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5-(Methoxymethyl)-2-methylpyrimidine

中文名称
——
中文别名
——
英文名称
5-(Methoxymethyl)-2-methylpyrimidine
英文别名
5-(methoxymethyl)-2-methylpyrimidine
5-(Methoxymethyl)-2-methylpyrimidine化学式
CAS
——
化学式
C7H10N2O
mdl
——
分子量
138.17
InChiKey
BKCJLEABVDUETF-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):
    0.3
  • 重原子数:
    10
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    35
  • 氢给体数:
    0
  • 氢受体数:
    3

文献信息

  • [EN] PROTEIN KINASE INHIBITORS<br/>[FR] INHIBITEURS DE PROTÉINES KINASES
    申请人:PHARMASCIENCE INC
    公开号:WO2015074138A1
    公开(公告)日:2015-05-28
    The present invention relates to a novel family of protein kinase inhibitors, more specifically the present invention is directed to inhibitors of the Tec or Src protein kinase families. The present invention also relates to the processes of preparation of these compounds, to pharmaceutical compositions comprising them, and to their use in the treatment of proliferative, inflammatory, autoimmune or infectious diseases, disorders, or conditions in which protein kinase activity is implicated.
    本发明涉及一种新型蛋白激酶抑制剂家族,更具体地说,本发明涉及Tec或Src蛋白激酶家族的抑制剂。本发明还涉及这些化合物的制备过程,包括含有它们的药物组合物,以及它们在治疗与蛋白激酶活性有关的增殖性、炎症性、自身免疫性或传染性疾病、紊乱或病况中的用途。
  • [EN] PROTEIN KINASE INHIBITORS<br/>[FR] INHIBITEURS DE PROTÉINE KINASES
    申请人:PHARMASCIENCE INC
    公开号:WO2013177668A1
    公开(公告)日:2013-12-05
    The present invention relates to a novel family of inhibitors of protein kinases. In particular, the present invention relates to inhibitors of the members of the Tec and Src protein kinase families.
    本发明涉及一种新型的蛋白激酶抑制剂家族。具体而言,本发明涉及Tec和Src蛋白激酶家族成员的抑制剂。
  • PROTEIN KINASE INHIBITORS
    申请人:Pharmascience, Inc.
    公开号:US20150191473A1
    公开(公告)日:2015-07-09
    The present invention relates to a novel family of inhibitors of protein kinases. In particular, the present invention relates to inhibitors of the members of the Tec and Src protein kinase families.
    本发明涉及一种新型的蛋白激酶抑制剂家族。具体而言,本发明涉及Tec和Src蛋白激酶家族成员的抑制剂。
  • 1-[4-(3-PHENOXY)-PHENYL]-1H-PYRAZOLO[4,3-D]PYRIMIDIN-7-YL-AMINE DERIVATIVES AS BRUTON'S TYROSINE KINASE (BTK) INHIBITORS FOR THE TREATMENT OF E.G. PROLIFERATIVE DISEASES
    申请人:Pharmascience Inc.
    公开号:EP2870158B1
    公开(公告)日:2017-05-31
  • Protein Kinase Inhibitors
    申请人:PHARMASCIENCE INC.
    公开号:US20160289236A1
    公开(公告)日:2016-10-06
    The present invention relates to a novel family of protein kinase inhibitors, more specifically the present invention is directed to inhibitors of the members of the Tec or Src protein kinase families. The present invention also relates to the processes of preparation of these compounds, their intermediates, to pharmaceutical compositions comprising them, and to their use in the treatment of proliferative, inflammatory, autoimmune, or infectious diseases, disorders, or conditions in which protein kinase activity is implicated.
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