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tert-Butyl 4-(1-aminopropyl)piperidine-1-carboxylate | 1290046-62-6

中文名称
——
中文别名
——
英文名称
tert-Butyl 4-(1-aminopropyl)piperidine-1-carboxylate
英文别名
tert-butyl 4-(1-aminopropyl)piperidine-1-carboxylate
tert-Butyl 4-(1-aminopropyl)piperidine-1-carboxylate化学式
CAS
1290046-62-6
化学式
C13H26N2O2
mdl
——
分子量
242.36
InChiKey
PMAWBAFHGHQTEJ-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):
    1.9
  • 重原子数:
    17
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.92
  • 拓扑面积:
    55.6
  • 氢给体数:
    1
  • 氢受体数:
    3

文献信息

  • 1,3,4-OXADIAZOLONE COMPOUND AND MEDICINE
    申请人:Nippon Shinyaku Co., Ltd.
    公开号:EP3882239A1
    公开(公告)日:2021-09-22
    The purpose of the present invention is to provide a compound having PIM inhibitory activity. Examples of the present invention include 1,3,4-oxadiazolone compounds represented by the following formula [1], and pharmaceutically acceptable salts, and solvates thereof. The compounds of the present invention have PIM inhibitory activity. In addition, since the compounds of the present invention have PIM inhibitory activity, the compounds of the present invention are useful as therapeutic agents for systemic lupus erythematosus, lupus nephritis, etc.
    本发明的目的是提供一种具有 PIM 抑制活性的化合物。 本发明的实例包括下式[1]代表的 1,3,4-噁二唑酮化合物及其药学上可接受的盐和溶液。 本发明的化合物具有 PIM 抑制活性。此外,由于本发明的化合物具有 PIM 抑制活性,因此本发明的化合物可用作系统性红斑狼疮、狼疮肾炎等的治疗剂。
  • 1,3,4-OXADIAZOLONE COMPOUND AND PHARMACEUTICAL
    申请人:NIPPON SHINYAKU CO., LTD.
    公开号:US20220024921A1
    公开(公告)日:2022-01-27
    The purpose of the present invention is to provide a compound having PIM inhibitory activity. Examples of the present invention include 1,3,4-oxadiazolone compounds represented by the following formula [1], and pharmaceutically acceptable salts thereof, and solvates thereof. The compounds of the present invention have PIM inhibitory activity. In addition, since the compounds of the present invention have PIM inhibitory activity, the compounds of the present invention are useful as therapeutic agents for systemic lupus erythematosus, lupus nephritis, etc.
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