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(8-{2-[4-(2-methyl-5-quinolinyl)-1-piperazinyl]ethyl}-3-oxo-2,3-dihydro-4H-1,4-benzoxazin-4-yl)acetic acid | 876921-55-0

中文名称
——
中文别名
——
英文名称
(8-{2-[4-(2-methyl-5-quinolinyl)-1-piperazinyl]ethyl}-3-oxo-2,3-dihydro-4H-1,4-benzoxazin-4-yl)acetic acid
英文别名
2-[8-[2-[4-(2-methylquinolin-5-yl)piperazin-1-yl]ethyl]-3-oxo-1,4-benzoxazin-4-yl]acetic acid
(8-{2-[4-(2-methyl-5-quinolinyl)-1-piperazinyl]ethyl}-3-oxo-2,3-dihydro-4H-1,4-benzoxazin-4-yl)acetic acid化学式
CAS
876921-55-0
化学式
C26H28N4O4
mdl
——
分子量
460.533
InChiKey
XRPNNQIDJKKQMD-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):
    0.9
  • 重原子数:
    34
  • 可旋转键数:
    6
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    86.2
  • 氢给体数:
    1
  • 氢受体数:
    7

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

  • [EN] FUSED TRICYCLIC DERIVATIVES FOR THE TREATMENT OF PSYCHOTIC DISORDERS<br/>[FR] DERIVES TRICYCLIQUES ACCOLES POUR LE TRAITEMENT DE TROUBLES PSYCHOTIQUES
    申请人:GLAXO GROUP LTD
    公开号:WO2006024517A1
    公开(公告)日:2006-03-09
    Compounds of formula (I) wherein R1, R2, X, A, Y, B, Z1, Q, p, r and s are defined in the specification for treating inter alia psychotic disorders, depressive disorders, anxiety disorders and sexual dysfunctions.
    式中R1、R2、X、A、Y、B、Z1、Q、p、r和s在说明书中定义的用于治疗精神疾病、抑郁障碍、焦虑障碍和性功能障碍的(I)式化合物。
  • FUSED TRICYCLIC DERIVATIVES FOR THE TREATMENT OF PSYCHOTIC DISORDERS
    申请人:Bentley Jonathan
    公开号:US20120022056A1
    公开(公告)日:2012-01-26
    Compounds of formula (I) wherein R 1 , R 2 , X, A, Y, B, Z 1 , Q, p, r and s are defined in the specification for treating inter alia psychotic disorders, depressive disorders, anxiety disorders and sexual dysfunctions.
    式(I)中的化合物,其中R1、R2、X、A、Y、B、Z1、Q、p、r和s在规范中定义,用于治疗精神疾病、抑郁症、焦虑症和性功能障碍等疾病。
  • Design and Synthesis of Novel Tricyclic Benzoxazines as Potent 5-HT<sub>1A/B/D</sub> Receptor Antagonists Leading to the Discovery of 6-{2-[4-(2-methyl-5-quinolinyl)-1-piperazinyl]ethyl}-4<i>H</i>-imidazo[5,1-<i>c</i>][1,4]benzoxazine-3-carboxamide (GSK588045)
    作者:Steven M. Bromidge、Roberto Arban、Barbara Bertani、Silvia Bison、Manuela Borriello、Paolo Cavanni、Giovanna Dal Forno、Romano Di-Fabio、Daniele Donati、Stefano Fontana、Massimo Gianotti、Laurie J. Gordon、Enrica Granci、Colin P. Leslie、Luca Moccia、Alessandra Pasquarello、Ilaria Sartori、Anna Sava、Jeannette M. Watson、Angela Worby、Laura Zonzini、Valeria Zucchelli
    DOI:10.1021/jm100482n
    日期:2010.8.12
    Bioisoteric replacement of the metabolically labile N-methyl amide group of a series of benzoxazinones with small heterocyclic rings has led to novel series of fused tricyclic benzoxazines which are potent 5-HT1A/B/D receptor antagonists with and without concomitant human serotonin transporter (hSerT) activity. Optimizing against multiple parameters in parallel identified 6-2-[4-(2-methyl-5-quinolinyl)-1-piperazinyl]ethyl}-4H-imidazo[5,1-c][1,4]benzoxazine-3-carboxamide (GSK588045) as a potent 5-HT1A/B/D receptor antagonist with a high degree of selectivity over human ether-a-go-go related gene (hERG) potassium channels, favorable pharmacokinetics, and excellent activity in vivo in rodent pharmacodynamic (PD) models. On the basis of its outstanding overall profile, this compound was progressed as a clinical candidate with the ultimate aim to assess its potential as a faster acting antidepressant/anxiolytic with reduced side-effect burden.
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