摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

6-morpholin-4-yl-1'-(phenoxazine-10-carbonyl)spiro[3H-chromene-2,4'-piperidine]-4-one | 1131680-19-7

中文名称
——
中文别名
——
英文名称
6-morpholin-4-yl-1'-(phenoxazine-10-carbonyl)spiro[3H-chromene-2,4'-piperidine]-4-one
英文别名
——
6-morpholin-4-yl-1'-(phenoxazine-10-carbonyl)spiro[3H-chromene-2,4'-piperidine]-4-one化学式
CAS
1131680-19-7
化学式
C30H29N3O5
mdl
——
分子量
511.577
InChiKey
LVKSVDKDUFVPTH-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):
    3.7
  • 重原子数:
    38
  • 可旋转键数:
    1
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    71.6
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    6-morpholinospiro[chromane-2,4'-piperidin]-4-one hydrochloride 、 10H-phenoxazine-10-carbonyl chlorideN,N-二异丙基乙胺 作用下, 以 四氢呋喃 为溶剂, 生成 6-morpholin-4-yl-1'-(phenoxazine-10-carbonyl)spiro[3H-chromene-2,4'-piperidine]-4-one
    参考文献:
    名称:
    Synthesis of spiro[chroman-2,4′-piperidin]-4-one derivatives as acetyl-CoA carboxylase inhibitors
    摘要:
    Various spiro[chroman-2,4'-piperidin]-4-one derivatives (38a-m and 43a-j) have been designed, synthesized and evaluated for in vitro acetyl-CoA carboxylase (ACC) inhibitory activity. Several compounds have shown ACC inhibitory activity in low nanomolar range. Compound 38j reduced the respiratory quotient (RQ) in C57BL/6J mice indicating increase in whole body fat oxidation even in the presence of high carbohydrate diet. Structure-activity relationship (SAR) has been discussed. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2008.11.099
点击查看最新优质反应信息

文献信息

  • Synthesis of spiro[chroman-2,4′-piperidin]-4-one derivatives as acetyl-CoA carboxylase inhibitors
    作者:Pundlik Shinde、Sanjay K. Srivastava、Rajendra Odedara、Davinder Tuli、Siralee Munshi、Jitendra Patel、Shitalkumar P. Zambad、Rajesh Sonawane、Ramesh C. Gupta、Vijay Chauthaiwale、Chaitanya Dutt
    DOI:10.1016/j.bmcl.2008.11.099
    日期:2009.2
    Various spiro[chroman-2,4'-piperidin]-4-one derivatives (38a-m and 43a-j) have been designed, synthesized and evaluated for in vitro acetyl-CoA carboxylase (ACC) inhibitory activity. Several compounds have shown ACC inhibitory activity in low nanomolar range. Compound 38j reduced the respiratory quotient (RQ) in C57BL/6J mice indicating increase in whole body fat oxidation even in the presence of high carbohydrate diet. Structure-activity relationship (SAR) has been discussed. (C) 2008 Elsevier Ltd. All rights reserved.
查看更多