(±)-Cloprostenol sodium salt

Discontinued Product

2295 has been discontinued.

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说明: Water-soluble PGF2α analog and potent FP receptor agonist
化学名: (5Z)-rel-7-[(1R,2R,3R,5S)-2-[(1E,3R)-4-(3-chlorophenoxy)-3-hydroxy-1-butenyl]-3,5-dihydroxycyclopentyl]-5-heptenoic acid monosodium salt
纯度: ≥98% (HPLC)
说明书
引用文献
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生物活性 for (±)-Cloprostenol sodium salt

(±)-Cloprostenol sodium salt is a water-soluble prostaglandin F2α (PGF2α) analog; acts as a potent FP receptor agonist (EC50 = 0.84 nM). Potently inhibits differentiation of adipocyte precursor cells. Luteolytic agent in vivo.

技术数据 for (±)-Cloprostenol sodium salt

分子量 446.9
公式 C22H28ClNaO6
储存 Desiccate at -20°C
纯度 ≥98% (HPLC)
CAS Number 55028-72-3
PubChem ID 17756794
InChI Key IFEJLMHZNQJGQU-KXXGZHCCSA-M
Smiles [Na+].O[C@@H](COC1=CC(Cl)=CC=C1)\C=C\[C@H]1[C@H](O)C[C@H](O)[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.

产品说明书 for (±)-Cloprostenol sodium salt

参考文献 for (±)-Cloprostenol sodium salt

参考文献是支持产品生物活性的出版物。

Dukes et al (1974) Potent luteolytic agents related to prostaglandin F. Nature 250 330 PMID: 4853720

Griffin et al (1998) Pharmacological characterization of an FP prostaglandin receptor on rat vascular smooth muscle cells (A7r5) coupled to phosphoinositide turnover and intracellular calcium mobilization. J.Pharmacol.Exp.Ther. 286 411 PMID: 9655886

Serrero and Lepak (2002) Prostaglandin F receptor (FP receptor) agonists are potent adipose differentiation inhibitors for primary culture of adipocyte precursors in defined medium. Biochem.Biophys.Res.Comm. 233 200

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关键词: (±)-Cloprostenol sodium salt, (±)-Cloprostenol sodium salt supplier, Water-soluble, PGF2alpha, potent, FP, receptor, agonists, Receptors, Prostaglandin, Prostanoid, 2295, Tocris Bioscience

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