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1-(3-methoxycarbonylphenyl)quinazoline-2,4(1H,3H)-dione | 130985-16-9

中文名称
——
中文别名
——
英文名称
1-(3-methoxycarbonylphenyl)quinazoline-2,4(1H,3H)-dione
英文别名
3-(3,4-Dihydro-2,4-dioxo-1(2h)-quinazolinyl)benzoic acid methyl ester;methyl 3-(2,4-dioxoquinazolin-1-yl)benzoate
1-(3-methoxycarbonylphenyl)quinazoline-2,4(1H,3H)-dione化学式
CAS
130985-16-9
化学式
C16H12N2O4
mdl
——
分子量
296.282
InChiKey
GOUWLELLHQRVOH-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):
    2
  • 重原子数:
    22
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    75.7
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    间氨基苯甲酸盐酸 、 camphor-10-sulfonic acid 、 potassium carbonate 、 copper(I) bromide 作用下, 以 N,N-二甲基甲酰胺 、 xylene 为溶剂, 反应 187.5h, 生成 1-(3-methoxycarbonylphenyl)quinazoline-2,4(1H,3H)-dione
    参考文献:
    名称:
    Structure-activity relationship of quinazolinedione inhibitors of calcium-independent phosphodiesterase
    摘要:
    A series of quinazolinediones and azaquinazolinediones is described which possess potent inhibitory activity toward the calcium-independent phosphodiesterase enzyme (CaIPDE). In vivo testing showed that this in vitro activity translates to animal models predictive of chronic diseases such as depression and inflammation. These results support the hypothesis that inhibition of CaIPDE may lead to useful activity in such chronic diseases.
    DOI:
    10.1021/jm00106a024
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文献信息

  • [EN] 1-(ARYLMETHYL)QUINAZOLINE-2,4(1H,3H)-DIONES AS PARP INHIBITORS AND THE USE THEREOF<br/>[FR] 1-(ARYLMÉTHYL)QUINAZOLINE-2,4(1H,3H)-DIONES EN TANT QU'INHIBITEURS DE PARP ET UTILISATION DE CELLES-CI
    申请人:IMPACT THERAPEUTICS INC
    公开号:WO2012130166A1
    公开(公告)日:2012-10-04
    Disclosed are 1-(arylmethyl)quinazoline-2,4(1H,3H)-diones thereof, represented by the Formula (I) wherein Ar, R1-R6 are defined herein. Compounds having Formula (I) are PARP inhibitors. Therefore, compounds of the invention may be used to treat clinical conditions that are responsive to the inhibition of PARP activity.
    公开了其1-(芳基甲基)喹唑啉-2,4(1H,3H)-二酮,其由式(I)所表示,其中Ar,R1-R6在此定义。具有式(I)的化合物是PARP抑制剂。因此,本发明的化合物可用于治疗对PARP活性抑制敏感的临床状况。
  • 1-(Arylmethyl)quinazoline-2,4(1H,3H)-diones as PARP Inhibitors and the Use Thereof
    申请人:Cai Sui Xiong
    公开号:US20140023642A1
    公开(公告)日:2014-01-23
    Disclosed are 1-(arylmethyl)quinazoline-2,4(1H,3H)-diones thereof, represented by the Formula (I) wherein Ar, R 1 -R 6 are defined herein. Compounds having Formula (I) are PARP inhibitors. Therefore, compounds of the invention may be used to treat clinical conditions that are responsive to the inhibition of PARP activity.
    公开的是其1-(芳基甲基)喹唑啉-2,4(1H,3H)-二酮,由式(I)所代表,其中Ar,R1-R6在此定义。具有式(I)的化合物为PARP抑制剂。因此,本发明的化合物可用于治疗对PARP活性抑制有响应的临床病况。
  • 1-(Arylmethyl)quinazoline-2,4(1H,3H)-Diones as PARP Inhibitors and the Use Thereof
    申请人:Impact Therapeutics, Inc.
    公开号:US20160237070A1
    公开(公告)日:2016-08-18
    Disclosed are 1-(arylmethyl)quinazoline-2,4(1H,3H)-diones represented by the Formula (I): wherein Ar, R 1 -R 6 are defined herein. Compounds having Formula (I) are PARP inhibitors. Therefore, compounds of the invention may be used to treat clinical conditions that are responsive to the inhibition of PARP activity.
    本发明涉及一种由式(I)表示的1-(芳基甲基)喹唑啉-2,4(1H,3H)-二酮,其中Ar,R1-R6如本文所定义。具有式(I)的化合物是PARP抑制剂。因此,本发明的化合物可以用于治疗对PARP活性抑制有反应的临床病症。
  • 1-(arylmethyl)quinazoline-2,4(1H,3H)-diones as PARP inhibitors and the use thereof
    申请人:IMPACT Therapeutics, Inc.
    公开号:US10316027B2
    公开(公告)日:2019-06-11
    Disclosed are 1-(arylmethyl)quinazoline-2,4(1H,3H)-diones represented by the Formula (I): wherein Ar, R1-R6, are defined herein. Compounds having Formula (I) are PARP inhibitors. Therefore, compounds of the invention may be used to treat clinical conditions that are responsive to the inhibition of PARP activity.
    本发明公开了由式 (I) 代表的 1-(芳基甲基)喹唑啉-2,4(1H,3H)-二酮: 其中 Ar、R1-R6 在本文中定义。具有式(I)的化合物是 PARP 抑制剂。因此,本发明的化合物可用于治疗对抑制 PARP 活性有反应的临床病症。
  • LOWE, JOHN A. (III);ARCHER, ROBERT L.;CHAPIN, DOUGLAS S.;CHENG, JOHN B.;H+, J. MED. CHEM., 34,(1991) N, C. 624-628
    作者:LOWE, JOHN A. (III)、ARCHER, ROBERT L.、CHAPIN, DOUGLAS S.、CHENG, JOHN B.、H+
    DOI:——
    日期:——
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