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6-[4-[ (2-phenylpyrrolidin-1-yl)methyl]phenoxy]pyridine-3-carboxamide

中文名称
——
中文别名
——
英文名称
6-[4-[ (2-phenylpyrrolidin-1-yl)methyl]phenoxy]pyridine-3-carboxamide
英文别名
(+/-)-6-[4-(2-phenyl-pyrrolidin-1-ylmethyl)-phenoxy]-nicotinamide;6-[4-[(2-Phenyl-1-pyrrolidinyl)methyl]phenoxy]-3-pyridinecarboxamide;6-[4-[(2-phenylpyrrolidin-1-yl)methyl]phenoxy]pyridine-3-carboxamide
6-[4-[ (2-phenylpyrrolidin-1-yl)methyl]phenoxy]pyridine-3-carboxamide化学式
CAS
——
化学式
C23H23N3O2
mdl
——
分子量
373.455
InChiKey
WZVUQWRQADDXOE-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):
    3.4
  • 重原子数:
    28
  • 可旋转键数:
    6
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    68.4
  • 氢给体数:
    1
  • 氢受体数:
    4

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

  • 作为反应物:
    描述:
    6-[4-[ (2-phenylpyrrolidin-1-yl)methyl]phenoxy]pyridine-3-carboxamide盐酸 作用下, 以 1,4-二氧六环 为溶剂, 以3.9%的产率得到(+/-)-6-[4-(2-phenyl-pyrrolidin-1-ylmethyl)-phenoxy]-nicotinamide hydrochloride
    参考文献:
    名称:
    [EN] DIARYL ETHERS AS OPIOID RECEPTOR ANTAGONIST
    [FR] DIARYLE ETHERS UTILISES EN TANT QU'ANTAGONISTES DE RECEPTEUR OPIOIDES
    摘要:
    公式(I)的化合物,其中变量X1至X10,R1至R7包括R3',E,v,y,z,A和B如所述,或其药用盐,溶剂化物,对映体,消旋体,非对映异构体或其混合物,用于治疗、预防或改善肥胖和相关疾病。
    公开号:
    WO2004026305A1
  • 作为产物:
    参考文献:
    名称:
    Discovery of Aminobenzyloxyarylamides as κ Opioid Receptor Selective Antagonists: Application to Preclinical Development of a κ Opioid Receptor Antagonist Receptor Occupancy Tracer
    摘要:
    Arylphenylpyrrolidinylmethylphenoxybenzamides were found to have high affinity and selectivity for K opioid receptors. On the basis of receptor binding assays in Chinese hamster ovary (CHO) cells expressing cloned human opioid receptors, (S)-3-fluoro-4-(4-((2-(3-fluorophenyppyrrolidin-1-yl)methyl)phenoxy)benzamide (25) had a K-i = 0.565 nM for kappa opioid receptor binding while having a K-i = 35.8 nM for mu opioid receptors and a K-i = 211 nM for delta opioid receptor binding. Compound 25 was also a potent antagonist of K opioid receptors when tested in vitro using a [S-35]-guanosine 5'O-[3-thiotriphosphate] ([S-35]GTP-gamma-S) functional assay in CHO cells expressing cloned human opioid receptors. Compounds were also evaluated for potential use as receptor occupancy tracers. Tracer evaluation was done in vivo, using liquid chromatography-tandem mass spectrometry (LC/MS/MS) methods, precluding the need for radiolabeling. (S)-3-Chloro-4-(4-((2-(pyridine-3-yl(pyrrolidin-1-yl)methyl)phenoxy)benzamide (18) was found to have favorable properties for a tracer for receptor occupancy, including good specific versus nonspecific binding and good brain uptake.
    DOI:
    10.1021/jm200789r
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文献信息

