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17-phenyl trinor Prostaglandin F2α-d4
本半岛bd体育手机客户端 不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
17-phenyl trinor Prostaglandin F2α-d4图片
CAS NO: 58976-50-4
包装与价格:
包装 价格(元)
25 μg 电议
50 μg 电议
100 μg 电议
1mg 电议

半岛bd体育手机客户端 介绍
An internal standard for the quantification of bimatoprost (free acid)
Cas No. 58976-50-4
Canonical SMILES O[C@@H](CCC1=CC=CC=C1)/C=C/[C@H]2[C@H](O)C[C@H](O)[C@@H]2C/C=C\C([2H])([2H])C([2H])([2H])CC(O)=O
分子式 C23H28D4O5
分子量 392.5
溶解度 DMF: 25 mg/ml,DMSO: 25 mg/ml,Ethanol: 30 mg/ml,PBS (pH 7.2): .5 mg/ml
储存条件 Store at -20°C
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.
Shipping Condition Evaluation sample solution : ship with blue ice
All other available size: ship with RT , or blue ice upon request
半岛bd体育手机客户端 描述

17-phenyl trinor Prostaglandin F-d4(17-phenyl trinor PGF-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 17-phenyl trinor PGFby GC-or LC-mass spectrometry. 17-phenyl trinor PGFis a metabolically stable analog of PGFand is a potent agonist for the FP receptor. It binds to the FP receptor on ovine luteal cells with a relative potency of 756% compared to that of PGF.1At the rat recombinant FP receptor expressed in CHO cells 17-phenyl trinor PGFinhibits PGFbinding with a Kiof 1.1 nM.2The isopropyl ester of 17-phenyl trinor PGF-d4is slightly better than PGFisopropyl ester in reducing the intraocular pressure in the cat eye without any irritation.3

1.Balapure, A.K., Rexroad, C.E., Jr., Kawada, K., et al.Structural requirements for prostaglandin analog interaction with the ovine corpus luteum prostaglandin F2α receptorBiochem. Pharmacol.38(14)2375-2381(1989) 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.Stjernschantz, J., and Resul, B.Phenyl substituted prostaglandin analogs for glaucoma treatmentDrugs of the Future17691-704(1992)

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