5α,6α-epoxycholest-7-en-3β-ol | 95841-65-9

• 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
• 英文名称: 5α,6α-epoxycholest-7-en-3β-ol
• 英文别名: 5α,6α-epoxycholest-7-en-3-ol；5,6α-epoxycholest-7-en-3β-ol；(1S,2R,5S,7R,9S,12R,15R,16R)-2,16-dimethyl-15-[(2R)-6-methylheptan-2-yl]-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-10-en-5-ol
• CAS: 95841-65-9
• 化学式: C₂₇H₄₄O₂
• 分子量: 400.645
• InChiKey: HQJPDAPYXZGRSF-SVPSOKIXSA-N

物化性质

• 沸点：
  506.1±50.0 °C(Predicted)
• 密度：
  1.05±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  7.1
• 重原子数：
  29
• 可旋转键数：
  5
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.93
• 拓扑面积：
  32.8
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  5α,6α-epoxycholest-7-en-3β-ol 在 吡啶 、 氢氧化钾 、 mercury(II) diacetate 、 溶剂黄146 作用下， 以 甲醇 、 二氯甲烷 为溶剂， 反应 48.0h， 生成 5α-cholest-7,9(11)-diene-3β,5,6α-triol-3,6-diacetate
  参考文献：
  名称：

  合成硬皮甾醇，两种具有细胞毒性的多氧化海绵类固醇

  摘要：

  据报道，两种细胞毒性海洋类固醇硬皮甾醇A和B的合成。

  DOI：

  10.1016/0040-4039(96)00932-x
• 作为产物：
  描述：

  7-去氢胆固醇 在 间氯过氧苯甲酸 作用下， 以 二氯甲烷 为溶剂， 生成 5α,6α-epoxycholest-7-en-3β-ol
  参考文献：
  名称：

  合成硬皮甾醇，两种具有细胞毒性的多氧化海绵类固醇

  摘要：

  据报道，两种细胞毒性海洋类固醇硬皮甾醇A和B的合成。

  DOI：

  10.1016/0040-4039(96)00932-x

文献信息

• [EN] PROCESS FOR THE PREPARATION OF STEROL DERIVATIVES<br/>[FR] PROCÉDÉ POUR LA PRÉPARATION DE DÉRIVÉS DE STÉROL
  申请人：INST NAT SANTE RECH MED

  公开号：WO2013076257A1

  公开（公告）日：2013-05-30

  The present invention relates to a process for the preparation of sterol derivatives comprising the reaction of an α-epoxy compound with an amine in an alcohol comprising 3 to 5 carbon atoms as a solvent.

  本发明涉及一种用于制备甾醇衍生物的方法，包括在含有3至5个碳原子的醇溶剂中，将α-环氧化合物与胺反应的过程。
• Synthesis of New Alkylaminooxysterols with Potent Cell Differentiating Activities: Identification of Leads for the Treatment of Cancer and Neurodegenerative Diseases
  作者：Philippe de Medina、Michael R. Paillasse、Bruno Payré、Sandrine Silvente-Poirot、Marc Poirot

  DOI：10.1021/jm901063e

  日期：2009.12.10

  We describe here the syntheses and the biological properties of new alkylaminooxysterols. Compounds were synthesized through the trans-diaxial aminolysis of 5,6-alpha-epoxysterols with various natural amines including histamine, putrescine, spermidine, or spermine. The regioselective synthesis of these 16 new 5 alpha-hydroxyl-6 beta-aminoalkylsterols is presented. Compounds were first screened for dendrite outgrowth and cytotoxicity in vitro, and two leads were selected and further characterized. 5 alpha-Hydroxy-6 beta-[2-(1-H-imidazol-4-yl)ethylamino]cholestan -3 beta-ol, called dendrogenin A, induced growth control, differentiation, and the death of tumor cell lines representative of various cancers including metastatic melanoma and breast cancer. 5 alpha-hydroxyl-6 beta-[3-(4-aminobutylamino)propylamino]cholest-7-en-3 beta-ol, called dendrogenin B, induced neurite outgrowth on various cell lines, neuronal differentiation in pluripotent cells, and survival of normal neurones at nanomolar concentrations. In summary, we report that two new alkylaminooxysterols, dendrogenin A and dendrogenin B, are the first members of a class of compounds that induce cell differentiation at nanomolar concentrations and represent promising new leads for the treatment of cancer or neurodegenerative diseases.
• Stereoselective synthesis and solvolytic behavior of the isomeric 7-dehydrocholesterol 5,6-oxides
  作者：Dennis P. Michaud、Nashaat T. Nashed、Donald M. Jerina

  DOI：10.1021/jo00211a009

  日期：1985.5