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5,7-Dihydroxy-6-methoxy-2-phenyl-8-(pyrrolidin-1-ylmethyl)chromen-4-one | 1021312-36-6

中文名称
——
中文别名
——
英文名称
5,7-Dihydroxy-6-methoxy-2-phenyl-8-(pyrrolidin-1-ylmethyl)chromen-4-one
英文别名
——
5,7-Dihydroxy-6-methoxy-2-phenyl-8-(pyrrolidin-1-ylmethyl)chromen-4-one化学式
CAS
1021312-36-6
化学式
C21H21NO5
mdl
——
分子量
367.401
InChiKey
HLCLPIQUDJBLCT-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):
    3.3
  • 重原子数:
    27
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    79.2
  • 氢给体数:
    2
  • 氢受体数:
    6

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:
    参考文献:
    名称:
    Synthesis and biological evaluation of novel 8-aminomethylated oroxylin A analogues as α-glucosidase inhibitors
    摘要:
    A series of 8-aminomethylated derivatives (1a-1j) were prepared by Mannich reaction of oroxylin A (1) with appropriate primary or secondary amines and para-formaldehyde. All the compounds were tested for their alpha-glucosidase inhibition activity against both yeast and rat intestinal alpha-glucosidase. Some of the compounds demonstrated significantly better alpha-glucosidase inhibitory activity than the parent compound (oroxylin A). (c) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2008.01.055
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文献信息

  • Synthesis and biological evaluation of novel 8-aminomethylated oroxylin A analogues as α-glucosidase inhibitors
    作者:T. Hari Babu、V. Rama Subba Rao、Ashok K. Tiwari、K. Suresh Babu、P.V. Srinivas、Amtul Z. Ali、J. Madhusudana Rao
    DOI:10.1016/j.bmcl.2008.01.055
    日期:2008.3
    A series of 8-aminomethylated derivatives (1a-1j) were prepared by Mannich reaction of oroxylin A (1) with appropriate primary or secondary amines and para-formaldehyde. All the compounds were tested for their alpha-glucosidase inhibition activity against both yeast and rat intestinal alpha-glucosidase. Some of the compounds demonstrated significantly better alpha-glucosidase inhibitory activity than the parent compound (oroxylin A). (c) 2008 Elsevier Ltd. All rights reserved.
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