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Tert-butyl 3,9-diazabicyclo[3.3.2]decane-9-carboxylate | 1050890-68-0

中文名称
——
中文别名
——
英文名称
Tert-butyl 3,9-diazabicyclo[3.3.2]decane-9-carboxylate
英文别名
——
Tert-butyl 3,9-diazabicyclo[3.3.2]decane-9-carboxylate化学式
CAS
1050890-68-0
化学式
C13H24N2O2
mdl
MFCD10686963
分子量
240.34
InChiKey
SEBKQWOUTPGSCS-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:
    331.7±15.0 °C(Predicted)
  • 密度:
    1.032±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.6
  • 重原子数:
    17
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.923
  • 拓扑面积:
    41.6
  • 氢给体数:
    1
  • 氢受体数:
    3

文献信息

  • FUSED HETEROCYCLIC COMPOUNDS AS CAM KINASE INHIBITORS
    申请人:Gilead Sciences, Inc.
    公开号:US20180148457A1
    公开(公告)日:2018-05-31
    The present disclosure relates to compounds that are CaM Kinase inhibitors and to their use in the treatment of various disease states, including atrial fibrillation and myocardial infarction. In particular embodiments, the general structure of the compounds is given by Formula I: wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 9 and R 10 are as described herein, to methods for the preparation and use of the compounds and to pharmaceutical compositions containing the same.
    本公开涉及的化合物是CaM激酶抑制剂,用于治疗各种疾病状态,包括心房颤动和心肌梗死。在特定实施例中,化合物的一般结构由公式I给出:其中R1、R2、R3、R4、R5、R6、R9和R10如本文所述,涉及化合物的制备和使用方法以及含有相同化合物的药物组合物。
  • Fused heterocyclic compounds as CaM kinase inhibitors
    申请人:Gilead Sciences, Inc.
    公开号:US10100058B2
    公开(公告)日:2018-10-16
    The present disclosure relates to compounds that are CaM Kinase inhibitors and to their use in the treatment of various disease states, including atrial fibrillation and myocardial infarction. In particular embodiments, the general structure of the compounds is given by Formula I: wherein R1, R2, R3, R4, R5, R6, R9 and R10 are as described herein, to methods for the preparation and use of the compounds and to pharmaceutical compositions containing the same.
    本公开涉及作为 CaM 激酶抑制剂的化合物及其在治疗包括心房颤动和心肌梗塞在内的各种疾病状态中的用途。在特定的实施方案中,化合物的一般结构由式 I 给出: 其中 R1、R2、R3、R4、R5、R6、R9 和 R10 如本文所述。
  • PYRAZOLOPYRIMIDINE DERIVATIVES AS CAM KINASE INHIBITORS
    申请人:Gilead Sciences, Inc.
    公开号:EP3548495A1
    公开(公告)日:2019-10-09
  • [EN] PYRAZOLOPYRIMIDINE DERIVATIVES AS CAM KINASE INHIBITORS<br/>[FR] DÉRIVÉS DE PYRAZOLOPYRIMIDINE EN TANT QU'INHIBITEURS DE KINASE CAM
    申请人:GILEAD SCIENCES INC
    公开号:WO2018102384A1
    公开(公告)日:2018-06-07
    The present disclosure relates to compounds that are CaM Kinase inhibitors and to their use in the treatment of various disease states, including atrial fibrillation and myocardial infarction. In particular embodiments, the general structure of the compounds is given by Formula I: (I) wherein R1, R2, R3, R4, R5, R6, R9 and R10 are as described herein, to methods for the preparation and use of the compounds and to pharmaceutical compositions containing the same.
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