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关于此项目
经验公式(希尔记法):
C19H19N5O
化学文摘社编号:
分子量:
333.39
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77
产品名称
CH-223191,
方案
≥98% (HPLC)
质量水平
表单
powder
颜色
orange-brown
溶解性
DMSO: ≥20 mg/mL
储存温度
2-8°C
SMILES字符串
Cc1cc(ccc1NC(=O)c2ccnn2C)\N=N\c3ccccc3C
InChI
1S/C19H19N5O/c1-13-6-4-5-7-17(13)23-22-15-8-9-16(14(2)12-15)21-19(25)18-10-11-20-24(18)3/h4-12H,1-3H3,(H,21,25)/b23-22+
InChI key
LKTNEXPODAWWFM-GHVJWSGMSA-N
相关类别
应用
CH-223191已被用作肝素细胞、TH17-白细胞介素-10+细胞和有机类中的芳香烃受体(AHR)拮抗剂。
生化/生理作用
CH-223191是一种强效特异性芳香烃受体(AhR)拮抗剂。
CH-223191是一种强效特异性芳香烃受体(AhR)拮抗剂。它抑制TCDD介导的核转位和AhR的脱氧核糖核酸结合,并抑制TCDD诱导的荧光素酶活性,IC50为30纳米。与其他在高浓度下显示激动剂活性的AhR拮抗剂不同,CH-223191即使在100微摩尔时也不能刺激AhR依赖性转录。它也对AhR有特异性,对雌激素受体没有亲和力,就像其他拮抗剂一样。
特点和优势
该化合物在受体分类和信号转导手册中 核受体(非甾体化合物) 页面中进行了详细介绍。欲浏览其他手册页面,请 点击这里。
这种化合物是基因调控研究的特色产品。点击此处发现更多特色基因调控产品。在sigma.com/discover-bsm可了解更多关于生物活性小分子的其他研究领域。
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
An immunoregulatory and tissue-residency program modulated by c-MAF in human TH 17 cells
Aschenbrenner D, et al.
Nature Immunology, 19(10), 1126-1126 (2018)
Lei Dong et al.
Scientific reports, 6, 36598-36598 (2016-11-04)
Understanding of T helper 17 lineage (T
Michela Zago et al.
PloS one, 8(9), e74953-e74953 (2013-10-03)
The aryl hydrocarbon receptor (AhR), a ligand-activated transcription factor that responds to man-made environmental toxicants, has emerged as an endogenous regulator of cyclooxygenase-2 (Cox-2) by a mechanism that is poorly understood. In this study, we first used AhR-deficient (AhR(-/-) )
Down-regulation of the expression of alcohol dehydrogenase 4 and CYP2E1 by the combination of alpha-endosulfan and dioxin in HepaRG human cells
Attignon E, et al.
Toxicology in vitro, 45, 309-317 (2017)
Qin Wang et al.
Environmental health perspectives, 121(11-12), 1334-1343 (2013-09-24)
The aryl hydrocarbon receptor (AHR) is a ligand-activated transcription factor that regulates the expression of xenobiotic detoxification genes and is a critical mediator of gene-environment interactions. Many AHR target genes identified by genome-wide gene expression profiling have morphogenetic functions, suggesting
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