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| 916483-27-7

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
916483-27-7
化学式
C52H86N4O18S
mdl
——
分子量
1087.34
InChiKey
AULCIWPRMKIJQR-WBDOEPRSSA-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):
    3.38
  • 重原子数:
    75.0
  • 可旋转键数:
    18.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.79
  • 拓扑面积:
    286.11
  • 氢给体数:
    6.0
  • 氢受体数:
    20.0

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:
    四氢吡咯四(三苯基膦)钯 作用下, 以 二氯甲烷 为溶剂, 生成
    参考文献:
    名称:
    Design, synthesis and in vivo activity of 9-(S)-dihydroerythromycin derivatives as potent anti-inflammatory agents
    摘要:
    The synthesis of a new class of 9-(S)-dihydroerythromycin derivatives and their anti-inflammatory activity on in vivo PMA assay are described. Modifying the desosamine sugar on the C-3' amino group, it was possible to differentiate between anti-biotic and anti-flammatory action. The compounds are completely devoid of anti-microbial effects but their anti-inflammatory properties are enhanced. These results strongly suggest the potential of macrolides as a new class of anti-inflammatory agents. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2006.08.076
  • 作为产物:
    描述:
    红霉素 在 sodium tetrahydroborate 、 DCC-resin 、 偶氮二甲酸二乙酯 作用下, 以 四氢呋喃二氯甲烷1,2-二氯乙烷 为溶剂, 反应 33.0h, 生成
    参考文献:
    名称:
    Design, synthesis and in vivo activity of 9-(S)-dihydroerythromycin derivatives as potent anti-inflammatory agents
    摘要:
    The synthesis of a new class of 9-(S)-dihydroerythromycin derivatives and their anti-inflammatory activity on in vivo PMA assay are described. Modifying the desosamine sugar on the C-3' amino group, it was possible to differentiate between anti-biotic and anti-flammatory action. The compounds are completely devoid of anti-microbial effects but their anti-inflammatory properties are enhanced. These results strongly suggest the potential of macrolides as a new class of anti-inflammatory agents. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2006.08.076
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