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6-[4-(2-oxo-propyl)-phenoxy]-nicotinamide | 189120-10-3

中文名称
——
中文别名
——
英文名称
6-[4-(2-oxo-propyl)-phenoxy]-nicotinamide
英文别名
6-[4-(2-Oxopropyl)phenoxy]pyridine-3-carboxamide
6-[4-(2-oxo-propyl)-phenoxy]-nicotinamide化学式
CAS
189120-10-3
化学式
C15H14N2O3
mdl
——
分子量
270.288
InChiKey
WQIKBKXJHGJQBA-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:
    20
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    82.3
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    6-[4-(2-oxo-propyl)-phenoxy]-nicotinamide(S)-4-[2-hydroxy-3-aminopropoxy]-1,3-dihydro-2H-benzimidazol-2-one 在 sodium cyanoborohydride 、 溶剂黄146 作用下, 以 甲醇 为溶剂, 反应 24.0h, 生成 6-[4-[2-[[(2S)-2-hydroxy-3-[(2-oxo-1,3-dihydrobenzimidazol-4-yl)oxy]propyl]amino]propyl]phenoxy]pyridine-3-carboxamide
    参考文献:
    名称:
    Potent benzimidazolone based human β3-adrenergic receptor agonists
    摘要:
    The synthesis and biological evaluation of a series of benzimidazolone beta(3) adrenergic receptor agonists are described. A trend toward the reduction of rat atrial tachycardia upon increasing steric bulk at the 3-position of the benzimidazolone moiety was observed. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2006.08.010
  • 作为产物:
    描述:
    6-氯烟酰胺4-羟基苯基丙酮potassium carbonate 作用下, 以 N,N-二甲基乙酰胺 为溶剂, 反应 2.5h, 以44%的产率得到6-[4-(2-oxo-propyl)-phenoxy]-nicotinamide
    参考文献:
    名称:
    Potent benzimidazolone based human β3-adrenergic receptor agonists
    摘要:
    The synthesis and biological evaluation of a series of benzimidazolone beta(3) adrenergic receptor agonists are described. A trend toward the reduction of rat atrial tachycardia upon increasing steric bulk at the 3-position of the benzimidazolone moiety was observed. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2006.08.010
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文献信息

  • [EN] DIARYL ETHERS AS OPIOID RECEPTOR ANTAGONIST<br/>[FR] DIARYLE ETHERS UTILISES EN TANT QU'ANTAGONISTES DE RECEPTEUR OPIOIDES
    申请人:LILLY CO ELI
    公开号:WO2004026305A1
    公开(公告)日:2004-04-01
    A compound of the formula (I) wherein the variables X1 to X10, R1 to R7 including R3', 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.
    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。
  • 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。
  • US7381719B2
    申请人:——
    公开号:US7381719B2
    公开(公告)日:2008-06-03
  • US7560463B2
    申请人:——
    公开号:US7560463B2
    公开(公告)日:2009-07-14
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