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3β,16α,20(R)-trihydroxy-25-acetoxy-2,11,22-trioxocucurbita-5,23(E)-diene | 89647-62-1

中文名称
——
中文别名
——
英文名称
3β,16α,20(R)-trihydroxy-25-acetoxy-2,11,22-trioxocucurbita-5,23(E)-diene
英文别名
3-epi-isocucurbitacin B;isocucurbitacin B;3-epicucurbitacin B;[(E,6R)-6-[(3R,8S,9R,10R,13R,14S,16R,17R)-3,16-dihydroxy-4,4,9,13,14-pentamethyl-2,11-dioxo-3,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-hydroxy-2-methyl-5-oxohept-3-en-2-yl] acetate
3β,16α,20(R)-trihydroxy-25-acetoxy-2,11,22-trioxocucurbita-5,23(E)-diene化学式
CAS
89647-62-1
化学式
C32H46O8
mdl
——
分子量
558.712
InChiKey
WTBZNVRBNJWSPF-KWPSBSMYSA-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):
    2.5
  • 重原子数:
    40
  • 可旋转键数:
    6
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    138
  • 氢给体数:
    3
  • 氢受体数:
    8

反应信息

  • 作为反应物:
    描述:
    3β,16α,20(R)-trihydroxy-25-acetoxy-2,11,22-trioxocucurbita-5,23(E)-diene乙酸酐 生成 [(3R,8S,9R,10R,13R,14S,16R,17R)-3-acetyloxy-17-[(E,2R)-2,6-diacetyloxy-6-methyl-3-oxohept-4-en-2-yl]-4,4,9,13,14-pentamethyl-2,11-dioxo-3,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-16-yl] acetate
    参考文献:
    名称:
    MATA, RACHEL;RIOS, LIZETH;CAMACHO, DEL RAYO;REGUERO, TERESA;LORENCE, DAVI+, PHYTOCHEMISTRY, 27,(1988) N 6, C. 1887-1889
    摘要:
    DOI:
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文献信息

  • Plant Anticancer Agents XXX: Cucurbitacins from Ipomopsis aggregata (Polemoniaceae)
    作者:Munehisa Arisawa、John M. Pezzuto、Geoffrey A. Cordell、Norman R. Farnsworth、A. Douglas Kinghorn
    DOI:10.1002/jps.2600730335
    日期:1984.3
    Isocucurbitacin B (I), 3-epi-isocucurbitacin B (II), and cucurbitacin B (III) were identified as the principal cytotoxic constituents of Ipomopsis aggregata (Pursh) V. Grant (Polemoniaceae). The structure of the new compound, II, was determined through analysis of its spectrometric characteristics.
    异葫芦素B(I),3-表异葫芦素B(II)和葫芦素B(III)被鉴定为Ipomopsis aaggregata(Pursh)V.Grant(Polemoniaceae)的主要细胞毒性成分。通过分析其光谱特征确定了新化合物II的结构。
  • MATA, RACHEL;RIOS, LIZETH;CAMACHO, DEL RAYO;REGUERO, TERESA;LORENCE, DAVI+, PHYTOCHEMISTRY, 27,(1988) N 6, C. 1887-1889
    作者:MATA, RACHEL、RIOS, LIZETH、CAMACHO, DEL RAYO、REGUERO, TERESA、LORENCE, DAVI+
    DOI:——
    日期:——
  • Chemosensory Receptor Ligand-Based Therapies
    申请人:BARON Alain D.
    公开号:US20120177730A1
    公开(公告)日:2012-07-12
    Provided herein are methods for treating conditions associated with a chemosensory receptor, including diabetes, obesity, and other metabolic diseases, disorders or conditions by administrating a composition comprising a chemosensory receptor ligand, such as a bitter receptor ligand. Also provided herein are chemosensory receptor ligand compositions, including bitter receptor ligand compositions, and methods for the preparation thereof for use in the methods of the present invention. Also provided herein are compositions comprising metformin and salts thereof and methods of use.
  • US9050292B2
    申请人:——
    公开号:US9050292B2
    公开(公告)日:2015-06-09
  • US9463170B2
    申请人:——
    公开号:US9463170B2
    公开(公告)日:2016-10-11
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