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tert-butyl 4-(((2RS)-7-((1R,2S)-1-cyclopropyl-3-methoxy-2-methyl-3-oxopropyl)-4-hydroxychroman-2-yl)methyl)piperidine-1-carboxylate

中文名称
——
中文别名
——
英文名称
tert-butyl 4-(((2RS)-7-((1R,2S)-1-cyclopropyl-3-methoxy-2-methyl-3-oxopropyl)-4-hydroxychroman-2-yl)methyl)piperidine-1-carboxylate
英文别名
tert-butyl 4-[[7-[(1R,2S)-1-cyclopropyl-3-methoxy-2-methyl-3-oxopropyl]-4-hydroxy-3,4-dihydro-2H-chromen-2-yl]methyl]piperidine-1-carboxylate
tert-butyl 4-(((2RS)-7-((1R,2S)-1-cyclopropyl-3-methoxy-2-methyl-3-oxopropyl)-4-hydroxychroman-2-yl)methyl)piperidine-1-carboxylate化学式
CAS
——
化学式
C28H41NO6
mdl
——
分子量
487.637
InChiKey
MVTVZVHNGXAZJO-HVOHCLKISA-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):
    4.8
  • 重原子数:
    35
  • 可旋转键数:
    9
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.71
  • 拓扑面积:
    85.3
  • 氢给体数:
    1
  • 氢受体数:
    6

反应信息

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文献信息

  • Antidiabetic heterocyclic compounds
    申请人:Merck Sharp & Dohme Corp.
    公开号:US11072602B2
    公开(公告)日:2021-07-27
    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,包括肥胖和脂质紊乱,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。
  • [EN] ANTIDIABETIC HETEROCYCLIC COMPOUNDS<br/>[FR] COMPOSÉS HÉTÉROCYCLIQUES ANTIDIABÉTIQUES
    申请人:MERCK SHARP & DOHME
    公开号:WO2018106518A1
    公开(公告)日:2018-06-14
    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可接受的盐是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介导的疾病方面有用。本发明的化合物可能在治疗2型糖尿病以及与该疾病常相关的病症方面有用,包括肥胖和与之相关的脂质紊乱,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。
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