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1β,2α,3β,11α-tetrahydroxyolean-12-ene | 252267-28-0

中文名称
——
中文别名
——
英文名称
1β,2α,3β,11α-tetrahydroxyolean-12-ene
英文别名
1β,2α,11α-tetrahydroxy-olean-12-ene;(1S,2S,3R,4aS,6aR,6bS,8aR,12aR,14R,14aS,14bS)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-1,2,3,14-tetrol
1β,2α,3β,11α-tetrahydroxyolean-12-ene化学式
CAS
252267-28-0
化学式
C30H50O4
mdl
——
分子量
474.725
InChiKey
RLHPTCMHCBNJKU-JCAJVAELSA-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):
    6.1
  • 重原子数:
    34
  • 可旋转键数:
    0
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.93
  • 拓扑面积:
    80.9
  • 氢给体数:
    4
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    乙酸酐1β,2α,3β,11α-tetrahydroxyolean-12-ene吡啶 作用下, 反应 2.0h, 生成 Acetic acid (4aR,6aS,6bR,8aS,10R,11R,12S,12aS,12bS,13R,14bR)-10,11-diacetoxy-12-hydroxy-2,2,4a,6a,6b,9,9,12a-octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydro-picen-13-yl ester
    参考文献:
    名称:
    Terpenoids from Salvia kronenburgii
    摘要:
    A new norditerpenoid and six new triterpenoids were isolated from the roots of Salvia kronenburgii The new diterpenoid was kronenquinone (1). The new triterpenoids were 1 beta,2 alpha,3 beta,11 alpha-tetrahydroxy-olean-12-ene (2), 1 beta,2 alpha,3 beta,11 alpha-tetrahydroxy-urs-12-ene (3), 2 alpha-acetoxy-urs-5,12-diene-3 beta,11 alpha-diol (4), 3 alpha-acetoxy-urs-12-ene-1 beta,11 alpha-diol (5), 1 beta,3 alpha,11 alpha-trihydroxy-urs-12-ene (6), 2 alpha,3 beta,11 alpha-trihydroxy-urs-12-ene (7), and the known triterpenes 3 beta-acetoxy-urs-12-ene-1 beta,2 alpha,11 alpha-triol (8) and 3 beta-acetoxyolean-12-ene-1 beta,2 alpha,11 alpha-triol (9). Structures were determined by NMR and MS techniques.
    DOI:
    10.1021/np990165p
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文献信息

  • ACCELERATOR FOR INITIAL INSULIN SECRETION
    申请人:Use-Techno Corporation
    公开号:EP1674089A1
    公开(公告)日:2006-06-28
    The present invention provides an early insulin secretion stimulator consisting of a triterpene represented by the following general formula (1) and/or a triterpene represented by the following general formula (2). [where R1 represents COOH, etc., R11 and R12 represent CH2OH, etc., X1 represents hydrogen or OH and X11, X12, X21 and X22 represent OH, etc.]
    本发明提供了一种早期胰岛素分泌刺激剂,由以下通式(1)代表的三萜和/或以下通式(2)代表的三萜组成。 [其中 R1 代表 COOH 等,R11 和 R12 代表 CH2OH 等,X1 代表氢或 OH,X11、X12、X21 和 X22 代表 OH 等。]
  • Insulin secretion potentiator
    申请人:Matsuyama Futoshi
    公开号:US20050143464A1
    公开(公告)日:2005-06-30
    The present invention provides early insulin secretion stimulators consisting of triterpenes represented by the following general formula (1) and/or triterpenes represented by the following general formula (2). [where R 1 represents COOH, etc., R 11 and R 12 represent CH 2 OH, etc., X 1 represents hydrogen or OH and X 11 , X 12 , X 21 and X 22 represent OH, etc.]
  • Terpenoids from <i>Salvia</i> <i>kronenburgii</i>
    作者:Gülaçtı Topçu、Ayhan Ulubelen
    DOI:10.1021/np990165p
    日期:1999.12.1
    A new norditerpenoid and six new triterpenoids were isolated from the roots of Salvia kronenburgii The new diterpenoid was kronenquinone (1). The new triterpenoids were 1 beta,2 alpha,3 beta,11 alpha-tetrahydroxy-olean-12-ene (2), 1 beta,2 alpha,3 beta,11 alpha-tetrahydroxy-urs-12-ene (3), 2 alpha-acetoxy-urs-5,12-diene-3 beta,11 alpha-diol (4), 3 alpha-acetoxy-urs-12-ene-1 beta,11 alpha-diol (5), 1 beta,3 alpha,11 alpha-trihydroxy-urs-12-ene (6), 2 alpha,3 beta,11 alpha-trihydroxy-urs-12-ene (7), and the known triterpenes 3 beta-acetoxy-urs-12-ene-1 beta,2 alpha,11 alpha-triol (8) and 3 beta-acetoxyolean-12-ene-1 beta,2 alpha,11 alpha-triol (9). Structures were determined by NMR and MS techniques.
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