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1-Indolyl-3-isopropylmethylamine | 299-24-1

中文名称
——
中文别名
——
英文名称
1-Indolyl-3-isopropylmethylamine
英文别名
(2-indol-3-yl-1-methyl-ethyl)-methyl-amine;3-(2-Methylamino-propyl)-indol;N,α-Dimethyltryptamine;3-(2-Methylaminopropyl)indol;1-(1H-indol-3-yl)-N-methylpropan-2-amine
1-Indolyl-3-isopropylmethylamine化学式
CAS
299-24-1
化学式
C12H16N2
mdl
——
分子量
188.272
InChiKey
HUWIYJREHSBOEO-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

计算性质

  • 辛醇/水分配系数(LogP):
    2.5
  • 重原子数:
    14
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    27.8
  • 氢给体数:
    2
  • 氢受体数:
    1

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    1-Indolyl-3-isopropylmethylamine炔丙基碘化物叔丁胺 作用下, 以 为溶剂, 反应 15.0h, 以95%的产率得到N-[1-(1H-吲哚-3-基)-2-丙基]-N-甲基-2-丙炔-1-胺
    参考文献:
    名称:
    Synthesis and antimonoamine oxidase activity of an indole analog of deprenyl
    摘要:
    DOI:
    10.1007/bf00764169
  • 作为产物:
    描述:
    DL-ALPHA-甲基色胺 在 lithium aluminium tetrahydride 、 三乙胺 作用下, 以 四氢呋喃氯仿 为溶剂, 反应 32.0h, 生成 1-Indolyl-3-isopropylmethylamine
    参考文献:
    名称:
    Synthesis and antimonoamine oxidase activity of an indole analog of deprenyl
    摘要:
    DOI:
    10.1007/bf00764169
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文献信息

