(20R,22S)-des-A,B-22-methyl-25-[(triethylsilyl)oxy]cholestan-8-one | 386743-50-6

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 异戊烯醇脂质
• 英文名称: (20R,22S)-des-A,B-22-methyl-25-[(triethylsilyl)oxy]cholestan-8-one
• 英文别名: (1R,3aR,7aR)-1-[(2R,3S)-3,6-dimethyl-6-triethylsilyloxyheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-one
• CAS: 386743-50-6
• 化学式: C₂₅H₄₈O₂Si
• 分子量: 408.74
• InChiKey: QVKXYRXPIDCURW-WUDUDLAESA-N

物化性质

• 沸点：
  447.5±18.0 °C(Predicted)
• 密度：
  0.919±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  7.62
• 重原子数：
  28
• 可旋转键数：
  10
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.96
• 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：

  (20R,22S)-des-A,B-22-methyl-25-[(triethylsilyl)oxy]cholestan-8-one 在 氢氟酸 、 苯基锂 作用下， 以 四氢呋喃 、 二丁醚 、 水 、 乙腈 为溶剂， 反应 0.5h， 生成 (20R,22S)-1α,25-dihydroxy-22-methyl-2-methylene-19-norvitamin D(3)
  参考文献：
  名称：

  A 20S Combined with a 22R Configuration Markedly Increases both in Vivo and in Vitro Biological Activity of 1α,25-Dihydroxy-22-methyl-2-methylene-19-norvitamin D₃

  摘要：

  Six new analogues of 1 alpha,25-dihydroxy-19-norvitamin D-3 (3a-4b, 5, and 6) were prepared by a convergent synthesis applying the Wittig-Horner reaction as a key step. The influence of methyl groups at C-22 on their biological activity was examined. It was established that both in vitro and in vivo activity is strongly dependent on the configuration of the stereogenic centers at C-20 and C-22. Introduction of the second methyl group at C-22 (analogues 5 and 6) generates the compounds that are slightly more potent than 1 alpha,25-(OH)(2)D-3 in the in vitro tests but much less potent in vivo. The greatest in vitro and in vivo biological activity was achieved when the C-20 is in the S configuration and the C-22 is in the R configuration. The building blocks for the synthesis, the respective (20R,22R)-, (20R,22S)-, (20S,22R)-, and (20S,22S)-diols, were obtained by fractional crystallization of mixtures of the corresponding diastereomers. Structures and absolute configurations of the diols 21a, 21b, and 22a as well as analogues 3a, 5, and 6 were confirmed by the X-ray crystallography.

  DOI：

  10.1021/jm300187x
• 作为产物：
  描述：

  4-bromo-2-methyl-2-(triethylsilyloxy)butane 在 吡啶 、 sodium tetrahydroborate 、 lithium aluminium tetrahydride 、 重铬酸吡啶 、 二异丁基氢化铝 、 lithium diisopropyl amide 作用下， 以 四氢呋喃 、 甲醇 、 乙醚 、 二氯甲烷 为溶剂， 反应 17.0h， 生成 (20R,22S)-des-A,B-22-methyl-25-[(triethylsilyl)oxy]cholestan-8-one
  参考文献：
  名称：

  (22R)-和(22S)-22-甲基-1α,25-二羟基维生素D3的立体选择性合成

  摘要：

  描述了构建 (22R)- 和 (22S)-22-烷基-1α,25-二羟基维生素 D3 侧链的有效、直接的方法。标题化合物通过Lythgoe's procedure合成。

  DOI：

  10.1055/s-2001-17446

文献信息

• DIASTEREOMERS OF 2-METHYLENE-19-NOR-22-METHYL-1ALPHA,25-DIHYDROXYVITAMIN D3
  申请人：DeLuca Hector F.

  公开号：US20110237557A1

  公开（公告）日：2011-09-29

  Compounds of formula I are provided where X 1 , X 2 , and X 3 are independently selected from H or hydroxy protecting groups. Such compounds may be used in preparing pharmaceutical compositions and are useful in treating a variety of biological conditions.

  提供了公式I的化合物，其中X1、X2和X3分别选自H或羟基保护基团。这些化合物可用于制备药物组合物，并可用于治疗各种生物状况。
• A 20<i>S</i> Combined with a 22<i>R</i> Configuration Markedly Increases both in Vivo and in Vitro Biological Activity of 1α,25-Dihydroxy-22-methyl-2-methylene-19-norvitamin D₃
  作者：Agnieszka Flores、Rafal R. Sicinski、Pawel Grzywacz、James B. Thoden、Lori A. Plum、Margaret Clagett-Dame、Hector F. DeLuca

  DOI：10.1021/jm300187x

  日期：2012.5.10

  Six new analogues of 1 alpha,25-dihydroxy-19-norvitamin D-3 (3a-4b, 5, and 6) were prepared by a convergent synthesis applying the Wittig-Horner reaction as a key step. The influence of methyl groups at C-22 on their biological activity was examined. It was established that both in vitro and in vivo activity is strongly dependent on the configuration of the stereogenic centers at C-20 and C-22. Introduction of the second methyl group at C-22 (analogues 5 and 6) generates the compounds that are slightly more potent than 1 alpha,25-(OH)(2)D-3 in the in vitro tests but much less potent in vivo. The greatest in vitro and in vivo biological activity was achieved when the C-20 is in the S configuration and the C-22 is in the R configuration. The building blocks for the synthesis, the respective (20R,22R)-, (20R,22S)-, (20S,22R)-, and (20S,22S)-diols, were obtained by fractional crystallization of mixtures of the corresponding diastereomers. Structures and absolute configurations of the diols 21a, 21b, and 22a as well as analogues 3a, 5, and 6 were confirmed by the X-ray crystallography.
• Stereoselective Synthesis of (22R)- and (22S)-22-Methyl-1α,25-Dihydroxyvitamin D3
  作者：Yagamare Fall、Carlos Fernandez、Victoria González、Antonio Mouriño

  DOI：10.1055/s-2001-17446

  日期：——

  An efficient, straightforward method for construction of the side chain of (22R)- and (22S)-22-alkyl-1α,25-dihydroxyvitamin D3 is described. The title compounds were synthesized by Lythgoe's procedure.

  描述了构建 (22R)- 和 (22S)-22-烷基-1α,25-二羟基维生素 D3 侧链的有效、直接的方法。标题化合物通过Lythgoe's procedure合成。