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17-phenyl trinor Prostaglandin F2αethyl amide-d4
本产品不向个人销售,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 F2αethyl amide-d4图片
规格:98%
分子量:419.6
包装与价格:
包装价格(元)
25ug电议
50ug电议
100ug电议
1mg电议

产品介绍
A neuropeptide with diverse biological activities
货号:ajcx21146
CAS:N/A
分子式:C25H33D4NO4
分子量:419.6
溶解度:DMF: 25 mg/ml,DMSO: 25 mg/ml,Ethanol: 30 mg/ml,PBS (pH 7.2): .3 mg/ml
纯度:98%
存储:Store at -20°C
库存:现货

Background:

17-phenyl trinor Prostaglandin Fethyl amide (17-phenyl trinor PGFethyl amide) is sold under the Allergan trade name Bimatoprost and is an F-series PG analog which has been approved for use as an ocular hypotensive drug.1Investigations in our lab have shown that 17-phenyl trinor PGFethyl amide is converted by an amidase enzymatic activity in the bovine and human cornea to yield the corresponding free acid, with a conversion rate of about 40 µg/g corneal tissue/24 hours.2The free acid, 17-phenyl trinor PGF, is a potent FP receptor agonist.3,4In human and animal models of glaucoma, FP receptor agonist activity corresponds very closely with intraocular hypotensive activity.


1.Woodward, D.F., Krauss, A.H.P., Chen, J., et al.The pharmacology of Bimatoprost (LumiganTM)Survey of Ophthalmology45S337-S345(2001) 2.Maxey, K.M., Johnson, J., Camras, C.B., et al.The hydrolysis of bimatoprost in corneal tissue generates a potent prostanoid FP receptor agonistSuv. Ophthalmol.47(4)S34-S40(2002) 3.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) 4.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)