  • Use of GAL3 receptor antagonists for the treatment of depression and/or anxiety and compounds useful in such methods
    申请人:——
    公开号:US20030078271A1
    公开(公告)日:2003-04-24
    This invention is directed to pyrimidine and indolone derivatives which are selective antagonists for the GAL3 receptor. The invention provides a pharmaceutical composition comprising a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. This invention also provides a pharmaceutical composition made by combining a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. This invention further provides a process for making a pharmaceutical composition comprising combining a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. This invention also provides a method of treating a subject suffering from depression and/or anxiety which comprises administering to the subject an amount of a compound of the invention effective to treat the subject's depression and/or anxiety. This invention also provides a method of treating depression and/or anxiety in a subject which comprises administering to the subject a composition comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of a GAL3 receptor antagonist.
    这项发明涉及嘧啶和吲哚酮衍生物,它们是选择性GAL3受体拮抗剂。该发明提供了一种包含该发明化合物的治疗有效量和药用载体的药物组合物。该发明还提供了通过结合该发明化合物的治疗有效量和药用载体制备的药物组合物。该发明进一步提供了一种制备药物组合物的方法,包括结合该发明化合物的治疗有效量和药用载体。该发明还提供了一种治疗患有抑郁症和/或焦虑症的受试者的方法,包括向受试者施用足以治疗受试者抑郁症和/或焦虑症的该发明化合物的量。该发明还提供了一种治疗受试者抑郁症和/或焦虑症的方法,包括向受试者施用包含药用载体和治疗有效量GAL3受体拮抗剂的组合物。
  • GAL3 antagonists for the treatment of neuropathic pain
    申请人:——
    公开号:US20040092570A1
    公开(公告)日:2004-05-13
    This invention is directed to pyrimidine and indolone derivatives which are selective antagonists for the GAL3 receptor and are useful for the treatment of neuropathic pain and other abnormalities. This invention also provides a method of treating a subject suffering from an abnormality which comprises administering to the subject an amount of a compound of the invention effective to treat the subject's abnormality. This invention also provides a method of treating an abnormality in a subject which comprises administering to the subject a composition comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of a GAL3 receptor antagonist.
    这项发明涉及嘧啶和吲哚酮衍生物,它们是选择性的GAL3受体拮抗剂,可用于治疗神经病痛和其他异常。这项发明还提供了一种治疗患有异常的受试者的方法,包括向受试者投予本发明中的化合物的有效剂量以治疗受试者的异常。这项发明还提供了一种治疗受试者异常的方法,包括向受试者投予包含药用载体和治疗有效量的GAL3受体拮抗剂的组合物。
  • GAL3 receptor antagonists for the treatment of affective disorders
    申请人:——
    公开号:US20040110821A1
    公开(公告)日:2004-06-10
    This invention is directed to pyrimidine and indolone derivatives which are selective antagonists for the GAL3 receptor. This invention provides a method of treating a subject suffering from an affective disorder which comprises administering to the subject an amount of a compound of the invention effective to treat the subject's affective disorder. This invention also provides a method of treating an affective disorder in a subject which comprises administering to the subject a composition comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of a GAL3 receptor antagonist. This invention further provides a process for making a pharmaceutical composition comprising combining a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier.
    这项发明涉及选择性拮抗剂对GAL3受体的嘧啶和吲哚酮衍生物。该发明提供了一种治疗患有情感障碍的受试者的方法,包括向受试者施用一定量的该发明化合物,以有效治疗受试者的情感障碍。该发明还提供了一种治疗受试者情感障碍的方法,包括向受试者施用包含药用可接受载体和治疗有效量GAL3受体拮抗剂的组合物。该发明进一步提供了一种制备药物组合物的方法,包括结合该发明化合物的治疗有效量和药用可接受载体。
  • Pyrimidine derivatives as ALK-5 inhibitors
    申请人:Novartis AG
    公开号:EP1878733A1
    公开(公告)日:2008-01-16
    Compounds of formula I in free or salt or solvate form, where T1, T2, K, Ra and Rb have the meanings as indicated in the specification, are useful for treating diseases mediated by the ALK-5 and/or ALK-4 receptor. Pharmaceutical compositions that contain the compounds and processes for preparing the compounds are also described.
    公式I中的化合物以自由形式、盐或溶剂形式存在,其中T1、T2、K、Ra和Rb的含义如规范中所示,可用于治疗由ALK-5和/或ALK-4受体介导的疾病。还描述了含有这些化合物的药物组合物以及制备这些化合物的过程。
  • Use of GAL3 antagonist for treatment of depression and/or anxiety and compounds useful in such methods
    申请人:Blackburn P. Thomas
    公开号:US20070259942A1
    公开(公告)日:2007-11-08
    This invention is directed to pyrimidine and indolone derivatives which are selective antagonists for the GAL3 receptor. The invention provides a pharmaceutical composition comprising a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. This invention also provides a pharmaceutical composition made by combining a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. This invention further provides a process for making a pharmaceutical composition comprising combining a therapeutically effective amount of a compound of the invention and a pharmaceutically acceptable carrier. This invention also provides a method of treating a subject suffering from depression and/or anxiety which comprises administering to the subject an amount of a compound of the invention effective to treat the subject's depression and/or anxiety. This invention also provides a method of treating depression and/or anxiety in a subject which comprises administering to the subject a composition comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of a GAL3 receptor antagonist.
    这项发明涉及选择性拮抗GAL3受体的嘧啶和吲哚酮衍生物。该发明提供了一种药物组合物,包括本发明化合物的治疗有效量和药学上可接受的载体。该发明还提供了一种由本发明化合物的治疗有效量和药学上可接受的载体组合而成的药物组合物。该发明进一步提供了一种制备药物组合物的方法,包括将本发明化合物的治疗有效量和药学上可接受的载体组合。该发明还提供了一种治疗患有抑郁和/或焦虑的受试者的方法,包括向受试者投予本发明化合物的治疗有效量。该发明还提供了一种治疗受试者抑郁和/或焦虑的方法,包括向受试者投予一种药学上可接受的载体和治疗有效量的GAL3受体拮抗剂的组合物。
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