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3-(1,3-Thiazol-4-yl)prop-2-enoic acid | 133047-17-3

中文名称
——
中文别名
——
英文名称
3-(1,3-Thiazol-4-yl)prop-2-enoic acid
英文别名
(E)-3-(1,3-thiazol-4-yl)prop-2-enoic acid
3-(1,3-Thiazol-4-yl)prop-2-enoic acid化学式
CAS
133047-17-3
化学式
C6H5NO2S
mdl
MFCD11180956
分子量
155.18
InChiKey
IXZOCDJVRALXCG-OWOJBTEDSA-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):
    0.9
  • 重原子数:
    10
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    78.4
  • 氢给体数:
    1
  • 氢受体数:
    4

文献信息

  • [EN] PYRIMIDINE PDE10 INHIBITORS<br/>[FR] INHIBITEURS PYRIMIDINES DE PDE10
    申请人:MERCK SHARP & DOHME
    公开号:WO2013028590A1
    公开(公告)日:2013-02-28
    The present invention is directed to pyrimidine compounds which are useful as therapeutic agents for the treatment of central nervous system disorders associated with phosphodiesterase 10 (PDE10). The present invention also relates to the use of such compounds for treating neurological and psychiatric disorders, such as schizophrenia, psychosis or Huntington's disease, and those associated with striatal hypofunction or basal ganglia dysfunction.
    本发明涉及嘧啶化合物,其可用作治疗与磷酸二酯酶10(PDE10)相关的中枢神经系统疾病的治疗剂。本发明还涉及利用这些化合物治疗神经系统和精神疾病,如精神分裂症、精神病或亨廷顿病,以及与纹状体功能不足或基底神经节功能障碍相关的疾病。
  • REAGENTS AND METHODS FOR REPLICATION, TRANSCRIPTION, AND TRANSLATION IN SEMI-SYNTHETIC ORGANISMS
    申请人:The Scripps Research Institute
    公开号:US20200392550A1
    公开(公告)日:2020-12-17
    Disclosed herein are compositions, methods, cells, engineered microorganisms, and kits for increasing the production of proteins or polypeptides comprising one or more unnatural amino acids. Further provided are compositions, cells, engineered microorganisms, and kits for increasing the retention of unnatural nucleic acids encoding the unnatural amino acids in an engineered cell, or semi-synthetic organism.
    本文揭示了一种用于增加含有一个或多个非天然氨基酸的蛋白质或多肽的生产的组合物、方法、细胞、工程微生物和试剂盒。此外,还提供了一种用于增加编码非天然氨基酸的非天然核酸在工程细胞或半合成生物体中的保留的组合物、细胞、工程微生物和试剂盒。
  • PYRIMIDINE PDE10 INHIBITORS
    申请人:Cox Christopher D.
    公开号:US20140228368A1
    公开(公告)日:2014-08-14
    The present invention is directed to pyrimidine compounds which are useful as therapeutic agents for the treatment of central nervous system disorders associated with phosphodiesterase 10 (PDE10). The present invention also relates to the use of such compounds for treating neurological and psychiatric disorders, such as schizophrenia, psychosis or Huntington's disease, and those associated with striatal hypofunction or basal ganglia dysfunction.
    本发明涉及嘧啶化合物,其作为治疗与磷酸二酯酶10(PDE10)相关的中枢神经系统疾病的治疗剂。本发明还涉及使用这些化合物治疗神经系统和精神疾病,例如精神分裂症、精神病或亨廷顿病以及与纹状体功能减退或基底节功能障碍相关的疾病。
  • Substituted 2,3-Dihydrobenzofuranyl Compounds And Uses Thereof
    申请人:KARYOPHARM THERAPEUTICS INC.
    公开号:US20160221994A1
    公开(公告)日:2016-08-04
    The invention generally relates to substituted 2,3-dihydrobenzofuranyl compounds, and more particularly to a compound represented by Structural Formula (I), or a pharmaceutically acceptable salt thereof, wherein the variables are as defined and described herein. The invention also includes the synthesis and use of a compound of Structural Formula (I), or a pharmaceutically acceptable salt or composition thereof, e.g., in the treatment of cancer (e.g., mantle cell lymphoma), and other diseases and disorders.
    本发明通常涉及取代的2,3-二氢苯并呋喃基化合物,更具体地涉及由结构式(I)表示的化合物,或其药学上可接受的盐,在此变量的定义和描述中。本发明还包括合成和使用结构式(I)的化合物,或其药学上可接受的盐或组合物,例如在治疗癌症(例如曼托细胞淋巴瘤)和其他疾病和障碍中。
  • Substituted benzofuranyl and benzoxazolyl compounds and uses thereof
    申请人:Karyopharm Therapeutics Inc.
    公开号:US11008309B2
    公开(公告)日:2021-05-18
    The invention generally relates to substituted benzofuranyl and substituted benzoxazolyl compounds, and more particularly to a compound represented by Structural Formula A: or a pharmaceutically acceptable salt thereof, wherein the variables are as defined and described herein. The invention also includes the synthesis and use of a compound of Structural Formula A, or a pharmaceutically acceptable salt or composition thereof, e.g., in the treatment of cancer (e.g., mantle cell lymphoma), and other diseases and disorders.
    本发明一般涉及取代的苯并呋喃基和取代的苯并恶唑基化合物,特别是结构式 A 所代表的化合物: 或其药学上可接受的盐,其中变量如本文所定义和描述。本发明还包括结构式 A 的化合物或其药学上可接受的盐或组合物的合成和使用,例如用于治疗癌症(如套细胞淋巴瘤)及其他疾病和失调。
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