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(S)-6-fluoro-2-[2-(2-fluoro-phenyl)-vinyl]-3-(2-methyl-pyridin-3-yl)-3H-quinazolin-4-one

中文名称
——
中文别名
——
英文名称
(S)-6-fluoro-2-[2-(2-fluoro-phenyl)-vinyl]-3-(2-methyl-pyridin-3-yl)-3H-quinazolin-4-one
英文别名
6-fluoro-2-[(E)-2-(2-fluorophenyl)ethenyl]-3-(2-methylpyridin-3-yl)quinazolin-4-one
(S)-6-fluoro-2-[2-(2-fluoro-phenyl)-vinyl]-3-(2-methyl-pyridin-3-yl)-3H-quinazolin-4-one化学式
CAS
——
化学式
C22H15F2N3O
mdl
——
分子量
375.377
InChiKey
BZXWTCCHDCVZBL-DHZHZOJOSA-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
  • 重原子数:
    28
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    45.6
  • 氢给体数:
    0
  • 氢受体数:
    5

文献信息

  • AMPA antagonists for the treatment of dyskinesias associated with dopamine agonist therapy
    申请人:Pfizer Products Inc.
    公开号:EP0900568A2
    公开(公告)日:1999-03-10
    The invention relates to a method of treating dyskinesias associated with dopamine agonist therapy in a mammal which comprises administering to said mammal a compound, as defined herein, which is an antagonist of the AMPA receptor. Dopamine agonist therapy, as referred to in the present invention, is generally used in the treatment of a central nervous system disorder such as Parkinson's disease.
    本发明涉及一种治疗哺乳动物多巴胺激动剂治疗相关运动障碍的方法,该方法包括向所述哺乳动物施用本文所定义的化合物,该化合物是 AMPA 受体的拮抗剂。本发明所述的多巴胺激动剂疗法通常用于治疗帕金森病等中枢神经系统疾病。
  • ATROPISOMERS OF 3-HETEROARYL-4(3H)-QUINAZOLINONES FOR THE TREATMENT OF NEURODEGENERATIVE AND CNS-TRAUMA RELATED CONDITIONS
    申请人:Pfizer Products Inc.
    公开号:EP0964860A1
    公开(公告)日:1999-12-22
  • JPH11158072A
    申请人:——
    公开号:JPH11158072A
    公开(公告)日:1999-06-15
  • Modulation of AMPA/kainate Receptors for the Treatment of Hypoglycemia
    申请人:Vanderklish Peter
    公开号:US20200397751A1
    公开(公告)日:2020-12-24
    Methods for modulating the levels of glucagon and blood glucose of a mammal are provided. In the subject methods, a positive allosteric modulator of AMPA/kainate receptors is administered to a host. The subject methods find use in applications where it is desired to increase one or both of the glucagon and blood glucose levels in a mammalian host. The subject methods find use in applications where it is desired to decrease the size, or breadth, of the circadian range of blood glucose levels in a mammalian host. The subject methods also find use in applications where it is desired to decrease the frequency, severity, or occurrence of hypoglycemia in a mammalian host. Finally, the subject method finds use in applications where it is desired to decrease the frequency, severity, or occurrence of nocturnal hypoglycemia in a mammalian host, particularly that which occurs in diabetics as a result of therapy with insulins or insulin analogs or other glucose lowering agents, or combinations of such agents.
  • US6136812A
    申请人:——
    公开号:US6136812A
    公开(公告)日:2000-10-24
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