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3-Ethoxycyclopentan-1-one | 64145-52-4

中文名称
——
中文别名
——
英文名称
3-Ethoxycyclopentan-1-one
英文别名
——
3-Ethoxycyclopentan-1-one化学式
CAS
64145-52-4
化学式
C7H12O2
mdl
——
分子量
128.17
InChiKey
UAFTUQCCPRMUPP-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):
    0.3
  • 重原子数:
    9
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.86
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • [EN] TETRAZOLE DERIVATIVES AND METHODS OF TREATMENT OF METABOLIC-RELATED DISORDERS THEREOF<br/>[FR] DERIVES DE TETRAZOLE ET METHODES DE TRAITEMENT DE TROUBLES LIES AU METABOLISME
    申请人:ARENA PHARM INC
    公开号:WO2005044816A1
    公开(公告)日:2005-05-19
    The present invention relates to certain tetrazole derivatives of Formula (I), and pharmaceutically acceptable salts thereof, which exhibit useful pharmacological properties, for example, as agonists for the RUP25 receptor. Also provided by the present invention are pharmaceutical compositions containing compounds of the invention, and methods of using the compounds and compositions of the invention in the treatment of metabolic-related disorders, including dyslipidemia, atherosclerosis, coronary heart disease, insulin resistance, type 2 diabetes, Syndrome-X and the like. In addition, the present invention also provides for the use of the compounds of the invention in combination with other active agents such as those belonging to the class of α-glucosidase inhibitors, aldose reductase inhibitors, biguanides, HMG-CoA reductase inhibitors, squalene synthesis inhibitors, fibrates, LDL catabolism enhancers, angiotensin converting enzyme (ACE) inhibitors, insulin secretion enhancers and the like.
    本发明涉及公式(I)的某些四唑衍生物及其药学上可接受的盐,这些衍生物表现出有用的药理特性,例如作为RUP25受体的激动剂。本发明还提供了含有本发明化合物的药物组合物,以及在治疗代谢相关疾病,包括脂质代谢异常、动脉粥样硬化、冠心病、胰岛素抵抗、2型糖尿病、X综合征等方面使用本发明化合物和组合物的方法。此外,本发明还提供了将本发明化合物与其他活性剂结合使用的方法,这些活性剂属于α-葡萄糖苷酶抑制剂、醛糖还原酶抑制剂、双胍类药物、HMG-CoA还原酶抑制剂、角鲨烯合成抑制剂、贝特类药物、LDL降解增强剂、血管紧张素转化酶(ACE)抑制剂、胰岛素分泌增强剂等类别。
  • Asymmetric 1,4-reductions of and 1,4-additions to enoates and related systems
    申请人:——
    公开号:US20030125563A1
    公开(公告)日:2003-07-03
    One aspect of the present invention relates to methods for the transition-metal-catalyzed asymmetric 1,4-addition of a nucleophile, e.g., hydride, to cyclic and acyclic enoates and enones. In certain embodiments of the methods of the present invention, the transition metal catalyst consists essentially of copper and an asymmetric bidentate bisphosphine ligand.
    本发明的一个方面涉及过渡金属催化的手性1,4-加成方法,用于将亲核试剂(例如氢化物)加成到环状和非环状烯酸酯和烯酮上。在本发明的某些实施方式中,过渡金属催化剂基本上由铜和手性双膦配体组成。
  • Tetrazole derivatives and methods of treatment of metabolic-related disorders thereof
    申请人:Semple Graeme
    公开号:US20060217562A1
    公开(公告)日:2006-09-28
    The present invention relates to certain tetrazole derivatives of Formula (I), and pharmaceutically acceptable salts thereof, which exhibit useful pharmacological properties, for example, as agonists for the RUP25 receptor. Also provided by the present invention are pharmaceutical compositions containing compounds of the invention, and methods of using the compounds and compositions of the invention in the treatment of metabolic-related disorders, including dyslipidemia, atherosclerosis, coronary heart disease, insulin resistance, type 2 diabetes, Syndrome-X and the like. In addition, the present invention also provides for the use of the compounds of the invention in combination with other active agents such as those belonging to the class of α-glucosidase inhibitors, aldose reductase inhibitors, biguanides, HMG-CoA reductase inhibitors, squalene synthesis inhibitors, fibrates, LDL catabolism enhancers, angiotensin converting enzyme (ACE) inhibitors, insulin secretion enhancers and the like.
    本发明涉及公式(I)的某些四唑衍生物及其药学上可接受的盐,这些化合物具有有用的药理学特性,例如作为RUP25受体激动剂。本发明还提供了含有本发明化合物的制药组合物,并提供了使用本发明化合物和组合物治疗代谢相关疾病的方法,包括血脂异常、动脉粥样硬化、冠心病、胰岛素抵抗、2型糖尿病、X综合症等。此外,本发明还提供了将本发明化合物与属于α-葡萄糖苷酶抑制剂、醛还原酶抑制剂、双胍类药物、HMG-CoA还原酶抑制剂、角鲨烷合成抑制剂、费布拉特类药物、LDL降解增强剂、血管紧张素转化酶(ACE)抑制剂、胰岛素分泌增强剂等类别的其他活性剂结合使用的方法。
  • Niacin receptor agonists, compositions containing such compounds and methods of treatment
    申请人:Imbriglio Jason E.
    公开号:US20090054423A1
    公开(公告)日:2009-02-26
    The present invention encompasses compounds of Formula I: as well as pharmaceutically acceptable salts and hydrates thereof, that are useful for treating dyslipidemias. Pharmaceutical compositions and methods of use are also included.
    本发明涵盖了I式化合物,以及其药学上可接受的盐和水合物,用于治疗血脂异常。此外,还包括药物组合物和使用方法。
  • TETRAZOLE DERIVATIVES AND METHODS OF TREATMENT OF METABOLIC-RELATED DISORDERS THEREOF
    申请人:Arena Pharmaceuticals, Inc.
    公开号:EP1599469A1
    公开(公告)日:2005-11-30
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