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1-(2-morpholinoethyl)-N-(naphthalen-1-yl)-2-oxo-1,2-dihydroquinazoline-3(4H)-carboxamide | 1039011-92-1

中文名称
——
中文别名
——
英文名称
1-(2-morpholinoethyl)-N-(naphthalen-1-yl)-2-oxo-1,2-dihydroquinazoline-3(4H)-carboxamide
英文别名
1-(2-morpholin-4-ylethyl)-N-naphthalen-1-yl-2-oxo-4H-quinazoline-3-carboxamide
1-(2-morpholinoethyl)-N-(naphthalen-1-yl)-2-oxo-1,2-dihydroquinazoline-3(4H)-carboxamide化学式
CAS
1039011-92-1
化学式
C25H26N4O3
mdl
——
分子量
430.506
InChiKey
HJLBLBURTOHNHG-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):
    2.9
  • 重原子数:
    32
  • 可旋转键数:
    4
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    65.1
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    1-萘胺对硝基苯基氯甲酸酯三乙胺 作用下, 以 二氯甲烷 为溶剂, 反应 3.0h, 以15%的产率得到1-(2-morpholinoethyl)-N-(naphthalen-1-yl)-2-oxo-1,2-dihydroquinazoline-3(4H)-carboxamide
    参考文献:
    名称:
    The SAR studies of novel CB2 selective agonists, benzimidazolone derivatives
    摘要:
    Benzimidazolone derivatives were discovered as novel CB2 selective agonists. Structure Activity Relationship (SAR) studies around them were examined to improve metabolic stability. Compound 39 exhibited excellent metabolic stability in human liver microsomes (HLM) and significant attenuation of the chronic colonic allodynia in the TNBS-treated rats by po administration. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2008.04.032
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文献信息

  • The SAR studies of novel CB2 selective agonists, benzimidazolone derivatives
    作者:Hirofumi Omura、Makoto Kawai、Akiko Shima、Yasuhiro Iwata、Fumitaka Ito、Tsutomu Masuda、Atsuko Ohta、Naoya Makita、Kiyoyuki Omoto、Hiromi Sugimoto、Akira Kikuchi、Hiroshi Iwata、Kazuo Ando
    DOI:10.1016/j.bmcl.2008.04.032
    日期:2008.6
    Benzimidazolone derivatives were discovered as novel CB2 selective agonists. Structure Activity Relationship (SAR) studies around them were examined to improve metabolic stability. Compound 39 exhibited excellent metabolic stability in human liver microsomes (HLM) and significant attenuation of the chronic colonic allodynia in the TNBS-treated rats by po administration. (C) 2008 Elsevier Ltd. All rights reserved.
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