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(S)-4-carboxyphenylglycine

中文名称
——
中文别名
——
英文名称
(S)-4-carboxyphenylglycine
英文别名
4-[(S)-amino(carboxy)methyl]benzoic acid
(S)-4-carboxyphenylglycine化学式
CAS
——
化学式
C9H9NO4
mdl
——
分子量
195.17
InChiKey
VTMJKPGFERYGJF-ZETCQYMHSA-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):
    -2.2
  • 重原子数:
    14
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    101
  • 氢给体数:
    3
  • 氢受体数:
    5

文献信息

  • DIMERIC IAP INHIBITORS
    申请人:STRAUB Christopher Sean
    公开号:US20110206690A1
    公开(公告)日:2011-08-25
    The present invention provides compounds of formula M-L-M′ (where M and M′ are each independently a monomeric moiety of Formula (I) and L is a linker). The dimeric compounds have been found to be effective in promoting apoptosis in rapidly dividing cells.
    本发明提供了公式M-L-M′的化合物(其中M和M′分别是公式(I)中的单体基团,L是连接物)。已发现二聚化合物在促进快速分裂细胞凋亡方面具有有效性。
  • Capture compounds, collections thereof and methods for analyzing the proteome and complex compositions
    申请人:Kõster Hubert
    公开号:US20100248264A1
    公开(公告)日:2010-09-30
    Capture compounds and collections thereof and methods using the compounds for the analysis of biomolecules are provided. In particular, collections, compounds and methods are provided for analyzing complex protein mixtures, such as the proteome. The compounds are multifunctional reagents that provide for the separation and isolation of complex protein mixtures. Automated systems for performing the methods also are provided.
    提供了捕获化合物及其集合以及使用这些化合物进行生物分子分析的方法。特别地,提供了用于分析复杂蛋白质混合物(如蛋白质组)的集合、化合物和方法。这些化合物是多功能试剂,可用于分离和分离复杂的蛋白质混合物。还提供了执行这些方法的自动化系统。
  • A method for treating tension-type headache
    申请人:HEADEXPLORER ApS
    公开号:EP1829539A2
    公开(公告)日:2007-09-05
    Tension-type headache is treated by interacting with neuronal transmission in relation to pain in connection with headache in a way which prevents or decreases sensitization of second order nociceptive neurons. In particular, treatment is performed by administration of an effective amount of a substance which prevents or decreases central sensitization. Important examples of such substances are substances which interact with glutamate neurotransmission, such as glutamate receptor antagonists, such as NMDA receptor antagonists, such as MK-801 or Amitriptylline or Imipramine or Desipramine or Mirtazaprine or Venlafaxine. Other examples are substances which interact with nitric oxide, such as nitric oxide synthase (NOS) inhibitors, such as L-NMMA or L-NAME or L-NIO or L-NNA. According to a broader aspect of the invention tension-type headache is treated by administration of substances which are effective in preventing or decreasing pain in connection with tension-type headache, such as the substances mentioned above. An additional aspect of the invention relates to treatment of tension-type headache by administration of substances which substantially inhibit the activity of nitric oxide synthase (NOS), such as NOS inhibitors, such as L-NMMA or L-NAME or L-NIO or L-NNA.
    治疗紧张型头痛的方法是,与头痛有关的疼痛神经元传递相互作用,防止或减少二阶痛觉神经元的敏化。具体来说,治疗方法是通过施用有效量的物质来防止或减少中枢敏化。这类物质的重要例子是与谷酸神经递质相互作用的物质,如谷酸受体拮抗剂,如NMDA受体拮抗剂,如MK-801或阿米替林丙咪嗪或地西普胺或米氮平文拉法辛。其他例子包括与一氧化氮相互作用的物质,如一氧化氮合酶(NOS)抑制剂,如L-NMMA或L-NAME或L-NIO或L-NNA。根据本发明更广泛的一个方面,治疗紧张型头痛的方法是施用能有效预防或减轻紧张型头痛相关疼痛的物质,如上述物质。本发明的另一个方面涉及通过施用实质上抑制一氧化氮合酶(NOS)活性的物质,如NOS抑制剂,如L-NMMA或L-NAME或L-NIO或L-NNA,来治疗紧张型头痛。
  • Method for treating tension-type headache
    申请人:——
    公开号:US20040097562A1
    公开(公告)日:2004-05-20
    NMDA receptor antagonists, especially mirtazapine, can be used to treat tension-type headaches.
  • TREATMENT OF TINNITUS USING GLUTAMATE RECEPTOR AGONISTS
    申请人:Northeast Ohio Medical University
    公开号:US20210251928A1
    公开(公告)日:2021-08-19
    A method of treating tinnitus in a subject is described that includes administering a therapeutically effective amount of a group II metabotropic glutamate receptor (mGluR) agonist to the subject. A method of screening a subject having tinnitus for treatment with a group II mGluR agonist that includes testing the use of residual inhibition to suppress tinnitus in the subject, wherein suppression of tinnitus by residual inhibition indicates that a group II mGluR agonist would be effective for treating tinnitus in the subject, is also described.
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