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methyl 4-[[3-(2-phenylethoxy)phenyl]methoxy]benzenepropanoate | 691901-85-6

中文名称
——
中文别名
——
英文名称
methyl 4-[[3-(2-phenylethoxy)phenyl]methoxy]benzenepropanoate
英文别名
Methyl 3-[4-[[3-(2-phenylethoxy)phenyl]methoxy]phenyl]propanoate
methyl 4-[[3-(2-phenylethoxy)phenyl]methoxy]benzenepropanoate化学式
CAS
691901-85-6
化学式
C25H26O4
mdl
——
分子量
390.479
InChiKey
GASZCJCPBYWQQC-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):
    5.4
  • 重原子数:
    29
  • 可旋转键数:
    11
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.24
  • 拓扑面积:
    44.8
  • 氢给体数:
    0
  • 氢受体数:
    4

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:
    methyl 4-[[3-(2-phenylethoxy)phenyl]methoxy]benzenepropanoatelithium hydroxide monohydrate 作用下, 以 四氢呋喃甲醇 为溶剂, 反应 3.0h, 以41%的产率得到3-(4-{[3-(2-phenylethoxy)benzyl]oxy}phenyl)propanoic acid
    参考文献:
    名称:
    Design, Synthesis, and Biological Activity of Potent and Orally Available G Protein-Coupled Receptor 40 Agonists
    摘要:
    G protein-coupled receptor 40 (GPR40) is being recently considered to be a new potential drug target for the treatment of type 2 diabetes because of its role in the enhancement of free fatty acid-regulated glucose-stimulated insulin secretion in pancreatic beta-cells. We initially identified benzyloxyphenylproparoic acid (1b) (EC50 = 510 nM), which was designed based on the structure of free fatty acids, as a promising lead compound with GPR40 agonist activity. Chemical modification of compound 1b led to the discovery of 3-{4-[(2',6'-dimethylbiphenyl-3-yl)methoxy]-2-fluorophenyl}propanoic acid (4p) as a potent GPR40 agonist (EC50 = 5,7 nM). Compound 4p exhibited acceptable pharmacokinetic profiles and significant glucose-lowering effects during an oral glucose tolerance test in diabetic rat;. Moreover, no hypoglycemic event was observed even after administration of a high dose of compound 4p to normal fasted rats. These pharmacological results suggest that GPR40 agonists might be novel glucose-dependent insulin secretagogues with little or no risk of hypoglycemia.
    DOI:
    10.1021/jm101405t
  • 作为产物:
    参考文献:
    名称:
    Design, Synthesis, and Biological Activity of Potent and Orally Available G Protein-Coupled Receptor 40 Agonists
    摘要:
    G protein-coupled receptor 40 (GPR40) is being recently considered to be a new potential drug target for the treatment of type 2 diabetes because of its role in the enhancement of free fatty acid-regulated glucose-stimulated insulin secretion in pancreatic beta-cells. We initially identified benzyloxyphenylproparoic acid (1b) (EC50 = 510 nM), which was designed based on the structure of free fatty acids, as a promising lead compound with GPR40 agonist activity. Chemical modification of compound 1b led to the discovery of 3-{4-[(2',6'-dimethylbiphenyl-3-yl)methoxy]-2-fluorophenyl}propanoic acid (4p) as a potent GPR40 agonist (EC50 = 5,7 nM). Compound 4p exhibited acceptable pharmacokinetic profiles and significant glucose-lowering effects during an oral glucose tolerance test in diabetic rat;. Moreover, no hypoglycemic event was observed even after administration of a high dose of compound 4p to normal fasted rats. These pharmacological results suggest that GPR40 agonists might be novel glucose-dependent insulin secretagogues with little or no risk of hypoglycemia.
    DOI:
    10.1021/jm101405t
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文献信息

  • Receptor Function Regulator
    申请人:Fukatsu Kohji
    公开号:US20090012093A1
    公开(公告)日:2009-01-08
    The GPR40 receptor function regulator of the present invention, which comprises a compound having an aromatic ring and a group capable of releasing cation is useful as an insulin secretagogue or an agent for the prophylaxis or treatment of diabetes and the like.
    本发明的GPR40受体功能调节剂包括具有芳香环和能够释放阳离子的基团的化合物,可用作胰岛素分泌剂或预防或治疗糖尿病等疾病的药剂。
  • GPR40 Receptor function regulator
    申请人:Takeda Pharmaceutical Company Limited
    公开号:EP2385032A1
    公开(公告)日:2011-11-09
    The GPR40 receptor function regulator of the present invention, which comprises a compound having an aromatic ring and a group capable of releasing cation is useful as an insulin secretagogue or an agent for the prophylaxis or treatment of diabetes and the like.
    本发明的 GPR40 受体功能调节剂由具有芳香环和能够释放阳离子的基团的化合物组成,可用作胰岛素分泌剂或预防或治疗糖尿病等的药物。
  • RECEPTOR FUNCTION CONTROLLING AGENT
    申请人:Takeda Pharmaceutical Company Limited
    公开号:EP1559422B1
    公开(公告)日:2014-04-30
  • US7960369B2
    申请人:——
    公开号:US7960369B2
    公开(公告)日:2011-06-14
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