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3,5-dihydroxy-3-n-pentadecylvaleric acid lactone | 95249-47-1

中文名称
——
中文别名
——
英文名称
3,5-dihydroxy-3-n-pentadecylvaleric acid lactone
英文别名
4-Hydroxy-4-pentadecyl-tetrahydro-pyran-2-one;4-hydroxy-4-pentadecyloxan-2-one
3,5-dihydroxy-3-n-pentadecylvaleric acid lactone化学式
CAS
95249-47-1
化学式
C20H38O3
mdl
——
分子量
326.52
InChiKey
DIDBIIFLZIVTON-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):
    7.1
  • 重原子数:
    23
  • 可旋转键数:
    14
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.95
  • 拓扑面积:
    46.5
  • 氢给体数:
    1
  • 氢受体数:
    3

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:
    棕榈酸乙酯chromium(VI) oxide 、 lithium aluminium tetrahydride 、 硫酸双氧水臭氧溶剂黄146 作用下, 以 四氢呋喃乙醚丙酮 为溶剂, 反应 20.0h, 生成 3,5-dihydroxy-3-n-pentadecylvaleric acid lactone
    参考文献:
    名称:
    3-Alkyl-3-hydroxyglutaric Acids: A New Class of Hypocholesterolemic HMG CoA Reductase Inhibitors. 1
    摘要:
    Derivatives of 3-hydroxy-3-methylglutaric acid (HMG), a portion of the substrate for HMG CoA reductase, were prepared and tested for their inhibitory action against rat liver HMG CoA reductase and for their hypocholesterolemic activity. Structure-dependent competitive inhibition was observed. Optimal structures had a free dicarboxylic acid with an alkyl group of 13-16 carbons at position 3. 3-n-Pentadecyl-3-hydroxyglutaric acid (3j) (IC50 = 50 microM) reduced serum cholesterol in the Triton-treated rat and HMG CoA reductase activity in the 20,25-diazacholesterol-treated rat.
    DOI:
    10.1021/jm50001a011
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文献信息

  • 3-Alkyl-3-hydroxyglutaric Acids: A New Class of Hypocholesterolemic HMG CoA Reductase Inhibitors. 1
    作者:John S. Baran、Ivar Laos、Donna D. Langford、James E. Miller、Charlene Jett、Beatrice Taite、Elaine Rohrbacher
    DOI:10.1021/jm50001a011
    日期:1985.5
    Derivatives of 3-hydroxy-3-methylglutaric acid (HMG), a portion of the substrate for HMG CoA reductase, were prepared and tested for their inhibitory action against rat liver HMG CoA reductase and for their hypocholesterolemic activity. Structure-dependent competitive inhibition was observed. Optimal structures had a free dicarboxylic acid with an alkyl group of 13-16 carbons at position 3. 3-n-Pentadecyl-3-hydroxyglutaric acid (3j) (IC50 = 50 microM) reduced serum cholesterol in the Triton-treated rat and HMG CoA reductase activity in the 20,25-diazacholesterol-treated rat.
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