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Postion:Product Catalog >AS1517499
AS1517499
  • AS1517499

AS1517499 NEW

Price $34 $48 $80
Package 1mg 2mg 5mg
Min. Order:
Supply Ability: 10g
Update Time: 2025-11-10

Product Details

Product Name: AS1517499 CAS No.: 919486-40-1
Purity: 98.31% Supply Ability: 10g
Release date: 2025/11/10

Product Introduction

Bioactivity

NameAS1517499
DescriptionAS1517499 is a blood-brain barrier permeable inhibitor of STAT6 phosphorylation (IC50= 21 nM).
Cell ResearchNormal human BSM cells (hBSMCs) are maintained in SmBM medium supplemented with 5% fetal bovine serum, 0.5 ng/mL human epidermal growth factor (hEGF), 5 μg/mL insulin, 2 ng/mL human fibroblast growth factor-basic (hFGFb), 50 μg/mL gentamicin, and 50 ng/mL amphotericin B. Cells are maintained at 37°C in a humidified atmosphere (5% CO2), fed every 48 to 72 hours, and passaged when cells reached 90 to 95% confluence. Then the hBSMCs (passages 7-9) are seeded in 6-well plates and 8-well chamber slides at a density of 3,500 cells/cm2 and, when 80 to 85% confluence observed, cells are cultured without serum for 24 hours before addition of recombin is ant human IL-13. AS1517499 (100 nM) or its vehicle (0.3% DMSO) is treated 30 minutes before the addition of IL-13 (100 ng/mL). In some experiments, AS1517499 is treated 0 (co-incubation), 3, or 12 hours after the addition of IL-13. In another series of experiments, a selective Rho-kinase inhibitor Y-27632 (1 μM) or its vehicle (0.3% DMSO) is also applied 15 minutes before the IL-13 application. At the indicated time after the IL-13 treatment, cells are washed with PBS, immediately collected, and disrupted with 1× SDS sample buffer (250 μL/well), and used for Western blot analyses[2] .
Animal ResearchMice[2]
In vitroMETHODS: Western Blot was used to detect the expression levels of AS1517499 in human BSM cells treated with 100 nM AS1517499. RESULTS: Treatment of BSM cells with AS1517499 inhibited IL-13-induced STAT6 phosphorylation and up-regulation of RhoA. [1]
In vivoMETHODS: To investigate the effect of AS1517499 on the development of antigen-induced BSM hyperreactivity, AS1517499 (10 mg/kg) was administered intraperitoneally to mice 1 hour before each ovalbumin exposure. RESULTS: AS1517499 completely inhibited the antigenicity induced upregulation of RhoA and BSM hyperreactivity. [1]
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information10% DMSO+40% PEG300+5% Tween 80+45% Saline : 5 mg/mL (12.57 mM), Sonication is recommended.
DMSO : 262.5 mg/mL (659.78 mM), Sonication is recommended.
KeywordsSTAT6 | STAT | Inhibitor | inhibit | AS-1517499 | AS1517499 | AS 1517499
Inhibitors RelatedStafia-1 | Nifuroxazide | Balsalazide disodium dihydrate | Fludarabine | Niclosamide | 2-(1,8-naphthyridin-2-yl)phenol | CASIN | Diosgenin | Niclosamide olamine | Artesunate | Alantolactone | Stattic
Related Compound LibrariesApoptosis Compound Library | Anti-Pancreatic Cancer Compound Library | Bioactive Compound Library | Anti-Diabetic Compound Library | Anti-Obesity Compound Library | CNS-Penetrant Compound Library | Inhibitor Library | Stem Cell Differentiation Compound Library | Immunology/Inflammation Compound Library | Bioactive Compounds Library Max | Preclinical Compound Library | 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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