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(R)-N-(2-(2-cyanopyrimidin-5-yl)ethyl)-1-(6-(4-ethylpiperazin-1-yl)-2-(trifluoromethyl)pyrimidin-4-yl)piperidine-3-carboxamide | 1595144-82-3

中文名称
——
中文别名
——
英文名称
(R)-N-(2-(2-cyanopyrimidin-5-yl)ethyl)-1-(6-(4-ethylpiperazin-1-yl)-2-(trifluoromethyl)pyrimidin-4-yl)piperidine-3-carboxamide
英文别名
(3R)-N-[2-(2-cyanopyrimidin-5-yl)ethyl]-1-[6-(4-ethylpiperazin-1-yl)-2-(trifluoromethyl)pyrimidin-4-yl]piperidine-3-carboxamide
(R)-N-(2-(2-cyanopyrimidin-5-yl)ethyl)-1-(6-(4-ethylpiperazin-1-yl)-2-(trifluoromethyl)pyrimidin-4-yl)piperidine-3-carboxamide化学式
CAS
1595144-82-3
化学式
C24H30F3N9O
mdl
——
分子量
517.557
InChiKey
MJKSBDOYJVJJGS-GOSISDBHSA-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):
    2.3
  • 重原子数:
    37
  • 可旋转键数:
    7
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.58
  • 拓扑面积:
    114
  • 氢给体数:
    1
  • 氢受体数:
    12

反应信息

  • 作为产物:
    描述:
    5-溴-2-氰基嘧啶 在 palladium diacetate 、 caesium carbonateN,N-二异丙基乙胺三氟乙酸 、 N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate 、 2-二环己基磷-2',6'-二异丙氧基-1,1'-联苯 作用下, 以 二氯甲烷N,N-二甲基甲酰胺甲苯 为溶剂, 反应 13.0h, 生成 (R)-N-(2-(2-cyanopyrimidin-5-yl)ethyl)-1-(6-(4-ethylpiperazin-1-yl)-2-(trifluoromethyl)pyrimidin-4-yl)piperidine-3-carboxamide
    参考文献:
    名称:
    Discovery of Trifluoromethyl(pyrimidin-2-yl)azetidine-2-carboxamides as Potent, Orally Bioavailable TGR5 (GPBAR1) Agonists: Structure–Activity Relationships, Lead Optimization, and Chronic In Vivo Efficacy
    摘要:
    Activation of the G-protein coupled receptor (GPCR) Takeda G-protein receptor 5 (TGR5), also known as G-protein bile acid receptor 1 (GPBAR1), has been shown to play a key role in pathways associated with diabetes, metabolic syndrome, and autoimmune disease. Nipecotamide 5 was identified as an attractive starting point after a high-throughput screen (HTS) for receptor agonists. A comprehensive hit-to-lead effort culminated in the discovery of 45h as a potent, selective, and bioavailable TGR5 agonist to test in preclinical metabolic disease models. In genetically obese mice (ob/ob), 45h was as effective as a dipeptidyl peptidase-4 (DPP-4) inhibitor at reducing peak glucose levels in an acute oral glucose tolerance test (OGTT), but this effect was lost upon chronic dosing.
    DOI:
    10.1021/jm401731q
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