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4-Methyl-N-(propan-2-yl)piperazin-1-amine | 670749-70-9

中文名称
——
中文别名
——
英文名称
4-Methyl-N-(propan-2-yl)piperazin-1-amine
英文别名
4-methyl-N-propan-2-ylpiperazin-1-amine
4-Methyl-N-(propan-2-yl)piperazin-1-amine化学式
CAS
670749-70-9
化学式
C8H19N3
mdl
——
分子量
157.26
InChiKey
KVRHHWSFMKTFGB-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):
    0.6
  • 重原子数:
    11
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    18.5
  • 氢给体数:
    1
  • 氢受体数:
    3

文献信息

  • PYRIDO [5, 4-D] PYRIMIDINES AS CELL PROLIFERATION INHIBITORS
    申请人:Mantoulidis Andreas
    公开号:US20120094975A1
    公开(公告)日:2012-04-19
    The present invention encompasses compounds of general formula (1) wherein the groups R 1 to R 4 , X 1 , X 1 , X 3 , L 1 and L 2 are defined as in claim 1 , which are suitable for the treatment of diseases characterised by excessive or anomalous cell pro-liferation, and the use thereof in such a treatment.
    本发明涵盖了一般式(1)中的化合物,其中基团R1至R4、X1、X1、X3、L1和L2如权利要求1中定义的那样,适用于治疗以细胞过度或异常增殖为特征的疾病,并且在此类治疗中的使用。
  • SUBSTITUTED DIAZEPINE SULFONAMIDES AS BOMBESIN RECEPTOR SUBTYPE-1 MODULATORS
    申请人:Baker Robert K.
    公开号:US20100317645A1
    公开(公告)日:2010-12-16
    Certain novel substituted diazepine sulfonamides are ligands of the human bombesin receptor and, in particular, are selective ligands of the human bombesin receptor subtype-3 (BRS-3). They are therefore useful for the treatment, control, or prevention of diseases and disorders responsive to the modulation of BRS-3, such as obesity, and diabetes.
    某些新型取代二氮杂环磺酰胺是人体炸弹素受体的配体,特别是人体炸弹素受体亚型-3(BRS-3)的选择性配体。因此,它们可用于治疗、控制或预防对BRS-3调节敏感的疾病和障碍,如肥胖和糖尿病。
  • Polyene macrolide derivative
    申请人:Shionogi & Co., Ltd.
    公开号:US10246478B2
    公开(公告)日:2019-04-02
    The present invention is the following Amphotericin B derivative: wherein each symbol is defined in description. The compound of the present invention has 16th position (X) is urea structure, cyclic structure, hydroxyalkyl or substituted monoalkylcarbamoyl. The compound of the present invention has antifungal activity.
    本发明是以下两性霉素 B生物: 其中各符号在说明中定义。本发明化合物的第 16 位(X)是结构、环状结构、羟烷基或取代的单烷基基甲酰基。本发明化合物具有抗真菌活性。
  • PYRIMIDO[5,4-D]PYRIMIDINES AS CELL PROLIFERATION INHIBITORS
    申请人:Boehringer Ingelheim International GmbH
    公开号:EP2350083B1
    公开(公告)日:2017-05-17
  • POLYENE MACROLIDE DERIVATIVE
    申请人:Shionogi & Co., Ltd.
    公开号:US20170190729A1
    公开(公告)日:2017-07-06
    The present invention is the following Amphotericin B derivative: wherein each symbol is defined in description. The compound of the present invention has 16th position (X) is urea structure, cyclic structure, hydroxyalkyl or substituted monoalkylcarbamoyl. The compound of the present invention has antifungal activity.
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