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Submit ReviewTreprostinil is a potent prostacyclin (PGI2) analog (EC50 values are 0.6, 1.9 and 6.2 nM at DP1, IP and EP2 receptors respectively). Causes vasodilation of human pulmonary arteries and inhibits NFκB nuclear translocation in human alveolar macrophages in vitro.
分子量 | 390.51 |
公式 | C23H34O5 |
储存 | Store at -20°C |
纯度 | ≥98% (HPLC) |
CAS Number | 81846-19-7 |
PubChem ID | 6918140 |
InChI Key | PAJMKGZZBBTTOY-ZFORQUDYSA-N |
Smiles | O[C@H](C3)[C@H](CC[C@@H](O)CCCCC)[C@@]([C@@]3([H])C2)([H])CC1=C2C(OCC(O)=O)=CC=C1 |
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.
溶剂 | 最高浓度 mg/mL | 最高浓度 mM | |
---|---|---|---|
溶解性 | |||
DMSO | 39.05 | 100 | |
ethanol | 19.53 | 50 |
以下数据基于产品分子量 390.51。 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.
浓度/溶剂体积/质量 | 1 mg | 5 mg | 10 mg |
---|---|---|---|
1 mM | 2.56 mL | 12.8 mL | 25.61 mL |
5 mM | 0.51 mL | 2.56 mL | 5.12 mL |
10 mM | 0.26 mL | 1.28 mL | 2.56 mL |
50 mM | 0.05 mL | 0.26 mL | 0.51 mL |
参考文献是支持产品生物活性的出版物。
Whittle et al (2012) Binding and activity of the prostacyclin receptor (IP) agonists, trepros. and iloprost, at human prostanoid receptors: trepros. is a potent DP1 and EP2 agonist. Biochem.Pharmacol. 84 68 PMID: 22480736
Raychaudhuri et al (2002) The prostacyclin analogue trepros. blocks NFκB nuclear translocation in human alveolar macrophages. J.Biol.Chem. 277 33344 PMID: 12082102
Fontana et al (2007) Treprostinil potentiates the positive inotropic effect of catecholamines in adult rat ventricular cardiomyocytes. Br.J.Pharmacol. 151 779 PMID: 17533419
If you know of a relevant reference for Treprostinil, please let us know.
关键词: Treprostinil, Treprostinil supplier, Potent, prostacyclin, PGI2, analogues, DP,IP, EP2, agonists, agonism, vasodilation, pulmonary, hypertension, PPH, Prostanoid, Receptors, 5349, Tocris Bioscience
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