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(S)-jalapinolic acid 11-O-(2-O-trans-cinnamoyl)-[(4-O-n-dodecanoyl)]-α-L-rhamnopyranosyl-(1->4)-O-(2-O-n-decanoyl)-α-L-rhamnopyranosyl-(1->4)-O-α-L-rhamnopyranosyl-(1->2)-O-β-D-fucopyranoside intramolecular 1,3''-ester | 1255952-66-9

中文名称
——
中文别名
——
英文名称
(S)-jalapinolic acid 11-O-(2-O-trans-cinnamoyl)-[(4-O-n-dodecanoyl)]-α-L-rhamnopyranosyl-(1->4)-O-(2-O-n-decanoyl)-α-L-rhamnopyranosyl-(1->4)-O-α-L-rhamnopyranosyl-(1->2)-O-β-D-fucopyranoside intramolecular 1,3''-ester
英文别名
ipomotaoside C;[(2S,3R,4R,5R,6S)-6-[(2S,3R,4R,5R,6S)-5-decanoyloxy-4-hydroxy-2-methyl-6-[[(1S,3R,4S,5R,6R,8R,10S,22S,23S,24S,26R)-4,5,26-trihydroxy-6,24-dimethyl-20-oxo-10-pentyl-2,7,9,21,25-pentaoxatricyclo[20.3.1.03,8]hexacosan-23-yl]oxy]oxan-3-yl]oxy-4-hydroxy-2-methyl-5-[(E)-3-phenylprop-2-enoyl]oxyoxan-3-yl] dodecanoate
(S)-jalapinolic acid 11-O-(2-O-trans-cinnamoyl)-[(4-O-n-dodecanoyl)]-α-L-rhamnopyranosyl-(1->4)-O-(2-O-n-decanoyl)-α-L-rhamnopyranosyl-(1->4)-O-α-L-rhamnopyranosyl-(1->2)-O-β-D-fucopyranoside intramolecular 1,3''-ester化学式
CAS
1255952-66-9
化学式
C71H116O21
mdl
——
分子量
1305.69
InChiKey
SUNFNBPOXNNWGR-RQSNGXSLSA-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

物化性质

  • 熔点:
    105-107 °C
  • 沸点:
    1168.3±65.0 °C(Predicted)
  • 密度:
    1.19±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    14.7
  • 重原子数:
    92
  • 可旋转键数:
    34
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.83
  • 拓扑面积:
    280
  • 氢给体数:
    5
  • 氢受体数:
    21

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

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文献信息

  • Ipomotaosides A−D, Resin Glycosides from the Aerial Parts of <i>Ipomoea batatas</i> and Their Inhibitory Activity against COX-1 and COX-2
    作者:Kazuko Yoshikawa、Chiho Yagi、Hiroshi Hama、Masami Tanaka、Shigenobu Arihara、Toshihiro Hashimoto
    DOI:10.1021/np100283t
    日期:2010.11.29
    Four new resin glycosides, namely, ipomotaosides A-D (1-4), were isolated from the dried aerial parts of Ipomoea batatas. The structures of 1-4 were elucidated by analysis of their spectroscopic data and by chemical derivatization and were tested for their anti-inflammatory activity against cyclooxygenase (COX)-1 and -2.
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