Indirubin-3'-monoxime, GSK, CDK kinase inhibitor

  • Catalog name: SIH-502-5MG
  • Supplier name: stressma
  • Size: 5 mg
  • Price: 160.00€
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  • Stock availabilitIn Stock In Stock
  • CAS number 160807-49-8
  • Molecular weight 277,3 g/mol
  • Primary research fields Cell Signaling, Cancer, Apoptosis, Cancer Growth Inhibitors, Tyrosine Kinase Inhibitors
  • Other name Indirubin-3'-monoxime, 3-[1,3-Dihydro-3-(hydroxyimino)-2H-indol-2-ylidene]-1,3-dihydro-2H-indol-2-one, Indirubin-3′-oxime
  • Product category Small Molecules
  • Product type Inhibitor
  • Chemical formula C16H11N3O2
  • Origin Synthetic
  • Purity pourcentage ≥98% (HPLC)
  • Soluble in Soluble to 100 mM in DMSO and to 100 mM in ethanol
  • Physical appearance Red solid
  • Storage recommendations -20ºC
  • Shipping recommendations Shipped Ambient
  • Safety information Classification: Not a hazardous substance or mixture. Safety Phrases: S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
  • PubChem number 5326739
  • Scientific context Indirubin-3'-monoxime is an inhibitor of protein kinases and cyclin-dependent kinases. Specifically, it is a potent inhibitor of glycogen synthase kinase-3β (GSK-3β).
  • Bibliography 1. Damiens E., Baratte B., Marie D., Eisenbrand G., & Meijer L. (2001) Oncogene. 20(29): 3786–3797.
  • Release date 1-Oct-2014
  • PubMed number Refer to PubMed
  • Tested applications To be tested
  • Tested reactivity To be tested
  • Representative figure legend Chemical structure of Indirubin-3'-monoxime (SIH-502), a GSK-3b and CDK kinase inhibitor. CAS #: 160807-49-8. Molecular Formula: C16H11N3O2. Molecular Weight: 277.3 g/mol. Chemical structure of Indirubin-3'-monoxime, a GSK-3b and CDK kinase inhibitor (SIH-502). CAS # 160807-49-8. Molecular Formula: C16H11N3O2.
  • Warning information Non-hazardous
  • Country of production Canada
  • Total weight (kg) 0.25
  • Net weight (g) 0.005
  • Additional description Tissue, pathway, proteinase, peptidase, protease ,acrosin, lipoprotein, activator, caspase, trypsin, papain, esterase inhibitors are proteins or receptor ligands or receptor antagonists that bind to an enzyme receptor and decreases its activity. Since blocking an enzyme's activity can kill a pathogen or correct a metabolic imbalance, many drugs are enzyme inhibitors. Not all receptor antagonist that bind to enzymes are inhibitors; enzyme activator ligands or agonists bind to enzymes and increase their enzymatic activity, while enzyme substrates bind and are converted to products in the normal catalytic cycle of the enzyme.