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(E)-3-(3-(hydrazinecarbonyl)phenyl)-N-hydroxyacrylamide | 1223593-85-8

中文名称
——
中文别名
——
英文名称
(E)-3-(3-(hydrazinecarbonyl)phenyl)-N-hydroxyacrylamide
英文别名
(e)-3-(3-(Hydrazinecarbonyl)phenyl)-n-hydroxyacrylamide;(E)-3-[3-(hydrazinecarbonyl)phenyl]-N-hydroxyprop-2-enamide
(E)-3-(3-(hydrazinecarbonyl)phenyl)-N-hydroxyacrylamide化学式
CAS
1223593-85-8
化学式
C10H11N3O3
mdl
——
分子量
221.216
InChiKey
OJVOPPSLXWPGMX-SNAWJCMRSA-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):
    -0.4
  • 重原子数:
    16
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    104
  • 氢给体数:
    4
  • 氢受体数:
    4

反应信息

点击查看最新优质反应信息

文献信息

  • CLASS- AND ISOFORM-SPECIFIC HDAC INHIBITORS AND USES THEREOF
    申请人:Mazitschek Ralph
    公开号:US20120208889A1
    公开(公告)日:2012-08-16
    HDAC inhibitors of the general formula (I) and (II) and pharmaceutically acceptable salts thereof, as described herein, are useful as inhibitors of histone deacetylases or other deacetylases, and thus are useful for the treatment of various diseases and disorders associated with acetylase/deacetylase activity as described herein (e.g., cancer). In certain embodiments, the compounds of the invention selectively target either a class or isoform of the HDAC family. Another aspect of the invention provides an assay for determining the inhibitory effect of a test compound on an HDAC protein comprising: incubating the HDAC protein with a substrate of general formula (IIIc) in the presence of a test compound; and determining the activity of the HDAC protein.
    本文描述的具有一般式(I)和(II)及其药学上可接受的盐的HDAC抑制剂,可用作组蛋白去乙酰化酶或其他去乙酰化酶的抑制剂,并因此可用于治疗与去乙酰化酶/乙酰化酶活性相关的各种疾病和疾病,如本文所述(例如癌症)。在某些实施例中,本发明的化合物有选择性地靶向HDAC家族的一类或同工酶。本发明的另一个方面提供了一种测定试验化合物对HDAC蛋白质抑制作用的测定方法,包括:在试验化合物的存在下,将HDAC蛋白质与一般式(IIIc)的底物孵育,并确定HDAC蛋白质的活性。
  • Class-and isoform-specific HDAC inhibitors and uses thereof
    申请人:President and Fellows of Harvard College
    公开号:US10059657B2
    公开(公告)日:2018-08-28
    HDAC inhibitors of the general formula (I) and (II) and pharmaceutically acceptable salts thereof, as described herein, are useful as inhibitors of histone deacetylases or other deacetylases, and thus are useful for the treatment of various diseases and disorders associated with acetylase/deacetylase activity as described herein (e.g., cancer). In certain embodiments, the compounds of the invention selectively target either a class or isoform of the HDAC family. Another aspect of the invention provides an assay for determining the inhibitory effect of a test compound on an HDAC protein comprising: incubating the HDAC protein with a substrate of general formula (IIIc) in the presence of a test compound; and determining the activity of the HDAC protein.
    本文所述通式(I)和(II)的HDAC抑制剂及其药学上可接受的盐类可作为组蛋白去乙酰化酶或其他去乙酰化酶的抑制剂,因此可用于治疗与本文所述乙酰化酶/去乙酰化酶活性相关的各种疾病和失调(如癌症)。在某些实施方案中,本发明的化合物选择性地靶向 HDAC 家族的一类或同工酶。本发明的另一方面提供了一种测定受试化合物对HDAC蛋白的抑制作用的方法,包括:在受试化合物存在下,将HDAC蛋白与通式(IIIc)的底物孵育;测定HDAC蛋白的活性。
  • CLASS-AND ISOFORM-SPECIFIC HDAC INHIBITORS AND USES THEREOF
    申请人:President and Fellows of Harvard College
    公开号:US20170267630A1
    公开(公告)日:2017-09-21
    HDAC inhibitors of the general formula (I) and (II) and pharmaceutically acceptable salts thereof, as described herein, are useful as inhibitors of histone deacetylases or other deacetylases, and thus are useful for the treatment of various diseases and disorders associated with acetylase/deacetylase activity as described herein (e.g., cancer). In certain embodiments, the compounds of the invention selectively target either a class or isoform of the HDAC family. Another aspect of the invention provides an assay for determining the inhibitory effect of a test compound on an HDAC protein comprising: incubating the HDAC protein with a substrate of general formula (IIIc) in the presence of a test compound; and determining the activity of the HDAC protein.
  • US8716344B2
    申请人:——
    公开号:US8716344B2
    公开(公告)日:2014-05-06
  • US9540317B2
    申请人:——
    公开号:US9540317B2
    公开(公告)日:2017-01-10
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