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5,7-Diisopropoxy-8-propionyl-4-propyl-chromen-2-one | 461695-36-3

中文名称
——
中文别名
——
英文名称
5,7-Diisopropoxy-8-propionyl-4-propyl-chromen-2-one
英文别名
5,7-Diisopropoxy-8-propanoyl-4-propyl-chromen-2-one;8-propanoyl-5,7-di(propan-2-yloxy)-4-propylchromen-2-one
5,7-Diisopropoxy-8-propionyl-4-propyl-chromen-2-one化学式
CAS
461695-36-3
化学式
C21H28O5
mdl
——
分子量
360.45
InChiKey
UFMTXGPEQOAODC-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):
    4.5
  • 重原子数:
    26
  • 可旋转键数:
    8
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.52
  • 拓扑面积:
    61.8
  • 氢给体数:
    0
  • 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:
    5,7-Diisopropoxy-8-propionyl-4-propyl-chromen-2-one 在 sodium tetrahydroborate 作用下, 以 乙醇 为溶剂, 以55%的产率得到8-(1-Hydroxy-propyl)-5,7-diisopropoxy-4-propyl-chromen-2-one
    参考文献:
    名称:
    Pyranocoumarin, a novel anti-TB pharmacophore: Synthesis and biological evaluation against Mycobacterium tuberculosis
    摘要:
    Pyranocoumarin compounds were identified to embody a novel and unique pharmacophore for anti-TB activity. A systematic approach was taken to investigate the structural characteristics. Focused libraries of compounds were synthesized and evaluated for their anti-TB activity in primary screening assays. Compounds shown to be active were further determined for MIC and MBC values. Three of the four bactericidal compounds (16, 17c, and 18f) were amino derivatives, with MIC values of 16 mu g/mL and respective MBC values of 32, 32, and 64 mu g/mL. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2006.02.017
  • 作为产物:
    描述:
    5,7-二羟基-8-丙酰-4-丙基-2H-色烯-2-酮2-溴丙烷potassium carbonate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 以56%的产率得到5,7-Diisopropoxy-8-propionyl-4-propyl-chromen-2-one
    参考文献:
    名称:
    Pyranocoumarin, a novel anti-TB pharmacophore: Synthesis and biological evaluation against Mycobacterium tuberculosis
    摘要:
    Pyranocoumarin compounds were identified to embody a novel and unique pharmacophore for anti-TB activity. A systematic approach was taken to investigate the structural characteristics. Focused libraries of compounds were synthesized and evaluated for their anti-TB activity in primary screening assays. Compounds shown to be active were further determined for MIC and MBC values. Three of the four bactericidal compounds (16, 17c, and 18f) were amino derivatives, with MIC values of 16 mu g/mL and respective MBC values of 32, 32, and 64 mu g/mL. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2006.02.017
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文献信息

  • Pyranocoumarin, a novel anti-TB pharmacophore: Synthesis and biological evaluation against Mycobacterium tuberculosis
    作者:Ze-Qi Xu、Krzysztof Pupek、William J. Suling、Livia Enache、Michael T. Flavin
    DOI:10.1016/j.bmc.2006.02.017
    日期:2006.7
    Pyranocoumarin compounds were identified to embody a novel and unique pharmacophore for anti-TB activity. A systematic approach was taken to investigate the structural characteristics. Focused libraries of compounds were synthesized and evaluated for their anti-TB activity in primary screening assays. Compounds shown to be active were further determined for MIC and MBC values. Three of the four bactericidal compounds (16, 17c, and 18f) were amino derivatives, with MIC values of 16 mu g/mL and respective MBC values of 32, 32, and 64 mu g/mL. (c) 2006 Elsevier Ltd. All rights reserved.
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