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7-[4-[[6-(cyclohexylamino)-7H-purin-2-yl]amino]phenoxy]-N-hydroxyheptanamide

中文名称
——
中文别名
——
英文名称
7-[4-[[6-(cyclohexylamino)-7H-purin-2-yl]amino]phenoxy]-N-hydroxyheptanamide
英文别名
——
7-[4-[[6-(cyclohexylamino)-7H-purin-2-yl]amino]phenoxy]-N-hydroxyheptanamide化学式
CAS
——
化学式
C24H33N7O3
mdl
——
分子量
467.6
InChiKey
LPHZEHLIRMVJSN-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):
    4.4
  • 重原子数:
    34
  • 可旋转键数:
    12
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    137
  • 氢给体数:
    5
  • 氢受体数:
    8

文献信息

  • [EN] HETEROCYCLIC HYDROXAMIC ACIDS AS PROTEIN DEACETYLASE INHIBITORS AND DUAL PROTEIN DEACETYLASE-PROTEIN KINASE INHIBITORS AND METHODS OF USE THEREOF<br/>[FR] ACIDES HYDROXAMIQUES HÉTÉROCYCLIQUES COMME INHIBITEURS DE PROTÉINE DÉSACÉTYLASE ET INHIBITEURS DOUBLES DE PROTÉINE KINASE-PROTÉINE DÉSACÉTYLASE, ET LEURS PROCÉDÉS D'UTILISATION
    申请人:UNIV COLORADO REGENTS
    公开号:WO2015175813A1
    公开(公告)日:2015-11-19
    The present invention relates to novel hydroxamic acids which are specific histone deacetylase (HDAC) inhibitors and/or TTK/Mpsl kinase inhibitors, including pharmaceutically acceptable salts thereof, which are useful for modulating HDAC and/or TTK/Mpsl kinase activity, pharmaceutical compositions comprising these compounds, and processes for their preparation.
    本发明涉及一种新型的羟羧胺酸,它们是特异的组蛋白去乙酰化酶(HDAC)抑制剂和/或TTK/Mps1激酶抑制剂,包括其药用盐,用于调节HDAC和/或TTK/Mps1激酶活性,包括这些化合物的制药组合物,以及其制备方法。
  • HETEROCYCLIC HYDROXAMIC ACIDS AS PROTEIN DEACETYLASE INHIBITORS AND DUAL PROTEIN DEACETYLASE-PROTEIN KINASE INHIBITORS AND METHODS OF USE THEREOF
    申请人:The Regents of the University of Colorado, a body corporate
    公开号:EP3142652A1
    公开(公告)日:2017-03-22
  • Heterocyclic Hydroxamic Acids as Protein Deacetylase Inhibitors and Dual Protein Deacetylase-Protein Kinase Inhibitors and Methods of Use Thereof
    申请人:The Regents of the University of Colorado, A Body Corporate
    公开号:US20170081343A1
    公开(公告)日:2017-03-23
    The present invention relates to novel hydroxamic acids which are specific histone deacetylase (HDAC) inhibitors and/or TTK/Mps1 kinase inhibitors, including pharmaceutically acceptable salts thereof, which are useful for modulating HDAC and/or TTK/Mps1 kinase activity, pharmaceutical compositions comprising these compounds, and processes for their preparation.
  • US9840520B2
    申请人:——
    公开号:US9840520B2
    公开(公告)日:2017-12-12
  • USRE47690E1
    申请人:——
    公开号:USRE47690E1
    公开(公告)日:2019-11-05
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