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  • Fluprostenol-d4
Fluprostenol-d4的可视化放大

Fluprostenol-d4

A neuropeptide with diverse biological activities

原价
¥737-5912
价格
590-4730
Fluprostenol-d4的二维码

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  • 库存: 现货
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  • 货号: ajcx22514
  • CAS: N/A
  • 别名: 16mtrifluoromethylphenoxy tetranor Prostaglandin F2αd4
  • 分子式: C23H25D4F3O6
  • 分子量: 462.5
  • 纯度: >98%
  • 溶解度: DMF: >100 mg/ml (from Fluprostenol),DMSO: >100 mg/ml (from Fluprostenol),Ethanol: >100 mg/ml (from Fluprostenol),PBS (7.2): 16 mg/ml (from Fluprostenol)
  • 储存: Store at -20°C
  • 库存: 现货

Background

Fluprostenol-d4 contains four deuterium atoms at the 3, 3', 4, and 4' positions. It is intended for use as an internal standard for the quantification of fluprostenol by GC- or LC-mass spectrometry. Fluprostenol is a metabolically stable analog of prostaglandin F (PGF) with potent FP receptor agonist activity.11,2 It inhibits PGF binding to human and rat FP receptors with IC50 values of 3.5 and 7.5 nM, respectively.1,2 Fluprostenol is a much more potent luteolytic agent than PGF in rats with a minimum fully effective dose of 270 . g/kg to terminate pregnancy.3 It is also an effective inhibitor of rat adipose precursor differentiation in primary cultures with an IC50 value of 3-10 x 10-11 M.4



1.Dukes, M., Russell, W., and Walpole, A.L.Potent luteolytic agents related to prostaglandin F2αNature250(464)330-331(1974) 2.Lake, S., Gullberg, H., Wahlqvist, J., et al.Cloning of the rat and human prostaglandin F2α receptors and the expression of the rat prostaglandin F2α receptorFEBS Letters355317-325(1994) 3.Abramovitz, M., Boie, Y., Nguyen, T., et al.Cloning and expression of a cDNA for the human prostanoid FP receptorThe Journal of Biological Chemisty2692632-2636(1994) 4.Serrero, G., and Lepak, N.M.Prostaglandin F2α receptor (FP receptor) agonists are potent adipose differentiation inhibitors for primary culture of adipocyte precursors in defined mediumBiochemical and Biophysical Research Communications233(1)200-202(1997)

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