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5-Methoxymethyl-2-methyl-pyridine | 34107-47-6

中文名称
——
中文别名
——
英文名称
5-Methoxymethyl-2-methyl-pyridine
英文别名
5-(Methoxymethyl)-2-methylpyridine
5-Methoxymethyl-2-methyl-pyridine化学式
CAS
34107-47-6
化学式
C8H11NO
mdl
——
分子量
137.181
InChiKey
YSFBAGSOKZIXIZ-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):
    0.9
  • 重原子数:
    10
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    22.1
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • [EN] PROTEIN KINASE INHIBITORS<br/>[FR] INHIBITEURS DE PROTÉINES KINASES
    申请人:PHARMASCIENCE INC
    公开号:WO2015077866A1
    公开(公告)日:2015-06-04
    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 processes for the preparation of these compounds, to the pharmaceutical composition comprising them, and to their use in the treatment of proliferative, inflammatory, infectious or autoimmune diseases, disorder or condition in which protein kinase activity is implicated. More particularly, the present invention relates to a compound of Formula I.
    本发明涉及一种新型蛋白激酶抑制剂家族,更具体地说,本发明是针对Tec或Src蛋白激酶家族成员的抑制剂。本发明还涉及制备这些化合物的方法,包括含有它们的药物组合物,以及它们在治疗蛋白激酶活性参与的增殖性、炎症性、感染性或自身免疫疾病、紊乱或病症中的用途。更具体地说,本发明涉及一种I式化合物。
  • [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。
  • [EN] TYK-2 INHIBITOR<br/>[FR] INHIBITEUR DE TYK -2
    申请人:BEIGENE LTD
    公开号:WO2021259208A1
    公开(公告)日:2021-12-30
    Disclosed herein is a compound of Formula (I) for inhibiting TYK2 and treating a disease associated with the undesirable tyk-2 activity (tyk-2 related diseases), a method of using the compounds disclosed herein for treating inflammatory or autoimmune disease, and a pharmaceutical composition comprising the same.
    本发明公开了一种式I化合物,用于抑制TYK2并治疗与不良tyk-2活性相关的疾病(tyk-2相关疾病),使用本发明所述化合物治疗炎症或自身免疫疾病的方法,以及包含所述化合物的药物组合物。
  • RING-FUSED 2-PYRIDONE DERIVATIVES AND HERBICIDES
    申请人:Takabe Fumiaki
    公开号:US20110287937A1
    公开(公告)日:2011-11-24
    Provided are 2-pyridone derivatives which have excellent herbicidal activity and exhibit high safety to useful crops and so on; salts thereof; and herbicides containing same. In more detail, 2-pyridone derivatives represented by general formula [I] or agrochemically acceptable salts thereof, and herbicides containing these compounds are provided. In general formula [I], X 1 is an oxygen atom or a sulfur atom; X 2 , X 3 , and X 4 are to each CH or N(O) m ; m is an integer of 0 or 1; R 1 is a hydrogen atom, a C 1-12 alkyl group, or the like; R 2 is a halogen atom, a cyano group, or the like; n is an integer of 0 to 4; R 3 is a hydroxyl group, a halogen atom, or the like; A 1 is C(R 11 R 12 ); A 2 is C(R 13 R 14 ) or C═O; A 3 is C(R 15 R 16 ); and R 11 , R 12 , R 13 , R 14 , R 15 , and R 16 are each independently a hydrogen atom or a C 1-6 alkyl group.
    提供了具有优异除草活性并对有用作物等表现出高安全性的2-吡啶酮衍生物;其盐;以及含有这些化合物的除草剂。更详细地说,提供了通式[I]所表示的2-吡啶酮衍生物或其农药可接受的盐,以及含有这些化合物的除草剂。在通式[I]中,X1是氧原子或硫原子;X2、X3和X4分别为CH或N(O)m;m是0或1的整数;R1是氢原子,C1-12烷基或类似物;R2是卤素原子,氰基或类似物;n是0到4的整数;R3是羟基,卤素原子或类似物;A1是C(R11R12);A2是C(R13R14)或C═O;A3是C(R15R16);R11、R12、R13、R14、R15和R16分别独立地是氢原子或C1-6烷基基团。
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