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5-(benzyloxy)-2-((3-hydroxyphenoxy)methyl)-4H-pyran-4-one | 1381864-92-1

中文名称
——
中文别名
——
英文名称
5-(benzyloxy)-2-((3-hydroxyphenoxy)methyl)-4H-pyran-4-one
英文别名
2-[(3-Hydroxyphenoxy)methyl]-5-phenylmethoxypyran-4-one;2-[(3-hydroxyphenoxy)methyl]-5-phenylmethoxypyran-4-one
5-(benzyloxy)-2-((3-hydroxyphenoxy)methyl)-4H-pyran-4-one化学式
CAS
1381864-92-1
化学式
C19H16O5
mdl
——
分子量
324.333
InChiKey
WSLAGRQURCPRHG-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:
    24
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    65
  • 氢给体数:
    1
  • 氢受体数:
    5

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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    5-(benzyloxy)-2-((3-hydroxyphenoxy)methyl)-4H-pyran-4-one三溴化硼 作用下, 以 二氯甲烷 为溶剂, 反应 24.0h, 以46%的产率得到5-hydroxy-2-((3-hydroxyphenoxy)methyl)-4H-pyran-4-one
    参考文献:
    名称:
    Synthesis of kojic acid-derived copper-chelating apoptosis inducing agents
    摘要:
    Three classes of kojic acid derivatives were synthesized and examined for their antiproliferative activity against HeLa cells. Both 8b and 11 co-treated with copper ion exhibited synergistic effect on the HeLa cell growth inhibition with GI(50) values of 11.9 and 7.1 mu M, respectively. Flow cytometric analysis of HeLa cells revealed that 11-Cu co-treatment induced the sub-G1 arrest in a dose-dependent manner, suggesting that the growth-inhibitory effect is attributed to DNA fragmentation. Moreover, western blot of HeLa cells cytosolic extracts displayed the cleavage of the 116-kDa protein poly(ADP-ribose) polymerase and activation of caspase-3 by the reduced level of the 32-kDa proenzyme, indicating that the caspase-dependent apoptotic pathway was involved. We further demonstrated that MAPK pathway regulators such as ERK and p38 were activated in response to 11-Cu co-treatment, suggesting that the intracellular oxidative stress was dramatically stimulated by the copper ion. Taken together, we have successfully synthesized kojic acid-derived copper-induced apoptotic agents.
    DOI:
    10.1007/s00044-012-0094-y
  • 作为产物:
    描述:
    曲酸potassium carbonate三乙胺 、 sodium bromide 作用下, 以 二氯甲烷N,N-二甲基甲酰胺丙酮 为溶剂, 反应 14.5h, 生成 5-(benzyloxy)-2-((3-hydroxyphenoxy)methyl)-4H-pyran-4-one
    参考文献:
    名称:
    Synthesis of kojic acid-derived copper-chelating apoptosis inducing agents
    摘要:
    Three classes of kojic acid derivatives were synthesized and examined for their antiproliferative activity against HeLa cells. Both 8b and 11 co-treated with copper ion exhibited synergistic effect on the HeLa cell growth inhibition with GI(50) values of 11.9 and 7.1 mu M, respectively. Flow cytometric analysis of HeLa cells revealed that 11-Cu co-treatment induced the sub-G1 arrest in a dose-dependent manner, suggesting that the growth-inhibitory effect is attributed to DNA fragmentation. Moreover, western blot of HeLa cells cytosolic extracts displayed the cleavage of the 116-kDa protein poly(ADP-ribose) polymerase and activation of caspase-3 by the reduced level of the 32-kDa proenzyme, indicating that the caspase-dependent apoptotic pathway was involved. We further demonstrated that MAPK pathway regulators such as ERK and p38 were activated in response to 11-Cu co-treatment, suggesting that the intracellular oxidative stress was dramatically stimulated by the copper ion. Taken together, we have successfully synthesized kojic acid-derived copper-induced apoptotic agents.
    DOI:
    10.1007/s00044-012-0094-y
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文献信息

  • DNA METHYLATION INHIBITORS
    申请人:Chen Ching-Shih
    公开号:US20120157465A1
    公开(公告)日:2012-06-21
    A number of DNA methylation inhibitors are described. The DNA methylation inhibitors were identified using a two-component enhanced green fluorescent protein reporter system to screen a compound library containing procainamide derivatives. The DNA methylation inhibitors can be used for cancer therapy and prevention.
  • US8546397B2
    申请人:——
    公开号:US8546397B2
    公开(公告)日:2013-10-01
  • [EN] DNA METHYLATION INHIBITORS<br/>[FR] INHIBITEURS DE MÉTHYLATION DE L'ADN
    申请人:UNIV OHIO STATE RES FOUND
    公开号:WO2012087889A2
    公开(公告)日:2012-06-28
    A number of DNA methylation inhibitors are described. The DNA methylation inhibitors were identified using a two-component enhanced green fluorescent protein reporter system to screen a compound library containing procainamide derivatives. The DNA methylation inhibitors can be used for cancer therapy and prevention.
  • Synthesis of kojic acid-derived copper-chelating apoptosis inducing agents
    作者:Yu-Hua Chen、Pei-Jung Lu、Christopher Hulme、Arthur Y. Shaw
    DOI:10.1007/s00044-012-0094-y
    日期:2013.2
    Three classes of kojic acid derivatives were synthesized and examined for their antiproliferative activity against HeLa cells. Both 8b and 11 co-treated with copper ion exhibited synergistic effect on the HeLa cell growth inhibition with GI(50) values of 11.9 and 7.1 mu M, respectively. Flow cytometric analysis of HeLa cells revealed that 11-Cu co-treatment induced the sub-G1 arrest in a dose-dependent manner, suggesting that the growth-inhibitory effect is attributed to DNA fragmentation. Moreover, western blot of HeLa cells cytosolic extracts displayed the cleavage of the 116-kDa protein poly(ADP-ribose) polymerase and activation of caspase-3 by the reduced level of the 32-kDa proenzyme, indicating that the caspase-dependent apoptotic pathway was involved. We further demonstrated that MAPK pathway regulators such as ERK and p38 were activated in response to 11-Cu co-treatment, suggesting that the intracellular oxidative stress was dramatically stimulated by the copper ion. Taken together, we have successfully synthesized kojic acid-derived copper-induced apoptotic agents.
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