CH 223191

Pricing Availability   Qty
说明: Potent aryl hydrocarbon receptor (AhR) antagonist
化学名: 1-Methyl-N-[2-methyl-4-[2-(2-methylphenyl)diazenyl]phenyl-1H-pyrazole-5-carboxamide
纯度: ≥98% (HPLC)
说明书
引用文献 (13)
评论

生物活性 for CH 223191

CH 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.

化合物库 for CH 223191

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。

技术数据 for CH 223191

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.

溶解性数据 for CH 223191

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
DMSO 33.34 100
ethanol 3.33 10

制备储备液 for CH 223191

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.

选择批次从而根据批次分子量重新计算:
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

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产品说明书 for CH 223191

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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

13 篇 CH 223191 的引用文献

引用文献是使用了 Tocris 产品的出版物。 CH 223191 的部分引用包括:

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

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

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

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

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

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

Sergio Costa et al (2022) STING is an intrinsic checkpoint inhibitor that restrains the TH17 cell pathogenic program. Cell Rep 39 110838 PMID: 35613599


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