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Methyl 3-cyclopropyl-3-(3-hydroxyphenyl)-2-methylpropanoate

中文名称
——
中文别名
——
英文名称
Methyl 3-cyclopropyl-3-(3-hydroxyphenyl)-2-methylpropanoate
英文别名
methyl 3-cyclopropyl-3-(3-hydroxyphenyl)-2-methylpropanoate
Methyl 3-cyclopropyl-3-(3-hydroxyphenyl)-2-methylpropanoate化学式
CAS
——
化学式
C14H18O3
mdl
——
分子量
234.29
InChiKey
XTKAMBAWNHTBEF-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):
    3.1
  • 重原子数:
    17
  • 可旋转键数:
    5
  • 环数:
    2.0
  • 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

文献信息

  • [EN] CYCLOHEXYL GPR40 AGONISTS FOR THE TREATMENT OF TYPE II DIABETES<br/>[FR] AGONISTES CYCLOHEXYLE DE GPR40 POUR LE TRAITEMENT DU DIABÈTE DE TYPE 2
    申请人:JANSSEN PHARMACEUTICA NV
    公开号:WO2018081047A1
    公开(公告)日:2018-05-03
    Disclosed are compounds, compositions and methods for treating of disorders that are affected by the modulation of the GPR40 receptor. Such compounds are represented by Formula (I) as follows: (Formula (I)) wherein R1, R2, R3, A, W, L, Ra, and G are defined herein: and by Formula (II) as follows: (Formula (II)) wherein R1B, WB, LB, and GB are defined herein.
    披露了用于治疗受GPR40受体调节影响的疾病的化合物、组合物和方法。这类化合物由公式(I)表示,如下所示:(公式(I)),其中R1、R2、R3、A、W、L、Ra和G在本文中定义;以及由公式(II)表示,如下所示:(公式(II)),其中R1B、WB、LB和GB在本文中定义。
  • [EN] GPR40 AGONISTS<br/>[FR] AGONISTES DE GPR40
    申请人:KALLYOPE INC
    公开号:WO2020242943A1
    公开(公告)日:2020-12-03
    This disclosure is directed, at least in part, to GPR40 agonists useful for the treatment of conditions or disorders involving the gut-brain axis. In some embodiments, the GPR40 agonists are gut-restricted compounds. In some embodiments, the GPR40 agonists are full agonists or partial agonists. In some embodiments, the condition or disorder is a metabolic disorder, such as diabetes, obesity, nonalcoholic steatohepatitis (NASH), or a nutritional disorder such as short bowel syndrome.
    这份公开信息至少部分涉及用于治疗涉及肠-脑轴的条件或疾病的GPR40激动剂。在某些实施例中,GPR40激动剂是肠道限制性化合物。在某些实施例中,GPR40激动剂是全激动剂或部分激动剂。在某些实施例中,所述条件或疾病是一种代谢紊乱,如糖尿病、肥胖、非酒精性脂肪肝炎(NASH)或一种营养紊乱,如短肠综合征。
  • [EN] ANTIDIABETIC BICYCLIC COMPOUNDS<br/>[FR] COMPOSÉS BICYCLIQUES ANTIDIABÉTIQUES
    申请人:MERCK SHARP & DOHME
    公开号:WO2016022742A1
    公开(公告)日:2016-02-11
    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)的新化合物及其药用盐是G蛋白偶联受体40(GPR40)的激动剂,可能对通过G蛋白偶联受体40介导的疾病的治疗、预防和抑制具有用处。本发明的化合物可能对2型糖尿病的治疗有用,以及对常与该疾病相关的疾病,包括肥胖和脂质紊乱,如混合型或糖尿病性脂质代谢异常、高脂血症、高胆固醇血症和高甘油三酯血症的治疗有用。
  • [EN] [5,6]-FUSED BICYCLIC ANTIDIABETIC COMPOUNDS<br/>[FR] COMPOSÉS ANTIDIABÉTIQUES BICYCLIQUES À FUSION [5,6]
    申请人:MERCK SHARP & DOHME
    公开号:WO2016022446A1
    公开(公告)日:2016-02-11
    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)的新化合物及其药用盐是G蛋白偶联受体40(GPR40)的激动剂,可能在治疗、预防和抑制由G蛋白偶联受体40介导的疾病方面具有用处。本发明的化合物可能在治疗2型糖尿病以及与该疾病经常相关的疾病,包括肥胖和脂质紊乱等条件中具有用处,如混合型或糖尿病性脂质代谢异常、高脂血症、高胆固醇血症和高甘油三酯血症。
  • ANTIDIABETIC BICYCLIC COMPOUNDS
    申请人:BROCKUNIER Linda L.
    公开号:US20160002255A1
    公开(公告)日:2016-01-07
    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)的新化合物及其药学上可接受的盐是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,以及与该疾病常见相关的疾病,包括肥胖和脂质紊乱,如混合型或糖尿病性脂质代谢异常、高脂血症、高胆固醇血症和高三酰甘油血症。
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