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3,7-diazabicyclo[3.3.1]nonane-3-carboxylic acid | 227941-21-1

中文名称
——
中文别名
——
英文名称
3,7-diazabicyclo[3.3.1]nonane-3-carboxylic acid
英文别名
3.7-Diazabicyclo[3.3.1]nonane-3-carboxylic Acid
3,7-diazabicyclo[3.3.1]nonane-3-carboxylic acid化学式
CAS
227941-21-1
化学式
C8H14N2O2
mdl
——
分子量
170.211
InChiKey
BJSBDAPLFVODIY-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:
    12
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.88
  • 拓扑面积:
    52.6
  • 氢给体数:
    2
  • 氢受体数:
    3

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

反应信息

点击查看最新优质反应信息

文献信息

  • Bispidine compounds useful in the treatment of cardiac arrythmias
    申请人:AstraZeneca AB
    公开号:US20040229900A1
    公开(公告)日:2004-11-18
    There is provided compounds of formula I, 1 wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 41 , R 42 , R 43 R 44 , R 45 , R 46 , A and B have meanings given in the description, which are useful in the prophylaxis and in the treatment of arrhythmias, in particular atrial and ventricular arrhythmias.
    提供了一种化合物I的公式,其中R1、R2、R3、R4、R5、R6、R7、R41、R42、R43、R44、R45、R46、A和B在描述中给出了含义,这些化合物在预防和治疗心律不齐方面特别是房性和室性心律不齐方面是有用的。
  • TRIAZINE COMPOUNDS AS PI3 KINASE AND MTOR INHIBITORS
    申请人:WYETH LLC
    公开号:US20170119778A1
    公开(公告)日:2017-05-04
    Compounds of formula I wherein: R 1 is and R 2 , R 4 , and R 6-9 are defined herein, and pharmaceutically acceptable salts and esters thereof. These compounds inhibit PI3 kinase and mTOR, and may be used to treat diseases mediated by PI3 kinase and mTOR, such as a variety of cancers. Methods for making and using the compounds of this invention are disclosed. Various compositions containing the compounds of this invention are also disclosed.
    式I化合物,其中:R1为,R2、R4和R6-9如本文所定义,以及其药学上可接受的盐和酯。这些化合物抑制PI3激酶和mTOR,并可用于治疗由PI3激酶和mTOR介导的疾病,例如多种癌症。本发明还公开了制备和使用这些化合物的方法。此外,还公开了含有本发明化合物的各种组合物。
  • [EN] PYRROLIDIN-2-ONE DERIVATIVES AS INHIBITORS OF FACTOR XA<br/>[FR] DERIVES PYRROLIDINE-2-UN COMME INHIBITEURS DE FACTEUR XA
    申请人:GLAXO GROUP LTD
    公开号:WO2002100886A1
    公开(公告)日:2002-12-19
    The invention relates to compounds of formula (Ic) processes for their preparation, pharmaceutical compositions containing them and to their use in medicine, particularly use in the amelioration of a clinical condition for which a Factor Xa inhibitor is indicated.
    本发明涉及式(Ic)化合物、其制备过程、含有它们的药物组合物以及它们在医学上的应用,特别是在改善适用于因子Xa抑制剂的临床状况方面的应用。
  • Chemical compounds
    申请人:Chan Chuen
    公开号:US20060160886A1
    公开(公告)日:2006-07-20
    The invention relates to compounds of formula (Ic) processes for their preparation, pharmaceutical compositions containing them and to their use in medicine, particularly use in the amelioration of a clinical condition for which a Factor Xa inhibitor is indicated.
    本发明涉及式(Ic)化合物,其制备方法,含有它们的药物组合物以及它们在医学上的应用,特别是在改善适应于Xa因子抑制剂的临床状况方面的应用。
  • Pyrrolidin-2-one derivatives as inhibitors of factor xa
    申请人:——
    公开号:US20040152697A1
    公开(公告)日:2004-08-05
    The invention relates to compounds of formula (Ic) processes for their preparation, pharmaceutical compositions containing them and to their use in medicine, particularly use in the amelioration of a clinical condition for which a Factor Xa inhibitor is indicated. 1
    本发明涉及公式(Ic)化合物,它们的制备过程,含有它们的药物组合物,以及它们在医学上的应用,特别是在改善适合使用因子Xa抑制剂的临床症状方面的应用。
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