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3,3-ethylenedioxy-5-cholen-24-al | 1432518-43-8

中文名称
——
中文别名
——
英文名称
3,3-ethylenedioxy-5-cholen-24-al
英文别名
(4R)-4-[(8S,9S,10R,13R,14S,17R)-10,13-dimethylspiro[1,2,4,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthrene-3,2'-1,3-dioxolane]-17-yl]pentanal
3,3-ethylenedioxy-5-cholen-24-al化学式
CAS
1432518-43-8
化学式
C26H40O3
mdl
——
分子量
400.602
InChiKey
SLVUOHSSEJFKRQ-DFRHSLQLSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    5.5
  • 重原子数:
    29
  • 可旋转键数:
    4
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.88
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 氢受体数:
    3

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    3,3-ethylenedioxy-5-cholen-24-al乙氧甲酰基甲基三苯基溴化膦碳酸氢钠 作用下, 以 二氯甲烷 为溶剂, 反应 3.0h, 以81.818%的产率得到
    参考文献:
    名称:
    27-Nor-Δ4-dafachronic acid is a synthetic ligand of Caenorhabditis elegans DAF-12 receptor
    摘要:
    27-Nor-Delta(4)-dafachronic acid was prepared in nine steps and 14% overall yield by two sequential 2-carbon homologations from 20 beta-carboxyaldehyde-4-pregnen-3-one. Its activity was evaluated in vivo, where it rescued the Mig phenotype of daf-9(rh50) Caenorhabditis elegans mutants and restored their normal resistance to oxidative stress. 27-Nor-Delta(4)-dafachronic acid was also able to directly bind and activate DAF-12 in a transactivation cell-based luciferase reporter assay, although it was less active than the corresponding 25R-and 255 dafachronic acids. The binding mode of the 27-Nor steroid was studied by molecular dynamics using a homology model of the CeDAF-12 receptor. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2013.03.071
  • 作为产物:
    描述:
    3,3-ethylenedioxy-5-cholenoic acid ethyl ester 在 lithium aluminium tetrahydride 、 barium carbonatepyridinium chlorochromate 作用下, 以 四氢呋喃二氯甲烷 为溶剂, 反应 4.0h, 生成 3,3-ethylenedioxy-5-cholen-24-al
    参考文献:
    名称:
    27-Nor-Δ4-dafachronic acid is a synthetic ligand of Caenorhabditis elegans DAF-12 receptor
    摘要:
    27-Nor-Delta(4)-dafachronic acid was prepared in nine steps and 14% overall yield by two sequential 2-carbon homologations from 20 beta-carboxyaldehyde-4-pregnen-3-one. Its activity was evaluated in vivo, where it rescued the Mig phenotype of daf-9(rh50) Caenorhabditis elegans mutants and restored their normal resistance to oxidative stress. 27-Nor-Delta(4)-dafachronic acid was also able to directly bind and activate DAF-12 in a transactivation cell-based luciferase reporter assay, although it was less active than the corresponding 25R-and 255 dafachronic acids. The binding mode of the 27-Nor steroid was studied by molecular dynamics using a homology model of the CeDAF-12 receptor. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2013.03.071
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文献信息

  • 27-Nor-Δ4-dafachronic acid is a synthetic ligand of Caenorhabditis elegans DAF-12 receptor
    作者:Gisela A. Samaja、Olga Castro、Lautaro D. Alvarez、María V. Dansey、Daiana S. Escudero、Adriana S. Veleiro、Adalí Pecci、Gerardo Burton
    DOI:10.1016/j.bmcl.2013.03.071
    日期:2013.5
    27-Nor-Delta(4)-dafachronic acid was prepared in nine steps and 14% overall yield by two sequential 2-carbon homologations from 20 beta-carboxyaldehyde-4-pregnen-3-one. Its activity was evaluated in vivo, where it rescued the Mig phenotype of daf-9(rh50) Caenorhabditis elegans mutants and restored their normal resistance to oxidative stress. 27-Nor-Delta(4)-dafachronic acid was also able to directly bind and activate DAF-12 in a transactivation cell-based luciferase reporter assay, although it was less active than the corresponding 25R-and 255 dafachronic acids. The binding mode of the 27-Nor steroid was studied by molecular dynamics using a homology model of the CeDAF-12 receptor. (C) 2013 Elsevier Ltd. All rights reserved.
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