TG 4-155

Discontinued Product

5052 has been discontinued.

View all Prostanoid Receptors products.
说明: High affinity and selective EP2 receptor antagonist
化学名: (2E)-N-[2-(2-Methyl-1H-indol-1-yl)ethyl]-3-(3,4,5-trimethoxyphenyl)-2-propenamide
纯度: ≥98% (HPLC)
说明书
引用文献 (2)
评论

生物活性 for TG 4-155

TG 4-155 is a high affinity and selective EP2 receptor antagonist (KB values are 2.4 and 34.5 nM for EP2 and DP1 receptors respectively). Exhibits >500-fold selectivity for EP2 over other prostanoid receptors. Inhibits butaprost-induced proinflammatory cytokine production, cell proliferation and invasion of PC-3 cells in vitro.

技术数据 for TG 4-155

分子量 394.46
公式 C23H26N2O4
储存 Store at +4°C
纯度 ≥98% (HPLC)
CAS Number 1164462-05-8
PubChem ID 5886965
InChI Key YBHUXHFZLMFETJ-MDZDMXLPSA-N
Smiles CC2=CC1=CC=CC=C1N2CCNC(/C=C/C3=CC(OC)=C(OC)C(OC)=C3)=O

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.

产品说明书 for TG 4-155

分析证书/产品说明书
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参考文献 for TG 4-155

参考文献是支持产品生物活性的出版物。

Jiang and Dingledine (2013) Role of prostaglandin receptor EP2 in the regulations of cancer cell proliferation, invasion, and inflammation. J.Pharmacol.Exp.Ther. 344 360 PMID: 23192657

Quan et al (2013) EP2 receptor signaling pathways regulate classical activation of microglia. J.Biol.Chem. 288 9293 PMID: 23404506

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关键词: TG 4-155, TG 4-155 supplier, TG4-155, high, affinity, selective, EP2, prostanoid, receptors, antagonists, Prostanoid, Receptors, 5052, Tocris Bioscience

2 篇 TG 4-155 的引用文献

引用文献是使用了 Tocris 产品的出版物。 TG 4-155 的部分引用包括:

Cuesto et al (2015) GSK3β inhibition promotes synaptogenesis in Drosophila and mammalian neurons. PLoS One 10 e0118475 PMID: 25764078

Donna A et al (2020) Aggregation of Human Mesenchymal Stromal Cells Eliminates Their Ability to Suppress Human T Cells. Front Immunol 11 143 PMID: 32158443


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