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(R)-(5-Chloro-thiophen-2-yl)-[(4aR,5S)-1-(4-fluoro-phenyl)-4a-methyl-4,4a,5,6,7,8-hexahydro-1H-benzo[f]indazol-5-yl]-methanol

中文名称
——
中文别名
——
英文名称
(R)-(5-Chloro-thiophen-2-yl)-[(4aR,5S)-1-(4-fluoro-phenyl)-4a-methyl-4,4a,5,6,7,8-hexahydro-1H-benzo[f]indazol-5-yl]-methanol
英文别名
(R)-[(4aR,5S)-1-(4-fluorophenyl)-4a-methyl-5,6,7,8-tetrahydro-4H-benzo[f]indazol-5-yl]-(5-chlorothiophen-2-yl)methanol
(R)-(5-Chloro-thiophen-2-yl)-[(4aR,5S)-1-(4-fluoro-phenyl)-4a-methyl-4,4a,5,6,7,8-hexahydro-1H-benzo[f]indazol-5-yl]-methanol化学式
CAS
——
化学式
C23H22ClFN2OS
mdl
——
分子量
428.958
InChiKey
DEOMFWBIPHAVQN-YSZBQJHXSA-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):
    5.7
  • 重原子数:
    29
  • 可旋转键数:
    3
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    66.3
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    (4aR,5S)-1-(4-fluorophenyl)-4a-methyl-4,4a,5,6,7,8-hexahydro-1H-benzo[f]indazole-5-carbaldehyde 、 以 四氢呋喃 为溶剂, 反应 0.75h, 生成 (S)-(5-Chloro-thiophen-2-yl)-[(4aR,5S)-1-(4-fluoro-phenyl)-4a-methyl-4,4a,5,6,7,8-hexahydro-1H-benzo[f]indazol-5-yl]-methanol 、 (R)-(5-Chloro-thiophen-2-yl)-[(4aR,5S)-1-(4-fluoro-phenyl)-4a-methyl-4,4a,5,6,7,8-hexahydro-1H-benzo[f]indazol-5-yl]-methanol
    参考文献:
    名称:
    Novel heterocyclic glucocorticoids: in vitro profile and in vivo efficacy
    摘要:
    A series of novel ligands for the glucocorticoid receptor containing two heterocycles were synthesized. These compounds were investigated for a dissociative profile using transrepression and transactivation assays. Several compounds were tested in vivo and showed the ability to reduce inflammation in a mouse. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2005.02.009
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文献信息

  • 1H-BENZO(F)INDAZOL-5-YL DERIVATIVES AS SELECTIVE GLUCOCORTICOID RECEPTOR MODULATORS
    申请人:Merck Sharp & Dohme Corp.
    公开号:EP1496892B1
    公开(公告)日:2011-01-26
  • 1H-benzo[F]indazol-5-YL derivatives as selective glucocorticoid receptor modulators
    申请人:Ali Amjad
    公开号:US20080076795A1
    公开(公告)日:2008-03-27
    The present invention encompasses compounds of Formula I: or pharmaceutically acceptable salts or hydrates thereof, which are useful as selective glucocorticoid receptor ligands for treating a variety of autoimmune and inflammatory diseases or conditions. Pharmaceutical compositions and methods of use are also included.
  • US7282591B2
    申请人:——
    公开号:US7282591B2
    公开(公告)日:2007-10-16
  • US7625937B2
    申请人:——
    公开号:US7625937B2
    公开(公告)日:2009-12-01
  • Novel heterocyclic glucocorticoids: in vitro profile and in vivo efficacy
    作者:Christopher F. Thompson、Nazia Quraishi、Amjad Ali、James R. Tata、Milton L. Hammond、James M. Balkovec、Monica Einstein、Lan Ge、Georgianna Harris、Theresa M. Kelly、Paul Mazur、Shilpa Pandit、Joseph Santoro、Ayesha Sitlani、Chuanlin Wang、Joanne Williamson、Douglas K. Miller、Ting-ting D. Yamin、Chris M. Thompson、Edward A. O’Neill、Dennis Zaller、Michael J. Forrest、Ester Carballo-Jane、Silvi Luell
    DOI:10.1016/j.bmcl.2005.02.009
    日期:2005.4
    A series of novel ligands for the glucocorticoid receptor containing two heterocycles were synthesized. These compounds were investigated for a dissociative profile using transrepression and transactivation assays. Several compounds were tested in vivo and showed the ability to reduce inflammation in a mouse. (c) 2005 Elsevier Ltd. All rights reserved.
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同类化合物

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