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3-(3-methyl-1,2,4,5-tetrahydro-3-benzazepin-7-yl)spiro[1,3-thiazolidine-2,3'-1H-indole]-2',4-dione | 1537907-16-6

中文名称
——
中文别名
——
英文名称
3-(3-methyl-1,2,4,5-tetrahydro-3-benzazepin-7-yl)spiro[1,3-thiazolidine-2,3'-1H-indole]-2',4-dione
英文别名
——
3-(3-methyl-1,2,4,5-tetrahydro-3-benzazepin-7-yl)spiro[1,3-thiazolidine-2,3'-1H-indole]-2',4-dione化学式
CAS
1537907-16-6
化学式
C21H21N3O2S
mdl
——
分子量
379.483
InChiKey
ZVZZZABVFDLSKE-UHFFFAOYSA-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

物化性质

  • 沸点:
    727.5±60.0 °C(Predicted)
  • 密度:
    1.41±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.7
  • 重原子数:
    27
  • 可旋转键数:
    1
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    78
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为产物:
    参考文献:
    名称:
    1-Thia-4,7-diaza-spiro[4.4]nonane-3,6-dione: A Structural Motif for 5-hydroxytryptamine 6 Receptor Antagonism
    摘要:
    A series of potent 5‐hydroxytryptamine 6 (5‐HT6) receptor antagonists based on 1‐thia‐4,7‐diaza‐spiro[4.4]nonane‐3,6‐dione motif has been disclosed. Enantiomers of potent racemate compound 8a (Ki = 26 nm) displayed difference in activity (Ki of 15 nm versus 855 nm) signaling the influence of the stereochemistry of the chiral center on potency. In addition, the potent enantiomer displayed significant selectivity in biological activities over several related family members.
    DOI:
    10.1111/cbdd.12240
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文献信息

  • 1-Thia-4,7-diaza-spiro[4.4]nonane-3,6-dione: A Structural Motif for 5-hydroxytryptamine 6 Receptor Antagonism
    作者:Greg Hostetler、Derek Dunn、Beth A. McKenna、Karla Kopec、Sankar Chatterjee
    DOI:10.1111/cbdd.12240
    日期:2014.2
    A series of potent 5‐hydroxytryptamine 6 (5‐HT6) receptor antagonists based on 1‐thia‐4,7‐diaza‐spiro[4.4]nonane‐3,6‐dione motif has been disclosed. Enantiomers of potent racemate compound 8a (Ki = 26 nm) displayed difference in activity (Ki of 15 nm versus 855 nm) signaling the influence of the stereochemistry of the chiral center on potency. In addition, the potent enantiomer displayed significant selectivity in biological activities over several related family members.
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