  • HETEROARYLPHENOXY BENZAMIDE KAPPA OPIOID LIGANDS
    申请人:Pfizer Inc.
    公开号:US20180148432A1
    公开(公告)日:2018-05-31
    The present invention provides compounds of Formula I: and pharmaceutically acceptable salts thereof wherein the variables R 1 , R 2 , R 3 , R 4 , R 9 , X, m and n are as defined herein; processes for the preparation of; intermediates used in the preparation of; and compositions containing such compounds or salts, and their uses for treating kappa opioid (κ-opioid) associated disorders including, e.g., a neurological disorder, or psychiatric disorder such as a neurocognitive disorder, substance abuse disorder, depressive disorder, anxiety disorder, trauma and stressor related disorder and feeding and eating disorder.
    本发明提供了Formula I的化合物及其药用盐,其中变量R1、R2、R3、R4、R9、X、m和n如本文所定义;制备方法;用于制备的中间体;含有这些化合物或盐的组合物,以及它们用于治疗κ-阿片受体相关疾病的用途,例如神经系统疾病,或精神障碍,如神经认知障碍、物质滥用障碍、抑郁障碍、焦虑障碍、创伤和应激相关障碍以及进食障碍。
  • Diaryl ethers as opioid receptor antagonist
    申请人:Blanco-Pillado Maria-Jesus
    公开号:US20060217372A1
    公开(公告)日:2006-09-28
    A compound of the formula (I) wherein the variables X 1 to X 10 , R 1 to R 7 including R 3′ , E, v, y, z, A and B are as described, or a pharmaceutically acceptable salt, solvate, enantiomer, racemate, diastereomer or mixtures thereof, useful for the treatment, prevention or amelioration of obesity and Related Diseases is disclosed.
    本发明公开了一种化合物(I)的公式,其中变量X1至X10,R1至R7包括R3',E,v,y,z,A和B如所述,或其药学上可接受的盐,溶剂合物,对映体,外消旋体,非对映体异构体或其混合物,用于治疗、预防或缓解肥胖和相关疾病。
  • DIARYL ETHERS AS OPIOID RECEPTOR ANTAGONISTS
    申请人:Blanco-Pillado Maria-Jesus
    公开号:US20080255152A1
    公开(公告)日:2008-10-16
    A compound of the formula (I) wherein the variables X 1 to X 10 , R 1 to R 7 including R 3′ , E, v, y, z, A and B are as described, or a pharmaceutically acceptable salt, solvate, enantiomer, racemate, diastereomer or mixtures thereof, useful for the treatment, prevention or amelioration of obesity and Related Diseases is disclosed.
    本发明揭示了一种式(I)的化合物,其中变量X1至X10,R1至R7包括R3′,E,v,y,z,A和B如所述,或其药学上可接受的盐,溶剂合物,对映体,外消旋体,非对映体异构体或其混合物,用于治疗、预防或改善肥胖和相关疾病。
  • Heteroarylphenoxy benzamide kappa opioid ligands
    申请人:Pfizer Inc.
    公开号:US10316021B2
    公开(公告)日:2019-06-11
    The present invention provides compounds of Formula I: and pharmaceutically acceptable salts thereof wherein the variables R1, R2, R3, R4, R9, X, m and n are as defined herein; processes for the preparation of; intermediates used in the preparation of; and compositions containing such compounds or salts, and their uses for treating kappa opioid (κ-opioid) associated disorders including, e.g., a neurological disorder, or psychiatric disorder such as a neurocognitive disorder, substance abuse disorder, depressive disorder, anxiety disorder, trauma and stressor related disorder and feeding and eating disorder.
    本发明提供了式 I 的化合物: 及其药学上可接受的盐,其中变量 R1、R2、R3、R4、R9、X、m 和 n 如本文所定义;制备工艺;制备工艺中使用的中间体;以及含有此类化合物或盐的组合物,及其用于治疗卡巴阿片(κ-阿片)相关紊乱的用途,例如包括神经紊乱或精神紊乱,如神经认知紊乱、药物滥用紊乱、抑郁紊乱、焦虑紊乱、创伤和应激相关紊乱以及进食和饮食紊乱。
  • US7381719B2
    申请人:——
    公开号:US7381719B2
    公开(公告)日:2008-06-03
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