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(2E,6S)-8-benzoyloxy-2,6-dimethyl-2-octenoic acid | 87442-13-5

中文名称
——
中文别名
——
英文名称
(2E,6S)-8-benzoyloxy-2,6-dimethyl-2-octenoic acid
英文别名
(2E,6S)-8-hydroxy-2,6-dimethyloct-2-enoic acid;(E,6S)-8-hydroxy-2,6-dimethyloct-2-enoic acid
(2E,6S)-8-benzoyloxy-2,6-dimethyl-2-octenoic acid化学式
CAS
87442-13-5
化学式
C10H18O3
mdl
——
分子量
186.251
InChiKey
CDAJACJYYZHNJA-MOIHINDBSA-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):
    1.9
  • 重原子数:
    13
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.7
  • 拓扑面积:
    57.5
  • 氢给体数:
    2
  • 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
  • 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:
    参考文献:
    名称:
    Acylated Iridoid Glycosides from Buddleja japonica HEMSL.
    摘要:
    从日本紫苑(Buddleja japonica HEMSL.)中分离出了十六种新的酰基化马兜铃苷,称为buddlejosides A1-A16,同时还分离出了四种已知的马兜铃苷;它们分别是6-香草酰-ajugol、6-阿魏酰-ajugol、verbascoside A和6-O-[α-L-(4-O-阿魏酰)-rhamnopyranosyl]-catalpol。这些新化合物的结构是基于化学和光谱证据确定的。Buddlejosides A1是与单萜酸酰化的ajugol衍生物,A2是sinusol,A3-A16是与肉桂酸衍生物和醋酸酰化的6-鼠李糖基-catalpol衍生物。
    DOI:
    10.1248/cpb.39.2944
  • 作为产物:
    参考文献:
    名称:
    Acylated Iridoid Glycosides from Buddleja japonica HEMSL.
    摘要:
    从日本紫苑(Buddleja japonica HEMSL.)中分离出了十六种新的酰基化马兜铃苷,称为buddlejosides A1-A16,同时还分离出了四种已知的马兜铃苷;它们分别是6-香草酰-ajugol、6-阿魏酰-ajugol、verbascoside A和6-O-[α-L-(4-O-阿魏酰)-rhamnopyranosyl]-catalpol。这些新化合物的结构是基于化学和光谱证据确定的。Buddlejosides A1是与单萜酸酰化的ajugol衍生物,A2是sinusol,A3-A16是与肉桂酸衍生物和醋酸酰化的6-鼠李糖基-catalpol衍生物。
    DOI:
    10.1248/cpb.39.2944
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文献信息

  • (2<i>E</i>,6<i>R</i>)-8-Hydroxy-2,6-dimethyl-2-octenoic Acid, a Novel<i>Anti</i>-osteoporotic Monoterpene, Isolated from<i>Cistanche salsa</i>
    作者:Kohji YAMAGUCHI、Chikara SHINOHARA、Sachiko KOJIMA、Mikiko SODEOKA、Tomoko TSUJI
    DOI:10.1271/bbb.63.731
    日期:1999.1
    (2E,6R)-8-Hydroxy-2,6-dimethyl-2-octenoic acid [(R)-HDOA], a novel monoterpene from Cistanche salsa, a Chinese herb, was found to be an anti-osteoporotic compound. The extract of Cistanche salsa significantly suppressed the bone weight loss in ovariectomized mice, a postmenopausal osteoporosis model. The active substance was then purified by using this osteoporotic model and the chemical structure was determined. The active compound from Cistanche salsa, (R)-HDOA, suppressed the decrease of bone weight and the mechanical strength in the ovariectomized mice. Furthermore, (R)- and (S)-HDOA were synthesized and the activity of each was evaluated. (R)-HDOA suppressed the bone weight loss, although (S)-HDOA did not showed any activity.
    (2E,6R)-8-羟基-2,6-二甲基-2-辛烯酸[(R)-HDOA]是从中国草药肉苁蓉中发现的一种新型单萜化合物,具有抗骨质疏松特性。肉苁蓉提取物显著抑制了卵巢切除小鼠(一种绝经后骨质疏松模型)的骨重量损失。通过利用这一骨质疏松模型对该活性物质进行纯化,并确定了其化学结构。肉苁蓉中的活性化合物(R)-HDOA抑制了卵巢切除小鼠骨重量的减少和力学强度的下降。进一步合成了(R)-和(S)-HDOA,并对它们各自的活性进行了评估。(R)-HDOA抑制了骨重量损失,而(S)-HDOA未显示出任何活性。
  • A bitter monoterpene diglycoside from viburnum urceolatum
    作者:Tetsuo Iwagawa、Tsunao Hase
    DOI:10.1016/s0031-9422(00)80101-6
    日期:1983.1
    Abstract From the methanolic extract of the leaves of Viburnum urceolatum a new bitter monoterpene diglycoside, urceolide, has been isolated in addition to several known compounds. The structures were elucidated by spectroscopic and chemical methods.
    摘要 除了几种已知的化合物外,还从紫堇属植物叶的甲醇提取物中分离出了一种新的苦味单萜二糖苷,紫杉内酯。通过光谱和化学方法阐明了结构。
  • Three New Monoterpene Glucosides from<i>Lamium amplexicaule</i>
    作者:Masao Kikuchi、Rie Onoguchi、Yasunori Yaoita
    DOI:10.1002/hlca.200900158
    日期:2009.10
    Three new monoterpene glucosides, lamiuamplexosides A–C (1–3), along with thirteen known glucosides, were isolated from the whole plant of Lamium amplexicaule L. The structures of 1–3 were elucidated on the basis of spectroscopic, chemical, and physicochemical evidence.
    三个新单萜葡糖苷,lamiuamplexosides A-C(1 - 3)中,用13个已知的葡糖苷一起,被从全植物分离宝盖草L.的结构1 - 3分别鉴定光谱学,化学,和物理化学的基础上证据。
  • Acylated Iridoid Glycosides from Buddleja japonica HEMSL.
    作者:Toshio MIYASE、Chiko AKAHORI、Hiromi KOHSAKA、Akira UENO
    DOI:10.1248/cpb.39.2944
    日期:——
    Sixteen new acylated iridoid glycosides, called buddlejosides A1-A16, were isolated from Buddleja japonica HEMSL., together with four known iridoid glycosides; 6-vanilloyl-ajugol, 6-feruloyl-ajugol, verbascoside A, and 6-O-[α-L-(4-O-feruloyl)-rhamnopyranosyl]-catalpol. Structures of the new compounds were determined on the basis of chemical and spectroscopic evidence. Buddlejosides A1 was an ajugol derivative acylated with monoterpenic acid, A2 was an sinuatol and A3-A16 were 6-rhamnopyranosyl-catalpol derivatives acylated with cinnamic acid derivative and acetic acid.
    从日本紫苑(Buddleja japonica HEMSL.)中分离出了十六种新的酰基化马兜铃苷,称为buddlejosides A1-A16,同时还分离出了四种已知的马兜铃苷;它们分别是6-香草酰-ajugol、6-阿魏酰-ajugol、verbascoside A和6-O-[α-L-(4-O-阿魏酰)-rhamnopyranosyl]-catalpol。这些新化合物的结构是基于化学和光谱证据确定的。Buddlejosides A1是与单萜酸酰化的ajugol衍生物,A2是sinusol,A3-A16是与肉桂酸衍生物和醋酸酰化的6-鼠李糖基-catalpol衍生物。
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