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5-(imidazo[1,2-b]pyridazine-3-yl)-4-(morpholine-4-yl)-7H-pyrrolo[2,3-d]pyrimidine | 1527475-55-3

中文名称
——
中文别名
——
英文名称
5-(imidazo[1,2-b]pyridazine-3-yl)-4-(morpholine-4-yl)-7H-pyrrolo[2,3-d]pyrimidine
英文别名
5-(imidazolo[1,2-b]pyridazin-3-yl)-4-(morpholin-4-yl)-7H-pyrrolo[2,3-d]pyrimidine;5-(imidazo[1,2-b]pyridazin-3-yl)-4-(morpholin-4-yl)-7H-pyrrolo[2,3-d]pyrimidine;5-(Imidazo[1,2-b]pyridazin-3-yl)-4-(morpholin-4-yl)-7H-pyrrolo[2,3-d]pyrimidin;4-(5-imidazo[1,2-b]pyridazin-3-yl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)morpholine
5-(imidazo[1,2-b]pyridazine-3-yl)-4-(morpholine-4-yl)-7H-pyrrolo[2,3-d]pyrimidine化学式
CAS
1527475-55-3
化学式
C16H15N7O
mdl
——
分子量
321.341
InChiKey
BISAHRSNHGARQL-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):
    0.8
  • 重原子数:
    24
  • 可旋转键数:
    2
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    84.2
  • 氢给体数:
    1
  • 氢受体数:
    6

文献信息

  • Novel 4-(Substituted Amino)-7H-Pyrrolo[2,3-d] Pyrimidines As LRRK2 Inhibitors
    申请人:Pfizer Inc.
    公开号:US20140005183A1
    公开(公告)日:2014-01-02
    The present invention provides novel 4,5-disubstituted-7H-pyrrolo[2,3-d]pyrimidine derivatives of Formula I, and the pharmaceutically acceptable salts thereof wherein R 1 , R 2 , R 3 , R 4 and R 5 are as defined in the specification. The invention is also directed to pharmaceutical compositions comprising the compounds of formula I and to use of the compounds in the treatment of diseases associated with LRRK2, such as neurodegenerative diseases including Parkinson's disease or Alzheimer's disease, cancer, Crohn's disease or leprosy.
    本发明提供了一种新型的4,5-二取代-7H-吡咯并[2,3-d]嘧啶生物I式,以及其药学上可接受的盐,其中R1、R2、R3、R4和R5如规范所定义。本发明还涉及含有I式化合物的制药组合物,以及用于治疗与LRRK2相关的疾病,如神经退行性疾病,包括帕森病或阿尔茨海默病,癌症,克隆病或麻风病的化合物的用途。
  • Novel 4-(Substituted Amino)-7H-Pyrrolo[2,3-d]Pyrimidines As LRRK2 Inhibitors
    申请人:Pfizer Inc.
    公开号:US20150366874A1
    公开(公告)日:2015-12-24
    The present invention provides novel 4,5-disubstituted-7H-pyrrolo[2,3-d]pyrimidine derivatives of Formula I, and the pharmaceutically acceptable salts thereof wherein R 1 , R 2 , R 3 , R 4 and R 5 are as defined in the specification. The invention is also directed to pharmaceutical compositions comprising the compounds of formula I and to use of the compounds in the treatment of diseases associated with LRRK2, such as neurodegenerative diseases including Parkinson's disease or Alzheimer's disease, cancer, Crohn's disease or leprosy.
    本发明提供了新型的4,5-二取代-7H-吡咯并[2,3-d]嘧啶生物I式及其药物可接受的盐,其中R1、R2、R3、R4和R5如规范中所定义。本发明还涉及包括I式化合物的制药组合物以及在治疗与LRRK2相关的疾病,如神经退行性疾病(包括帕森病或阿尔茨海默病)、癌症、克罗恩病或麻风病中使用该化合物的用途。
  • NOVEL 4-(SUBSTITUTED-AMINO)-7H-PYRROLO[2,3-D]PYRIMIDINES AS LRRK2 INHIBITORS
    申请人:Pfizer Inc.
    公开号:EP2867236B1
    公开(公告)日:2017-06-14
  • PHOSPHO-RAB ANTIBODIES, ASSAYS AND METHODS OF USE THEREOF
    申请人:Denali Therapeutics Inc.
    公开号:US20210147573A1
    公开(公告)日:2021-05-20
    In one aspect, antibodies that specifically bind to a phosphorylated Rab protein are provided. In some embodiments, the antibody is a monoclonal antibody that specifically binds to a phosphorylated human Rab10 protein and recognizes an epitope within or comprising the sequence AGQERFH(pT)ITTSYYR. In some embodiments, the antibody is a monoclonal antibody that specifically binds to a phosphorylated human Rab8a protein and recognizes an epitope within or comprising the sequence QERFR(pT)ITTAY. Methods and materials for detecting LRRK2 and Rab protein are also provided.
  • US9156845B2
    申请人:——
    公开号:US9156845B2
    公开(公告)日:2015-10-13
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