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5-Butan-2-yl-1,2-thiazol-3-one

中文名称
——
中文别名
——
英文名称
5-Butan-2-yl-1,2-thiazol-3-one
英文别名
5-butan-2-yl-1,2-thiazol-3-one
5-Butan-2-yl-1,2-thiazol-3-one化学式
CAS
——
化学式
C7H11NOS
mdl
——
分子量
157.24
InChiKey
DAJBESJFILGAKK-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):
    1.3
  • 重原子数:
    10
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    54.4
  • 氢给体数:
    1
  • 氢受体数:
    2

文献信息

  • [EN] HISTONE DEMETHYLASE INHIBITORS FOR TREATING CANCERS<br/>[FR] INHIBITEURS D'HISTONE DÉMÉTHYLASE POUR LE TRAITEMENT DE CANCERS
    申请人:UNIV TEXAS
    公开号:WO2020257733A1
    公开(公告)日:2020-12-24
    The present disclosure provides a new series of 8-hydroxyquinoline derivatives/analogs that are potent KDM4 inhibitors with high activity and selectivity against KDM4 enzymes. Also disclosed are the pharmaceutical compositions comprising such 8-hydroxyquinoline-based potent KDM4 inhibitors, or a pharmaceutically acceptable salt thereof, and method of use thereof, for treating cancer and neoplastic diseases and the like.
    本公开提供了一系列新的8-羟基喹啉生物/类似物,它们是有效的KDM4抑制剂,对KDM4酶具有高活性和选择性。还公开了包含这些基于8-羟基喹啉的有效KDM4抑制剂或其药用盐的药物组合物,以及使用方法,用于治疗癌症、肿瘤性疾病等。
  • Bromodomain inhibitors
    申请人:CELGENE QUANTICEL RESEARCH, INC.
    公开号:US10941160B2
    公开(公告)日:2021-03-09
    The present invention relates to substituted heterocyclic derivative compounds, compositions comprising said compounds, and the use of said compounds and compositions for epigenetic regulation by inhibition of bromodomain-mediated recognition of acetyl lysine regions of proteins, such as histones. Said compositions and methods are useful for the treatment of cancer and neoplastic disease.
    本发明涉及取代的杂环衍生物化合物、包含所述化合物的组合物,以及所述化合物和组合物通过抑制域介导的对蛋白质(如组蛋白)乙酰赖氨酸区的识别来进行表观遗传调控的用途。所述组合物和方法可用于治疗癌症和肿瘤性疾病。
  • BROMODOMAIN INHIBITORS
    申请人:CELGENE QUANTICEL RESEARCH, INC.
    公开号:US20200148703A1
    公开(公告)日:2020-05-14
    The present invention relates to substituted heterocyclic derivative compounds, compositions comprising said compounds, and the use of said compounds and compositions for epigenetic regulation by inhibition of bromodomain-mediated recognition of acetyl lysine regions of proteins, such as histones. Said compositions and methods are useful for the treatment of cancer and neoplastic disease.
  • US9771329B2
    申请人:——
    公开号:US9771329B2
    公开(公告)日:2017-09-26
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