U 46619

Pricing Availability   Qty
说明: Potent, stable thromboxane A2 (TP) receptor agonist
别名: 9,11-Dideoxy-9a,11a-methanoepoxy prostaglandin F2a
化学名: (5Z)-7-[(1R,4S,5S,6R)-6-[(1E,3S)-3-Hydroxy-1-octenyl]-2-oxabicyclo[2.2.1]hept-5-yl]-5-heptenoic acid
纯度: ≥98% (HPLC)
说明书
引用文献 (9)
评论

生物活性 for U 46619

U 46619 is a PGH2 (TXA2) analog that is a potent and stable thromboxane A2 (TP) receptor agonist (EC50 = 0.035 μM). Potently stimulates TP receptor-mediated, but not other prostaglandin receptor-mediated responses in various in vitro preparations. Activates ERK-1 and ERK-2 in HEK 293 cells expressing TPα and TPβ receptors.

技术数据 for U 46619

分子量 350.5
公式 C21H34O4
储存 Store at -20°C
纯度 ≥98% (HPLC)
CAS Number 56985-40-1
PubChem ID 5311493
InChI Key LQANGKSBLPMBTJ-BRSNVKEHSA-N
Smiles O[C@@H](CCCCC)/C=C/[C@H]1[C@@H]2OC[C@@H](C2)[C@@H]1C/C=C\CCCC(O)=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.

溶解性数据 for U 46619

溶解性 Soluble in methyl acetate (supplied pre-dissolved -10mg/ml)

产品说明书 for U 46619

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参考文献 for U 46619

参考文献是支持产品生物活性的出版物。

Coleman et al (1981) Comparison of the actions of U-46619, a prostaglandin H2-analogue, with those of prostaglandin H2 and thromboxane A2 on some isolated smooth muscle preparations. Br.J.Pharmacol. 73 773 PMID: 7248665

Morinelli et al (1987) Receptor-mediated effects of a PGH2 analogue (U 46619) on human platelets. Am.J.Physiol. 253 H1035 PMID: 3688248

Miggin and Kinsella (2002) Regulation of extracellular signal-regulated kinase cascades by α- and β-isoforms of the human thromboxane A2 receptor. Mol.Pharmacol. 61 817 PMID: 11901221


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关键词: U 46619, U 46619 supplier, Potent, stable, thromboxane, A2, TP, receptor, agonists, TXA2, Prostanoid, prostaglandins, prostacyclins, eicosanoids, U46619, 9, 11-Dideoxy-9a, 11a-methanoepoxy, prostaglandinF2a, 9,11-Dideoxy-9a,11a-methanoepoxy, prostaglandin, F2a, Receptors, 1932, Tocris Bioscience

9 篇 U 46619 的引用文献

引用文献是使用了 Tocris 产品的出版物。 U 46619 的部分引用包括:

Seto et al (2013) Acute SimV. inhibits K ATP channels of porcine coronary artery myocytes. Diabetes 8 e66404 PMID: 23799098

Lee and Diamond (2015) A human platelet calcium calculator trained by pairwise agonist scanning. PLoS One 11 e1004118 PMID: 25723389

Davis et al (2013) Potent vasorelaxant activity of the TMEM16A inhibitor T16A(inh) -A01. Br J Pharmacol 168 773 PMID: 22946562

White et al (2013) Hydrogen sulphide-mediated vasodilatation involves the release of neurotransmitters from sensory nerves in pressurized mesenteric small arteries isolated from rats. Br J Pharmacol 168 785 PMID: 22928888


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