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5-(azidecarbonyl)nicotinic acid methyl ester | 915391-81-0

中文名称
——
中文别名
——
英文名称
5-(azidecarbonyl)nicotinic acid methyl ester
英文别名
methyl 5-(azidocarbonyl)nicotinate;Methyl 5-(azidocarbonyl)nicotinate;methyl 5-carbonazidoylpyridine-3-carboxylate
5-(azidecarbonyl)nicotinic acid methyl ester化学式
CAS
915391-81-0
化学式
C8H6N4O3
mdl
——
分子量
206.161
InChiKey
JTFBJGCXRXIYRK-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):
    1.5
  • 重原子数:
    15
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    70.6
  • 氢给体数:
    0
  • 氢受体数:
    5

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

反应信息

点击查看最新优质反应信息

文献信息

  • Pyrrolidine derivative or salt thereof
    申请人:Hachiya Shunichiro
    公开号:US20090062366A1
    公开(公告)日:2009-03-05
    [Problem] To provide a compound which may be used in treating diseases in which a calcium sensing receptor (CaSR) is concerned, particularly hyperparathyroidism. [Means for Resolution] It was found that novel pyrrolidine derivatives which are characterized by the possession of aminomethyl group substituted with arylalkyl group or the like, or salts thereof, have excellent CaSR agonistic regulatory activity and also have excellent selectivity with CYP2D6 inhibitory activity having a possibility of causing drug interaction. Based on the above, these novel pyrrolidine derivatives are useful as therapeutic agents for treating diseases in which CaSR is concerned (hyperparathyroidism, renal osteodystrophy, hypercalcemia and the like).
    [问题] 提供一种可用于治疗钙敏感受体(CaSR)相关疾病,特别是甲状旁腺功能亢进症的化合物。 [解决方法] 发现了一种新型吡咯烷衍生物,其特征在于具有氨甲基基团,该基团被芳基烷基或类似物取代,或其盐,具有出色的CaSR激动调节活性,并且具有出色的选择性与CYP2D6抑制活性,可能导致药物相互作用。基于以上发现,这些新型吡咯烷衍生物可用作治疗CaSR相关疾病(甲状旁腺功能亢进症,肾性骨营养不良,高钙血症等)的治疗剂。
  • UREA COMPOUND OR SALT THEREOF
    申请人:Ishii Takahiro
    公开号:US20110172230A1
    公开(公告)日:2011-07-14
    [Object] To provide a compound which can be used for the treatment of a disease associated with fatty acid amide hydrolase (FAAH), particularly urinary frequency, urinary incontinence and/or overactive bladder. [Means for solution] It is confirmed that a urea compound chemical-structurally characterized by having a piperidine or piperazine ring or a salt thereof has an excellent FAAH-inhibitory activity, and thus the present invention is completed. The urea compound or its pharmaceutically acceptable salt of the present invention can increase the effective bladder capacity and ameliorate the state of urinary frequency, and is therefore useful as an agent for treating urinary frequency, urinary incontinence and/or overactive bladder.
    [目的] 提供一种化合物,可用于治疗与脂肪酸酰胺水解酶(FAAH)相关的疾病,特别是尿频、尿失禁和/或膀胱过度活动。 [解决方案] 确认具有哌啶或哌嗪环或其盐的尿素化合物在化学结构上具有出色的FAAH抑制活性,因此完成了本发明。本发明的尿素化合物或其药学上可接受的盐可以增加有效膀胱容量,改善尿频状态,因此可用作治疗尿频、尿失禁和/或膀胱过度活动的药物。
  • PYRROLIDINE DERIVATIVE OR SALT THEREOF
    申请人:Astellas Pharma Inc.
    公开号:EP1882684A1
    公开(公告)日:2008-01-30
    [Problem] To provide a compound which may be used in treating diseases in which a calcium sensing receptor (CaSR) is concerned, particularly hyperparathyroidism. [Means for Resolution] It was found that novel pyrrolidine derivatives which are characterized by the possession of aminomethyl group substituted with arylalkyl group or the like, or salts thereof, have excellent CaSR agonistic regulatory activity and also have excellent selectivity with CYP2D6 inhibitory activity having a possibility of causing drug interaction. Based on the above, these novel pyrrolidine derivatives are useful as therapeutic agents for treating diseases in which CaSR is concerned (hyperparathyroidism, renal osteodystrophy, hypercalcemia and the like).
    [问题]提供一种可用于治疗钙传感受体(CaSR)相关疾病,特别是甲状旁腺机能亢进症的化合物。 [解决方法] 研究发现,新型吡咯烷衍生物(其特征在于具有被芳基烷基或类似基团取代的氨甲基)或其盐具有优异的 CaSR 激动调节活性,同时还具有优异的选择性和 CYP2D6 抑制活性,但有可能引起药物相互作用。基于以上所述,这些新型吡咯烷衍生物可作为治疗剂用于治疗与 CaSR 有关的疾病(甲状旁腺机能亢进症、肾性骨营养不良症、高钙血症等)。
  • US7585886B2
    申请人:——
    公开号:US7585886B2
    公开(公告)日:2009-09-08
  • WO2006/123725
    申请人:——
    公开号:——
    公开(公告)日:——
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