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5-Chloro-2,4-di-t-butylpyrimidin | 69050-88-0

中文名称
——
中文别名
——
英文名称
5-Chloro-2,4-di-t-butylpyrimidin
英文别名
2,4-di-tert-butyl-5-chloro-pyrimidine;2,4-Ditert-butyl-5-chloropyrimidine
5-Chloro-2,4-di-t-butylpyrimidin化学式
CAS
69050-88-0
化学式
C12H19ClN2
mdl
——
分子量
226.749
InChiKey
FEVLHZKUXPNSAP-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):
    4.2
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    25.8
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • Rho-associated protein kinase inhibitor, pharmaceutical composition comprising the same, as well as preparation method and use thereof
    申请人:Beijing Tide Pharmaceutical Co., Ltd.
    公开号:US10329282B2
    公开(公告)日:2019-06-25
    The present invention relates to a Rho-associated protein kinase inhibitor of Formula (I), a pharmaceutical composition comprising the same, a preparation method thereof, and use thereof for the prevention or treatment of a disease mediated by the Rho-associated protein kinase (ROCK).
    本发明涉及一种式(I)的Rho相关蛋白激酶抑制剂、一种包含其的药物组合物、其制备方法以及其用于预防或治疗由Rho相关蛋白激酶(ROCK)介导的疾病的用途。
  • RHO-ASSOCIATED PROTEIN KINASE INHIBITOR, PHARMACEUTICAL COMPOSITION COMPRISING SAME, AND PREPARATION METHOD AND USE THEREOF
    申请人:BEIJING TIDE PHARMACEUTICAL CO., LTD.
    公开号:US20190276440A1
    公开(公告)日:2019-09-12
    The present invention relates to a Rho-associated protein kinase inhibitor of formula (I), a pharmaceutical composition comprising the same, a preparation method thereof, and a use of the same in preventing or treating a disease mediated by Rho-associated protein kinase (ROCK).
  • METHOD FOR TREATING FATTY LIVER DISEASE AND/OR STEATOHEPATITIS
    申请人:BEIJING TIDE PHARMACEUTICAL CO., LTD.
    公开号:US20220378743A1
    公开(公告)日:2022-12-01
    The present invention falls within the field of biological medicine, and specifically relates to a method for preventing, alleviating and/or treating fatty liver disease and/or steatohepatitis. The method comprises administering, to an individual in need thereof, an effective amount of a compound of formula (I) or a pharmaceutically acceptable salt, an ester, a stereoisomer, a polymorph, a solvate, an N-oxide, an isotopically labeled compound, a metabolite or a prodrug thereof.
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