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(R)-2-cyclopropyl-piperazine | 1240589-80-3

中文名称
——
中文别名
——
英文名称
(R)-2-cyclopropyl-piperazine
英文别名
(2R)-2-cyclopropylpiperazine
(R)-2-cyclopropyl-piperazine化学式
CAS
1240589-80-3
化学式
C7H14N2
mdl
——
分子量
126.202
InChiKey
SXGUFQFMTFDRMC-ZETCQYMHSA-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:
    214.9±8.0 °C(Predicted)
  • 密度:
    1.006±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0
  • 重原子数:
    9
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    24.1
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

点击查看最新优质反应信息

文献信息

  • [EN] THERAPEUTICALLY ACTIVE COMPOSITIONS AND THEIR METHODS OF USE<br/>[FR] COMPOSITIONS THÉRAPEUTIQUEMENT ACTIVES ET LEURS PROCÉDÉS D'UTILISATION
    申请人:AGIOS PHARMACEUTICALS INC
    公开号:WO2012171337A1
    公开(公告)日:2012-12-20
    Provided are compounds with the following structure, formula (I) pharmaceutically acceptable salts thereof, use of those compounds for treating cancer and pharmaceutical compositions comprising those compounds.
    提供具有以下结构、式(I)的化合物,其药学上可接受的盐,以及利用这些化合物治疗癌症的用途和包含这些化合物的药物组合物。
  • [EN] COMPOUNDS, THEIR PHARMACEUTICAL COMPOSITIONS AND THEIR USES AS IDH1 MUTANTS INHIBITORS FOR TREATING CANCERS<br/>[FR] COMPOSÉS, COMPOSITIONS PHARMACEUTIQUES DE CEUX-CI ET UTILISATION DE CES COMPOSÉS COMME INHIBITEURS MUTANTS D'IDH1 DANS LE TRAITEMENT DE CANCERS
    申请人:AGIOS PHARMACEUTICALS INC
    公开号:WO2012171506A1
    公开(公告)日:2012-12-20
    Provided are compounds of formula (I), wherein X, Y, Z, W, V, R2, R3 and m are defined as in the description. Their pharmaceutical compositions and their uses as IDH1 mutants inhibitors for treating cancers are also provided.
    提供了公式(I)的化合物,其中X、Y、Z、W、V、R2、R3和m的定义如描述中所述。还提供了它们的药物组合物以及它们作为IDH1突变体抑制剂用于治疗癌症的用途。
  • COMPOUNDS THAT INTERACT WITH GLUCOKINASE REGULATORY PROTEIN FOR THE TREATMENT OF DIABETES
    申请人:Ashton Kate
    公开号:US20120225854A1
    公开(公告)日:2012-09-06
    The present invention relates to compounds of Formula I, or pharmaceutically acceptable salts thereof, that interact with glucokinase regulatory protein. In addition, the present invention relates to methods of treating type 2 diabetes, and other diseases and/or conditions where glucokinase regulatory protein is involved using the compounds, or pharmaceutically acceptable salts thereof, and pharmaceutical compositions that contain the compounds, or pharmaceutically acceptable salts thereof.
    本发明涉及公式I的化合物或其药学上可接受的盐,其与葡萄糖激酶调节蛋白相互作用。此外,本发明涉及使用这些化合物或其药学上可接受的盐以及含有这些化合物或其药学上可接受的盐的药物组合物治疗2型糖尿病以及其他与葡萄糖激酶调节蛋白有关的疾病和/或病况的方法。
  • Compounds that interact with glucokinase regulatory protein for the treatment of diabetes
    申请人:Ashton Kate
    公开号:US08431563B2
    公开(公告)日:2013-04-30
    The present invention relates to compounds of Formula I, or pharmaceutically acceptable salts thereof, that interact with glucokinase regulatory protein. In addition, the present invention relates to methods of treating type 2 diabetes, and other diseases and/or conditions where glucokinase regulatory protein is involved using the compounds, or pharmaceutically acceptable salts thereof, and pharmaceutical compositions that contain the compounds, or pharmaceutically acceptable salts thereof.
    本发明涉及式I的化合物或其药学上可接受的盐,该化合物与葡萄糖激酶调节蛋白相互作用。此外,本发明涉及使用该化合物或其药学上可接受的盐以及含有该化合物或其药学上可接受的盐的制药组合物治疗2型糖尿病和其他涉及葡萄糖激酶调节蛋白的疾病和/或病状的方法。
  • TRI-CYCLIC PYRAZOLOPYRIDINE KINASE INHIBITORS
    申请人:Vertex Pharmaceuticals Incorporated
    公开号:US20130252939A1
    公开(公告)日:2013-09-26
    The present invention relates to compounds useful as inhibitors of protein kinase. The invention also provides pharmaceutically acceptable compositions comprising said compounds and methods of using the compositions in the treatment of various disease, conditions, or disorders. The invention also provides processes for preparing compounds of the inventions.
    本发明涉及作为蛋白激酶抑制剂有用的化合物。本发明还提供了包含该化合物的药学上可接受的组合物以及使用该组合物治疗各种疾病、病况或疾患的方法。本发明还提供了制备本发明中化合物的方法。
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