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methyl 2-[4-({(tert-butoxycarbonyl)[(1R)-1-(1-naphthyl)ethyl]amino}methyl)-3-(3-fluorophenyl)piperidin-1-yl]-1,3-benzoxazole-5-carboxylate | 1027707-35-2

中文名称
——
中文别名
——
英文名称
methyl 2-[4-({(tert-butoxycarbonyl)[(1R)-1-(1-naphthyl)ethyl]amino}methyl)-3-(3-fluorophenyl)piperidin-1-yl]-1,3-benzoxazole-5-carboxylate
英文别名
methyl 2-[3-(3-fluorophenyl)-4-[[(2-methylpropan-2-yl)oxycarbonyl-[(1R)-1-naphthalen-1-ylethyl]amino]methyl]piperidin-1-yl]-1,3-benzoxazole-5-carboxylate
methyl 2-[4-({(tert-butoxycarbonyl)[(1R)-1-(1-naphthyl)ethyl]amino}methyl)-3-(3-fluorophenyl)piperidin-1-yl]-1,3-benzoxazole-5-carboxylate化学式
CAS
1027707-35-2
化学式
C38H40FN3O5
mdl
——
分子量
637.751
InChiKey
OBKNXWYFFDDORN-SPWTXMEKSA-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):
    8.3
  • 重原子数:
    47
  • 可旋转键数:
    10
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.34
  • 拓扑面积:
    85.1
  • 氢给体数:
    0
  • 氢受体数:
    8

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

文献信息

  • PIPERIDINE DERIVATIVE OR SALT THEREOF
    申请人:Hachiya Shunichiro
    公开号:US20100029687A1
    公开(公告)日:2010-02-04
    [Problem] To provide a compound which can be used for treating diseases in which a calcium sensing receptor (CaSR) participates, particularly hyperparathyroidism. [Means for Resolution] It was found that a novel piperidine derivative which is characterized in that one of a 3-position and a 4-position is substituted with an aminomethyl group substituted with an arylalkyl group or the like and the other position is substituted with aryl, heteroaryl or the like, or a salt thereof, has an excellent CaSR agonistic regulatory action, and also has excellent selectivity with a CYP2D6 inhibitory action having a possibility of causing drug interaction. Based on the above, this novel piperidine derivative is useful as a therapeutic agent for diseases in which CaSR participates (hyperparathyroidism, renal osteodystrophy, hypercalcemia, and the like).
    【问题】提供一种化合物,可用于治疗感受受体(CaSR)参与的疾病,特别是甲状旁腺功能亢进症。【解决方法】发现一种新的哌啶生物,其特征在于3位和4位中的一个位置被取代为含有芳基烷基等基团的甲基基团,另一个位置被取代为芳基、杂环芳基等,或其盐,具有出色的CaSR激动调节作用,并且具有出色的选择性,具有可能引起药物相互作用的CYP2D6抑制作用。基于以上发现,这种新的哌啶生物可用作治疗CaSR参与的疾病(甲状旁腺功能亢进症、肾性骨营养不良、高血症等)的治疗剂。
  • Piperidine derivative or salt thereof
    申请人:Astellas Pharma, Inc.
    公开号:US08153658B2
    公开(公告)日:2012-04-10
    To provide a compound which can be used for treating diseases in which a calcium sensing receptor (CaSR) participates, particularly hyperparathyroidism. It was found that a novel piperidine derivative which is characterized in that one of a 3-position and a 4-position is substituted with an aminomethyl group substituted with an arylalkyl group or the like and the other position is substituted with aryl, heteroaryl or the like, or a salt thereof, has an excellent CaSR agonistic regulatory action, and also has excellent selectivity with a CYP2D6 inhibitory action having a possibility of causing drug interaction. Based on the above, this novel piperidine derivative is useful as a therapeutic agent for diseases in which CaSR participates (hyperparathyroidism, renal osteodystrophy, hypercalcemia, and the like).
    提供一种可以用于治疗感受受体(CaSR)参与的疾病,特别是甲状旁腺功能亢进症的化合物。发现一种新的哌啶生物,其特征在于3位和4位之一被取代为甲基基团,该甲基基团被取代为芳基烷基基团或类似物,另一位置被取代为芳基,杂环芳基或类似物,或其盐,具有出色的CaSR激动调节作用,并且具有出色的选择性,具有可能引起药物相互作用的CYP2D6抑制作用。基于以上发现,这种新的哌啶生物可用作治疗CaSR参与的疾病(甲状旁腺功能亢进症,肾性骨营养不良,高血症等)的治疗剂。
  • PIPERIDINE DERIVATIVES OR SALTS THEREOF
    申请人:Astellas Pharma Inc.
    公开号:EP2085383A1
    公开(公告)日:2009-08-05
    [Problem] To provide a compound which can be used for treating diseases in which a calcium sensing receptor (CaSR) participates, particularly hyperparathyroidism. [Means for Resolution] It was found that a novel piperidine derivative which is characterized in that one of a 3-position and a 4-position is substituted with an aminomethyl group substituted with an arylalkyl group or the like and the other position is substituted with aryl, heteroaryl or the like, or a salt thereof, has an excellent CaSR agonistic regulatory action, and also has excellent selectivity with a CYP2D6 inhibitory action having a possibility of causing drug interaction. Based on the above, this novel piperidine derivative is useful as a therapeutic agent for diseases in which CaSR participates (hyperparathyroidism, renal osteodystrophy, hypercalcemia, and the like).
    [问题]提供一种可用于治疗传感受体(CaSR)参与的疾病,特别是甲状旁腺机能亢进的化合物。 [解决方法]发现一种新型哌啶生物,其特征在于 3 位和 4 位中的一个被甲基取代,另一个被芳基、杂芳基等取代,或其盐具有极好的 CaSR 激动调节作用,同时还具有极好的选择性,具有 CYP2D6 抑制作用,但有可能引起药物相互作用。基于以上所述,这种新型哌啶生物可作为治疗剂用于治疗 CaSR 参与的疾病(甲状旁腺功能亢进症、肾性骨营养不良症、高血症等)。
  • US8153658B2
    申请人:——
    公开号:US8153658B2
    公开(公告)日:2012-04-10
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