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(12S,13S)-(E)-9-oxo-12,13-bis(tert-butyldimethylsilyloxy)-10-octadecenoic acid tert-butyl ester | 401901-46-0

中文名称
——
中文别名
——
英文名称
(12S,13S)-(E)-9-oxo-12,13-bis(tert-butyldimethylsilyloxy)-10-octadecenoic acid tert-butyl ester
英文别名
(12S,13S)-(E)-12,13-di-tert-butyldimethylsiloxy-9-oxo-10-octadecaenoic Acid t-butyl Ester;tert-butyl (E,12S,13S)-12,13-bis[[tert-butyl(dimethyl)silyl]oxy]-9-oxooctadec-10-enoate
(12S,13S)-(E)-9-oxo-12,13-bis(tert-butyldimethylsilyloxy)-10-octadecenoic acid tert-butyl ester化学式
CAS
401901-46-0
化学式
C34H68O5Si2
mdl
——
分子量
613.082
InChiKey
WBLXWZYPCFIPIS-YMXFUWPXSA-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):
    10.55
  • 重原子数:
    41
  • 可旋转键数:
    23
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.88
  • 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

点击查看最新优质反应信息

文献信息

  • Total synthesis of pinellic acid, a potent oral adjuvant for nasal influenza vaccine. Determination of the relative and absolute configuration
    作者:Toshiaki Sunazuka、Tatsuya Shirahata、Kiminari Yoshida、Daisuke Yamamoto、Yoshihiro Harigaya、Takayuki Nagai、Hiroaki Kiyohara、Haruki Yamada、Isao Kuwajima、Satoshi Ōmura
    DOI:10.1016/s0040-4039(01)02348-6
    日期:2002.2
    from a medicinal plant Pinelliae tuber, has potent adjuvant activity. The absolute configuration of pinellic acid was expected by derivatization of this compound and CD exciton chirality method. A convergent synthetic route to pinellic acid has been developed via regioselective asymmetric dihydroxylation and stereoselective reduction. The absolute configuration of pinellic acid was determined to be 9S
    从药用植物半夏中分离出的松香酸(1)具有有效的佐剂活性。通过该化合物的衍生化和CD激子手性法可以预期到松果酸的绝对构型。通过区域选择性的不对称二羟基化和立体选择性的还原,已经开发出一种聚合的合成壬二酸的途径。通过与天然和合成化合物的光谱数据进行比较,确定了半乳糖酸的绝对构型为9 S,12 S,13 S。
  • Total synthesis and adjuvant activity of all stereoisomers of pinellic acid
    作者:Tatsuya Shirahata、Toshiaki Sunazuka、Kiminari Yoshida、Daisuke Yamamoto、Yoshihiko Harigaya、Takayuki Nagai、Hiroaki Kiyohara、Haruki Yamada、Isao Kuwajima、Satoshi Ōmura
    DOI:10.1016/s0960-894x(02)01069-7
    日期:2003.3
    Pinellic acid is a novel and potentially useful oral adjuvant when used in conjunction with intranasal inoculation of influenza HA vaccines. All stereoisomers of pinellic acid have been synthesized via regioselective asymmetric dihydroxylation, regioselective inversion, and stereoselective reduction, and their adjuvant activities were characterized. Among this series of isomers, 9S, 12S, 13S compound
    松果酸与鼻内接种HA流感疫苗一起使用时,是一种新颖且可能有用的口服佐剂。已通过区域选择性不对称二羟基化,区域选择性反转和立体选择性还原合成了所有松果酸立体异构体,并对其佐剂活性进行了表征。在这一系列异构体中,9S,12S,13S化合物具有最强的佐剂活性。讨论了构效关系。
  • Vaccine preparation containing fatty acid as component
    申请人:——
    公开号:US20040024058A1
    公开(公告)日:2004-02-05
    The present invention provides an adjuvant that is a hydroxy unsaturated fatty acid or a derivative thereof, as well as a vaccine preparation containing the adjuvant as a constituent. For example, a vaccine shows sufficient activity to enhance the immunity when a hydroxy unsaturated fatty acid having the following structure is administered: 1
    本发明提供了一种辅助剂,其为羟基不饱和脂肪酸或其衍生物,以及包含该辅助剂作为组成部分的疫苗制剂。例如,当给予具有以下结构的羟基不饱和脂肪酸时,疫苗显示出足够的活性以增强免疫力:1
  • Vaccine preparation containing fatty acid as a constituent
    申请人:The Kitasato Institute
    公开号:US07560484B2
    公开(公告)日:2009-07-14
    The present invention provides an adjuvant that is a hydroxy unsaturated fatty acid or a derivative thereof, as well as a vaccine preparation containing the adjuvant as a constituent. For example, a vaccine shows sufficient activity to enhance the immunity when a hydroxy unsaturated fatty acid having the following structure is administered:
    本发明提供了一种辅助剂,它是一种羟基不饱和脂肪酸或其衍生物,以及包含该辅助剂作为组分的疫苗制备。例如,当给予具有以下结构的羟基不饱和脂肪酸时,疫苗显示出足够的活性以增强免疫力:
  • Total synthesis, elucidation of absolute stereochemistry, and adjuvant activity of trihydroxy fatty acids
    作者:Tatsuya Shirahata、Toshiaki Sunazuka、Kiminari Yoshida、Daisuke Yamamoto、Yoshihiro Harigaya、Isao Kuwajima、Takayuki Nagai、Hiroaki Kiyohara、Haruki Yamada、Satoshi Ōmura
    DOI:10.1016/j.tet.2006.06.088
    日期:2006.10
    Pinellic acid from the tuber of Pinellia ternate, an active herbal component of the traditional Japanese herbal (Kampo) medicine Sho-seiryu-to, is a C18 trihydroxy fatty acid whose absolute stereochernistry has now been determined. All stereoisomers of pinellic acid were synthesized via regioselective asymmetric dihydroxylation, regioselective inversion, and stereoselective reduction in order to determine their absolute stereochemistries and adjuvant activities. Among this series of isomers, the (9S,12S,13S)-compound, which is a natural product, exhibited the most potent adjuvant activity. Spectral data for all of the stereoisomers of the 1,2-allylic diols were compared and related to their stereochemistries. (c) 2006 Published by Elsevier Ltd.
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