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(1'R,2R,2'S,3R,3aS,6S,7aR,10'S,11'R,14'S)-3,6,6',11'-tetramethylspiro[3a,4,5,6,7,7a-hexahydro-3H-furo[3,2-b]pyridine-2,5'-pentacyclo[8.8.0.02,8.06,8.011,16]octadec-16-ene]-14'-ol | 878204-85-4

中文名称
——
中文别名
——
英文名称
(1'R,2R,2'S,3R,3aS,6S,7aR,10'S,11'R,14'S)-3,6,6',11'-tetramethylspiro[3a,4,5,6,7,7a-hexahydro-3H-furo[3,2-b]pyridine-2,5'-pentacyclo[8.8.0.02,8.06,8.011,16]octadec-16-ene]-14'-ol
英文别名
——
(1'R,2R,2'S,3R,3aS,6S,7aR,10'S,11'R,14'S)-3,6,6',11'-tetramethylspiro[3a,4,5,6,7,7a-hexahydro-3H-furo[3,2-b]pyridine-2,5'-pentacyclo[8.8.0.02,8.06,8.011,16]octadec-16-ene]-14'-ol化学式
CAS
878204-85-4
化学式
C28H43NO2
mdl
——
分子量
425.655
InChiKey
QMNVCSWLZHZJLT-UHIKDDTDSA-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):
    4.8
  • 重原子数:
    31
  • 可旋转键数:
    0
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.93
  • 拓扑面积:
    41.5
  • 氢给体数:
    2
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    (1'R,2R,2'S,3R,3aS,6S,7aR,10'S,11'R,14'S)-3,6,6',11'-tetramethylspiro[3a,4,5,6,7,7a-hexahydro-3H-furo[3,2-b]pyridine-2,5'-pentacyclo[8.8.0.02,8.06,8.011,16]octadec-16-ene]-14'-ol三乙酰氧基硼氢化钠 作用下, 以 乙腈 为溶剂, 反应 16.0h, 生成 N-[2-[(1'R,2R,2'S,3R,3aS,6S,7aR,10'S,11'R,14'S)-14'-hydroxy-3,6,6',11'-tetramethylspiro[3,3a,5,6,7,7a-hexahydrofuro[3,2-b]pyridine-2,5'-pentacyclo[8.8.0.02,8.06,8.011,16]octadec-16-ene]-4-yl]ethyl]-6-(3-phenylpropanoylamino)hexanamide
    参考文献:
    名称:
    [EN] CYCLOPAMINE ANALOGUES AND METHODS OF USE THEREOF
    [FR] ANALOGUES DE CYCLOPAMINE ET PROCEDES D'UTILISATION DE CEUX-CI
    摘要:
    公开号:
    WO2006026430A3
  • 作为产物:
    描述:
    9H-fluoren-9-ylmethyl (1'R,2R,2'S,3R,3aS,6S,7aR,10'S,11'R,14'S)-14'-hydroxy-3,6,6',11'-tetramethylspiro[3,3a,5,6,7,7a-hexahydrofuro[3,2-b]pyridine-2,5'-pentacyclo[8.8.0.02,8.06,8.011,16]octadec-16-ene]-4-carboxylate 在 二乙胺 作用下, 以 二氯甲烷 为溶剂, 以95%的产率得到(1'R,2R,2'S,3R,3aS,6S,7aR,10'S,11'R,14'S)-3,6,6',11'-tetramethylspiro[3a,4,5,6,7,7a-hexahydro-3H-furo[3,2-b]pyridine-2,5'-pentacyclo[8.8.0.02,8.06,8.011,16]octadec-16-ene]-14'-ol
    参考文献:
    名称:
    [EN] CYCLOPAMINE ANALOGUES AND METHODS OF USE THEREOF
    [FR] ANALOGUES DE CYCLOPAMINE ET PROCEDES D'UTILISATION DE CEUX-CI
    摘要:
    公开号:
    WO2006026430A3
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文献信息

  • Cyclopamine analogues and methods of use thereof
    申请人:Infinity Pharmaceuticals, Inc.
    公开号:EP2316832B1
    公开(公告)日:2017-03-08
  • CYCLOPAMINE ANALOGUES AND METHODS OF USE THEREOF
    申请人:ADAMS Julian
    公开号:US20070191410A1
    公开(公告)日:2007-08-16
    The present invention provides compositions and methods for modulating smoothened-dependent pathway activation. The present invention provides analogs of cyclopamine that can be used to counteract the phenotypic effects of unwanted activation of a hedgehog pathway, such as resulting from hedgehog gain-of-function, Ptc loss-of-function or smoothened gain-of-function mutations. The compounds of the present invention are particularly useful in treating cancers.
  • Cyclopamine Analogues and Methods of Use Thereof
    申请人:Adams Julian
    公开号:US20110166353A1
    公开(公告)日:2011-07-07
    The present invention provides compositions and methods for modulating smoothened-dependent pathway activation. The present invention provides analogs of cyclopamine that can be used to counteract the phenotypic effects of unwanted activation of a hedgehog pathway, such as resulting from hedgehog gain-of-function, Ptc loss-of-function or smoothened gain-of-function mutations. The compounds of the present invention are particularly useful in treating cancers.
  • US7230004B2
    申请人:——
    公开号:US7230004B2
    公开(公告)日:2007-06-12
  • US7407967B2
    申请人:——
    公开号:US7407967B2
    公开(公告)日:2008-08-05
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