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ID-8

Catalog No. T2431   CAS 147591-46-6
Synonyms: ID8

ID-8, a DYRK inhibitor, sustains embryonic stem cell self-renewal in long-term culture.

All products from TargetMol are for Research Use Only. Not for Human or Veterinary or Therapeutic Use.
ID-8 Chemical Structure
ID-8, CAS 147591-46-6
Pack Size Availability Price/USD Quantity
5 mg In stock $ 41.00
10 mg In stock $ 57.00
25 mg In stock $ 103.00
50 mg In stock $ 166.00
100 mg In stock $ 296.00
200 mg In stock $ 384.00
1 mL * 10 mM (in DMSO) In stock $ 45.00
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Purity: 99.77%
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Biological Description
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Storage & Solubility Information
Description ID-8, a DYRK inhibitor, sustains embryonic stem cell self-renewal in long-term culture.
In vivo ID-8 maintains the expression of the Nanog gene through the activation of Sox2-Oct3/4, enabling the reversible maintenance of ESC (Embryonic Stem Cells) cultures for prolonged periods. In the presence of Wnt, ID-8 modulates the Wnt/β-catenin signaling pathway, enhancing CBP/β-catenin levels to preserve the undifferentiated state of hESCs (human Embryonic Stem Cells), thereby supporting cell proliferation and survival.
Kinase Assay In Vitro Enzymatic Assay for Histone Deacetylases: In vitro activities of the 11 recombinant human zinc-dependent HDAC enzymes are detected by ?uorigenic release of 7-amino-4-methylcoumarin from substrate upon deacetylase enzymatic activity. A series of dilutions of the unique HDAC6 compound, tubacin, and SAHA are prepared with 10% DMSO in HDAC assay buffer, and 5 μL of the dilution was added to a 50-μL reaction so that the ?nal concentration of DMSO is 1% in all of the reactions. The enzymatic reactions are conducted in duplicate at 37 °C for 30 min in a 50-μL mixture containing HDAC assay buffer, 5 μg BSA, an HDAC substrate, an HDAC enzyme, and a test compound. After enzymatic reactions, 50 μL of 2× HDAC developer is added to each well, and the plate is incubated at room temperature for an additional 15 min. Fluorescence intensity is measured at an excitation of 360 nm and an emission of 460 nm using a Synergy microplate reader. Negative (no enzyme, no inhibitor, a drug with no HDAC inhibition activity) and positive controls (known HDAC inhibitor SAHA) are included in the assays. IC50 is determined at the drug concentration that results in 50% reduction of HDAC activity compared with the control.
Cell Research Briefly, the hESCs in feeder-free culture are dissociated completely with 0.05% trypsin-EDTA and seeded at 104 cells per well in Matrigel-coated 6-well culture plates and cultured in MEF-CM. Various concentrations of Wnt3, IQ-1, ID-8, and/or ICG-001 are supplemented into the culture media at the onset of seeding and then continuously until the end of culturing. For all assays, the cell and colony morphology are examined under a microscope, and the replating efficiency is examined by counting the number of colonies after 7 days of culture. (Only for Reference)
Synonyms ID8
Molecular Weight 298.29
Formula C16H14N2O4
CAS No. 147591-46-6

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 29.8 mg/mL (100 mM)

TargetMolReferences and Literature

1. Miyabayashi T, et al. Biosci Biotechnol Biochem. 2008 , 72(5), 1242-1248. 2. Hasegawa K, et al. Stem Cells Transl Med. 2012, 1(1), 18-28.

Related compound libraries

This product is contained In the following compound libraries:
Inhibitor Library Tyrosine Kinase Inhibitor Library Stem Cell Differentiation Compound Library Anti-Cancer Compound Library Anti-Aging Compound Library Kinase Inhibitor Library NO PAINS Compound Library Bioactive Compounds Library Max Cell Cycle Compound Library Bioactive Compound Library

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Keywords

ID-8 147591-46-6 Cell Cycle/Checkpoint Tyrosine Kinase/Adaptors DYRK cell embryonic dual-specificity ESC Inhibitor inhibit Dual specificity tyrosine phosphorylation regulated kinase stem regulated phosphorylation kinase tyrosine ID 8 ID8 Dual specificity tyrosine regulated kinase inhibitor

 

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