Free shipping on all orders over $ 500

CH-223191

Cat. No. M7727

All AbMole products are for research use only, cannot be used for human consumption.

CH-223191 Structure
Synonym:

CH223191

Size Price Availability Quantity
Free Sample (0.5-1 mg)  USD 0 In stock
2mg USD 35  USD35 In stock
5mg USD 55  USD55 In stock
10mg USD 100  USD100 In stock
50mg USD 300  USD300 In stock
Free Delivery on orders over USD 500 Bulk Inquiry?

Quality Control & Documentation
Biological Activity

CH-223191 is a potent and specific aryl hydrocarbon receptor (AhR) antagonist. CH-223191 inhibits TCDD-mediated nuclear translocation and DNA binding of AhR, and inhibits TCDD-induced luciferase activity with an IC50 of 0.03 μM.

*The compound is unstable in solutions, freshly prepared is recommended

Product Citations
Protocol (for reference only)
Cell Experiment
Cell lines
Preparation method
Concentrations
Incubation time
Animal Experiment
Animal models Male ICR mice (6 weeks old)
Formulation 10 mg/kg in corn oil
Dosages 10 mg/kg once a day for 25 days
Administration oral
Chemical Information
Molecular Weight 333.39
Formula C19H19N5O
CAS Number 301326-22-7
Solubility (25°C) DMSO ≥ 30 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Majid Keshavarzi, et al. Toxicol Res (Camb) . The interplay of aryl hydrocarbon receptor/WNT/CTNNB1/Notch signaling pathways regulate amyloid beta precursor mRNA/protein expression and effected the learning and memory of mice

[2] Kuo-Liang Wei, et al. Sorafenib is an antagonist of the aryl hydrocarbon receptor

[3] Jelena Kulas, et al. Aryl Hydrocarbon Receptor is Involved in the Proinflammatory Cytokine Response to Cadmium

[4] Theodoros Eleftheriadis, et al. Reoxygenation induces reactive oxygen species production and ferroptosis in renal tubular epithelial cells by activating aryl hydrocarbon receptor

[5] Lizath M Aguiniga, et al. Acyloxyacyl hydrolase regulates voiding activity

[6] Sun-Hee Kim, et al. Mol Pharmacol. Novel compound 2-methyl-2H-pyrazole-3-carboxylic acid (2-methyl-4-o-tolylazo-phenyl)-amide (CH-223191) prevents 2,3,7,8-TCDD-induced toxicity by antagonizing the aryl hydrocarbon receptor

Related Aryl hydrocarbon Receptor Products
AHR antagonist 5 

AHR antagonist 5, a potent and orally active aryl hydrocarbon receptor (AHR) antagonist, has an IC50 of < 0.5 µΜ.

AHR antagonist 5 free base 

AHR antagonist 5 free base is a selective and orally active aryl hydrocarbon receptor (AHR) inhibitor.

KYN-101

KYN-101 is a potent, selective and orally active AHR inhibitor.

AHR agonist 4

AHR agonist 4 is an agonist of Aryl hydrocarbon receptor (AHR), assocaited with the immune balance of Th17/22 and Treg cells.

Benzyl butyl phthalate

Benzyl butyl phthalate can trigger the migration and invasion of hemangioma (HA) cells via upregulation of Zeb1. Benzyl butyl phthalate activates aryl hydrocarbon receptor (AhR) in breast cancer cells to stimulate SPHK1/S1P/S1PR3 signaling and enhances formation of metastasis-initiating breast cancer stem cells (BCSCs).

  Catalog
Abmole Inhibitor Catalog




Keywords: CH-223191, CH223191 supplier, Aryl hydrocarbon Receptor, inhibitors, activators

All AbMole products are for research use only, cannot be used for human consumption or veterinary use. We do not provide products or services to individuals. Please comply with the intended use and do not use AbMole products for any other purpose.



Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2024 AbMole BioScience. All Rights Reserved.