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(E)-3-(1-(naphthalen-1-ylmethyl)-1H-indol-3-yl)acrylic acid | 1376447-03-8

中文名称
——
中文别名
——
英文名称
(E)-3-(1-(naphthalen-1-ylmethyl)-1H-indol-3-yl)acrylic acid
英文别名
(E)-3-[1-(naphthalen-1-ylmethyl)indol-3-yl]prop-2-enoic acid
(E)-3-(1-(naphthalen-1-ylmethyl)-1H-indol-3-yl)acrylic acid化学式
CAS
1376447-03-8
化学式
C22H17NO2
mdl
——
分子量
327.382
InChiKey
CQWZYWLMEPQXMH-OUKQBFOZSA-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):
    4.8
  • 重原子数:
    25
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    42.2
  • 氢给体数:
    1
  • 氢受体数:
    2

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

  • 作为产物:
    描述:
    1-(1-萘基甲基)-1H-吲哚-3-甲醛丙二酸哌啶吡啶盐酸 作用下, 以 为溶剂, 反应 12.0h, 以78.2%的产率得到(E)-3-(1-(naphthalen-1-ylmethyl)-1H-indol-3-yl)acrylic acid
    参考文献:
    名称:
    Design, synthesis and biological evaluation of thiazole- and indole-based derivatives for the treatment of type II diabetes
    摘要:
    Present studies have shown that the lipid carrier has a significant role in several aspects of metabolic syndrome in A-FABP/ap2-deficient mice, including type 2 diabetes and atherosclerosis. 38 Thiazole- and indole-based derivatives were synthesized and investigated for their inhibitory effects on the production of LPS-stimulated TNF-alpha. Among them, 12b exhibited an excellent inhibitory efficiency compared to BMS309403 (95% vs. 85%) at the concentration of 10 mu M and a binding affinity for ap2 with the apparent K-i values 33 nM. Oral administration of 12b at a dosage of 50 mg/kg effectively reduced the levels of plasma blood glucose, triglycerides, insulin, total cholesterol and alanine aminotransferase in high-fat/diet-induced obesity model. The results highlighted that 12b was a potent anti-diabetic agent. (C) 2012 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2012.03.006
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文献信息

  • Design, synthesis and biological evaluation of thiazole- and indole-based derivatives for the treatment of type II diabetes
    作者:Qinyuan Xu、Li Huang、Juan Liu、Liang Ma、Tao Chen、Jinying Chen、Fei Peng、Dong Cao、Zhuang Yang、Neng Qiu、Jingxiang Qiu、Guangcheng Wang、Xiaolin Liang、Aihua Peng、Mingli Xiang、Yuquan Wei、Lijuan Chen
    DOI:10.1016/j.ejmech.2012.03.006
    日期:2012.6
    Present studies have shown that the lipid carrier has a significant role in several aspects of metabolic syndrome in A-FABP/ap2-deficient mice, including type 2 diabetes and atherosclerosis. 38 Thiazole- and indole-based derivatives were synthesized and investigated for their inhibitory effects on the production of LPS-stimulated TNF-alpha. Among them, 12b exhibited an excellent inhibitory efficiency compared to BMS309403 (95% vs. 85%) at the concentration of 10 mu M and a binding affinity for ap2 with the apparent K-i values 33 nM. Oral administration of 12b at a dosage of 50 mg/kg effectively reduced the levels of plasma blood glucose, triglycerides, insulin, total cholesterol and alanine aminotransferase in high-fat/diet-induced obesity model. The results highlighted that 12b was a potent anti-diabetic agent. (C) 2012 Elsevier Masson SAS. All rights reserved.
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