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(4-fluoro-3-methylphenyl(3R,5R,8R,9S,10S,13S,14S,17S)-3-hydroxy-3,10,13-trimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)methanone

中文名称
——
中文别名
——
英文名称
(4-fluoro-3-methylphenyl(3R,5R,8R,9S,10S,13S,14S,17S)-3-hydroxy-3,10,13-trimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)methanone
英文别名
(4-fluoro-3-methylphenyl)-[(3R,5R,8R,9S,10S,13S,14S,17S)-3-hydroxy-3,10,13-trimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]methanone
(4-fluoro-3-methylphenyl(3R,5R,8R,9S,10S,13S,14S,17S)-3-hydroxy-3,10,13-trimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)methanone化学式
CAS
——
化学式
C28H39FO2
mdl
——
分子量
426.615
InChiKey
JUNSUEWXZPTWIN-NABSQCQYSA-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):
    7.2
  • 重原子数:
    31
  • 可旋转键数:
    2
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    37.3
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

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文献信息

  • COMPOSITIONS FOR INDUCING SEDATION
    申请人:Sage Therapeutics, Inc.
    公开号:EP3719029A1
    公开(公告)日:2020-10-07
    Described herein are neuroactive steroids of the Formula (II): or a pharmaceutically acceptable salt thereof; wherein A, R1, R2a, R2b, R3a, R3b, R4a, R4b, R5, R6 and ------ are as defined herein. Such compounds are envisioned, in certain embodiments, to behave as GABA modulators. The present invention also provides pharmaceutical compositions comprising a compound of the present invention and methods of use and treatment, e.g., such for inducing sedation and/or anesthesia.
    本文描述的是式 (II) 的神经活性类固醇: 或其药学上可接受的盐;其中 A、R1、R2a、R2b、R3a、R3b、R4a、R4b、R5、R6 和 ------ 如本文所定义。在某些实施方案中,此类化合物被设想为 GABA 调节剂。本发明还提供了包含本发明化合物的药物组合物以及使用和治疗方法,例如用于诱导镇静和/或麻醉的方法。
  • Compositions and methods for treating CNS disorders
    申请人:Sage Therapeutics, Inc.
    公开号:US10774108B2
    公开(公告)日:2020-09-15
    Described herein are neuroactive steroids of the Formula (II): or a pharmaceutically acceptable salt thereof; wherein A, R1, R2a, R2b, R3a, R3b, R4a, R4b, R5, R6 and are as defined herein. Such compounds are envisioned, in certain embodiments, to behave as GABA modulators. The present invention also provides pharmaceutical compositions comprising a compound of the present invention and methods of use and treatment, e.g., such for inducing sedation and/or anesthesia.
    本文描述的是式 (II) 的神经活性类固醇:或其药学上可接受的盐;其中 A、R1、R2a、R2b、R3a、R3b、R4a、R4b、R5、R6 和如本文所定义。在某些实施方案中,此类化合物被设想为 GABA 调节剂。本发明还提供了包含本发明化合物的药物组合物以及使用和治疗方法,例如用于诱导镇静和/或麻醉的方法。
  • COMPOSITIONS AND METHODS FOR TREATING CNS DISORDERS
    申请人:Sage Therapeutics, Inc.
    公开号:EP3224269B1
    公开(公告)日:2020-02-26
  • [EN] COMPOSITIONS AND METHODS FOR TREATING CNS DISORDERS<br/>[FR] COMPOSITIONS ET PROCÉDÉS POUR TRAITER DES TROUBLES DU SNC
    申请人:SAGE THERAPEUTICS INC
    公开号:WO2016082789A1
    公开(公告)日:2016-06-02
    Described herein are neuroactive steroids of the Formula (II) : or a pharmaceutically acceptable salt thereof; wherein A, R1, R2a, R2b, R3a, R3b, R4a, R4b, R5, R6 and ----- are as defined herein. Such compounds are envisioned, in certain embodiments, to behave as GABA modulators. The present invention also provides pharmaceutical compositions comprising a compound of the present invention and methods of use and treatment, e. g., such for inducing sedation and/or anesthesia.
    本文描述了Formula (II)的神经活性类固醇:或其药用可接受的盐;其中A、R1、R2a、R2b、R3a、R3b、R4a、R4b、R5、R6和-----如本文所定义。在某些实施例中,这些化合物被设想为GABA调节剂。本发明还提供了包括本发明化合物的药物组合物以及使用和治疗方法,例如用于诱导镇静和/或麻醉。
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