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cis-2,5-Diaethyl-tetrahydrofuran | 5921-97-1

中文名称
——
中文别名
——
英文名称
cis-2,5-Diaethyl-tetrahydrofuran
英文别名
(2R,5S)-2,5-diethyloxolane
cis-2,5-Diaethyl-tetrahydrofuran化学式
CAS
5921-97-1
化学式
C8H16O
mdl
——
分子量
128.214
InChiKey
YKWLEIXVUHRKEF-OCAPTIKFSA-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):
    2.5
  • 重原子数:
    9
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    1

文献信息

  • Macrocyclic Modulators of the Ghrelin Receptor
    申请人:Ocera Therapeutics, Inc.
    公开号:US20180110824A1
    公开(公告)日:2018-04-26
    The present invention provides novel conformationally-defined macrocyclic compounds that have been demonstrated to be selective modulators of the ghrelin receptor (growth hormone secretagogue receptor, GHS-R1a and subtypes, isoforms and variants thereof). Methods of synthesizing the novel compounds are also described herein. These compounds are useful as agonists of the ghrelin receptor and as medicaments for treatment and prevention of a range of medical conditions including, but not limited to, metabolic and/or endocrine disorders, gastrointestinal disorders, cardiovascular disorders, obesity and obesity-associated disorders, central nervous system disorders, genetic disorders, hyperproliferative disorders and inflammatory disorders.
    本发明提供了一种新颖的构象定义明确的大环化合物,已经证明是生长激素分泌素受体(GHS-R1a及其亚型、异构体和变体)的选择性调节剂。本文还描述了合成这些新型化合物的方法。这些化合物可用作生长激素分泌素受体的激动剂,用于治疗和预防一系列医疗状况,包括但不限于代谢和/或内分泌紊乱、胃肠道紊乱、心血管疾病、肥胖和与肥胖相关的疾病、中枢神经系统疾病、遗传疾病、过度增殖性疾病和炎症性疾病。
  • MACROCYCLIC MODULATORS OF THE GHRELIN RECEPTOR
    申请人:TRANZYME PHARMA INC.
    公开号:US20130211045A1
    公开(公告)日:2013-08-15
    The present invention provides novel conformationally-defined macrocyclic compounds that have been demonstrated to be selective modulators of the ghrelin receptor (growth hormone secretagogue receptor, GHS-R1a and subtypes, isoforms and variants thereof). Methods of synthesizing the novel compounds are also described herein. These compounds are useful as agonists of the ghrelin receptor and as medicaments for treatment and prevention of a range of medical conditions including, but not limited to, metabolic and/or endocrine disorders, gastrointestinal disorders, cardiovascular disorders, obesity and obesity-associated disorders, central nervous system disorders, genetic disorders, hyperproliferative disorders and inflammatory disorders.
    本发明提供了一种新型构象定义的大环化合物,已经被证明是生长激素分泌肽受体(GHS-R1a和其亚型、同工异构体和变异体)的选择性调节剂。本文还描述了合成这些新化合物的方法。这些化合物可用作生长激素分泌肽受体的激动剂,以及用于治疗和预防一系列医学疾病,包括但不限于代谢和/或内分泌紊乱、胃肠道疾病、心血管疾病、肥胖和肥胖相关疾病、中枢神经系统疾病、遗传疾病、过度增生性疾病和炎症性疾病。
  • Spatially-defined macrocyclic compounds useful for drug discovery
    申请人:Tranzyme Pharma Inc.
    公开号:EP2319859A2
    公开(公告)日:2011-05-11
    Spatially-defined macrocyclic compounds containing specific conformational control elements are disclosed. Libraries of these macrocycles are then used to select one or more macrocycle species that exhibit a specific interaction with a particular biological target. In particular, compounds according to the invention are disclosed as agonists or antagonists of a mammalian motilin receptor and a mammalian ghrelin receptor.
    本研究公开了含有特定构象控制元件的空间定义大环化合物。这些大环化合物库可用于选择一种或多种与特定生物靶标发生特定相互作用的大环化合物。特别是,根据本发明的化合物被公开为哺乳动物动情素受体和哺乳动物胃泌素受体的激动剂或拮抗剂。
  • Methods of using macrocyclic modulators of the ghrelin receptor
    申请人:Fraser L. Graeme
    公开号:US20070021331A1
    公开(公告)日:2007-01-25
    The present invention provides novel conformationally-defined macrocyclic compounds that have been demonstrated to be selective modulators of the ghrelin receptor (growth hormone secretagogue receptor, GHS-R1a and subtypes, isoforms and variants thereof). Methods of synthesizing the novel compounds are also described herein. These compounds are useful as agonists of the ghrelin receptor and as medicaments for treatment and prevention of a range of medical conditions including, but not limited to, metabolic and/or endocrine disorders, gastrointestinal disorders, cardiovascular disorders, obesity and obesity-associated disorders, central nervous system disorders, genetic disorders, hyperproliferative disorders and inflammatory disorders.
  • METHODS OF USING MACROCYCLIC MODULATORS OF THE GHRELIN RECEPTOR
    申请人:Fraser Graeme L.
    公开号:US20090170757A1
    公开(公告)日:2009-07-02
    The present invention provides novel conformationally-defined macrocyclic compounds that have been demonstrated to be selective modulators of the ghrelin receptor (growth hormone secretagogue receptor, GHS-R1a and subtypes, isoforms and variants thereof). Methods of synthesizing the novel compounds are also described herein. These compounds are useful as agonists of the ghrelin receptor and as medicaments for treatment and prevention of a range of medical conditions including, but not limited to, metabolic and/or endocrine disorders, gastrointestinal disorders, cardiovascular disorders, obesity and obesity-associated disorders, central nervous system disorders, genetic disorders, hyperproliferative disorders and inflammatory disorders.
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