embedded image ;In the formula, substituent R is H, alkanoyl or alkenoyl having 2 to 22 carbon atoms or stereoisomers thereof; substituent R′ can be H, alkanoyl or alkenoyl having 2 to 4 carbon atoms or stereoisomers thereof; such an aliphatic ester compound being used as a pro-drug can improve the stability of a compound, meanwhile the decrease of polarity can enable them to be easily made into preparations like lipid emulsion, microsphere etc., and avoid the degradation of the compound caused by factors like high temperature etc. and the use of an organic solution during preparation process."/> Ester derivatives of 7-alpha-9-(4,4,5,5,5-pentafluoropentylsulfinyl)nonyl)-estra-1,3,5(10)-triene-3,17beta-diol having anticancer activity and preparation method thereof
首页> 外国专利> Ester derivatives of 7-alpha-9-(4,4,5,5,5-pentafluoropentylsulfinyl)nonyl)-estra-1,3,5(10)-triene-3,17beta-diol having anticancer activity and preparation method thereof

Ester derivatives of 7-alpha-9-(4,4,5,5,5-pentafluoropentylsulfinyl)nonyl)-estra-1,3,5(10)-triene-3,17beta-diol having anticancer activity and preparation method thereof

机译:具有抗癌活性的7-α-[9-(4,4,5,5,5-五氟戊基亚磺酰基)壬基)-雌二醇-1,3,5(10)-三烯-3,17β-二醇的酯衍生物及其制备方法其中

摘要

The present invention provides a class of fulvestrant ester derivatives and preparation method thereof. Such a compound is an aliphatic ester formed by esterifying the —OH at positions C-3 and C-17 of fulvestrant, having a structure of the following formula:; embedded image ;In the formula, substituent R is H, alkanoyl or alkenoyl having 2 to 22 carbon atoms or stereoisomers thereof; substituent R′ can be H, alkanoyl or alkenoyl having 2 to 4 carbon atoms or stereoisomers thereof; such an aliphatic ester compound being used as a pro-drug can improve the stability of a compound, meanwhile the decrease of polarity can enable them to be easily made into preparations like lipid emulsion, microsphere etc., and avoid the degradation of the compound caused by factors like high temperature etc. and the use of an organic solution during preparation process.
机译:本发明提供了一种氟司威特酯衍生物及其制备方法。这样的化合物是通过酯化夫弗司特的C-3和C-17位处的-OH形成的脂族酯,具有下式结构: “嵌入式图像” 式中,取代基R为H,碳数2至22的链烷酰基或链烯酰基或其立体异构体。取代基R'可以是H,具有2-4个碳原子的链烷酰基或链烯酰基或其立体异构体;这样的脂族酯化合物用作前药可以提高化合物的稳定性,同时极性的降低可以使它们易于制成脂质乳剂,微球等制剂,并且避免了化合物的降解。受高温等因素影响,以及在制备过程中使用有机溶液。

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