing Jin Ming Biotechnology Co., Ltd.
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TargetMol Chemicals Inc.
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