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3-(4-Hydroxy-2-oxo-2H-chromen-3-yl)-3-phenyl-propionic acid methyl ester | 6081-84-1

中文名称
——
中文别名
——
英文名称
3-(4-Hydroxy-2-oxo-2H-chromen-3-yl)-3-phenyl-propionic acid methyl ester
英文别名
Methyl 3-(4-hydroxy-2-oxochromen-3-yl)-3-phenylpropanoate
3-(4-Hydroxy-2-oxo-2H-chromen-3-yl)-3-phenyl-propionic acid methyl ester化学式
CAS
6081-84-1
化学式
C19H16O5
mdl
——
分子量
324.333
InChiKey
IOQFFVWYRWJEKD-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):
    2.9
  • 重原子数:
    24
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.16
  • 拓扑面积:
    72.8
  • 氢给体数:
    1
  • 氢受体数:
    5

文献信息

  • Materials and methods for treating coagulation disorders
    申请人:——
    公开号:US20040220258A1
    公开(公告)日:2004-11-04
    This invention is drawn to compounds which are more easily metabolized by the metabolic drug detoxification systems. Particularly, warfarin analogs which have been designed to include esters within the structure of the compounds are taught. The invention teaches methods of reducing the toxicity of drugs comprising the introduction of ester groups into drugs during the synthesis of the drug. This invention is also drawn to methods of treating coagulation disorders comprising the administration of compounds which have been designed to be metabolized by serum or intracellular hydrolases and esterases. Pharmaceutical compositions of the ester containing warfarin, analogs are also taught.
    这项发明涉及一种更容易被代谢药物解毒系统代谢的化合物。特别是,设计了包含酯基的华法林类似物的结构。该发明教导了在药物合成过程中引入酯基以减少药物毒性的方法。这项发明还涉及治疗凝血障碍的方法,包括给予设计为通过血清或细胞内酯酶代谢的化合物。还教导了含有酯基华法林类似物的药物组合物。
  • Materials and Methods for Treating Coagulation Disorders
    申请人:Druzgala Pascal
    公开号:US20080221204A1
    公开(公告)日:2008-09-11
    This invention is drawn to compounds which are more easily metabolized by the metabolic drug detoxification systems. Particularly, warfarin analogs which have been designed to include esters within the structure of the compounds are taught. The invention teaches methods of reducing the toxicity of drugs comprising the introduction of ester groups into drugs during the synthesis of the drug. This invention is also drawn to methods of treating coagulation disorders comprising the administration of compounds which have been designed to be metabolized by serum or intracellular hydrolases and esterases. Pharmaceutical compositions of the ester containing warfarin, analogs are also taught.
    本发明涉及化合物,这些化合物更容易被代谢药物解毒系统代谢。特别地,本发明涉及华法林类似物,其已被设计为在化合物的结构中包含酯基。本发明教导了在药物合成过程中引入酯基来减少药物毒性的方法。本发明还涉及治疗凝血障碍的方法,包括给予被设计为被血清或细胞内酯酶代谢的化合物。本发明还教导了含有酯基华法林类似物的药物组成物。
  • Materials And Methods For Treating Coagulation Disorders
    申请人:Druzgala Pascal
    公开号:US20070129429A1
    公开(公告)日:2007-06-07
    This invention is drawn to compounds which are more easily metabolized by the metabolic drug detoxification systems. Particularly, warfarin analogs which have been designed to include esters within the structure of the compounds are taught. The invention teaches methods of reducing the toxicity of drugs comprising the introduction of ester groups into drugs during the synthesis of the drug. This invention is also drawn to methods of treating coagulation disorders comprising the administration of compounds which have been designed to be metabolized by serum or intracellular hydrolases and esterases. Pharmaceutical compositions of the ester containing warfarin, analogs are also taught.
    本发明涉及一种化合物,该化合物更易于被代谢药物解毒系统代谢。特别是,本发明教授了设计在化合物结构中包含酯基的华法林类似物。本发明教授了一种通过在药物合成过程中引入酯基来减少药物毒性的方法。本发明还涉及一种治疗凝血障碍的方法,该方法包括给予已经设计成可以被血清或细胞内水解酶和酯酶代谢的化合物。本发明还涉及含有酯基华法林类似物的制药组合物。
  • Materials and methods for treating coagulation disorders
    申请人:ARYx Therapeutics
    公开号:EP2161261A1
    公开(公告)日:2010-03-10
    A compound according to Formula VI, or a pharmaceutically acceptable salt thereof, for the treatment of coagulation disorders, wherein, R is C1-C8 alkyl substituted with at least one halogen; R is C2-C8 alkyl substituted with at least one halogen; R is C3-C7 alkyl substituted with at least one halogen; R is C3-C6 alkyl substituted with at least one halogen.
    用于治疗凝血障碍的符合式 VI 的化合物或其药学上可接受的盐、 其中 R 是被至少一种卤素取代的 C1-C8 烷基; R 是被至少一种卤素取代的 C2-C8 烷基 R 是被至少一种卤素取代的 C3-C7 烷基 R 是被至少一种卤素取代的 C3-C6 烷基。
  • PYRANONE COMPOUNDS USEFUL TO TREAT RETROVIRAL INFECTIONS
    申请人:PHARMACIA & UPJOHN COMPANY
    公开号:EP0758327A1
    公开(公告)日:1997-02-19
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