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Postion:Product Catalog >AS2863619
AS2863619
  • AS2863619

AS2863619 NEW

Price $133 $189 $289
Package 1mg 2mg 5mg
Min. Order:
Supply Ability: 10g
Update Time: 2025-11-09

Product Details

Product Name: AS2863619 CAS No.: 2241300-51-4
Purity: 100.00% Supply Ability: 10g
Release date: 2025/11/09

Product Introduction

Bioactivity

NameAS2863619
DescriptionAS2863619 is an oral inhibitor of cyclin-dependent kinase 8 (CDK8) and CDK19. Inhibition of CDK8/19 can enhance the activation of STAT5, thereby activating the Foxp3 gene. It can convert antigen-specific effector/memory T cells into Foxp3+ regulatory T cells to study various immune diseases.
In vitroMETHODS: Mouse CD4 T cells were treated with AS2863619 (1 μM; 22 hours), and the possible effects of AS2863619 on STAT5 phosphorylation during Foxp3 induction in Tconv cells were investigated. RESULTS AS2863619 inhibited the PSP motif serine phosphorylation of STAT5b to about 40%, while increasing the tyrosine phosphorylation of the C-terminal domain to about 160%; the inhibitory effect of AS2863619 on STAT5b serine phosphorylation was dose-dependent with Foxp3 induction. [1]
In vivoMETHODS: Mice were orally treated with AS2863619 (3, 10, or 30 mg/kg). Plasma samples were collected from mice at 1, 2, 4, 8, and 24 hours after administration, and drug levels were determined by high-performance liquid chromatography-tandem mass spectrometry. RESULTS Compared with control mice, AS2863619 treatment after 2,4-dinitrofluorobenzene (DNFB) sensitization suppressed the extent of secondary responses, with less inflammatory cell infiltration into the skin and a lower proportion of interferon-γ (IFN-γ) cells in regional lymph nodes; depletion of Tregs abolished AS2863619-induced suppression before the induction of secondary responses. [1]
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility InformationDMSO : 245 mg/mL (604.58 mM), Sonication is recommended.
10% DMSO+40% PEG300+5% Tween 80+45% Saline : 5 mg/mL (12.34 mM), Sonication is recommended.
KeywordsSTAT5 | STAT | Inhibitor | inhibit | Cyclin dependent kinase | CDK8 | CDK19 | CDK | AS-2863619 | AS2863619 | AS 2863619
Inhibitors RelatedRibociclib | Nifuroxazide | Balsalazide disodium dihydrate | Abemaciclib | Fludarabine | Niclosamide | CASIN | Diosgenin | Niclosamide olamine | Artesunate | Dinaciclib | Abemaciclib methanesulfonate
Related Compound LibrariesAnti-Pancreatic Cancer Compound Library | Bioactive Compound Library | Kinase Inhibitor Library | Anti-Cancer Metabolism Compound Library | JAK-STAT Compound Library | Inhibitor Library | NO PAINS Compound Library | Stem Cell Differentiation Compound Library | Anti-Aging Compound Library | Immunology/Inflammation Compound Library | Bioactive Compounds Library Max | Transcription Factor-Targeted Compound Library

Company Profile Introduction

Target Molecule Corp. (TargetMol) is a global high-tech enterprise, headquartered in Boston, MA, specializing in chemical and biological research product and service to meet the research needs of global customers. TargetMol has evolved into one of the biggest global compound library and small molecule suppliers and a customer based on 40+ countries. TargetMol offers over 80 types of compound libraries and a wide range of high-quality research chemicals including inhibitors, activator, natural compounds, peptides, inhibitory antibodies, and novel life-science kits, for laboratory and scientific use. Besides, virtual screening service is also available for customers who would like to conduct the computer-aided drug discovery.

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TargetMol Chemicals Inc.

6YR United StatesUnited States
  • Since: 2011-01-07
  • Address: 36 Washington Street, Wellesley Hill, MA
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