摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

4-(cyclopropylamino)-1-methylcyclohexanol | 1346555-37-0

中文名称
——
中文别名
——
英文名称
4-(cyclopropylamino)-1-methylcyclohexanol
英文别名
4-(cyclopropylamino)-1-methylcyclohexan-1-ol
4-(cyclopropylamino)-1-methylcyclohexanol化学式
CAS
1346555-37-0
化学式
C10H19NO
mdl
——
分子量
169.267
InChiKey
ZVNBKTDGJXJERI-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):
    1.2
  • 重原子数:
    12
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    32.3
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    4-(cyclopropylamino)-1-methylcyclohexanol 在 O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate 、 N,N-二异丙基乙胺 作用下, 以 乙腈 为溶剂, 生成 N-cyclopropyl-N-((1r,4r)-4-hydroxy-4-methylcyclohexyl)-6-(piperidin-1-yl)picolinamide
    参考文献:
    名称:
    吡啶甲酰胺类强效抑制剂11β-羟类固醇脱氢酶(11β-HSD1)的合成和生物学评估
    摘要:
    描述了一系列6-取代的吡啶甲酰胺衍生物的合成及其对1β-11β-羟基类固醇脱氢酶的抑制活性。初始命中化合物的优化,ñ -环己基-6-(哌啶-1-基)吡啶甲酰胺(1从高吞吐量内部文库的筛选)导致高度有效的和代谢稳定的化合物的发现25,这是有效在小鼠离体药效学模型中降低剂量,并在口服后降低了HF / STZ小鼠模型中的空腹血糖和胰岛素水平。
    DOI:
    10.1016/j.bmcl.2014.11.074
  • 作为产物:
    参考文献:
    名称:
    吡啶甲酰胺类强效抑制剂11β-羟类固醇脱氢酶(11β-HSD1)的合成和生物学评估
    摘要:
    描述了一系列6-取代的吡啶甲酰胺衍生物的合成及其对1β-11β-羟基类固醇脱氢酶的抑制活性。初始命中化合物的优化,ñ -环己基-6-(哌啶-1-基)吡啶甲酰胺(1从高吞吐量内部文库的筛选)导致高度有效的和代谢稳定的化合物的发现25,这是有效在小鼠离体药效学模型中降低剂量,并在口服后降低了HF / STZ小鼠模型中的空腹血糖和胰岛素水平。
    DOI:
    10.1016/j.bmcl.2014.11.074
点击查看最新优质反应信息

