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7-Methoxy-6-(5-oxazolyl)-2-phenyl-4(1H)-quinolinone | 371249-67-1

中文名称
——
中文别名
——
英文名称
7-Methoxy-6-(5-oxazolyl)-2-phenyl-4(1H)-quinolinone
英文别名
7-methoxy-6-(1,3-oxazol-5-yl)-2-phenyl-1H-quinolin-4-one
7-Methoxy-6-(5-oxazolyl)-2-phenyl-4(1H)-quinolinone化学式
CAS
371249-67-1
化学式
C19H14N2O3
mdl
——
分子量
318.332
InChiKey
HHMIBIGHTIBSRR-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):
    3.2
  • 重原子数:
    24
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    64.4
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    (E)-3-(3-Methoxy-4-oxazol-5-yl-phenylamino)-3-phenyl-acrylic acid ethyl ester 以 xylene 为溶剂, 以66%的产率得到7-Methoxy-6-(5-oxazolyl)-2-phenyl-4(1H)-quinolinone
    参考文献:
    名称:
    Novel inhibitors of IMPDH
    摘要:
    A series of novel quinolone-based small molecule inhibitors of inosine monophosphate dehydrogenase (IMPDH) was explored. The synthesis and the structure-activity relationships (SARs) derived from in vitro studies are described. (C) 2002 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(02)00944-7
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文献信息

  • Heterocycles that are inhibitors of IMPDH enzyme
    申请人:——
    公开号:US20020040022A1
    公开(公告)日:2002-04-04
    Compounds of the formula 1 wherein X 1 is C(O), —S(O)—, or —S(O) 2 —; X 2 is CR 3 or N; X 3 is —NH—, —O—, or —S—; X 4 is CR 4 or N; X 5 is CR 5 or N; and X 6 is CR 6 or N are useful as inhibitors of IMPDH enzyme. Thus, these compounds can be used as therapeutic agents for IMPDH-associated disorders.
    公式1中的化合物,其中X1是C(O)、—S(O)—或—S(O)2—;X2是CR3或N;X3是—NH—、—O—或—S—;X4是CR4或N;X5是CR5或N;X6是CR6或N,可用作IMPDH酶的抑制剂。因此,这些化合物可作为治疗IMPDH相关疾病的治疗剂。
  • HETEROCYCLES THAT ARE INHIBITORS OF IMPDH ENZYME
    申请人:Bristol-Myers Squibb Co.
    公开号:EP1276739A2
    公开(公告)日:2003-01-22
  • US6919335B2
    申请人:——
    公开号:US6919335B2
    公开(公告)日:2005-07-19
  • [EN] HETEROCYCLES THAT ARE INHIBITORS OF IMPDH ENZYME<br/>[FR] HETEROCYCLES UTILES EN TANT QU'INHIBITEURS DE L'ENZYME IMPDH
    申请人:BRISTOL MYERS SQUIBB CO
    公开号:WO2001081340A2
    公开(公告)日:2001-11-01
    Compounds of formula (I) wherein X1 is C(O), -S(O)-, or -S(O)¿2?-; X?2 is CR3¿ or N; X3 is -NH-, -O-, or -S-; X?4 is CR4¿ or N; X?5 is CR5¿ or N; and X?6 is CR6¿ or N are useful as inhibitors of IMPDH enzyme. Thus, these compounds can be used as therapeutic agents for IMPDH- associated disorders.
  • Novel inhibitors of IMPDH
    作者:Scott H. Watterson、Marianne Carlsen、T.G. Murali Dhar、Zhongqi Shen、William J. Pitts、Junqing Guo、Henry H. Gu、Derek Norris、John Chorba、Ping Chen、Daniel Cheney、Mark Witmer、Catherine A. Fleener、Katherine Rouleau、Robert Townsend、Diane L. Hollenbaugh、Edwin J. Iwanowicz
    DOI:10.1016/s0960-894x(02)00944-7
    日期:2003.2
    A series of novel quinolone-based small molecule inhibitors of inosine monophosphate dehydrogenase (IMPDH) was explored. The synthesis and the structure-activity relationships (SARs) derived from in vitro studies are described. (C) 2002 Elsevier Science Ltd. All rights reserved.
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