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5-[4-[2-(5-methyl-2-pyridyl)ethoxy]benzyl]-2,4-thiazolidinedione | 105355-35-9

中文名称
——
中文别名
——
英文名称
5-[4-[2-(5-methyl-2-pyridyl)ethoxy]benzyl]-2,4-thiazolidinedione
英文别名
5-{4-[2-(5-Methyl-2pyridyl)ethoxy]benzyl}-2,4-thiazolidinedione;5-[[4-[2-(5-methylpyridin-2-yl)ethoxy]phenyl]methyl]-1,3-thiazolidine-2,4-dione
5-[4-[2-(5-methyl-2-pyridyl)ethoxy]benzyl]-2,4-thiazolidinedione化学式
CAS
105355-35-9
化学式
C18H18N2O3S
mdl
——
分子量
342.419
InChiKey
SJRYOPKADFWPBS-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

物化性质

  • 熔点:
    192-193 °C
  • 沸点:
    568.5±45.0 °C(Predicted)
  • 密度:
    1.286±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.3
  • 重原子数:
    24
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    93.6
  • 氢给体数:
    1
  • 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

反应信息

点击查看最新优质反应信息

文献信息

  • Thiazolidinedione derivatives, useful as antidiabetic agents
    申请人:Takeda Chemical Industries, Ltd.
    公开号:US04687777A1
    公开(公告)日:1987-08-18
    Thiazolidinedione derivatives of the formula: ##STR1## and pharmacologically acceptable salts thereof are novel compounds, which exhibit in mammals blood sugar- and lipid-lowering activity, and are of value as a therapeutic agent for treatment of diabetes and hyperlipemia.
    Thiazolidinedione衍生物的化学式为:##STR1##及其药理学上可接受的盐是新颖的化合物,对哺乳动物具有降血糖和降脂活性,并且作为治疗糖尿病和高脂血症的治疗剂具有价值。
  • Thiazolidinedione derivatives, their production and their use
    申请人:TAKEDA CHEMICAL INDUSTRIES, LTD.
    公开号:EP0508740A1
    公开(公告)日:1992-10-14
    There is disclosed a novel thiazolidinedione derivative of the general formula (I): wherein R1 and R2 are the same or different and are a hydrogen atom or a lower alkyl group, or a salt thereof. The thiazolidinedione derivative has hypoglycemic activity and hypolipidemic activity.
    本发明公开了一种通式为(I)的新型噻唑烷二酮衍生物: 其中 R1 和 R2 相同或不同,且为氢原子或低级烷基,或其盐。该噻唑烷二酮衍生物具有降血糖活性和降血脂活性。
  • Thiazolidinedione derivatives, their production and use
    申请人:Takeda Chemical Industries, Ltd.
    公开号:EP0193256B1
    公开(公告)日:1989-04-05
  • SOHDA, T.;MOMOSE, Y.;MEGURO, K.;KAWAMATSU, Y.;SUGIYAMA, Y.;IKEDA, H., ARZNEIM.-FOSRCH, 40,(1990) N, C. 37-42
    作者:SOHDA, T.、MOMOSE, Y.、MEGURO, K.、KAWAMATSU, Y.、SUGIYAMA, Y.、IKEDA, H.
    DOI:——
    日期:——
  • MODULATION OF NEUROGENESIS BY PPAR AGENTS
    申请人:Barlow Carrolee
    公开号:US20100184806A1
    公开(公告)日:2010-07-22
    The instant disclosure describes methods for treating diseases and conditions of the central and peripheral nervous system including by stimulating or increasing neurogenesis, neuroproliferation, and/or neurodifferentiation. The disclosure includes compositions and methods based on use of a peroxisome proliferator-activated receptor (PPAR) agent, optionally in combination with one or more neurogenic agents, to stimulate or increase a neurogenic response and/or to treat a nervous system disease or disorder.
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