文献信息

  • PICOLINAMIDE AND PYRIMIDINE-4-CARBOXAMIDE COMPOUNDS, PROCESS FOR PREPARING AND PHAMACEUTICAL COMPOSITION COMPRISING THE SAME
    申请人:Ryu Je Ho
    公开号:US20130210811A1
    公开(公告)日:2013-08-15
    Provided are picolinamide and pyrimidine-4-carboxamide compounds, a method for preparing the same, a pharmaceutical composition containing the same, and a medical use using the compound as an agent for preventing, regulating, and treating diseases related to regulation of glucocorticoids by using selective inhibitory activity of the compound for an 11β-HSD1 enzyme. The picolinamide and pyrimidine-4-carboxamide compounds of the present invention are selective inhibitors of human-derived 11β-HSD1 enzymes, and are useful in an agent for preventing, regulating, and treating diseases related to glucocorticoid regulation in which human-derived 11β-HSD1 enzymes are involved, for example, metabolic syndromes such as, type 1 and type 2 diabetes, diabetes later complications, latent autoimmune diabetes adult (LADA), insulin tolerance syndromes, obesity, impaired glucose tolerance (IGT), impaired fasting glucose (IFG), damaged glucose tolerance, dyslipidemia, atherosclerosis, hypertension, etc.
    本发明提供了吡啶甲酰胺和嘧啶-4-羧酰胺化合物、制备方法、含有该化合物的制药组合物以及使用该化合物作为11β-HSD1酶的选择性抑制剂,用于预防、调节和治疗与糖皮质激素调节相关的疾病的医疗用途。本发明的吡啶甲酰胺和嘧啶-4-羧酰胺化合物是人源11β-HSD1酶的选择性抑制剂,可用于预防、调节和治疗与人源11β-HSD1酶参与的糖皮质激素调节相关疾病,例如代谢综合征,如1型和2型糖尿病、糖尿病后并发症、成人隐形自身免疫性糖尿病(LADA)、胰岛素耐受综合征、肥胖症、糖耐量受损(IGT)、空腹血糖受损(IFG)、糖耐量受损、血脂异常、动脉粥样硬化、高血压等。
  • Picolinamide and pyrimidine-4-carboxamide compounds, process for preparing and pharmaceutical composition comprising the same
    申请人:Ryu Je Ho
    公开号:US09096571B2
    公开(公告)日:2015-08-04
    Provided are picolinamide and pyrimidine-4-carboxamide compounds, a method for preparing the same, a pharmaceutical composition containing the same, and a medical use using the compound as an agent for preventing, regulating, and treating diseases related to regulation of glucocorticoids by using selective inhibitory activity of the compound for an 11β-HSD1 enzyme. The picolinamide and pyrimidine-4-carboxamide compounds of the present invention are selective inhibitors of human-derived 11β-HSD1 enzymes, and are useful in an agent for preventing, regulating, and treating diseases related to glucocorticoid regulation in which human-derived 11β-HSD1 enzymes are involved, for example, metabolic syndromes such as, type 1 and type 2 diabetes, diabetes later complications, latent autoimmune diabetes adult (LADA), insulin tolerance syndromes, obesity, impaired glucose tolerance (IGT), impaired fasting glucose (IFG), damaged glucose tolerance, dyslipidemia, atherosclerosis, hypertension, etc.
    本发明提供了吡啶甲酰胺和嘧啶-4-羧酰胺化合物、其制备方法、含有该化合物的药物组合物,以及使用该化合物作为11β-HSD1酶的选择性抑制活性的药剂来预防、调节和治疗与糖皮质激素调节相关的疾病的医疗用途。本发明的吡啶甲酰胺和嘧啶-4-羧酰胺化合物是人源11β-HSD1酶的选择性抑制剂,在预防、调节和治疗与人源11β-HSD1酶相关的糖皮质激素调节疾病中非常有用,例如代谢综合征、1型和2型糖尿病、糖尿病后并发症、成人潜在自身免疫性糖尿病、胰岛素耐量综合征、肥胖症、糖耐量受损、空腹血糖受损、糖耐量受损、血脂异常、动脉硬化和高血压等。
  • [EN] PICOLINAMIDE AND PYRIMIDINE-4-CARBOXAMIDE COMPOUNDS, PROCESS FOR PREPARING AND PHAMACEUTICAL COMPOSITION COMPRISING THE SAME<br/>[FR] COMPOSÉS DE PICOLINAMIDE ET DE PYRIMIDINE-4-CARBOXAMIDE, LEUR PROCÉDÉ DE PRÉPARATION ET COMPOSITION PHARMACEUTIQUE LES COMPRENANT
    申请人:SK CHEMICALS CO LTD
    公开号:WO2011139107A3
    公开(公告)日:2012-05-18
  • Optimization of novel di-substituted cyclohexylbenzamide derivatives as potent 11β-HSD1 inhibitors
    作者:Dustin L. McMinn、Yosup Rew、Athena Sudom、Seb Caille、Michael DeGraffenreid、Xiao He、Randall Hungate、Ben Jiang、Juan Jaen、Lisa D. Julian、Jacob Kaizerman、Perry Novak、Daqing Sun、Hua Tu、Stefania Ursu、Nigel P.C. Walker、Xuelei Yan、Qiuping Ye、Zhulun Wang、Jay P. Powers
    DOI:10.1016/j.bmcl.2009.01.026
    日期:2009.3
    Novel 4,4-disubstituted cyclohexylbenzamide inhibitors of 11beta-HSD1 were optimized to account for liabilities relating to in vitro pharmacokinetics, cytotoxicity and protein-related shifts in potency. A representative compound showing favorable in vivo pharmacokinetics was found to be an efficacious inhibitor of 11beta-HSD1 in a rat pharmacodynamic model (ED(50)=10mg/kg).
  • PICOLINAMIDE AND PYRIMIDINE-4-CARBOXAMIDE COMPOUNDS, PROCESS FOR PREPARING AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME
    申请人:Sk Chemicals Co., Ltd.
    公开号:EP2566859B1
    公开(公告)日:2016-12-21
查看更多