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

3-({[(1R)-1-(2,4-difluorophenyl)propyl](pyrazolo[1,5-a]pyridin-2-ylcarbonyl)amino}methyl)benzoic acid | 1398582-68-7

中文名称
——
中文别名
——
英文名称
3-({[(1R)-1-(2,4-difluorophenyl)propyl](pyrazolo[1,5-a]pyridin-2-ylcarbonyl)amino}methyl)benzoic acid
英文别名
3-[[[(1R)-1-(2,4-difluorophenyl)propyl]-(pyrazolo[1,5-a]pyridine-2-carbonyl)amino]methyl]benzoic acid
3-({[(1R)-1-(2,4-difluorophenyl)propyl](pyrazolo[1,5-a]pyridin-2-ylcarbonyl)amino}methyl)benzoic acid化学式
CAS
1398582-68-7
化学式
C25H21F2N3O3
mdl
——
分子量
449.457
InChiKey
LWTRPOBSYVDNTC-HSZRJFAPSA-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):
    4.5
  • 重原子数:
    33
  • 可旋转键数:
    7
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.16
  • 拓扑面积:
    74.9
  • 氢给体数:
    1
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    3-甲醛苯甲酸甲酯 在 sodium tetrahydroborate 、 、 O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate 、 三乙胺 、 sodium hydroxide 作用下, 以 甲醇二氯甲烷 为溶剂, 反应 3.17h, 生成 3-({[(1R)-1-(2,4-difluorophenyl)propyl](pyrazolo[1,5-a]pyridin-2-ylcarbonyl)amino}methyl)benzoic acid
    参考文献:
    名称:
    Discovery of a Selective TRPM8 Antagonist with Clinical Efficacy in Cold-Related Pain
    摘要:
    The transient receptor potential (TRP) family of ion channels comprises nonselective cation channels that respond to a wide range of chemical and thermal stimuli. TRPM8, a member of the melastatin subfamily, is activated by cold temperatures (<28 degrees C), and antagonists of this channel have the potential to treat cold induced allodynia and hyperalgesia. However, TRPM8 has also been implicated in mammalian thermoregulation and antagonists have the potential to induce hypothermia in patients. We report herein the identification and optimization of a series of TRPM8 antagonists that ultimately led to the discovery of PF-05105679. The clinical finding with this compound will be discussed, including both efficacy and its ability to affect thermoregulation processes in humans.
    DOI:
    10.1021/ml500479v
点击查看最新优质反应信息

文献信息

  • [EN] ARYL SUBSTITUTED CARBOXAMIDE DERIVATIVES AS TRPM8 MODULATORS<br/>[FR] DÉRIVÉS DE CARBOXAMIDE SUBSTITUÉS PAR ARYLE EN TANT QUE MODULATEURS DE TRPM8
    申请人:PFIZER LTD
    公开号:WO2012120398A1
    公开(公告)日:2012-09-13
    The invention provides a compound of the formula (I): wherein A, R1, R2 and R3 are as defined herein, or a pharmaceutically acceptable salt thereof. Such compounds are small molecule TRPM8 blockers and therefore useful in the propylaxis or treatment of a wide range of diseases, conditions or syndromes, including cold allodynia and Raynaulds syndrome.
    本发明提供了一种化合物,其化学式为(I):其中A、R1、R2和R3如本文所定义,或其药学上可接受的盐。这些化合物是小分子TRPM8阻断剂,因此在预防或治疗包括寒冷痛觉异常和雷诺综合征在内的各种疾病、症状或综合征中有用。
  • Discovery of a Selective TRPM8 Antagonist with Clinical Efficacy in Cold-Related Pain
    作者:Mark D. Andrews、Kerry af Forselles、Kevin Beaumont、Sébastien R. G. Galan、Paul A. Glossop、Mathilde Grenie、Alan Jessiman、Amy S. Kenyon、Graham Lunn、Graham Maw、Robert M. Owen、David C. Pryde、Dannielle Roberts、Thien Duc Tran
    DOI:10.1021/ml500479v
    日期:2015.4.9
    The transient receptor potential (TRP) family of ion channels comprises nonselective cation channels that respond to a wide range of chemical and thermal stimuli. TRPM8, a member of the melastatin subfamily, is activated by cold temperatures (<28 degrees C), and antagonists of this channel have the potential to treat cold induced allodynia and hyperalgesia. However, TRPM8 has also been implicated in mammalian thermoregulation and antagonists have the potential to induce hypothermia in patients. We report herein the identification and optimization of a series of TRPM8 antagonists that ultimately led to the discovery of PF-05105679. The clinical finding with this compound will be discussed, including both efficacy and its ability to affect thermoregulation processes in humans.
查看更多

同类化合物

西卡唑酯 维利西呱 盐酸依他唑酯 月桂41-2272 月桂-41-8543 异丁司特 吡唑并[5,1-f]吡啶-6-甲醛 吡唑并[1,5-a]吡啶-7-羧酸 吡唑并[1,5-a]吡啶-7-甲醇 吡唑并[1,5-a]吡啶-7-甲胺 吡唑并[1,5-a]吡啶-5-醇 吡唑并[1,5-a]吡啶-5-胺 吡唑并[1,5-a]吡啶-5-羧醛 吡唑并[1,5-a]吡啶-5-羧酸 吡唑并[1,5-a]吡啶-5-基甲醇 吡唑并[1,5-a]吡啶-4-醇 吡唑并[1,5-a]吡啶-4-羧酸乙酯 吡唑并[1,5-a]吡啶-4-羧酸 吡唑并[1,5-a]吡啶-4-甲醛 吡唑并[1,5-a]吡啶-3-胺盐酸盐 吡唑并[1,5-a]吡啶-3-胺 吡唑并[1,5-a]吡啶-3-羧酸甲酯 吡唑并[1,5-a]吡啶-3-羧酸 吡唑并[1,5-a]吡啶-3-甲醛 吡唑并[1,5-a]吡啶-3-甲酰胺 吡唑并[1,5-a]吡啶-3-甲胺 吡唑并[1,5-a]吡啶-3-基甲醇 吡唑并[1,5-a]吡啶-3-基乙腈 吡唑并[1,5-a]吡啶-3,7-二醇 吡唑并[1,5-a]吡啶-3,7-二胺 吡唑并[1,5-a]吡啶-3,6-二胺 吡唑并[1,5-a]吡啶-3,5-二胺 吡唑并[1,5-a]吡啶-3,4-二胺 吡唑并[1,5-a]吡啶-2-羧醛 吡唑并[1,5-a]吡啶-2-碳酰肼 吡唑并[1,5-a]吡啶-2-甲醇 吡唑并[1,5-a]吡啶-2-甲酸甲酯 吡唑并[1,5-a]吡啶-2-甲酸 吡唑并[1,5-a]吡啶-2-甲胺 吡唑并[1,5-a]吡啶-2,3-二胺 吡唑并[1,5-a]吡啶-2,3-二甲酸二甲酯 吡唑并[1,5-a]吡啶-2,3-二甲酸二乙酯 吡唑并[1,5-a]吡啶-2(1H)-酮 吡唑并[1,5-a]吡啶 吡唑并[1,5-A〕吡啶-3,5-二羧酸-3-乙基 吡唑并[1,5-A]吡啶-7-甲酰胺 吡唑并[1,5-A]吡啶-7-甲腈 吡唑并[1,5-A]吡啶-5-甲腈 吡唑并[1,5-A]吡啶-3-硼酸 吡唑并[1,5-A]吡啶-3-硫代甲酰胺