(20S)-21-[[三(异丙基l)硅烷基]氧基]-20-甲基-孕甾-4-烯-3-酮 | 356063-47-3

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 类固醇和类固醇衍生物
• 中文名称: (20S)-21-[[三(异丙基l)硅烷基]氧基]-20-甲基-孕甾-4-烯-3-酮
• 英文名称: (20S)-20-[((triisopropylsilyl)oxy)methyl]-pregna-4-en-3-one
• 英文别名: (20S)-20-(triisopropylsilyloxymethyl)-pregn-4-en-3-one；(20S)-21-[[Tris(isopropyll)silyl]oxy]-20-methyl-pregn-4-en-3-one；(8S,9S,10R,13S,14S,17R)-10,13-dimethyl-17-[(2S)-1-tri(propan-2-yl)silyloxypropan-2-yl]-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
• CAS: 356063-47-3
• 化学式: C₃₁H₅₄O₂Si
• 分子量: 486.854
• InChiKey: MCSRTMAXJYKTHU-OLEFNNLGSA-N

物化性质

• 沸点：
  529.1±19.0 °C(Predicted)
• 密度：
  0.97±0.1 g/cm3(Predicted)
• 溶解度：
  溶于二氯甲烷、乙酸乙酯、甲醇

计算性质

• 辛醇/水分配系数(LogP)：
  8.96
• 重原子数：
  34
• 可旋转键数：
  7
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.9
• 拓扑面积：
  26.3
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  (20S)-21-[[三(异丙基l)硅烷基]氧基]-20-甲基-孕甾-4-烯-3-酮 在 吡啶 、 2,4,6-三甲基吡啶 、 4-二甲氨基吡啶 、 lithium aluminium tetrahydride 、 1,3-二溴-5,5-二甲基海因 、 Li₂CuCl₃ 、 硫酸 、 potassium tert-butylate 、 四丁基氟化铵 作用下， 以 四氢呋喃 、 1,4-二氧六环 、 正己烷 、 甲苯 、 叔丁醇 、 苯 为溶剂， 反应 77.5h， 生成 (3R,5S,10S,13S,17S)-4,4,10,13-四甲基-17-[(2R)-6-甲基庚-5-烯-2-基]-1,2,3,5,6,7,11,12,16,17-十氢环戊烯并[a]菲-3-醇
  参考文献：
  名称：

  Two Syntheses of FF-MAS

  摘要：

  Follicular fluid-meiosis activating sterol (FF-MAS) has been shown to be an efficient inducer of meiotic maturation. It can potentially be used for improvements of in vitro fertilization techniques. Two short synthesis of FF-MAS are presented in this article. Both syntheses are based on microbiological degradations of sterol side chains. FF-MAS can be synthesized in nine steps from commercially available starting materials by both routes.

  DOI：

  10.1021/ol0343156
• 作为产物：
  描述：

  三异丙基氯硅烷 、 (20S)-21-羟基-20-甲基孕甾-4-烯-3-酮 在 咪唑 作用下， 以 二氯甲烷 为溶剂， 反应 4.0h， 生成 (20S)-21-[[三(异丙基l)硅烷基]氧基]-20-甲基-孕甾-4-烯-3-酮
  参考文献：
  名称：

  Two Syntheses of FF-MAS

  摘要：

  Follicular fluid-meiosis activating sterol (FF-MAS) has been shown to be an efficient inducer of meiotic maturation. It can potentially be used for improvements of in vitro fertilization techniques. Two short synthesis of FF-MAS are presented in this article. Both syntheses are based on microbiological degradations of sterol side chains. FF-MAS can be synthesized in nine steps from commercially available starting materials by both routes.

  DOI：

  10.1021/ol0343156

文献信息

• Steroid derivatives with an additional ring annulated to ring A and use of these derivatives for the preparation of meiosis regulating medicaments
  申请人：SCHERING AKTIENGESELLSCHAFT

  公开号：EP1127890A1

  公开（公告）日：2001-08-29

  The present invention relates to pharmaceutically active steroid derivatives with an additional ring annulated to ring A, to pharmaceutical compositions comprising and to the use of these compounds for the preparation of medicaments. More particularly it has been found that the described steroids of the invention can be used for regulating meiosis.

  本发明涉及具有额外环并接到环A的药用活性类固醇衍生物，以及包含这些化合物的药物组合物，以及利用这些化合物制备药物的用途。更具体地，已经发现本发明中描述的类固醇可以用于调节减数分裂。
• Steroid compounds, use of these compounds for the preparation of meiosis-regulating medicaments and method for the preparation of these compounds
  申请人：Schering AG

  公开号：US20020188143A1

  公开（公告）日：2002-12-12

  The present invention relates to steroid compounds of general formula X, which may advantageously be employed to stimulate meiosis in human oocytes, the steroid being specifically characterized by amino nitrogen bonded to C 17 of the steroid skeleton via a spacer A. 1

  本发明涉及一般式X的类固醇化合物，这些化合物可以优势地用于刺激人卵母细胞的减数分裂，该类固醇化合物的特殊特征是氨基氮通过间隔物A.1与类固醇骨架的C17键合。
• Thiomorpholino steroid compounds, the use thereof for the preparation of meiosis-regulating medicaments and method for the preparation thereof
  申请人：Blume Thorsten

  公开号：US20070078262A1

  公开（公告）日：2007-04-05

  The present invention relates to thiomorpholino steroid compounds of general formula I, which may advantageously be employed to stimulate meiosis in human oocytes, the steroid being specifically characterized by a thiomorpholino moiety bonded to C 17 of the steroid skeleton via an alkylen spacer.

  本发明涉及到一般式I的硫代吗啡基类固醇化合物，可以优势地用于刺激人类卵母细胞的减数分裂，该类固醇特别的特征是通过烷基间隔将硫代吗啡基与类固醇骨架的C17键合。