L-798,106

Pricing Availability   Qty
说明: Potent and highly selective EP3 antagonist
化学名: N-[(5-Bromo-2-methoxyphenyl)sulfonyl]-3-[2-(2-naphthalenylmethyl)phenyl]-2-propenamide
纯度: ≥99% (HPLC)
说明书
引用文献 (7)
评论

生物活性 for L-798,106

L-798,106 is a potent and highly selective prostanoid EP3 receptor antagonist (Ki values are 0.3, 916, > 5000 and > 5000 nM at EP3, EP4, EP1 and EP2 respectively). Attenuates sulprostone-induced inhibition of EFS-evoked twitch and contractile responses in vivo.

化合物库 for L-798,106

L-798,106 is also offered as part of the Tocriscreen 2.0 Max. 了解 Tocris 化合物库的更多信息。

技术数据 for L-798,106

分子量 536.44
公式 C27H22BrNO4S
储存 Store at RT
纯度 ≥99% (HPLC)
CAS Number 244101-02-8
PubChem ID 15551229
InChI Key ODTKFNUPVBULRJ-NTCAYCPXSA-N
Smiles O=C(NS(C4=C(OC)C=CC(Br)=C4)(=O)=O)/C=C/C1=CC=CC=C1CC3=CC2=CC=CC=C2C=C3

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 L-798,106

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
DMSO 53.64 100

制备储备液 for L-798,106

以下数据基于产品分子量 536.44。 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 1.86 mL 9.32 mL 18.64 mL
5 mM 0.37 mL 1.86 mL 3.73 mL
10 mM 0.19 mL 0.93 mL 1.86 mL
50 mM 0.04 mL 0.19 mL 0.37 mL

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产品说明书 for L-798,106

分析证书/产品说明书
选择另一批次:

参考文献 for L-798,106

参考文献是支持产品生物活性的出版物。

Juteau et al (2001) Structure-activity relationships of cinnamic acylsulfonamide analogues on human EP3 prostanoid receptor. Bioorg.Med.Chem. 9 1977 PMID: 11504634

Clarke et al (2004) E-ring 8-isoprostanes inhibit ACh release from parasympathetic nerves innervating guinea-pig trachea through agonism of prostanoid receptors of the EP3-subtype. Br.J.Pharmacol. 141 600 PMID: 14744812

Bassil et al (2008) Activation of prostaglandin EP receptors by lubipro. in rat and human stomach and colon. Br.J.Pharmacol. 154 126 PMID: 18332851


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关键词: L-798,106, L-798,106 supplier, Potent, selective, EP3, antagonists, Receptors, Prostanoid, prostaglandins, prostacyclins, eicosanoids, L798106, 3342, Tocris Bioscience

7 篇 L-798,106 的引用文献

引用文献是使用了 Tocris 产品的出版物。 L-798,106 的部分引用包括:

Yang et al (2015) Exposure to 50 Hz magnetic field modulates GABAA currents in cerebellar granule neurons through an EP receptor-mediated PKC pathway. J Cell Mol Med 19 2413 PMID: 26176998

Chia et al (2011) Protection of protease-activated receptor 2 mediated vasodilatation against angiotensin II-induced vascular dysfunction in mice. BMC Pharmacol 11 10 PMID: 21955547

Fernández-Galilea et al (2012) Effects of lipoic acid on lipolysis in 3T3-L1 adipocytes. J Lipid Res 53 2296 PMID: 22941773

Ye et al (2018) Prostaglandin E2 receptor 3 signaling is induced in placentas with unexplained recurrent pregnancy losses. Endocr Connect 7 749 PMID: 29700097


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