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Submit ReviewU 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.
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 | Soluble in methyl acetate (supplied pre-dissolved -10mg/ml) |
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
If you know of a relevant reference for U 46619, please let us know.
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
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
Lacar et al (2012) S phase entry of neural progenitor cells correlates with increased blood flow in the young subventricular zone. PLoS One 7 e31960 PMID: 22359646
Chapman et al (2012) Platelets present antigen in the context of MHC class I. J Immunol 189 916 PMID: 22706078
Choi et al (2016) Inhibition of endoplasmic reticulum stress improves coronary artery function in the spontaneously hypertensive rats. Scientific Reports 6 31925 PMID: 27550383
Pike et al (2014) Prenatal development is linked to bronchial reactivity: epidemiological and animal model evidence. Sci Rep 4 4705 PMID: 24740086
Coleman et al (2014) New positive Ca2+-activated K+ channel gating modulators with selectivity for KCa3.1. Mol Pharmacol 86 342 PMID: 24958817
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