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N-[2-[(4R)-2-amino-5-methoxy-4-methyl-5,6-dihydro-1,3-thiazin-4-yl]pyridin-4-yl]-5-(fluoromethyl)pyrazine-2-carboxamide

中文名称
——
中文别名
——
英文名称
N-[2-[(4R)-2-amino-5-methoxy-4-methyl-5,6-dihydro-1,3-thiazin-4-yl]pyridin-4-yl]-5-(fluoromethyl)pyrazine-2-carboxamide
英文别名
——
N-[2-[(4R)-2-amino-5-methoxy-4-methyl-5,6-dihydro-1,3-thiazin-4-yl]pyridin-4-yl]-5-(fluoromethyl)pyrazine-2-carboxamide化学式
CAS
——
化学式
C17H19FN6O2S
mdl
——
分子量
390.4
InChiKey
DWWRGGBNUYQAJI-FBMWCMRBSA-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:
    27
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    141
  • 氢给体数:
    2
  • 氢受体数:
    8

文献信息

  • PYRIDINE DERIVATIVES AND A PHARMACEUTICAL COMPOSITION FOR INHIBITING BACE1 CONTAINING THEM
    申请人:Tada Yukio
    公开号:US20140235626A1
    公开(公告)日:2014-08-21
    The present invention provides a compound of formula (I): wherein ring B is substituted or unsubstituted carbocycle or heterocycle, R 1 is substituted or unsubstituted alkyl or the like, R 2a and R 2b are each independently hydrogen, substituted or unsubstituted alkyl or the like, R 3 , R 4a and R 4b are each independently hydrogen, halogen, substituted or unsubstituted alkyl or the like, a dashed line represents a presence or absence of a bond, R 5 is hydrogen, substituted or unsubstituted alkyl or the like, R 6 is halogen, hydroxy, substituted or unsubstituted alkyl or the like, p is an integer of 0 to 3, or a pharmaceutically acceptable salt thereof which has an effect of inhibiting amyloid β production, especially an effect of inhibiting BACE1, and which is useful as a therapeutic or prophylactic agent for diseases induced by production, secretion and/or deposition of amyloid β proteins.
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