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(S)-methyl 3-(4-hydroxyphenyl)heptanoate | 1073546-39-0

中文名称
——
中文别名
——
英文名称
(S)-methyl 3-(4-hydroxyphenyl)heptanoate
英文别名
methyl (3S)-3-(4-hydroxyphenyl)heptanoate
(S)-methyl 3-(4-hydroxyphenyl)heptanoate化学式
CAS
1073546-39-0
化学式
C14H20O3
mdl
——
分子量
236.311
InChiKey
QUAMJUVDJRMPDQ-LBPRGKRZSA-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):
    3.6
  • 重原子数:
    17
  • 可旋转键数:
    7
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    46.5
  • 氢给体数:
    1
  • 氢受体数:
    3

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

  • IMINOTHIADIAZINE DIOXIDE COMPOUNDS AS BACE INHIBITORS, COMPOSITIONS, AND THEIR USE
    申请人:Merck Sharp & Dohme Corp.
    公开号:US20140206675A1
    公开(公告)日:2014-07-24
    In its many embodiments, the present invention provides certain iminothiadiazine dioxide compounds, including compounds Formula (I): (I) and include stereoisomers thereof, and pharmaceutically acceptable salts of said compounds stereoisomers, wherein each of R 1 , R 2 , R 3 , R 4 , R 5 , R 9 , ring A, ring B, m, n, p, -L 1 -, L 2 -, and L 3 - is selected independently and as defined herein. The novel iminothiadiazine dioxide compounds of the invention have surprisingly been found to exhibit properties which are expected to render them advantageous as BACE inhibitors and/or for the treatment and prevention of various pathologies related to β-amyloid (Aβ) production. Pharmaceutical compositions comprising one or more such compounds (alone and in combination nation with one or more other active agents), and methods for their preparation and use in treating pathologies associated with amyloid beta (Aβ) protein, including Alzheimers disease, are also disclosed.
    在其不同实施例中,本发明提供某些亚氨基噻二嗪二氧化物化合物,包括化合物公式(I):(I),并包括其立体异构体和药学上可接受的盐,其中R1、R2、R3、R4、R5、R9、环A、环B、m、n、p、-L1-、L2-和L3-各自独立选择并按照定义选定。本发明的新型亚氨基噻二嗪二氧化物化合物出人意料地发现具有预期的性质,这些性质使它们有望成为BACE抑制剂和/或用于治疗和预防与β-淀粉样蛋白(Aβ)产生相关的各种病理的优势。本发明还揭示了包括一个或多个此类化合物(独立和与一个或多个其他活性剂联合使用)的药物组合物,并揭示了用于制备和治疗与淀粉样β(Aβ)蛋白相关的病理,包括阿尔茨海默病的方法。
  • Antidiabetic bicyclic compounds
    申请人:Merck Sharp & Dohme Corp.
    公开号:US10662171B2
    公开(公告)日:2020-05-26
    Novel compounds of the structural formula (I), and the pharmaceutically acceptable salts thereof, are agonists of G-protein coupled receptor 40 (GPR40) and may be useful in the treatment, prevention and suppression of diseases mediated by the G-protein-coupled receptor 40. The compounds of the present invention may be useful in the treatment of Type 2 diabetes mellitus, and of conditions that are often associated with this disease, including obesity and lipid disorders, such as mixed or diabetic dyslipidemia, hyperlipidemia, hypercholesterolemia, and hypertriglyceridemia.
    结构式(I)的新型化合物及其药学上可接受的盐类是G-蛋白偶联受体40(GPR40)的激动剂,可用于治疗、预防和抑制由G-蛋白偶联受体40介导的疾病。本发明的化合物可用于治疗 2 型糖尿病以及通常与这种疾病相关的病症,包括肥胖和血脂紊乱,如混合性或糖尿病性血脂异常、高脂血症、高胆固醇血症和高甘油三酯血症。
  • SUBSTITUTED BIPHENYL PHENOXY-, THIOPHENYL- AND AMINOPHENYLPROPANOIC ACID GPR40 MODULATORS
    申请人:Amgen, Inc
    公开号:EP2139843B1
    公开(公告)日:2013-12-25
  • ANTIDIABETIC BICYCLIC COMPOUNDS
    申请人:Merck Sharp & Dohme Corp.
    公开号:US20170217920A1
    公开(公告)日:2017-08-03
    Novel compounds of the structural formula (I), and the pharmaceutically acceptable salts thereof, are agonists of G-protein coupled receptor 40 (GPR40) and may be useful in the treatment, prevention and suppression of diseases mediated by the G-protein-coupled receptor 40. The compounds of the present invention may be useful in the treatment of Type 2 diabetes mellitus, and of conditions that are often associated with this disease, including obesity and lipid disorders, such as mixed or diabetic dyslipidemia, hyperlipidemia, hypercholesterolemia, and hypertriglyceridemia.
  • US7572934B2
    申请人:——
    公开号:US7572934B2
    公开(公告)日:2009-08-11
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