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Submit ReviewCH 223191 is a potent aryl hydrocarbon receptor (AhR) antagonist (IC50 = 30 nM). Exhibits no AhR agonist-like activity (at concentrations up to 100 μM). Inhibits 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD)-induced AhR-dependent transcription in vitro and reduces TCDD-induced toxicity in vivo. Attenuates Th17 differentiation of naive CD4 T cells and promotes expansion of hematopoietic stem cells in vitro.
CH 223191 is also offered as part of the Tocriscreen Stem Cell Library. 了解 Tocris 化合物库的更多信息。
分子量 | 333.39 |
公式 | C19H19N5O |
储存 | Store at +4°C |
纯度 | ≥98% (HPLC) |
CAS Number | 301326-22-7 |
PubChem ID | 3091786 |
InChI Key | LKTNEXPODAWWFM-UHFFFAOYSA-N |
Smiles | CC1=C(/N=N/C2=CC=C(NC(C3=CC=NN3C)=O)C(C)=C2)C=CC=C1 |
上方提供的技术数据仅供参考。批次相关数据请参见分析证书。
Tocris products are intended for laboratory research use only, unless stated otherwise.
溶剂 | 最高浓度 mg/mL | 最高浓度 mM | |
---|---|---|---|
溶解性 | |||
DMSO | 33.34 | 100 | |
ethanol | 3.33 | 10 |
以下数据基于产品分子量 333.39。 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
浓度/溶剂体积/质量 | 1 mg | 5 mg | 10 mg |
---|---|---|---|
1 mM | 3 mL | 15 mL | 29.99 mL |
5 mM | 0.6 mL | 3 mL | 6 mL |
10 mM | 0.3 mL | 1.5 mL | 3 mL |
50 mM | 0.06 mL | 0.3 mL | 0.6 mL |
参考文献是支持产品生物活性的出版物。
Kim et al (2006) 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. Mol.Pharmacol. 69 1871 PMID: 16540597
Veldhoen et al (2009) Natural agonists for aryl hydrocarbon receptor in culture medium are essential for optimal differentiation of TH17 T cells. J.Exp.Med. 206 43 PMID: 19114668
Dubrovska et al (2012) CXCR4 activation maintains a stem cell population in tamoxifen-resistant breast cancer cells through AhR signalling. Br.J.Cancer. 107 43 PMID: 22644306
Boitano et al (2010) Aryl hydrocarbon receptor antagonists promote the expansion of human hematopoietic stem cells. Science 329 1345 PMID: 20688981
If you know of a relevant reference for CH 223191, please let us know.
关键词: CH 223191, CH 223191 supplier, CH223191, potent, specific, agonists, aryl, hydrocarbon, receptors, AhR, stem, cells, hematopoietic, expansion, haematopoietic, HSC, Aryl, Hydrocarbon, Receptors, Stem, Cell, Proliferation, Other, Differentiation, Products, Hematopoietic, Cells, 3858, Tocris Bioscience
引用文献是使用了 Tocris 产品的出版物。 CH 223191 的部分引用包括:
Yuecheng et al (2021) Hypoxia-Inducible Factor 1α (HIF1α) Suppresses Virus Replication in Human Cytomegalovirus Infection by Limiting Kynurenine Synthesis. MBio 12 PMID: 33758082
Brian T et al (2021) Vitamin D Inhibits IL-22 Production Through a Repressive Vitamin D Response Element in the il22 Promoter. Front Immunol 12 715059 PMID: 34408754
Stephen et al (2015) Aryl Hydrocarbon Receptor Activity of Tryptophan Metabolites in Young Adult Mouse Colonocytes. Drug Metab Dispos 43 1536-43 PMID: 25873348
D'Amato et al (2015) A TDO2-AhR Signaling Axis Facilitates Anoikis Resistance and Metastasis in Triple-Negative Breast Cancer. Cancer Res 75 4651 PMID: 26363006
Liu et al (2014) Regulation of plasmacytoid dendritic cell development in mice by aryl hydrocarbon receptor. Immunol Cell Biol 92 200 PMID: 24165981
Alexandra E et al (2017) Mechanisms of Skin Toxicity Associated with Metabotropic Glutamate Receptor 5 Negative Allosteric Modulators. Cell Chem Biol 24 858-869.e5 PMID: 28669525
Rao et al (2016) Effects of Cigarette Smoke Condensate on Oxidative Stress, Apoptotic Cell Death, and HIV Replication in Human Monocytic Cells. PLoS One 11 e0155791 PMID: 27203850
Howard L et al (2019) Control of tumor-associated macrophages and T cells in glioblastoma via AHR and CD39. Nat Neurosci 22 729-740 PMID: 30962630
Gimenez-Gomez et al (2018) Increasing kynurenine brain levels reduces ethanol consumption in mice by inhibiting dopamine release in nucleus accumbens. Neuropharmacology 135 581 PMID: 29705534
Nicholas C et al (2018) Gut Microbiota-Produced Tryptamine Activates an Epithelial G-Protein-Coupled Receptor to Increase Colonic Secretion. Cell Host Microbe 23 775-785.e5 PMID: 29902441
Sergio Costa et al (2022) STING is an intrinsic checkpoint inhibitor that restrains the TH17 cell pathogenic program. Cell Rep 39 110838 PMID: 35613599
Beom K et al (2020) Targeting Actomyosin Contractility Suppresses Malignant Phenotypes of Acute Myeloid Leukemia Cells. Int J Mol Sci 21 PMID: 32422910
Matino et al (2015) IDO1 suppresses inhibitor development in hemophilia A treated with factor VIII. Br J Pharmacol 125 3766 PMID: 26426076
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