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15-methoxycarbonylmethyloxyisocupressic acid | 540777-55-7

中文名称
——
中文别名
——
英文名称
15-methoxycarbonylmethyloxyisocupressic acid
英文别名
——
15-methoxycarbonylmethyloxyisocupressic acid化学式
CAS
540777-55-7
化学式
C23H36O5
mdl
——
分子量
392.536
InChiKey
LKPHRYSCJBRCTK-QGERIXNMSA-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):
    4.77
  • 重原子数:
    28.0
  • 可旋转键数:
    8.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.74
  • 拓扑面积:
    72.83
  • 氢给体数:
    1.0
  • 氢受体数:
    4.0

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:
    15-methoxycarbonylmethyloxyisocupressic acidsodium hydroxideN,N'-二环己基碳二亚胺 作用下, 以 甲醇氯仿 为溶剂, 反应 18.0h, 生成 (1S,4aR,5S,8aR)-5-[(E)-5-(2,5-Dioxo-pyrrolidin-1-yloxycarbonylmethoxy)-3-methyl-pent-3-enyl]-1,4a-dimethyl-6-methylene-decahydro-naphthalene-1-carboxylic acid
    参考文献:
    名称:
    Development of Enzyme-Linked Immunosorbent Assays for Isocupressic Acid and Serum Metabolites of Isocupressic Acid
    摘要:
    The consumption of ponderosa pine (Pinus ponderosa), lodgepole pine (Pinus contorta), common juniper (Juniperus communis), and Monterey cypress (Cupressus macrocarpa) causes abortions in pregnant cattle. Recent studies have identified isocupressic acid (1) as the primary abortificient compound in these plants. In vitro and in vivo studies using rumen and blood have shown isocupressic acid (1) is rapidly metabolized to agathic acid (3), dihydroagathic acid (4), and tetrahydroagathic acid (5). Rapid and sensitive diagnostic techniques are needed to identify poisoned animals, to study toxicokinetics, and to elucidate the mechanism of isocupressic acid-induced abortion in cattle. In this study, four competitive inhibition enzyme-linked immunosorbent assays for isocupressic acid and its sera metabolites were developed using polyclonal antibodies. One assay is specific to 1, whereas the other three assays show cross-reactivity to 3-5 in addition to 1. The assay specific to 1 had a limit of detection of 44.1 pg. The other assays which demonstrated cross-reactivity to the isocupressic acid blood metabolites also had comparably low limits of detection. One assay was used to follow the absorption and elimination profile of isocupressic acid metabolites in both cow serum and urine after oral dosage of a cow with common juniper.
    DOI:
    10.1021/jf021095m
  • 作为产物:
    描述:
    异柏烯酸溴乙酸甲酯 在 sodium hydride 作用下, 以 四氢呋喃 为溶剂, 反应 18.0h, 以61%的产率得到15-methoxycarbonylmethyloxyisocupressic acid
    参考文献:
    名称:
    Development of Enzyme-Linked Immunosorbent Assays for Isocupressic Acid and Serum Metabolites of Isocupressic Acid
    摘要:
    The consumption of ponderosa pine (Pinus ponderosa), lodgepole pine (Pinus contorta), common juniper (Juniperus communis), and Monterey cypress (Cupressus macrocarpa) causes abortions in pregnant cattle. Recent studies have identified isocupressic acid (1) as the primary abortificient compound in these plants. In vitro and in vivo studies using rumen and blood have shown isocupressic acid (1) is rapidly metabolized to agathic acid (3), dihydroagathic acid (4), and tetrahydroagathic acid (5). Rapid and sensitive diagnostic techniques are needed to identify poisoned animals, to study toxicokinetics, and to elucidate the mechanism of isocupressic acid-induced abortion in cattle. In this study, four competitive inhibition enzyme-linked immunosorbent assays for isocupressic acid and its sera metabolites were developed using polyclonal antibodies. One assay is specific to 1, whereas the other three assays show cross-reactivity to 3-5 in addition to 1. The assay specific to 1 had a limit of detection of 44.1 pg. The other assays which demonstrated cross-reactivity to the isocupressic acid blood metabolites also had comparably low limits of detection. One assay was used to follow the absorption and elimination profile of isocupressic acid metabolites in both cow serum and urine after oral dosage of a cow with common juniper.
    DOI:
    10.1021/jf021095m
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同类化合物

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