Inibitor of phosphoinositide-dependent kinase 1 and GSK
Inhibitor of phosphoinositide-dependent kinase 1 (PDK1). Potent, reversible and ATP-competitive inhibitor of glycogen synthase kinase-3α/β (GSK-3α/β) (IC50=5nM). Maintains self-renewal and pluripotency in embryonic stem cells via activation of Wnt in vitro. Promotes proliferation and dedifferentiation in cardiomyocytes.
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Product Details
Appearance |
Dark red solid. |
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CAS |
667463-62-9 |
Couple Target |
GSK, Phosphoinositide-dependent protein kinase |
Couple Type |
Inhibitor |
Formula |
C16H10BrN3O2 |
MW |
356.2 |
Purity |
≥98% (HPLC) |
Solubility |
Soluble in DMSO. |
Handling & Storage
Use/Stability |
As indicated on product label or CoA when stored as recommended. |
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Handling |
Protect from light. |
Long Term Storage |
+4°C |
Shipping |
Ambient Temperature |
Regulatory Status |
RUO – Research Use Only |
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- Adipose-derived mesenchymal stem cells promote salivary duct regeneration via a paracrine effect: S. Kang, et al.; J. Oral. Biosci. 65, 104 (2023), Abstract
- Wnt/β-Catenin Protects Lymphocytes from HIV-Mediated Apoptosis via Induction of Bcl-xL: Y.A. Albalawi, et al.; Viruses 14, 1469 (2022), Abstract
- Liquidambaric acid inhibits Wnt/β-catenin signaling and colon cancer via targeting TNF receptor-associated factor 2: Yan, R., Zhu, H., et al.; Cell Rep. 38, 110319 (2022), Abstract
- Axitinib blocks Wnt/β-catenin signaling and directs asymmetric cell division in cancer: Qu, Y., Gharbi, N., et al.; PNAS 113, 9339 (2016), Abstract
- GSK3β-dependent phosphorylation alters DNA binding, transactivity and half-life of the transcription factor USF2: Horbach, T., Chi, T. F., et al.; PLoS One 9, e107914 (2014), Abstract
- Glycogen synthase kinase-3 inhibition reduces ischemic cerebral damage, restores impaired mitochondrial biogenesis and prevents ROS production: A. Valerio, et al.; J. Neurochem. 116, 1148 (2011), Abstract
- Anticancer effects and antimetastatic mechanisms of novel indirubin derivatives: C.A. Kressirer; , (2010), (PhD thesis), Full Text
- Wnt/beta-catenin and retinoic acid receptor signaling pathways interact to regulate chondrocyte function and matrix turnover: R. Yasuhara, et al.; J. Biol. Chem. 285, 317 (2010), Abstract — Full Text
- Inhibition of glycogen synthase kinase-3beta downregulates total tau proteins in cultured neurons and its reversal by the blockade of protein phosphatase-2A: L. Martin, et al.; Brain Res. 1252, 66 (2009), Abstract
- An integrated computational approach to the phenomenon of potent and selective inhibition of aurora kinases B and C by a series of 7-substituted indirubins: V. Myrianthopoulos, et al.; J. Med. Chem. 50, 4027 (2007), Abstract
- Inverse in silico screening for identification of kinase inhibitor targets: S. Zahler, et al.; Chem. Biol. 14, 1207 (2007), Abstract
- 7-Bromoindirubin-3’-oxime induces caspase-independent cell death: J. Ribas, et al.; Oncogene 25, 6304 (2006), Abstract
- The GSK-3 inhibitor BIO promotes proliferation in mammalian cardiomyocytes: A.S. Tseng, et al.; Chem. Biol. 13, 957 (2006), Abstract
- Structural basis for the synthesis of indirubins as potent and selective inhibitors of glycogen synthase kinase-3 and cyclin-dependent kinases: P. Polychronopoulos, et al.; J. Med. Chem. 47, 935 (2004), Abstract
- GSK-3-selective inhibitors derived from Tyrian purple indirubins: L. Meijer, et al.; Chem. Biol. 10, 1255 (2003), Abstract
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Last modified: May 29, 2024
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