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1-Carbamoylpiperidine-3-carboxylic acid | 871478-82-9

中文名称
——
中文别名
——
英文名称
1-Carbamoylpiperidine-3-carboxylic acid
英文别名
——
1-Carbamoylpiperidine-3-carboxylic acid化学式
CAS
871478-82-9
化学式
C7H12N2O3
mdl
MFCD06799728
分子量
172.18
InChiKey
CRCXZDRNTOBHLY-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:
    372.8±52.0 °C(Predicted)
  • 密度:
    1.343±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.8
  • 重原子数:
    12
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.714
  • 拓扑面积:
    83.6
  • 氢给体数:
    2
  • 氢受体数:
    3

文献信息

  • ARYLMETHYLENE UREA DERIVATIVE AND USE THEREOF
    申请人:Ohno Michihiro
    公开号:US20100016319A1
    公开(公告)日:2010-01-21
    This invention relates to a pharmaceutical comprising as an effective ingredient an arylmethylene urea exemplified by the following formula: or a pharmaceutically acceptable salt thereof. The arylmethylene urea and the pharmaceutically acceptable salts thereof are useful for therapy or prophylaxis of inflammatory bowel disease and overactive bladder.
    本发明涉及一种药物,其有效成分为以下式子所示的芳基亚甲基脲或其药学上可接受的盐: 该芳基亚甲基脲及其药学上可接受的盐可用于治疗或预防炎症性肠病和过度活跃的膀胱。
  • TRICYCLIC PYRAZOLE DERIVATIVES AS CANNABINOID RECEPTOR MODULATORS
    申请人:CADILA HEALTHCARE LIMITED
    公开号:EP1781668A2
    公开(公告)日:2007-05-09
  • SUBSTITUTED 5-HETEROARYL-1-PHENYL-PYRAZOLE CANNABINOID MODULATORS
    申请人:Janssen Pharmaceutica NV
    公开号:EP1966194A2
    公开(公告)日:2008-09-10
  • Pharmaceutical compositions comprising CBx cannabinoid receptor modulators and potassium channel modulators
    申请人:Antel Jochen
    公开号:US20070254862A1
    公开(公告)日:2007-11-01
    Described herein are pharmaceutical compositions comprising therapeutically effective quantities of (i) a K ATP channel modulator; and (ii) a CB x modulator. Also described herein are methods of making and using these compositions.
  • TDO2 and IDO1 Inhibitors
    申请人:Genentech, Inc.
    公开号:US20200123163A1
    公开(公告)日:2020-04-23
    Presently provided are inhibitors of cellularly expressed TD02 and IDO1, and pharmaceutical compositions thereof, useful for modulating an activity of tryptophan 2,3 dioxygenase and indoleamine 2,3-dioxygenase 1; treating immunosuppression; treating a medical conditions that benefit from the inhibition of tryptophan degradation; enhancing the effectiveness of an anti-cancer treatment comprising administering an anti-cancer agent; and treating tumor-specific immunosuppression associated with cancer.
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