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3-[4-[2-(5-Methyl-2-phenyl-4-oxazolyl)ethoxy]benzylidene]pentane-2,4-dione | 199794-75-7

中文名称
——
中文别名
——
英文名称
3-[4-[2-(5-Methyl-2-phenyl-4-oxazolyl)ethoxy]benzylidene]pentane-2,4-dione
英文别名
3-[[4-[2-(5-methyl-2-phenyl-1,3-oxazol-4-yl)ethoxy]phenyl]methylidene]pentane-2,4-dione
3-[4-[2-(5-Methyl-2-phenyl-4-oxazolyl)ethoxy]benzylidene]pentane-2,4-dione化学式
CAS
199794-75-7
化学式
C24H23NO4
mdl
——
分子量
389.451
InChiKey
XGDVDMCKNUYLJY-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):
    4.4
  • 重原子数:
    29
  • 可旋转键数:
    8
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.21
  • 拓扑面积:
    69.4
  • 氢给体数:
    0
  • 氢受体数:
    5

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    3-[4-[2-(5-Methyl-2-phenyl-4-oxazolyl)ethoxy]benzylidene]pentane-2,4-dionepalladium-carbon 作用下, 以 甲醇 为溶剂, 以87%的产率得到3-[4-[2-(5-Methyl-2-phenyl-4-oxazolyl)ethoxy]benzyl]pentane-2,4-dione
    参考文献:
    名称:
    Propionic acid derivatives and applications thereof
    摘要:
    一种具有式(I)的新型丙酸衍生物及其药学上可接受的盐,以及含有该衍生物的药物组合物。该丙酸衍生物及其药学上可接受的盐具有卓越的降血糖作用,并预期表现出降血脂作用,可作为治疗糖尿病及其并发症以及相关疾病如高脂血症的治疗剂。
    公开号:
    US06204277B1
  • 作为产物:
    描述:
    4-[2-(5-甲基-2-苯基-1,3-恶唑-4-基)乙氧基]苯甲醛乙酰丙酮哌啶乙酸盐 作用下, 以 甲苯 为溶剂, 反应 5.0h, 以60%的产率得到3-[4-[2-(5-Methyl-2-phenyl-4-oxazolyl)ethoxy]benzylidene]pentane-2,4-dione
    参考文献:
    名称:
    Isoxazolidine-3,5-dione and Noncyclic 1,3-Dicarbonyl Compounds as Hypoglycemic Agents
    摘要:
    Isoxazolidine-3,5-dione 2 (JTT-501), one of the cyclic malonic acid derivatives, was found to decrease blood glucose at an oral dose of 38 mg/kg/day in KKA(y) mice and is currently undergoing evaluation in phase II clinical trials. Further studies on a series of malonic acids and related compounds showed that the 1,3-dicarbonyl structure was important for insulin-sensitizing activity. Dimethyl malonate 10, which was selected as a successor for 2, was the optimum compound in a series of 1,3-dicarbonyl compounds and was more potent than the corresponding thiazolidine-2,4-dione 1.
    DOI:
    10.1021/jm970771m
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文献信息

  • Propionic acid derivatives and applications thereof
    申请人:Japan Tobacco Inc.
    公开号:US06204277B1
    公开(公告)日:2001-03-20
    A novel propionic acid derivative of the formula (I): and a pharmaceutically acceptable salt thereof, and pharmaceutical compositions containing the derivative. The propionic acid derivative and a pharmaceutically acceptable salt thereof have superior hypoglycemic action and are expected to show hypolipidemic action and to be useful as therapeutic agents for diabetes and complications of diabetes, as well as related diseases such as hyperlipemia.
    一种具有式(I)的新型丙酸衍生物及其药学上可接受的盐,以及含有该衍生物的药物组合物。该丙酸衍生物及其药学上可接受的盐具有卓越的降血糖作用,并预期表现出降血脂作用,可作为治疗糖尿病及其并发症以及相关疾病如高脂血症的治疗剂。
  • PROPIONIC ACID DERIVATIVES AND APPLICATIONS THEREOF
    申请人:Japan Tobacco Inc.
    公开号:EP0930299A1
    公开(公告)日:1999-07-21
    A novel propionic acid derivative of the formula (I): and a pharmaceutically acceptable salt thereof, and pharmaceutical compositions containing the derivative. The propionic acid derivative and a pharmaceutically acceptable salt thereof have superior hypoglycemic action and are expected to show hypolipidemic action and to be useful as therapeutic agents for diabetes and complications of diabetes, as well as related diseases such as hyperlipemia.
    一种新颖的式 (I) 丙酸衍生物: 及其药学上可接受的盐,以及含有该衍生物的药物组合物。该丙酸衍生物及其药学上可接受的盐具有卓越的降血糖作用,并有望显示出降血脂作用,可用作糖尿病和糖尿病并发症以及高脂血症等相关疾病的治疗剂。
  • US6204277B1
    申请人:——
    公开号:US6204277B1
    公开(公告)日:2001-03-20
  • Isoxazolidine-3,5-dione and Noncyclic 1,3-Dicarbonyl Compounds as Hypoglycemic Agents
    作者:Hisashi Shinkai、Syoji Onogi、Masahiro Tanaka、Tsutomu Shibata、Megumi Iwao、Korekiyo Wakitani、Itsuo Uchida
    DOI:10.1021/jm970771m
    日期:1998.5.1
    Isoxazolidine-3,5-dione 2 (JTT-501), one of the cyclic malonic acid derivatives, was found to decrease blood glucose at an oral dose of 38 mg/kg/day in KKA(y) mice and is currently undergoing evaluation in phase II clinical trials. Further studies on a series of malonic acids and related compounds showed that the 1,3-dicarbonyl structure was important for insulin-sensitizing activity. Dimethyl malonate 10, which was selected as a successor for 2, was the optimum compound in a series of 1,3-dicarbonyl compounds and was more potent than the corresponding thiazolidine-2,4-dione 1.
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