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7-Mercapto-indol | 89942-92-7

中文名称
——
中文别名
——
英文名称
7-Mercapto-indol
英文别名
indole-7-thiole;1H-indole-7-thiol
7-Mercapto-indol化学式
CAS
89942-92-7
化学式
C8H7NS
mdl
MFCD19221973
分子量
149.216
InChiKey
BEPKJAXROVBBID-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:
    326.6±15.0 °C(Predicted)
  • 密度:
    1.303±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3
  • 重原子数:
    10
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    16.8
  • 氢给体数:
    2
  • 氢受体数:
    1

文献信息

  • Indole derivatives comprising an acetylene group
    申请人:Ackermann Jean
    公开号:US20060035956A1
    公开(公告)日:2006-02-16
    This invention is directed to compounds of the formula (I): wherein one of R 6 , R 7 , R 8 and R 9 is and X, R 1 to R 12 , m, n and o are as defined in the description, and pharmaceutically acceptable salts and/or esters thereof. The invention is also directed to pharmaceutical compositions containing such compounds, to a process for their preparation and to their use for the treatment and/or prevention of diseases which are modulated by PPARδ and/or PPARα agonists.
    这项发明涉及式(I)的化合物:其中R6、R7、R8和R9中的一个是X,R1到R12,m,n和o如描述中所定义,并且其药学上可接受的盐和/或酯。该发明还涉及含有这种化合物的药物组合物,以及用于治疗和/或预防由PPARδ和/或PPARα激动剂调节的疾病的方法。
  • Modulators of sphingosine phosphate receptors
    申请人:The Scripps Research Institute
    公开号:US10544136B2
    公开(公告)日:2020-01-28
    Compounds that activate a sphingosine-1-phosphate receptor of the subtype 1 are provided. Certain compounds selectively activate the receptor subtype 1 in relation to the sphinogosine-1-phosphate receptor subtype 3. Uses and methods of inventive compounds for treatment of malconditions wherein activation, agonism, inhibition or antagonism of the S1P1 is medically indicated are provided.
    本研究提供了能激活亚型 1 的鞘氨醇-1-磷酸受体的化合物。与鞘氨醇-1-磷酸受体亚型 3 相比,某些化合物可选择性地激活受体亚型 1。本发明提供了本发明化合物的用途和方法,用于治疗S1P1的活化、激动、抑制或拮抗在医学上适用的不良病症。
  • INDOLE DERIVATIVES COMPRISING AN ACETYLENE GROUP AS PPAR ACTIVATORS
    申请人:F.HOFFMANN-LA ROCHE AG
    公开号:EP1781608A1
    公开(公告)日:2007-05-09
  • NOVEL MODULATORS OF SPHINGOSINE PHOSPHATE RECEPTORS
    申请人:The Scripps Research Institute
    公开号:US20190084947A1
    公开(公告)日:2019-03-21
    Compounds that activate a sphingosine-1-phosphate receptor of the subtype 1 are provided. Certain compounds selectively activate the receptor subtype 1 in relation to the sphinogosine- 1 -phosphate receptor subtype 3. Uses and methods of inventive compounds for treatment of malconditions wherein activation, agonism, inhibition or antagonism of the S1P1 is medically indicated are provided.
  • OPTICAL PRODUCT AND OPTICAL FILTER INCLUDING SAME
    申请人:LMS Co., Ltd.
    公开号:US20200241185A1
    公开(公告)日:2020-07-30
    The present invention relates to an optical article, and an optical filter and an imaging device including the same. The optical article comprises: a near-infrared absorption glass substrate including a divalent copper ion as a chromatic ingredient; and a pigment dispersion layer formed on one surface or both surfaces of the near-infrared absorption glass substrate and having a near-infrared absorption pigment and an ultraviolet absorption pigment dispersed across the resin matrix thereof. Provided with a first and a second transmission cut-off region, the optical article has the advantage of allowing the fabrication of an excellent near-infrared cut-off filter that can effectively block light in near-infrared and ultraviolet bands and does not permit a difference in color sense with the change of incident angles.
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