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22β-methoxy-3β,24-isopropylidenedioxyolean-12-ene | 187393-96-0

中文名称
——
中文别名
——
英文名称
22β-methoxy-3β,24-isopropylidenedioxyolean-12-ene
英文别名
(1R,2R,5S,10S,11R,14R,15S,18R,19R,23S)-19-methoxy-2,7,7,10,14,15,18,21,21-nonamethyl-6,8-dioxahexacyclo[12.12.0.02,11.05,10.015,24.018,23]hexacos-24-ene
22β-methoxy-3β,24-isopropylidenedioxyolean-12-ene化学式
CAS
187393-96-0
化学式
C34H56O3
mdl
——
分子量
512.817
InChiKey
JTBFEQZUMKZLNW-JCKMBJOBSA-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):
    8.5
  • 重原子数:
    37
  • 可旋转键数:
    1
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.94
  • 拓扑面积:
    27.7
  • 氢给体数:
    0
  • 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

反应信息

  • 作为反应物:
    描述:
    22β-methoxy-3β,24-isopropylidenedioxyolean-12-ene盐酸 作用下, 以 甲醇二氯甲烷 为溶剂, 生成 22β-methoxyolean-12-ene-3β,24-diol
    参考文献:
    名称:
    Synthesis and hepatoprotective effects of soyasapogenol B derivatives
    摘要:
    Derivatives of soyasapogenol B (1), which is the aglycon moiety of soyasaponins from soybean, were synthesized and evaluated for their hepatoprotective effects in vitro. Copyright (C) 1996 Elsevier Science Ltd
    DOI:
    10.1016/s0960-894x(96)00572-0
  • 作为产物:
    描述:
    (4aS,4bR,6aR,6bS,8aR,12aS,14aR,14bR,16aS)-2,2,4a,6a,6b,8a,11,11,14b-nonamethyl-4b,5,6,6a,6b,7,8,8a,10,11,12,12a,14,14a,14b,15,16,16a-octadecahydro-4H-piceno[3,4-d][1,3]dioxin-9(4aH)-one 在 sodium 、 sodium hydride 作用下, 以 四氢呋喃甲苯叔丁醇 为溶剂, 反应 42.0h, 生成 22β-methoxy-3β,24-isopropylidenedioxyolean-12-ene
    参考文献:
    名称:
    Preventive effects of soyasapogenol B derivatives on liver injury in a concanavalin A-induced hepatitis model
    摘要:
    To shed light on the structure-activity relationship, various so soyasapogenol B derivatives were synthesized and evaluated for preventive effects on liver injury in the concanavalin A (Con A)-induced hepatitis model in mice, Con A injection into mice induces some pathophysiology of human liver disease such as autoimmune or viral hepatitis, Two hydroxyl groups on the A ring of soyasapogenol B are required for amelioration of liver damage, Modification of the C-22 hydroxyl moiety with an acyloxy or alkyloxy group, or removal of the hydroxyl group. resulted in I greatly enhanced percentage of alleviation. Among the series of soyasapogenol B derivatives examined, six compounds exhibited preventive effects on liver damage. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2005.04.074
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文献信息

  • Synthesis and hepatoprotective effects of soyasapogenol B derivatives
    作者:Kazue Sasaki、Nobuto Minowa、Hiroyuki Kuzuhara、Shoji Nishiyama、Shoji Omoto
    DOI:10.1016/s0960-894x(96)00572-0
    日期:1997.1
    Derivatives of soyasapogenol B (1), which is the aglycon moiety of soyasaponins from soybean, were synthesized and evaluated for their hepatoprotective effects in vitro. Copyright (C) 1996 Elsevier Science Ltd
  • Preventive effects of soyasapogenol B derivatives on liver injury in a concanavalin A-induced hepatitis model
    作者:Kazue Sasaki、Nobuto Minowa、Hiroyuki Kuzuhara、Shoji Nishiyama
    DOI:10.1016/j.bmc.2005.04.074
    日期:2005.8
    To shed light on the structure-activity relationship, various so soyasapogenol B derivatives were synthesized and evaluated for preventive effects on liver injury in the concanavalin A (Con A)-induced hepatitis model in mice, Con A injection into mice induces some pathophysiology of human liver disease such as autoimmune or viral hepatitis, Two hydroxyl groups on the A ring of soyasapogenol B are required for amelioration of liver damage, Modification of the C-22 hydroxyl moiety with an acyloxy or alkyloxy group, or removal of the hydroxyl group. resulted in I greatly enhanced percentage of alleviation. Among the series of soyasapogenol B derivatives examined, six compounds exhibited preventive effects on liver damage. (c) 2005 Elsevier Ltd. All rights reserved.
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